CNRS Nantes University US2B US2B
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***  Serum Amyloid A1  ***

elNémo ID: 240722144403682667

Job options:

ID        	=	 240722144403682667
JOBID     	=	 Serum Amyloid A1
USERID    	=	 unknown
PRIVAT    	=	 0

NMODES    	=	 5
DQMIN     	=	 -100
DQMAX     	=	 100
DQSTEP    	=	 20
DOGRAPHS  	=	 on

DOPROJMODS	=	 on
DORMSD    	=	 on

NRBL      	=	 0
CUTOFF    	=	 0
CAONLY    	=	 0


Input data for this run:

HEADER Serum Amyloid A1

CRYST1   93.850   93.850  130.520  90.00  90.00 120.00 H 3 2         3
ATOM      1  N   ARG A   1     -23.982   2.835  35.374  1.00 89.90           N  
ANISOU    1  N   ARG A   1     9443  12653  12061   2685    280   2074       N  
ATOM      2  CA  ARG A   1     -22.979   3.037  36.425  1.00 87.93           C  
ANISOU    2  CA  ARG A   1     9547  12069  11792   2567    474   1772       C  
ATOM      3  C   ARG A   1     -22.425   1.704  36.958  1.00 87.82           C  
ANISOU    3  C   ARG A   1     9564  12232  11572   2025    445   1709       C  
ATOM      4  O   ARG A   1     -21.281   1.656  37.427  1.00 84.59           O  
ANISOU    4  O   ARG A   1     9510  11502  11129   1816    490   1542       O  
ATOM      5  CB  ARG A   1     -23.534   3.902  37.574  1.00 93.04           C  
ANISOU    5  CB  ARG A   1    10092  12759  12500   2975    752   1509       C  
ATOM      6  CG  ARG A   1     -22.450   4.492  38.480  1.00103.00           C  
ANISOU    6  CG  ARG A   1    11796  13549  13789   2964    901   1165       C  
ATOM      7  CD  ARG A   1     -23.033   5.130  39.722  1.00115.91           C  
ANISOU    7  CD  ARG A   1    13320  15335  15388   3324   1175    826       C  
ATOM      8  NE  ARG A   1     -23.478   6.501  39.476  1.00125.28           N  
ANISOU    8  NE  ARG A   1    14536  16206  16857   3918   1236    748       N  
ATOM      9  CZ  ARG A   1     -23.522   7.455  40.400  1.00138.70           C  
ANISOU    9  CZ  ARG A   1    16347  17731  18622   4309   1445    350       C  
ATOM     10  NH1 ARG A   1     -23.141   7.200  41.647  1.00120.85           N1+
ANISOU   10  NH1 ARG A   1    14174  15638  16104   4157   1616    -10       N1+
ATOM     11  NH2 ARG A   1     -23.935   8.673  40.083  1.00130.56           N  
ANISOU   11  NH2 ARG A   1    15355  16344  17908   4870   1469    299       N  
ATOM     12  N   SER A   2     -23.225   0.621  36.872  1.00 84.29           N  
ANISOU   12  N   SER A   2     8735  12275  11017   1790    348   1862       N  
ATOM     13  CA  SER A   2     -22.784  -0.713  37.298  1.00 81.24           C  
ANISOU   13  CA  SER A   2     8360  12021  10487   1277    283   1860       C  
ATOM     14  C   SER A   2     -21.631  -1.252  36.426  1.00 81.10           C  
ANISOU   14  C   SER A   2     8699  11656  10461    975     66   1889       C  
ATOM     15  O   SER A   2     -20.791  -2.007  36.930  1.00 79.67           O  
ANISOU   15  O   SER A   2     8703  11361  10207    643     60   1806       O  
ATOM     16  CB  SER A   2     -23.954  -1.696  37.423  1.00 86.38           C  
ANISOU   16  CB  SER A   2     8507  13224  11089   1077    211   2046       C  
ATOM     17  OG  SER A   2     -24.724  -1.891  36.248  1.00 95.99           O  
ANISOU   17  OG  SER A   2     9482  14613  12377   1104    -43   2248       O  
ATOM     18  N   PHE A   3     -21.536  -0.761  35.162  1.00 75.92           N  
ANISOU   18  N   PHE A   3     8142  10839   9864   1135    -91   2009       N  
ATOM     19  CA  PHE A   3     -20.478  -1.116  34.211  1.00 72.77           C  
ANISOU   19  CA  PHE A   3     8060  10170   9420    935   -260   2038       C  
ATOM     20  C   PHE A   3     -19.092  -0.618  34.643  1.00 71.76           C  
ANISOU   20  C   PHE A   3     8339   9596   9330    898   -117   1885       C  
ATOM     21  O   PHE A   3     -18.125  -1.373  34.510  1.00 69.47           O  
ANISOU   21  O   PHE A   3     8243   9176   8975    605   -191   1833       O  
ATOM     22  CB  PHE A   3     -20.800  -0.641  32.779  1.00 76.97           C  
ANISOU   22  CB  PHE A   3     8574  10725   9947   1158   -433   2241       C  
ATOM     23  CG  PHE A   3     -22.167  -0.969  32.208  1.00 82.66           C  
ANISOU   23  CG  PHE A   3     8883  11897  10628   1207   -635   2403       C  
ATOM     24  CD1 PHE A   3     -22.784  -2.188  32.480  1.00 86.75           C  
ANISOU   24  CD1 PHE A   3     9136  12732  11093    861   -775   2378       C  
ATOM     25  CD2 PHE A   3     -22.812  -0.083  31.349  1.00 88.51           C  
ANISOU   25  CD2 PHE A   3     9495  12735  11399   1574   -722   2608       C  
ATOM     26  CE1 PHE A   3     -24.044  -2.490  31.949  1.00 91.21           C  
ANISOU   26  CE1 PHE A   3     9288  13721  11646    859   -996   2525       C  
ATOM     27  CE2 PHE A   3     -24.062  -0.395  30.800  1.00 94.77           C  
ANISOU   27  CE2 PHE A   3     9874  13987  12148   1609   -949   2761       C  
ATOM     28  CZ  PHE A   3     -24.671  -1.595  31.106  1.00 93.14           C  
ANISOU   28  CZ  PHE A   3     9385  14108  11897   1236  -1087   2704       C  
ATOM     29  N   PHE A   4     -18.987   0.635  35.157  1.00 67.19           N  
ANISOU   29  N   PHE A   4     7878   8775   8879   1198     69   1798       N  
ATOM     30  CA  PHE A   4     -17.704   1.192  35.612  1.00 64.92           C  
ANISOU   30  CA  PHE A   4     7948   8053   8664   1143    179   1638       C  
ATOM     31  C   PHE A   4     -17.228   0.557  36.894  1.00 63.39           C  
ANISOU   31  C   PHE A   4     7792   7923   8372    888    266   1421       C  
ATOM     32  O   PHE A   4     -16.024   0.387  37.070  1.00 59.74           O  
ANISOU   32  O   PHE A   4     7574   7219   7906    668    252   1336       O  
ATOM     33  CB  PHE A   4     -17.752   2.710  35.776  1.00 70.42           C  
ANISOU   33  CB  PHE A   4     8771   8420   9567   1521    311   1579       C  
ATOM     34  CG  PHE A   4     -17.978   3.444  34.485  1.00 74.92           C  
ANISOU   34  CG  PHE A   4     9390   8817  10258   1755    217   1858       C  
ATOM     35  CD1 PHE A   4     -16.916   3.722  33.629  1.00 77.46           C  
ANISOU   35  CD1 PHE A   4     9991   8810  10629   1626    166   1998       C  
ATOM     36  CD2 PHE A   4     -19.254   3.869  34.121  1.00 81.05           C  
ANISOU   36  CD2 PHE A   4     9908   9797  11091   2114    182   2018       C  
ATOM     37  CE1 PHE A   4     -17.129   4.418  32.433  1.00 80.90           C  
ANISOU   37  CE1 PHE A   4    10473   9124  11141   1840     88   2320       C  
ATOM     38  CE2 PHE A   4     -19.466   4.556  32.919  1.00 85.69           C  
ANISOU   38  CE2 PHE A   4    10544  10245  11771   2345     73   2328       C  
ATOM     39  CZ  PHE A   4     -18.405   4.823  32.084  1.00 82.78           C  
ANISOU   39  CZ  PHE A   4    10479   9551  11422   2200     30   2489       C  
ATOM     40  N   SER A   5     -18.171   0.221  37.801  1.00 59.89           N  
ANISOU   40  N   SER A   5     7079   7841   7835    923    357   1358       N  
ATOM     41  CA  SER A   5     -17.863  -0.461  39.052  1.00 57.48           C  
ANISOU   41  CA  SER A   5     6768   7695   7377    684    438   1218       C  
ATOM     42  C   SER A   5     -17.280  -1.799  38.676  1.00 56.98           C  
ANISOU   42  C   SER A   5     6739   7660   7253    281    256   1341       C  
ATOM     43  O   SER A   5     -16.186  -2.127  39.129  1.00 54.32           O  
ANISOU   43  O   SER A   5     6612   7152   6876     73    243   1247       O  
ATOM     44  CB  SER A   5     -19.118  -0.668  39.888  1.00 62.84           C  
ANISOU   44  CB  SER A   5     7085   8853   7938    789    576   1224       C  
ATOM     45  OG  SER A   5     -19.535   0.559  40.459  1.00 78.16           O  
ANISOU   45  OG  SER A   5     9011  10760   9926   1212    770   1035       O  
ATOM     46  N   PHE A   6     -17.944  -2.506  37.741  1.00 52.39           N  
ANISOU   46  N   PHE A   6     5966   7255   6685    195     88   1532       N  
ATOM     47  CA  PHE A   6     -17.489  -3.809  37.273  1.00 49.75           C  
ANISOU   47  CA  PHE A   6     5668   6909   6326   -151   -116   1611       C  
ATOM     48  C   PHE A   6     -16.025  -3.773  36.782  1.00 51.66           C  
ANISOU   48  C   PHE A   6     6254   6778   6595   -230   -169   1531       C  
ATOM     49  O   PHE A   6     -15.240  -4.667  37.121  1.00 49.25           O  
ANISOU   49  O   PHE A   6     6052   6393   6270   -483   -236   1496       O  
ATOM     50  CB  PHE A   6     -18.426  -4.342  36.178  1.00 52.30           C  
ANISOU   50  CB  PHE A   6     5766   7438   6668   -177   -319   1764       C  
ATOM     51  CG  PHE A   6     -18.195  -5.797  35.853  1.00 52.66           C  
ANISOU   51  CG  PHE A   6     5807   7489   6713   -542   -546   1799       C  
ATOM     52  CD1 PHE A   6     -18.889  -6.797  36.530  1.00 56.58           C  
ANISOU   52  CD1 PHE A   6     6050   8221   7229   -807   -601   1901       C  
ATOM     53  CD2 PHE A   6     -17.272  -6.173  34.882  1.00 53.19           C  
ANISOU   53  CD2 PHE A   6     6121   7318   6771   -615   -701   1732       C  
ATOM     54  CE1 PHE A   6     -18.680  -8.143  36.229  1.00 57.30           C  
ANISOU   54  CE1 PHE A   6     6163   8226   7383  -1148   -841   1930       C  
ATOM     55  CE2 PHE A   6     -17.043  -7.527  34.605  1.00 55.73           C  
ANISOU   55  CE2 PHE A   6     6465   7589   7122   -911   -921   1707       C  
ATOM     56  CZ  PHE A   6     -17.760  -8.499  35.265  1.00 55.10           C  
ANISOU   56  CZ  PHE A   6     6160   7662   7113  -1180  -1008   1803       C  
ATOM     57  N   LEU A   7     -15.661  -2.730  36.012  1.00 48.62           N  
ANISOU   57  N   LEU A   7     6023   6179   6270     -9   -133   1535       N  
ATOM     58  CA  LEU A   7     -14.298  -2.572  35.504  1.00 46.93           C  
ANISOU   58  CA  LEU A   7     6083   5664   6086    -77   -146   1501       C  
ATOM     59  C   LEU A   7     -13.294  -2.217  36.583  1.00 48.66           C  
ANISOU   59  C   LEU A   7     6470   5673   6347   -157    -27   1345       C  
ATOM     60  O   LEU A   7     -12.199  -2.774  36.583  1.00 47.90           O  
ANISOU   60  O   LEU A   7     6498   5456   6247   -345    -77   1307       O  
ATOM     61  CB  LEU A   7     -14.227  -1.588  34.333  1.00 48.28           C  
ANISOU   61  CB  LEU A   7     6344   5700   6298    144   -142   1629       C  
ATOM     62  CG  LEU A   7     -14.800  -2.079  33.007  1.00 54.91           C  
ANISOU   62  CG  LEU A   7     7080   6756   7026    177   -316   1775       C  
ATOM     63  CD1 LEU A   7     -14.312  -1.213  31.898  1.00 56.28           C  
ANISOU   63  CD1 LEU A   7     7401   6797   7187    345   -296   1936       C  
ATOM     64  CD2 LEU A   7     -14.387  -3.547  32.694  1.00 56.77           C  
ANISOU   64  CD2 LEU A   7     7330   7084   7158    -92   -478   1693       C  
ATOM     65  N   GLY A   8     -13.683  -1.327  37.493  1.00 44.93           N  
ANISOU   65  N   GLY A   8     5983   5183   5904      0    113   1234       N  
ATOM     66  CA  GLY A   8     -12.872  -0.955  38.644  1.00 45.10           C  
ANISOU   66  CA  GLY A   8     6152   5058   5925    -73    198   1032       C  
ATOM     67  C   GLY A   8     -12.646  -2.168  39.545  1.00 46.93           C  
ANISOU   67  C   GLY A   8     6318   5507   6007   -335    144   1009       C  
ATOM     68  O   GLY A   8     -11.517  -2.426  39.949  1.00 46.41           O  
ANISOU   68  O   GLY A   8     6388   5312   5935   -508    102    935       O  
ATOM     69  N   GLU A   9     -13.701  -2.959  39.799  1.00 42.07           N  
ANISOU   69  N   GLU A   9     5472   5223   5289   -380    126   1117       N  
ATOM     70  CA  GLU A   9     -13.634  -4.209  40.576  1.00 42.37           C  
ANISOU   70  CA  GLU A   9     5423   5465   5210   -648     58   1192       C  
ATOM     71  C   GLU A   9     -12.662  -5.192  39.878  1.00 47.08           C  
ANISOU   71  C   GLU A   9     6134   5867   5888   -859   -128   1266       C  
ATOM     72  O   GLU A   9     -11.897  -5.873  40.557  1.00 44.94           O  
ANISOU   72  O   GLU A   9     5923   5575   5578  -1044   -190   1273       O  
ATOM     73  CB  GLU A   9     -15.019  -4.887  40.686  1.00 44.64           C  
ANISOU   73  CB  GLU A   9     5405   6115   5439   -689     56   1362       C  
ATOM     74  CG  GLU A   9     -16.067  -4.142  41.503  1.00 52.13           C  
ANISOU   74  CG  GLU A   9     6165   7373   6267   -479    267   1304       C  
ATOM     75  CD  GLU A   9     -17.517  -4.572  41.318  1.00 74.44           C  
ANISOU   75  CD  GLU A   9     8622  10573   9089   -460    282   1493       C  
ATOM     76  OE1 GLU A   9     -17.803  -5.390  40.416  1.00 62.53           O  
ANISOU   76  OE1 GLU A   9     7012   9056   7691   -624     90   1659       O  
ATOM     77  OE2 GLU A   9     -18.379  -4.063  42.070  1.00 79.68           O1-
ANISOU   77  OE2 GLU A   9     9080  11558   9635   -271    483   1453       O1-
ATOM     78  N   ALA A  10     -12.684  -5.232  38.522  1.00 44.23           N  
ANISOU   78  N   ALA A  10     5798   5388   5621   -799   -216   1314       N  
ATOM     79  CA  ALA A  10     -11.828  -6.104  37.728  1.00 43.04           C  
ANISOU   79  CA  ALA A  10     5748   5079   5525   -926   -369   1331       C  
ATOM     80  C   ALA A  10     -10.342  -5.737  37.867  1.00 50.30           C  
ANISOU   80  C   ALA A  10     6853   5771   6486   -941   -329   1238       C  
ATOM     81  O   ALA A  10      -9.550  -6.614  38.227  1.00 49.22           O  
ANISOU   81  O   ALA A  10     6756   5575   6370  -1091   -423   1234       O  
ATOM     82  CB  ALA A  10     -12.273  -6.103  36.270  1.00 43.43           C  
ANISOU   82  CB  ALA A  10     5775   5141   5585   -818   -452   1375       C  
ATOM     83  N   PHE A  11      -9.975  -4.439  37.666  1.00 49.03           N  
ANISOU   83  N   PHE A  11     6787   5473   6368   -797   -203   1181       N  
ATOM     84  CA  PHE A  11      -8.596  -3.969  37.822  1.00 49.74           C  
ANISOU   84  CA  PHE A  11     7010   5358   6532   -850   -167   1109       C  
ATOM     85  C   PHE A  11      -8.082  -4.214  39.238  1.00 48.92           C  
ANISOU   85  C   PHE A  11     6918   5290   6381   -992   -188   1011       C  
ATOM     86  O   PHE A  11      -6.949  -4.660  39.411  1.00 47.03           O  
ANISOU   86  O   PHE A  11     6712   4980   6179  -1114   -258    997       O  
ATOM     87  CB  PHE A  11      -8.453  -2.488  37.429  1.00 55.16           C  
ANISOU   87  CB  PHE A  11     7788   5850   7320   -706    -46   1100       C  
ATOM     88  CG  PHE A  11      -8.423  -2.235  35.943  1.00 60.15           C  
ANISOU   88  CG  PHE A  11     8440   6433   7980   -602    -34   1254       C  
ATOM     89  CD1 PHE A  11      -7.261  -2.455  35.207  1.00 65.19           C  
ANISOU   89  CD1 PHE A  11     9120   7006   8644   -679    -34   1309       C  
ATOM     90  CD2 PHE A  11      -9.553  -1.771  35.274  1.00 66.36           C  
ANISOU   90  CD2 PHE A  11     9182   7289   8742   -408    -17   1361       C  
ATOM     91  CE1 PHE A  11      -7.235  -2.222  33.822  1.00 68.00           C  
ANISOU   91  CE1 PHE A  11     9490   7394   8953   -573     -1   1470       C  
ATOM     92  CE2 PHE A  11      -9.522  -1.522  33.890  1.00 70.94           C  
ANISOU   92  CE2 PHE A  11     9785   7879   9290   -306    -19   1534       C  
ATOM     93  CZ  PHE A  11      -8.363  -1.749  33.175  1.00 68.78           C  
ANISOU   93  CZ  PHE A  11     9572   7567   8996   -393     -2   1588       C  
ATOM     94  N   ASP A  12      -8.942  -3.975  40.240  1.00 44.69           N  
ANISOU   94  N   ASP A  12     6328   4917   5734   -959   -129    955       N  
ATOM     95  CA  ASP A  12      -8.645  -4.204  41.652  1.00 44.69           C  
ANISOU   95  CA  ASP A  12     6331   5051   5598  -1077   -145    874       C  
ATOM     96  C   ASP A  12      -8.460  -5.699  41.935  1.00 48.95           C  
ANISOU   96  C   ASP A  12     6796   5714   6088  -1262   -288   1039       C  
ATOM     97  O   ASP A  12      -7.557  -6.064  42.686  1.00 47.47           O  
ANISOU   97  O   ASP A  12     6646   5535   5855  -1385   -373   1031       O  
ATOM     98  CB  ASP A  12      -9.725  -3.585  42.550  1.00 47.38           C  
ANISOU   98  CB  ASP A  12     6612   5608   5782   -952    -11    774       C  
ATOM     99  CG  ASP A  12      -9.660  -2.074  42.683  1.00 54.30           C  
ANISOU   99  CG  ASP A  12     7611   6296   6725   -765    104    539       C  
ATOM    100  OD1 ASP A  12      -8.661  -1.466  42.218  1.00 55.07           O  
ANISOU  100  OD1 ASP A  12     7848   6083   6993   -803     65    470       O  
ATOM    101  OD2 ASP A  12     -10.587  -1.501  43.254  1.00 62.07           O1-
ANISOU  101  OD2 ASP A  12     8542   7432   7610   -583    232    427       O1-
ATOM    102  N   GLY A  13      -9.292  -6.534  41.303  1.00 46.79           N  
ANISOU  102  N   GLY A  13     6419   5510   5848  -1280   -340   1190       N  
ATOM    103  CA  GLY A  13      -9.211  -7.989  41.389  1.00 46.46           C  
ANISOU  103  CA  GLY A  13     6327   5485   5840  -1456   -504   1356       C  
ATOM    104  C   GLY A  13      -7.895  -8.481  40.807  1.00 49.14           C  
ANISOU  104  C   GLY A  13     6768   5583   6319  -1478   -624   1325       C  
ATOM    105  O   GLY A  13      -7.217  -9.326  41.405  1.00 48.00           O  
ANISOU  105  O   GLY A  13     6633   5404   6199  -1591   -749   1407       O  
ATOM    106  N   ALA A  14      -7.498  -7.872  39.668  1.00 45.60           N  
ANISOU  106  N   ALA A  14     6381   4992   5951  -1347   -571   1226       N  
ATOM    107  CA  ALA A  14      -6.238  -8.100  38.952  1.00 44.53           C  
ANISOU  107  CA  ALA A  14     6305   4691   5923  -1317   -619   1179       C  
ATOM    108  C   ALA A  14      -5.047  -7.756  39.839  1.00 45.58           C  
ANISOU  108  C   ALA A  14     6455   4794   6069  -1381   -619   1137       C  
ATOM    109  O   ALA A  14      -4.100  -8.529  39.895  1.00 45.85           O  
ANISOU  109  O   ALA A  14     6471   4766   6183  -1410   -725   1160       O  
ATOM    110  CB  ALA A  14      -6.201  -7.270  37.671  1.00 45.26           C  
ANISOU  110  CB  ALA A  14     6434   4728   6034  -1171   -511   1133       C  
ATOM    111  N   ARG A  15      -5.124  -6.638  40.581  1.00 42.14           N  
ANISOU  111  N   ARG A  15     6045   4406   5560  -1392   -524   1057       N  
ATOM    112  CA  ARG A  15      -4.061  -6.211  41.511  1.00 42.84           C  
ANISOU  112  CA  ARG A  15     6148   4492   5638  -1483   -561    975       C  
ATOM    113  C   ARG A  15      -3.932  -7.196  42.695  1.00 47.56           C  
ANISOU  113  C   ARG A  15     6703   5248   6119  -1598   -707   1067       C  
ATOM    114  O   ARG A  15      -2.809  -7.545  43.046  1.00 47.53           O  
ANISOU  114  O   ARG A  15     6665   5230   6162  -1661   -826   1087       O  
ATOM    115  CB  ARG A  15      -4.329  -4.800  42.030  1.00 42.26           C  
ANISOU  115  CB  ARG A  15     6145   4401   5512  -1458   -450    809       C  
ATOM    116  CG  ARG A  15      -4.214  -3.711  40.975  1.00 53.18           C  
ANISOU  116  CG  ARG A  15     7582   5562   7061  -1375   -334    770       C  
ATOM    117  CD  ARG A  15      -4.920  -2.448  41.425  1.00 55.79           C  
ANISOU  117  CD  ARG A  15     8004   5817   7378  -1288   -230    615       C  
ATOM    118  NE  ARG A  15      -4.329  -1.880  42.638  1.00 48.15           N  
ANISOU  118  NE  ARG A  15     7094   4844   6356  -1393   -288    402       N  
ATOM    119  CZ  ARG A  15      -5.023  -1.507  43.709  1.00 62.81           C  
ANISOU  119  CZ  ARG A  15     8998   6843   8024  -1336   -257    221       C  
ATOM    120  NH1 ARG A  15      -6.343  -1.643  43.732  1.00 52.27           N1+
ANISOU  120  NH1 ARG A  15     7620   5676   6564  -1175   -148    261       N1+
ATOM    121  NH2 ARG A  15      -4.405  -0.970  44.756  1.00 43.94           N  
ANISOU  121  NH2 ARG A  15     6680   4462   5554  -1434   -336    -18       N  
ATOM    122  N   ASP A  16      -5.082  -7.649  43.285  1.00 44.44           N  
ANISOU  122  N   ASP A  16     6282   5027   5574  -1626   -698   1165       N  
ATOM    123  CA  ASP A  16      -5.144  -8.636  44.382  1.00 46.44           C  
ANISOU  123  CA  ASP A  16     6490   5460   5695  -1750   -822   1344       C  
ATOM    124  C   ASP A  16      -4.592  -9.995  43.933  1.00 51.77           C  
ANISOU  124  C   ASP A  16     7142   5967   6561  -1787  -1001   1521       C  
ATOM    125  O   ASP A  16      -3.955 -10.664  44.728  1.00 53.45           O  
ANISOU  125  O   ASP A  16     7335   6231   6744  -1862  -1150   1662       O  
ATOM    126  CB  ASP A  16      -6.582  -8.846  44.871  1.00 49.06           C  
ANISOU  126  CB  ASP A  16     6756   6027   5858  -1783   -737   1463       C  
ATOM    127  CG  ASP A  16      -7.264  -7.629  45.435  1.00 57.20           C  
ANISOU  127  CG  ASP A  16     7792   7264   6679  -1693   -550   1276       C  
ATOM    128  OD1 ASP A  16      -6.632  -6.913  46.235  1.00 60.17           O  
ANISOU  128  OD1 ASP A  16     8237   7715   6910  -1691   -548   1100       O  
ATOM    129  OD2 ASP A  16      -8.453  -7.435  45.135  1.00 62.54           O1-
ANISOU  129  OD2 ASP A  16     8391   8040   7332  -1618   -422   1293       O1-
ATOM    130  N   MET A  17      -4.861 -10.407  42.668  1.00 46.58           N  
ANISOU  130  N   MET A  17     6494   5114   6090  -1712  -1001   1505       N  
ATOM    131  CA  MET A  17      -4.296 -11.623  42.086  1.00 45.60           C  
ANISOU  131  CA  MET A  17     6377   4776   6174  -1690  -1165   1579       C  
ATOM    132  C   MET A  17      -2.763 -11.426  41.956  1.00 50.79           C  
ANISOU  132  C   MET A  17     7016   5357   6923  -1603  -1199   1490       C  
ATOM    133  O   MET A  17      -1.996 -12.303  42.345  1.00 50.80           O  
ANISOU  133  O   MET A  17     6989   5286   7028  -1600  -1363   1600       O  
ATOM    134  CB  MET A  17      -4.915 -11.924  40.709  1.00 46.17           C  
ANISOU  134  CB  MET A  17     6477   4704   6362  -1609  -1152   1494       C  
ATOM    135  CG  MET A  17      -6.323 -12.532  40.785  1.00 49.06           C  
ANISOU  135  CG  MET A  17     6809   5109   6722  -1735  -1208   1627       C  
ATOM    136  SD  MET A  17      -6.457 -14.108  41.683  1.00 53.56           S  
ANISOU  136  SD  MET A  17     7363   5561   7426  -1932  -1446   1923       S  
ATOM    137  CE  MET A  17      -5.586 -15.218  40.588  1.00 50.19           C  
ANISOU  137  CE  MET A  17     7038   4731   7301  -1797  -1639   1784       C  
ATOM    138  N   TRP A  18      -2.323 -10.250  41.464  1.00 46.64           N  
ANISOU  138  N   TRP A  18     6487   4854   6379  -1541  -1049   1323       N  
ATOM    139  CA  TRP A  18      -0.892  -9.952  41.352  1.00 46.50           C  
ANISOU  139  CA  TRP A  18     6395   4814   6459  -1501  -1061   1262       C  
ATOM    140  C   TRP A  18      -0.203  -9.993  42.723  1.00 51.92           C  
ANISOU  140  C   TRP A  18     7025   5631   7072  -1614  -1202   1330       C  
ATOM    141  O   TRP A  18       0.895 -10.551  42.844  1.00 53.85           O  
ANISOU  141  O   TRP A  18     7167   5861   7433  -1576  -1331   1387       O  
ATOM    142  CB  TRP A  18      -0.641  -8.583  40.669  1.00 43.62           C  
ANISOU  142  CB  TRP A  18     6030   4440   6102  -1480   -875   1130       C  
ATOM    143  CG  TRP A  18       0.818  -8.298  40.507  1.00 45.11           C  
ANISOU  143  CG  TRP A  18     6089   4631   6418  -1482   -879   1106       C  
ATOM    144  CD1 TRP A  18       1.675  -7.819  41.453  1.00 48.58           C  
ANISOU  144  CD1 TRP A  18     6446   5149   6865  -1612   -966   1085       C  
ATOM    145  CD2 TRP A  18       1.608  -8.560  39.344  1.00 45.94           C  
ANISOU  145  CD2 TRP A  18     6096   4708   6651  -1348   -805   1103       C  
ATOM    146  CE2 TRP A  18       2.938  -8.202  39.653  1.00 50.08           C  
ANISOU  146  CE2 TRP A  18     6442   5303   7282  -1412   -832   1114       C  
ATOM    147  CE3 TRP A  18       1.320  -9.069  38.061  1.00 47.29           C  
ANISOU  147  CE3 TRP A  18     6300   4840   6828  -1173   -719   1077       C  
ATOM    148  NE1 TRP A  18       2.951  -7.766  40.953  1.00 48.53           N  
ANISOU  148  NE1 TRP A  18     6263   5156   7019  -1588   -956   1098       N  
ATOM    149  CZ2 TRP A  18       3.981  -8.345  38.735  1.00 50.95           C  
ANISOU  149  CZ2 TRP A  18     6375   5469   7515  -1298   -740   1129       C  
ATOM    150  CZ3 TRP A  18       2.355  -9.187  37.145  1.00 49.90           C  
ANISOU  150  CZ3 TRP A  18     6493   5230   7236  -1040   -625   1057       C  
ATOM    151  CH2 TRP A  18       3.665  -8.821  37.482  1.00 51.53           C  
ANISOU  151  CH2 TRP A  18     6493   5529   7558  -1098   -617   1099       C  
ATOM    152  N   ARG A  19      -0.854  -9.393  43.738  1.00 47.81           N  
ANISOU  152  N   ARG A  19     6557   5272   6335  -1727  -1180   1314       N  
ATOM    153  CA  ARG A  19      -0.364  -9.284  45.108  1.00 49.25           C  
ANISOU  153  CA  ARG A  19     6711   5658   6345  -1840  -1313   1345       C  
ATOM    154  C   ARG A  19      -0.133 -10.661  45.730  1.00 54.16           C  
ANISOU  154  C   ARG A  19     7284   6322   6971  -1854  -1521   1615       C  
ATOM    155  O   ARG A  19       0.866 -10.860  46.427  1.00 57.13           O  
ANISOU  155  O   ARG A  19     7577   6802   7327  -1884  -1694   1681       O  
ATOM    156  CB  ARG A  19      -1.325  -8.414  45.935  1.00 50.59           C  
ANISOU  156  CB  ARG A  19     6966   6019   6237  -1904  -1208   1235       C  
ATOM    157  CG  ARG A  19      -0.823  -8.007  47.328  1.00 59.80           C  
ANISOU  157  CG  ARG A  19     8130   7444   7149  -2011  -1328   1160       C  
ATOM    158  CD  ARG A  19      -1.692  -6.927  47.965  1.00 58.81           C  
ANISOU  158  CD  ARG A  19     8105   7475   6764  -2012  -1185    925       C  
ATOM    159  NE  ARG A  19      -3.130  -7.153  47.773  1.00 69.62           N  
ANISOU  159  NE  ARG A  19     9497   8915   8042  -1940  -1012   1015       N  
ATOM    160  CZ  ARG A  19      -3.894  -7.866  48.591  1.00 86.29           C  
ANISOU  160  CZ  ARG A  19    11571  11320   9895  -1983  -1013   1219       C  
ATOM    161  NH1 ARG A  19      -5.190  -8.011  48.342  1.00 80.24           N1+
ANISOU  161  NH1 ARG A  19    10771  10630   9085  -1937   -850   1307       N1+
ATOM    162  NH2 ARG A  19      -3.369  -8.437  49.668  1.00 74.24           N  
ANISOU  162  NH2 ARG A  19    10018  10043   8148  -2083  -1183   1372       N  
ATOM    163  N   ALA A  20      -1.016 -11.614  45.428  1.00 49.62           N  
ANISOU  163  N   ALA A  20     6753   5642   6457  -1838  -1529   1785       N  
ATOM    164  CA  ALA A  20      -0.929 -12.989  45.911  1.00 51.75           C  
ANISOU  164  CA  ALA A  20     7005   5853   6806  -1861  -1735   2085       C  
ATOM    165  C   ALA A  20       0.353 -13.659  45.393  1.00 57.13           C  
ANISOU  165  C   ALA A  20     7614   6325   7770  -1711  -1883   2095       C  
ATOM    166  O   ALA A  20       1.077 -14.268  46.178  1.00 57.14           O  
ANISOU  166  O   ALA A  20     7549   6378   7783  -1708  -2085   2296       O  
ATOM    167  CB  ALA A  20      -2.156 -13.773  45.477  1.00 52.04           C  
ANISOU  167  CB  ALA A  20     7100   5743   6931  -1905  -1714   2220       C  
ATOM    168  N   TYR A  21       0.651 -13.509  44.078  1.00 53.71           N  
ANISOU  168  N   TYR A  21     7170   5699   7536  -1563  -1774   1884       N  
ATOM    169  CA  TYR A  21       1.858 -14.100  43.497  1.00 55.49           C  
ANISOU  169  CA  TYR A  21     7293   5775   8015  -1369  -1864   1853       C  
ATOM    170  C   TYR A  21       3.128 -13.381  43.897  1.00 57.87           C  
ANISOU  170  C   TYR A  21     7421   6274   8294  -1367  -1886   1800       C  
ATOM    171  O   TYR A  21       4.149 -14.033  44.104  1.00 58.39           O  
ANISOU  171  O   TYR A  21     7347   6321   8518  -1243  -2048   1897       O  
ATOM    172  CB  TYR A  21       1.734 -14.378  41.987  1.00 56.95           C  
ANISOU  172  CB  TYR A  21     7520   5747   8372  -1190  -1743   1658       C  
ATOM    173  CG  TYR A  21       0.553 -15.277  41.702  1.00 61.46           C  
ANISOU  173  CG  TYR A  21     8244   6100   9007  -1219  -1807   1711       C  
ATOM    174  CD1 TYR A  21       0.487 -16.562  42.234  1.00 65.96           C  
ANISOU  174  CD1 TYR A  21     8858   6452   9753  -1222  -2042   1926       C  
ATOM    175  CD2 TYR A  21      -0.543 -14.811  40.980  1.00 61.16           C  
ANISOU  175  CD2 TYR A  21     8295   6072   8872  -1272  -1659   1580       C  
ATOM    176  CE1 TYR A  21      -0.633 -17.363  42.053  1.00 68.32           C  
ANISOU  176  CE1 TYR A  21     9283   6527  10148  -1318  -2127   1998       C  
ATOM    177  CE2 TYR A  21      -1.675 -15.599  40.802  1.00 62.85           C  
ANISOU  177  CE2 TYR A  21     8609   6118   9152  -1351  -1748   1637       C  
ATOM    178  CZ  TYR A  21      -1.713 -16.883  41.332  1.00 72.60           C  
ANISOU  178  CZ  TYR A  21     9884   7115  10585  -1394  -1984   1840       C  
ATOM    179  OH  TYR A  21      -2.803 -17.702  41.148  1.00 69.40           O  
ANISOU  179  OH  TYR A  21     9564   6506  10299  -1523  -2099   1910       O  
ATOM    180  N   SER A  22       3.049 -12.049  44.067  1.00 52.73           N  
ANISOU  180  N   SER A  22     6768   5798   7469  -1509  -1751   1651       N  
ATOM    181  CA  SER A  22       4.152 -11.227  44.547  1.00 52.89           C  
ANISOU  181  CA  SER A  22     6626   5999   7469  -1589  -1800   1579       C  
ATOM    182  C   SER A  22       4.526 -11.696  45.969  1.00 57.61           C  
ANISOU  182  C   SER A  22     7170   6793   7925  -1670  -2067   1764       C  
ATOM    183  O   SER A  22       5.694 -11.965  46.228  1.00 57.57           O  
ANISOU  183  O   SER A  22     6965   6879   8031  -1622  -2234   1832       O  
ATOM    184  CB  SER A  22       3.757  -9.753  44.522  1.00 54.02           C  
ANISOU  184  CB  SER A  22     6844   6200   7482  -1743  -1629   1373       C  
ATOM    185  OG  SER A  22       4.818  -8.943  45.002  1.00 59.12           O  
ANISOU  185  OG  SER A  22     7337   6977   8151  -1869  -1708   1284       O  
ATOM    186  N   ASP A  23       3.505 -11.911  46.836  1.00 56.51           N  
ANISOU  186  N   ASP A  23     7186   6750   7536  -1773  -2105   1883       N  
ATOM    187  CA  ASP A  23       3.656 -12.416  48.207  1.00 59.96           C  
ANISOU  187  CA  ASP A  23     7602   7428   7752  -1854  -2342   2117       C  
ATOM    188  C   ASP A  23       4.189 -13.858  48.245  1.00 67.41           C  
ANISOU  188  C   ASP A  23     8467   8227   8918  -1705  -2562   2436       C  
ATOM    189  O   ASP A  23       5.012 -14.181  49.105  1.00 68.86           O  
ANISOU  189  O   ASP A  23     8528   8596   9038  -1703  -2807   2620       O  
ATOM    190  CB  ASP A  23       2.323 -12.316  48.978  1.00 61.77           C  
ANISOU  190  CB  ASP A  23     7998   7831   7642  -1986  -2262   2192       C  
ATOM    191  CG  ASP A  23       1.976 -10.924  49.495  1.00 65.88           C  
ANISOU  191  CG  ASP A  23     8584   8585   7860  -2107  -2133   1890       C  
ATOM    192  OD1 ASP A  23       2.847 -10.018  49.410  1.00 65.03           O  
ANISOU  192  OD1 ASP A  23     8408   8495   7807  -2143  -2160   1642       O  
ATOM    193  OD2 ASP A  23       0.847 -10.748  50.020  1.00 66.40           O1-
ANISOU  193  OD2 ASP A  23     8760   8819   7649  -2165  -2013   1901       O1-
ATOM    194  N   MET A  24       3.727 -14.712  47.308  1.00 65.56           N  
ANISOU  194  N   MET A  24     8308   7649   8954  -1570  -2497   2486       N  
ATOM    195  CA  MET A  24       4.156 -16.109  47.158  1.00 69.07           C  
ANISOU  195  CA  MET A  24     8719   7827   9696  -1387  -2697   2732       C  
ATOM    196  C   MET A  24       5.676 -16.177  46.925  1.00 74.78           C  
ANISOU  196  C   MET A  24     9204   8574  10637  -1182  -2810   2675       C  
ATOM    197  O   MET A  24       6.352 -17.015  47.528  1.00 78.57           O  
ANISOU  197  O   MET A  24     9583   9042  11230  -1067  -3068   2943       O  
ATOM    198  CB  MET A  24       3.394 -16.782  46.001  1.00 70.91           C  
ANISOU  198  CB  MET A  24     9094   7667  10181  -1287  -2590   2649       C  
ATOM    199  CG  MET A  24       3.610 -18.283  45.906  1.00 78.75           C  
ANISOU  199  CG  MET A  24    10119   8292  11512  -1114  -2817   2878       C  
ATOM    200  SD  MET A  24       2.466 -19.050  44.729  1.00 83.01           S  
ANISOU  200  SD  MET A  24    10866   8373  12301  -1080  -2746   2742       S  
ATOM    201  CE  MET A  24       3.453 -20.417  44.203  1.00 83.82           C  
ANISOU  201  CE  MET A  24    10946   8024  12878   -720  -2979   2770       C  
ATOM    202  N   ARG A  25       6.206 -15.267  46.082  1.00 67.80           N  
ANISOU  202  N   ARG A  25     8205   7748   9809  -1142  -2616   2365       N  
ATOM    203  CA  ARG A  25       7.631 -15.147  45.774  1.00 68.39           C  
ANISOU  203  CA  ARG A  25     7987   7920  10077   -981  -2661   2294       C  
ATOM    204  C   ARG A  25       8.406 -14.667  46.994  1.00 74.27           C  
ANISOU  204  C   ARG A  25     8547   9021  10650  -1133  -2881   2404       C  
ATOM    205  O   ARG A  25       9.507 -15.159  47.232  1.00 78.48           O  
ANISOU  205  O   ARG A  25     8824   9643  11352   -975  -3077   2532       O  
ATOM    206  CB  ARG A  25       7.864 -14.174  44.602  1.00 65.10           C  
ANISOU  206  CB  ARG A  25     7496   7522   9718   -976  -2365   1991       C  
ATOM    207  CG  ARG A  25       7.502 -14.743  43.243  1.00 76.13           C  
ANISOU  207  CG  ARG A  25     8974   8646  11307   -730  -2188   1859       C  
ATOM    208  CD  ARG A  25       7.866 -13.793  42.115  1.00 85.73           C  
ANISOU  208  CD  ARG A  25    10076   9960  12538   -712  -1899   1633       C  
ATOM    209  NE  ARG A  25       6.674 -13.126  41.599  1.00 89.37           N  
ANISOU  209  NE  ARG A  25    10787  10342  12829   -856  -1701   1511       N  
ATOM    210  CZ  ARG A  25       6.388 -11.847  41.779  1.00 99.59           C  
ANISOU  210  CZ  ARG A  25    12114  11757  13967  -1095  -1579   1443       C  
ATOM    211  NH1 ARG A  25       7.196 -11.075  42.493  1.00 93.51           N1+
ANISOU  211  NH1 ARG A  25    11162  11180  13186  -1263  -1646   1456       N1+
ATOM    212  NH2 ARG A  25       5.273 -11.334  41.279  1.00 82.05           N  
ANISOU  212  NH2 ARG A  25    10107   9448  11620  -1166  -1414   1355       N  
ATOM    213  N   GLU A  26       7.837 -13.706  47.755  1.00 68.39           N  
ANISOU  213  N   GLU A  26     7924   8496   9566  -1419  -2860   2326       N  
ATOM    214  CA  GLU A  26       8.442 -13.114  48.946  1.00 70.62           C  
ANISOU  214  CA  GLU A  26     8079   9146   9607  -1604  -3081   2347       C  
ATOM    215  C   GLU A  26       8.593 -14.151  50.066  1.00 79.95           C  
ANISOU  215  C   GLU A  26     9244  10473  10660  -1551  -3403   2724       C  
ATOM    216  O   GLU A  26       9.697 -14.337  50.572  1.00 82.70           O  
ANISOU  216  O   GLU A  26     9340  11040  11042  -1507  -3667   2844       O  
ATOM    217  CB  GLU A  26       7.626 -11.895  49.415  1.00 70.24           C  
ANISOU  217  CB  GLU A  26     8224   9244   9220  -1873  -2951   2102       C  
ATOM    218  CG  GLU A  26       8.365 -10.979  50.388  1.00 79.43           C  
ANISOU  218  CG  GLU A  26     9262  10753  10166  -2084  -3155   1962       C  
ATOM    219  CD  GLU A  26       7.520  -9.868  50.988  1.00 87.00           C  
ANISOU  219  CD  GLU A  26    10450  11841  10765  -2300  -3061   1689       C  
ATOM    220  OE1 GLU A  26       7.800  -8.684  50.693  1.00 86.63           O  
ANISOU  220  OE1 GLU A  26    10385  11743  10789  -2447  -2977   1370       O  
ATOM    221  OE2 GLU A  26       6.571 -10.179  51.743  1.00 68.65           O1-
ANISOU  221  OE2 GLU A  26     8320   9663   8102  -2315  -3065   1800       O1-
ATOM    222  N   ALA A  27       7.484 -14.831  50.421  1.00 77.95           N  
ANISOU  222  N   ALA A  27     9234  10112  10272  -1564  -3388   2946       N  
ATOM    223  CA  ALA A  27       7.389 -15.869  51.447  1.00 81.87           C  
ANISOU  223  CA  ALA A  27     9761  10710  10635  -1541  -3661   3392       C  
ATOM    224  C   ALA A  27       8.419 -16.984  51.241  1.00 92.72           C  
ANISOU  224  C   ALA A  27    10942  11887  12401  -1252  -3901   3659       C  
ATOM    225  O   ALA A  27       9.094 -17.375  52.206  1.00 96.71           O  
ANISOU  225  O   ALA A  27    11310  12638  12798  -1221  -4215   3962       O  
ATOM    226  CB  ALA A  27       5.985 -16.461  51.463  1.00 81.10           C  
ANISOU  226  CB  ALA A  27     9929  10439  10446  -1619  -3536   3587       C  
ATOM    227  N   ASN A  28       8.543 -17.483  49.983  1.00 89.64           N  
ANISOU  227  N   ASN A  28    10539  11074  12447  -1015  -3758   3529       N  
ATOM    228  CA  ASN A  28       9.432 -18.578  49.565  1.00 93.02           C  
ANISOU  228  CA  ASN A  28    10804  11230  13312   -658  -3928   3692       C  
ATOM    229  C   ASN A  28       9.184 -19.878  50.373  1.00101.75           C  
ANISOU  229  C   ASN A  28    12022  12151  14490   -577  -4223   4207       C  
ATOM    230  O   ASN A  28      10.084 -20.697  50.559  1.00105.62           O  
ANISOU  230  O   ASN A  28    12335  12546  15248   -301  -4483   4452       O  
ATOM    231  CB  ASN A  28      10.914 -18.134  49.539  1.00 96.04           C  
ANISOU  231  CB  ASN A  28    10790  11897  13802   -525  -4036   3587       C  
ATOM    232  CG  ASN A  28      11.861 -19.051  48.787  1.00113.27           C  
ANISOU  232  CG  ASN A  28    12751  13819  16467    -91  -4085   3600       C  
ATOM    233  ND2 ASN A  28      11.395 -19.669  47.707  1.00100.08           N  
ANISOU  233  ND2 ASN A  28    11245  11716  15064    110  -3879   3423       N  
ATOM    234  OD1 ASN A  28      13.021 -19.226  49.175  1.00110.14           O  
ANISOU  234  OD1 ASN A  28    12021  13629  16198     88  -4316   3749       O  
ATOM    235  N   TYR A  29       7.932 -20.049  50.837  1.00 98.40           N  
ANISOU  235  N   TYR A  29    11873  11672  13841   -818  -4174   4396       N  
ATOM    236  CA  TYR A  29       7.454 -21.196  51.603  1.00102.53           C  
ANISOU  236  CA  TYR A  29    12534  12018  14406   -835  -4411   4943       C  
ATOM    237  C   TYR A  29       7.029 -22.304  50.644  1.00108.96           C  
ANISOU  237  C   TYR A  29    13510  12150  15739   -648  -4396   4966       C  
ATOM    238  O   TYR A  29       6.238 -22.069  49.731  1.00105.60           O  
ANISOU  238  O   TYR A  29    13230  11502  15389   -716  -4139   4635       O  
ATOM    239  CB  TYR A  29       6.278 -20.794  52.517  1.00103.08           C  
ANISOU  239  CB  TYR A  29    12779  12420  13968  -1208  -4330   5141       C  
ATOM    240  CG  TYR A  29       6.186 -21.636  53.766  1.00110.55           C  
ANISOU  240  CG  TYR A  29    13749  13511  14743  -1277  -4626   5793       C  
ATOM    241  CD1 TYR A  29       6.794 -21.230  54.950  1.00115.83           C  
ANISOU  241  CD1 TYR A  29    14278  14772  14958  -1344  -4827   5978       C  
ATOM    242  CD2 TYR A  29       5.516 -22.856  53.761  1.00114.01           C  
ANISOU  242  CD2 TYR A  29    14349  13494  15476  -1286  -4731   6246       C  
ATOM    243  CE1 TYR A  29       6.755 -22.025  56.095  1.00122.28           C  
ANISOU  243  CE1 TYR A  29    15112  15775  15573  -1393  -5111   6631       C  
ATOM    244  CE2 TYR A  29       5.466 -23.658  54.901  1.00120.57           C  
ANISOU  244  CE2 TYR A  29    15197  14447  16168  -1357  -5009   6930       C  
ATOM    245  CZ  TYR A  29       6.070 -23.229  56.073  1.00131.65           C  
ANISOU  245  CZ  TYR A  29    16458  16500  17064  -1403  -5187   7138       C  
ATOM    246  OH  TYR A  29       6.017 -24.011  57.204  1.00139.18           O  
ANISOU  246  OH  TYR A  29    17427  17633  17822  -1469  -5463   7858       O  
ATOM    247  N   ILE A  30       7.572 -23.506  50.839  1.00111.70           N  
ANISOU  247  N   ILE A  30    13835  12151  16453   -402  -4696   5344       N  
ATOM    248  CA  ILE A  30       7.267 -24.661  49.991  1.00113.34           C  
ANISOU  248  CA  ILE A  30    14217  11636  17211   -197  -4750   5351       C  
ATOM    249  C   ILE A  30       5.873 -25.204  50.334  1.00116.42           C  
ANISOU  249  C   ILE A  30    14882  11787  17564   -537  -4757   5686       C  
ATOM    250  O   ILE A  30       5.525 -25.312  51.509  1.00118.22           O  
ANISOU  250  O   ILE A  30    15129  12289  17501   -775  -4892   6205       O  
ATOM    251  CB  ILE A  30       8.373 -25.759  50.048  1.00122.58           C  
ANISOU  251  CB  ILE A  30    15266  12452  18858    239  -5081   5612       C  
ATOM    252  CG1 ILE A  30       9.786 -25.180  50.349  1.00124.06           C  
ANISOU  252  CG1 ILE A  30    15077  13120  18941    480  -5158   5521       C  
ATOM    253  CG2 ILE A  30       8.385 -26.576  48.754  1.00124.79           C  
ANISOU  253  CG2 ILE A  30    15680  12014  19722    569  -5054   5298       C  
ATOM    254  CD1 ILE A  30      10.245 -25.302  51.808  1.00136.27           C  
ANISOU  254  CD1 ILE A  30    16479  15092  20207    399  -5485   6087       C  
ATOM    255  N   GLY A  31       4.928 -25.539  49.397  1.00110.61           N  
ANISOU  255  N   GLY A  31    14334  10590  17101   -566  -4614   5397       N  
ATOM    256  CA  GLY A  31       3.414 -25.757  49.608  1.00111.16           C  
ANISOU  256  CA  GLY A  31    14623  10409  17202   -915  -4611   5666       C  
ATOM    257  C   GLY A  31       2.218 -24.681  49.472  1.00111.28           C  
ANISOU  257  C   GLY A  31    14646  10946  16692  -1294  -4311   5543       C  
ATOM    258  O   GLY A  31       0.836 -24.674  49.508  1.00111.43           O  
ANISOU  258  O   GLY A  31    14772  10926  16642  -1624  -4285   5837       O  
ATOM    259  N   SER A  32       2.807 -23.560  49.237  1.00103.94           N  
ANISOU  259  N   SER A  32    13583  10494  15416  -1244  -4081   5112       N  
ATOM    260  CA  SER A  32       2.102 -22.378  49.254  1.00 99.38           C  
ANISOU  260  CA  SER A  32    13005  10395  14359  -1525  -3789   4916       C  
ATOM    261  C   SER A  32       1.326 -22.350  48.112  1.00 98.88           C  
ANISOU  261  C   SER A  32    13057  10073  14441  -1586  -3571   4533       C  
ATOM    262  O   SER A  32       0.428 -21.743  48.120  1.00 96.52           O  
ANISOU  262  O   SER A  32    12784  10043  13844  -1844  -3370   4500       O  
ATOM    263  CB  SER A  32       3.125 -21.363  49.241  1.00100.40           C  
ANISOU  263  CB  SER A  32    12969  11029  14149  -1448  -3672   4600       C  
ATOM    264  OG  SER A  32       4.149 -21.861  48.477  1.00108.37           O  
ANISOU  264  OG  SER A  32    13890  11845  15440  -1156  -3616   4183       O  
ATOM    265  N   ASP A  33       1.643 -23.074  47.121  1.00 94.80           N  
ANISOU  265  N   ASP A  33    12594   9066  14360  -1322  -3614   4230       N  
ATOM    266  CA  ASP A  33       0.996 -22.737  45.989  1.00 91.94           C  
ANISOU  266  CA  ASP A  33    12342   8435  14154  -1313  -3459   3815       C  
ATOM    267  C   ASP A  33      -0.307 -22.718  46.203  1.00 91.73           C  
ANISOU  267  C   ASP A  33    12396   8492  13967  -1678  -3348   3921       C  
ATOM    268  O   ASP A  33      -0.811 -21.813  45.900  1.00 88.39           O  
ANISOU  268  O   ASP A  33    11945   8360  13279  -1750  -3093   3619       O  
ATOM    269  CB  ASP A  33       1.037 -23.700  44.943  1.00 97.47           C  
ANISOU  269  CB  ASP A  33    13157   8486  15391  -1041  -3653   3675       C  
ATOM    270  CG  ASP A  33       2.248 -23.863  44.524  1.00111.95           C  
ANISOU  270  CG  ASP A  33    14872  10299  17366   -607  -3641   3363       C  
ATOM    271  OD1 ASP A  33       3.023 -23.665  45.384  1.00116.33           O  
ANISOU  271  OD1 ASP A  33    15302  10896  18002   -439  -3814   3628       O  
ATOM    272  OD2 ASP A  33       2.453 -24.187  43.427  1.00114.84           O1-
ANISOU  272  OD2 ASP A  33    15245  10637  17750   -427  -3460   2877       O1-
ATOM    273  N   LYS A  34      -0.935 -23.647  46.800  1.00 88.55           N  
ANISOU  273  N   LYS A  34    12062   7859  13723  -1911  -3537   4394       N  
ATOM    274  CA  LYS A  34      -2.341 -23.525  46.996  1.00 86.91           C  
ANISOU  274  CA  LYS A  34    11871   7737  13412  -2290  -3458   4597       C  
ATOM    275  C   LYS A  34      -2.769 -22.542  47.891  1.00 86.05           C  
ANISOU  275  C   LYS A  34    11633   8329  12732  -2477  -3197   4672       C  
ATOM    276  O   LYS A  34      -3.632 -21.926  47.626  1.00 83.85           O  
ANISOU  276  O   LYS A  34    11324   8234  12302  -2613  -2990   4469       O  
ATOM    277  CB  LYS A  34      -2.931 -24.832  47.378  1.00 93.92           C  
ANISOU  277  CB  LYS A  34    12829   8226  14628  -2516  -3735   5173       C  
ATOM    278  CG  LYS A  34      -2.754 -25.820  46.353  1.00 96.50           C  
ANISOU  278  CG  LYS A  34    13327   7764  15575  -2412  -3984   5010       C  
ATOM    279  CD  LYS A  34      -3.031 -27.138  46.896  1.00101.56           C  
ANISOU  279  CD  LYS A  34    14054   7916  16617  -2626  -4301   5629       C  
ATOM    280  CE  LYS A  34      -4.360 -27.315  47.467  1.00 97.06           C  
ANISOU  280  CE  LYS A  34    13473   7271  16135  -3110  -4308   5909       C  
ATOM    281  NZ  LYS A  34      -4.261 -28.664  47.316  1.00108.95           N1+
ANISOU  281  NZ  LYS A  34    15108   8077  18211  -3298  -4667   6406       N1+
ATOM    282  N   TYR A  35      -2.164 -22.349  48.985  1.00 81.77           N  
ANISOU  282  N   TYR A  35    11014   8187  11867  -2461  -3217   4931       N  
ATOM    283  CA  TYR A  35      -2.903 -21.326  49.708  1.00 79.62           C  
ANISOU  283  CA  TYR A  35    10643   8587  11024  -2600  -2985   4943       C  
ATOM    284  C   TYR A  35      -3.021 -20.087  48.855  1.00 80.07           C  
ANISOU  284  C   TYR A  35    10678   8844  10901  -2480  -2714   4352       C  
ATOM    285  O   TYR A  35      -3.818 -19.236  49.122  1.00 78.61           O  
ANISOU  285  O   TYR A  35    10449   8974  10444  -2618  -2486   4267       O  
ATOM    286  CB  TYR A  35      -2.235 -20.976  51.034  1.00 82.11           C  
ANISOU  286  CB  TYR A  35    10896   9291  11009  -2563  -3104   5233       C  
ATOM    287  CG  TYR A  35      -2.538 -19.743  51.767  1.00 81.49           C  
ANISOU  287  CG  TYR A  35    10745   9897  10321  -2649  -2874   5098       C  
ATOM    288  CD1 TYR A  35      -3.499 -19.634  52.498  1.00 85.28           C  
ANISOU  288  CD1 TYR A  35    11177  10785  10439  -2895  -2725   5395       C  
ATOM    289  CD2 TYR A  35      -1.764 -18.710  51.732  1.00 79.17           C  
ANISOU  289  CD2 TYR A  35    10422   9826   9833  -2483  -2789   4635       C  
ATOM    290  CE1 TYR A  35      -3.703 -18.605  53.083  1.00 85.06           C  
ANISOU  290  CE1 TYR A  35    11095  11376   9847  -2921  -2496   5190       C  
ATOM    291  CE2 TYR A  35      -2.042 -17.681  52.339  1.00 79.06           C  
ANISOU  291  CE2 TYR A  35    10376  10359   9302  -2549  -2592   4431       C  
ATOM    292  CZ  TYR A  35      -3.011 -17.659  52.978  1.00 86.70           C  
ANISOU  292  CZ  TYR A  35    11318  11729   9894  -2741  -2444   4685       C  
ATOM    293  OH  TYR A  35      -3.339 -16.624  53.609  1.00 85.51           O  
ANISOU  293  OH  TYR A  35    11148  12119   9225  -2755  -2243   4429       O  
ATOM    294  N   PHE A  36      -2.074 -19.842  47.976  1.00 74.88           N  
ANISOU  294  N   PHE A  36    10029   8022  10399  -2214  -2734   3982       N  
ATOM    295  CA  PHE A  36      -2.090 -18.507  47.373  1.00 71.15           C  
ANISOU  295  CA  PHE A  36     9539   7698   9798  -2105  -2495   3484       C  
ATOM    296  C   PHE A  36      -2.814 -18.399  46.210  1.00 70.99           C  
ANISOU  296  C   PHE A  36     9576   7447   9951  -2117  -2368   3244       C  
ATOM    297  O   PHE A  36      -3.334 -17.474  46.004  1.00 67.81           O  
ANISOU  297  O   PHE A  36     9154   7264   9345  -2131  -2142   2991       O  
ATOM    298  CB  PHE A  36      -0.729 -17.956  46.952  1.00 72.38           C  
ANISOU  298  CB  PHE A  36     9637   7816  10049  -1862  -2540   3233       C  
ATOM    299  CG  PHE A  36       0.067 -17.371  48.018  1.00 75.40           C  
ANISOU  299  CG  PHE A  36     9926   8584  10139  -1886  -2621   3349       C  
ATOM    300  CD1 PHE A  36      -0.382 -16.480  48.745  1.00 77.59           C  
ANISOU  300  CD1 PHE A  36    10182   9276  10020  -1995  -2454   3166       C  
ATOM    301  CD2 PHE A  36       1.239 -17.747  48.244  1.00 81.25           C  
ANISOU  301  CD2 PHE A  36    10600   9268  11002  -1788  -2889   3623       C  
ATOM    302  CE1 PHE A  36       0.335 -16.022  49.603  1.00 80.67           C  
ANISOU  302  CE1 PHE A  36    10500  10035  10117  -2033  -2566   3219       C  
ATOM    303  CE2 PHE A  36       1.838 -17.258  49.130  1.00 86.43           C  
ANISOU  303  CE2 PHE A  36    11155  10331  11356  -1822  -3004   3725       C  
ATOM    304  CZ  PHE A  36       1.389 -16.411  49.784  1.00 83.21           C  
ANISOU  304  CZ  PHE A  36    10740  10348  10529  -1959  -2847   3503       C  
ATOM    305  N   HIS A  37      -2.891 -19.463  45.515  1.00 68.45           N  
ANISOU  305  N   HIS A  37     9329   6675  10003  -2118  -2538   3334       N  
ATOM    306  CA  HIS A  37      -3.724 -19.502  44.490  1.00 66.90           C  
ANISOU  306  CA  HIS A  37     9187   6266   9966  -2165  -2485   3125       C  
ATOM    307  C   HIS A  37      -4.993 -19.307  45.113  1.00 70.92           C  
ANISOU  307  C   HIS A  37     9618   7080  10247  -2451  -2357   3325       C  
ATOM    308  O   HIS A  37      -5.791 -19.083  44.485  1.00 68.61           O  
ANISOU  308  O   HIS A  37     9294   6917   9857  -2459  -2188   3083       O  
ATOM    309  CB  HIS A  37      -3.737 -20.748  43.927  1.00 70.36           C  
ANISOU  309  CB  HIS A  37     9737   6132  10863  -2134  -2751   3174       C  
ATOM    310  CG  HIS A  37      -2.614 -21.017  43.076  1.00 73.40           C  
ANISOU  310  CG  HIS A  37    10185   6224  11481  -1785  -2822   2848       C  
ATOM    311  CD2 HIS A  37      -1.942 -20.263  42.266  1.00 71.86           C  
ANISOU  311  CD2 HIS A  37     9962   6162  11180  -1541  -2646   2443       C  
ATOM    312  ND1 HIS A  37      -2.092 -22.232  42.916  1.00 78.79           N  
ANISOU  312  ND1 HIS A  37    10952   6427  12556  -1653  -3090   2953       N  
ATOM    313  CE1 HIS A  37      -1.114 -22.234  42.077  1.00 77.25           C  
ANISOU  313  CE1 HIS A  37    10761   6132  12457  -1304  -3050   2576       C  
ATOM    314  NE2 HIS A  37      -1.017 -21.039  41.650  1.00 73.63           N  
ANISOU  314  NE2 HIS A  37    10226   6053  11694  -1246  -2778   2282       N  
ATOM    315  N   ALA A  38      -5.240 -19.404  46.371  1.00 69.32           N  
ANISOU  315  N   ALA A  38     9358   7060   9920  -2660  -2418   3785       N  
ATOM    316  CA  ALA A  38      -6.582 -19.142  46.830  1.00 69.65           C  
ANISOU  316  CA  ALA A  38     9273   7482   9707  -2926  -2275   4052       C  
ATOM    317  C   ALA A  38      -6.880 -17.977  47.569  1.00 71.36           C  
ANISOU  317  C   ALA A  38     9407   8270   9437  -2861  -1992   3877       C  
ATOM    318  O   ALA A  38      -7.856 -17.716  47.729  1.00 70.92           O  
ANISOU  318  O   ALA A  38     9242   8490   9215  -2951  -1798   3841       O  
ATOM    319  CB  ALA A  38      -7.039 -20.296  47.591  1.00 74.65           C  
ANISOU  319  CB  ALA A  38     9874   8117  10372  -3165  -2441   4652       C  
ATOM    320  N   ARG A  39      -5.975 -17.322  48.114  1.00 67.70           N  
ANISOU  320  N   ARG A  39     8981   7978   8764  -2704  -1985   3761       N  
ATOM    321  CA  ARG A  39      -6.033 -15.985  48.731  1.00 66.82           C  
ANISOU  321  CA  ARG A  39     8828   8348   8215  -2642  -1759   3542       C  
ATOM    322  C   ARG A  39      -6.303 -14.871  47.705  1.00 67.79           C  
ANISOU  322  C   ARG A  39     8967   8425   8364  -2490  -1561   3076       C  
ATOM    323  O   ARG A  39      -7.149 -14.000  47.941  1.00 67.32           O  
ANISOU  323  O   ARG A  39     8847   8684   8049  -2487  -1342   2954       O  
ATOM    324  CB  ARG A  39      -4.759 -15.691  49.550  1.00 67.21           C  
ANISOU  324  CB  ARG A  39     8910   8560   8068  -2553  -1866   3524       C  
ATOM    325  CG  ARG A  39      -4.946 -14.596  50.605  1.00 67.49           C  
ANISOU  325  CG  ARG A  39     8915   9136   7593  -2557  -1694   3384       C  
ATOM    326  CD  ARG A  39      -3.630 -13.932  50.972  1.00 70.41           C  
ANISOU  326  CD  ARG A  39     9324   9582   7846  -2445  -1796   3142       C  
ATOM    327  NE  ARG A  39      -3.207 -12.940  49.978  1.00 63.78           N  
ANISOU  327  NE  ARG A  39     8524   8516   7193  -2304  -1695   2681       N  
ATOM    328  CZ  ARG A  39      -2.076 -12.244  50.030  1.00 76.64           C  
ANISOU  328  CZ  ARG A  39    10157  10134   8828  -2233  -1772   2435       C  
ATOM    329  NH1 ARG A  39      -1.227 -12.413  51.040  1.00 71.48           N1+
ANISOU  329  NH1 ARG A  39     9468   9702   7991  -2272  -1975   2563       N1+
ATOM    330  NH2 ARG A  39      -1.784 -11.372  49.074  1.00 66.56           N  
ANISOU  330  NH2 ARG A  39     8903   8644   7741  -2139  -1658   2089       N  
ATOM    331  N   GLY A  40      -5.603 -14.922  46.576  1.00 62.41           N  
ANISOU  331  N   GLY A  40     8361   7368   7986  -2344  -1634   2840       N  
ATOM    332  CA  GLY A  40      -5.778 -13.961  45.492  1.00 58.75           C  
ANISOU  332  CA  GLY A  40     7920   6835   7567  -2200  -1471   2468       C  
ATOM    333  C   GLY A  40      -7.177 -14.017  44.925  1.00 61.72           C  
ANISOU  333  C   GLY A  40     8236   7236   7977  -2270  -1377   2482       C  
ATOM    334  O   GLY A  40      -7.776 -12.975  44.651  1.00 60.41           O  
ANISOU  334  O   GLY A  40     8037   7237   7677  -2187  -1183   2285       O  
ATOM    335  N   ASN A  41      -7.703 -15.250  44.741  1.00 59.59           N  
ANISOU  335  N   ASN A  41     7941   6778   7921  -2428  -1537   2726       N  
ATOM    336  CA  ASN A  41      -9.056 -15.495  44.244  1.00 59.28           C  
ANISOU  336  CA  ASN A  41     7800   6770   7955  -2555  -1508   2784       C  
ATOM    337  C   ASN A  41     -10.099 -15.004  45.242  1.00 65.19           C  
ANISOU  337  C   ASN A  41     8373   7992   8403  -2672  -1315   2973       C  
ATOM    338  O   ASN A  41     -11.106 -14.448  44.823  1.00 64.78           O  
ANISOU  338  O   ASN A  41     8200   8116   8299  -2651  -1176   2879       O  
ATOM    339  CB  ASN A  41      -9.256 -16.963  43.887  1.00 57.55           C  
ANISOU  339  CB  ASN A  41     7604   6181   8080  -2735  -1770   2989       C  
ATOM    340  CG  ASN A  41      -8.790 -17.304  42.491  1.00 65.13           C  
ANISOU  340  CG  ASN A  41     8698   6736   9310  -2583  -1906   2673       C  
ATOM    341  ND2 ASN A  41      -7.545 -17.690  42.382  1.00 53.09           N  
ANISOU  341  ND2 ASN A  41     7305   4956   7913  -2418  -2011   2579       N  
ATOM    342  OD1 ASN A  41      -9.531 -17.227  41.495  1.00 55.61           O  
ANISOU  342  OD1 ASN A  41     7466   5488   8176  -2591  -1918   2503       O  
ATOM    343  N   TYR A  42      -9.823 -15.123  46.550  1.00 65.20           N  
ANISOU  343  N   TYR A  42     8351   8248   8175  -2758  -1295   3221       N  
ATOM    344  CA  TYR A  42     -10.732 -14.682  47.614  1.00 68.33           C  
ANISOU  344  CA  TYR A  42     8577   9176   8210  -2840  -1085   3394       C  
ATOM    345  C   TYR A  42     -10.804 -13.164  47.670  1.00 71.36           C  
ANISOU  345  C   TYR A  42     8968   9827   8319  -2594   -836   3005       C  
ATOM    346  O   TYR A  42     -11.907 -12.612  47.676  1.00 72.81           O  
ANISOU  346  O   TYR A  42     8990  10301   8375  -2555   -636   2963       O  
ATOM    347  CB  TYR A  42     -10.353 -15.299  48.988  1.00 72.70           C  
ANISOU  347  CB  TYR A  42     9124   9957   8542  -2990  -1155   3781       C  
ATOM    348  CG  TYR A  42     -11.152 -14.761  50.162  1.00 77.51           C  
ANISOU  348  CG  TYR A  42     9563  11209   8677  -3035   -906   3929       C  
ATOM    349  CD1 TYR A  42     -12.381 -15.316  50.509  1.00 83.19           C  
ANISOU  349  CD1 TYR A  42    10042  12204   9361  -3265   -813   4317       C  
ATOM    350  CD2 TYR A  42     -10.677 -13.696  50.929  1.00 77.73           C  
ANISOU  350  CD2 TYR A  42     9656  11591   8288  -2852   -763   3666       C  
ATOM    351  CE1 TYR A  42     -13.121 -14.822  51.587  1.00 87.54           C  
ANISOU  351  CE1 TYR A  42    10403  13423   9435  -3274   -543   4451       C  
ATOM    352  CE2 TYR A  42     -11.415 -13.185  51.998  1.00 81.52           C  
ANISOU  352  CE2 TYR A  42     9989  12698   8285  -2846   -518   3736       C  
ATOM    353  CZ  TYR A  42     -12.628 -13.762  52.333  1.00 91.72           C  
ANISOU  353  CZ  TYR A  42    11026  14312   9513  -3041   -389   4139       C  
ATOM    354  OH  TYR A  42     -13.349 -13.267  53.391  1.00 96.55           O  
ANISOU  354  OH  TYR A  42    11460  15612   9611  -3005   -110   4210       O  
ATOM    355  N   ASP A  43      -9.635 -12.502  47.713  1.00 65.93           N  
ANISOU  355  N   ASP A  43     8451   9025   7575  -2430   -862   2728       N  
ATOM    356  CA  ASP A  43      -9.522 -11.045  47.750  1.00 64.75           C  
ANISOU  356  CA  ASP A  43     8356   9010   7238  -2215   -674   2338       C  
ATOM    357  C   ASP A  43     -10.178 -10.415  46.524  1.00 66.82           C  
ANISOU  357  C   ASP A  43     8595   9103   7692  -2069   -568   2120       C  
ATOM    358  O   ASP A  43     -10.964  -9.478  46.683  1.00 68.81           O  
ANISOU  358  O   ASP A  43     8779   9580   7785  -1927   -363   1956       O  
ATOM    359  CB  ASP A  43      -8.049 -10.605  47.855  1.00 65.24           C  
ANISOU  359  CB  ASP A  43     8585   8900   7304  -2138   -783   2126       C  
ATOM    360  CG  ASP A  43      -7.327 -11.005  49.125  1.00 74.39           C  
ANISOU  360  CG  ASP A  43     9762  10291   8213  -2242   -905   2302       C  
ATOM    361  OD1 ASP A  43      -7.934 -11.696  49.959  1.00 77.10           O  
ANISOU  361  OD1 ASP A  43    10006  10936   8352  -2379   -894   2632       O  
ATOM    362  OD2 ASP A  43      -6.141 -10.643  49.270  1.00 80.44           O1-
ANISOU  362  OD2 ASP A  43    10620  10960   8984  -2198  -1022   2141       O1-
ATOM    363  N   ALA A  44      -9.872 -10.937  45.309  1.00 58.98           N  
ANISOU  363  N   ALA A  44     7653   7735   7022  -2079   -713   2116       N  
ATOM    364  CA  ALA A  44     -10.441 -10.444  44.047  1.00 55.69           C  
ANISOU  364  CA  ALA A  44     7219   7180   6762  -1948   -657   1951       C  
ATOM    365  C   ALA A  44     -11.966 -10.584  44.055  1.00 59.16           C  
ANISOU  365  C   ALA A  44     7437   7882   7160  -2004   -570   2098       C  
ATOM    366  O   ALA A  44     -12.648  -9.609  43.779  1.00 58.54           O  
ANISOU  366  O   ALA A  44     7288   7932   7022  -1825   -411   1950       O  
ATOM    367  CB  ALA A  44      -9.850 -11.197  42.865  1.00 54.76           C  
ANISOU  367  CB  ALA A  44     7195   6688   6923  -1961   -847   1927       C  
ATOM    368  N   ALA A  45     -12.499 -11.764  44.455  1.00 56.92           N  
ANISOU  368  N   ALA A  45     7021   7686   6920  -2255   -675   2418       N  
ATOM    369  CA  ALA A  45     -13.943 -12.006  44.524  1.00 58.37           C  
ANISOU  369  CA  ALA A  45     6930   8161   7089  -2372   -606   2618       C  
ATOM    370  C   ALA A  45     -14.651 -11.046  45.479  1.00 62.54           C  
ANISOU  370  C   ALA A  45     7292   9180   7289  -2237   -316   2590       C  
ATOM    371  O   ALA A  45     -15.798 -10.667  45.214  1.00 62.32           O  
ANISOU  371  O   ALA A  45     7031   9399   7250  -2165   -190   2599       O  
ATOM    372  CB  ALA A  45     -14.219 -13.443  44.920  1.00 61.51           C  
ANISOU  372  CB  ALA A  45     7230   8522   7621  -2717   -783   3010       C  
ATOM    373  N   LYS A  46     -13.945 -10.620  46.563  1.00 59.57           N  
ANISOU  373  N   LYS A  46     7034   8960   6639  -2174   -219   2524       N  
ATOM    374  CA  LYS A  46     -14.459  -9.707  47.594  1.00 61.68           C  
ANISOU  374  CA  LYS A  46     7198   9699   6538  -2009     53   2416       C  
ATOM    375  C   LYS A  46     -14.725  -8.288  47.044  1.00 63.17           C  
ANISOU  375  C   LYS A  46     7426   9835   6742  -1661    216   2022       C  
ATOM    376  O   LYS A  46     -15.571  -7.573  47.580  1.00 65.27           O  
ANISOU  376  O   LYS A  46     7527  10476   6797  -1475    453   1928       O  
ATOM    377  CB  LYS A  46     -13.528  -9.697  48.824  1.00 65.17           C  
ANISOU  377  CB  LYS A  46     7798  10287   6676  -2044     45   2400       C  
ATOM    378  CG  LYS A  46     -14.160  -9.109  50.091  1.00 89.01           C  
ANISOU  378  CG  LYS A  46    10686  13906   9227  -1935    310   2356       C  
ATOM    379  CD  LYS A  46     -13.358  -9.417  51.362  1.00101.04           C  
ANISOU  379  CD  LYS A  46    12311  15681  10400  -2063    248   2490       C  
ATOM    380  CE  LYS A  46     -14.147  -9.056  52.599  1.00112.99           C  
ANISOU  380  CE  LYS A  46    13660  17887  11383  -1970    526   2490       C  
ATOM    381  NZ  LYS A  46     -13.666  -9.784  53.800  1.00122.60           N1+
ANISOU  381  NZ  LYS A  46    14889  19464  12231  -2177    452   2828       N1+
ATOM    382  N   ARG A  47     -14.026  -7.906  45.967  1.00 56.25           N  
ANISOU  382  N   ARG A  47     6751   8499   6122  -1561     94   1818       N  
ATOM    383  CA  ARG A  47     -14.156  -6.606  45.301  1.00 55.63           C  
ANISOU  383  CA  ARG A  47     6743   8270   6125  -1255    205   1515       C  
ATOM    384  C   ARG A  47     -15.538  -6.445  44.666  1.00 62.28           C  
ANISOU  384  C   ARG A  47     7319   9290   7053  -1136    290   1602       C  
ATOM    385  O   ARG A  47     -16.030  -5.316  44.543  1.00 63.20           O  
ANISOU  385  O   ARG A  47     7401   9460   7151   -832    452   1405       O  
ATOM    386  CB  ARG A  47     -13.079  -6.435  44.207  1.00 51.46           C  
ANISOU  386  CB  ARG A  47     6455   7250   5846  -1233     49   1389       C  
ATOM    387  CG  ARG A  47     -11.632  -6.462  44.693  1.00 58.64           C  
ANISOU  387  CG  ARG A  47     7585   7975   6720  -1329    -48   1289       C  
ATOM    388  CD  ARG A  47     -11.284  -5.287  45.578  1.00 61.65           C  
ANISOU  388  CD  ARG A  47     8087   8407   6930  -1177     78    993       C  
ATOM    389  NE  ARG A  47      -9.847  -5.212  45.809  1.00 63.53           N  
ANISOU  389  NE  ARG A  47     8511   8427   7201  -1280    -58    885       N  
ATOM    390  CZ  ARG A  47      -9.227  -4.171  46.347  1.00 76.91           C  
ANISOU  390  CZ  ARG A  47    10352  10044   8828  -1206    -29    591       C  
ATOM    391  NH1 ARG A  47      -9.918  -3.105  46.735  1.00 62.84           N1+
ANISOU  391  NH1 ARG A  47     8589   8347   6940   -995    139    341       N1+
ATOM    392  NH2 ARG A  47      -7.913  -4.183  46.501  1.00 66.68           N  
ANISOU  392  NH2 ARG A  47     9170   8576   7589  -1336   -181    528       N  
ATOM    393  N   GLY A  48     -16.115  -7.576  44.252  1.00 58.74           N  
ANISOU  393  N   GLY A  48     6688   8903   6730  -1375    153   1890       N  
ATOM    394  CA  GLY A  48     -17.414  -7.670  43.604  1.00 60.25           C  
ANISOU  394  CA  GLY A  48     6576   9291   7026  -1344    162   2020       C  
ATOM    395  C   GLY A  48     -17.387  -8.521  42.343  1.00 61.81           C  
ANISOU  395  C   GLY A  48     6786   9211   7486  -1530   -114   2126       C  
ATOM    396  O   GLY A  48     -16.387  -9.196  42.064  1.00 59.97           O  
ANISOU  396  O   GLY A  48     6785   8647   7354  -1692   -296   2122       O  
ATOM    397  N   PRO A  49     -18.474  -8.478  41.540  1.00 57.38           N  
ANISOU  397  N   PRO A  49     5973   8795   7033  -1483   -162   2195       N  
ATOM    398  CA  PRO A  49     -18.532  -9.289  40.311  1.00 56.55           C  
ANISOU  398  CA  PRO A  49     5882   8466   7138  -1659   -456   2243       C  
ATOM    399  C   PRO A  49     -17.372  -9.136  39.322  1.00 58.52           C  
ANISOU  399  C   PRO A  49     6490   8285   7460  -1556   -588   2033       C  
ATOM    400  O   PRO A  49     -16.970 -10.120  38.701  1.00 57.30           O  
ANISOU  400  O   PRO A  49     6443   7894   7433  -1754   -825   2037       O  
ATOM    401  CB  PRO A  49     -19.864  -8.881  39.695  1.00 60.66           C  
ANISOU  401  CB  PRO A  49     6063   9287   7699  -1533   -454   2303       C  
ATOM    402  CG  PRO A  49     -20.682  -8.467  40.848  1.00 67.44           C  
ANISOU  402  CG  PRO A  49     6626  10590   8408  -1441   -177   2408       C  
ATOM    403  CD  PRO A  49     -19.742  -7.757  41.752  1.00 61.42           C  
ANISOU  403  CD  PRO A  49     6146   9721   7470  -1261     32   2224       C  
ATOM    404  N   GLY A  50     -16.849  -7.923  39.181  1.00 54.30           N  
ANISOU  404  N   GLY A  50     6126   7650   6855  -1251   -434   1854       N  
ATOM    405  CA  GLY A  50     -15.711  -7.652  38.310  1.00 52.07           C  
ANISOU  405  CA  GLY A  50     6145   7019   6619  -1152   -503   1699       C  
ATOM    406  C   GLY A  50     -14.469  -8.386  38.780  1.00 53.81           C  
ANISOU  406  C   GLY A  50     6578   7006   6862  -1333   -569   1667       C  
ATOM    407  O   GLY A  50     -13.704  -8.907  37.963  1.00 50.38           O  
ANISOU  407  O   GLY A  50     6303   6334   6507  -1375   -717   1601       O  
ATOM    408  N   GLY A  51     -14.319  -8.469  40.107  1.00 51.72           N  
ANISOU  408  N   GLY A  51     6291   6854   6506  -1422   -465   1718       N  
ATOM    409  CA  GLY A  51     -13.233  -9.179  40.772  1.00 50.51           C  
ANISOU  409  CA  GLY A  51     6291   6543   6356  -1588   -539   1742       C  
ATOM    410  C   GLY A  51     -13.320 -10.674  40.541  1.00 55.00           C  
ANISOU  410  C   GLY A  51     6825   6999   7074  -1850   -772   1907       C  
ATOM    411  O   GLY A  51     -12.293 -11.304  40.275  1.00 54.77           O  
ANISOU  411  O   GLY A  51     6969   6691   7150  -1901   -910   1864       O  
ATOM    412  N   VAL A  52     -14.551 -11.246  40.612  1.00 51.04           N  
ANISOU  412  N   VAL A  52     6083   6698   6613  -2015   -826   2092       N  
ATOM    413  CA  VAL A  52     -14.820 -12.673  40.366  1.00 52.83           C  
ANISOU  413  CA  VAL A  52     6257   6775   7042  -2311  -1080   2260       C  
ATOM    414  C   VAL A  52     -14.378 -13.017  38.925  1.00 57.49           C  
ANISOU  414  C   VAL A  52     7015   7042   7785  -2246  -1288   2041       C  
ATOM    415  O   VAL A  52     -13.652 -13.990  38.704  1.00 57.36           O  
ANISOU  415  O   VAL A  52     7158   6703   7932  -2350  -1483   2012       O  
ATOM    416  CB  VAL A  52     -16.331 -13.027  40.599  1.00 59.28           C  
ANISOU  416  CB  VAL A  52     6724   7913   7886  -2514  -1085   2500       C  
ATOM    417  CG1 VAL A  52     -16.682 -14.413  40.051  1.00 60.74           C  
ANISOU  417  CG1 VAL A  52     6864   7865   8351  -2846  -1401   2632       C  
ATOM    418  CG2 VAL A  52     -16.710 -12.916  42.073  1.00 60.72           C  
ANISOU  418  CG2 VAL A  52     6727   8472   7873  -2589   -863   2741       C  
ATOM    419  N   TRP A  53     -14.829 -12.199  37.961  1.00 53.64           N  
ANISOU  419  N   TRP A  53     6490   6665   7228  -2042  -1243   1889       N  
ATOM    420  CA  TRP A  53     -14.537 -12.319  36.539  1.00 52.11           C  
ANISOU  420  CA  TRP A  53     6432   6297   7072  -1933  -1400   1679       C  
ATOM    421  C   TRP A  53     -13.018 -12.255  36.277  1.00 52.31           C  
ANISOU  421  C   TRP A  53     6736   6054   7087  -1784  -1367   1508       C  
ATOM    422  O   TRP A  53     -12.475 -13.139  35.613  1.00 51.62           O  
ANISOU  422  O   TRP A  53     6784   5729   7099  -1814  -1552   1374       O  
ATOM    423  CB  TRP A  53     -15.309 -11.226  35.780  1.00 50.94           C  
ANISOU  423  CB  TRP A  53     6165   6397   6793  -1712  -1312   1635       C  
ATOM    424  CG  TRP A  53     -14.989 -11.130  34.323  1.00 51.43           C  
ANISOU  424  CG  TRP A  53     6372   6375   6796  -1556  -1432   1448       C  
ATOM    425  CD1 TRP A  53     -15.411 -11.965  33.334  1.00 56.15           C  
ANISOU  425  CD1 TRP A  53     6959   6947   7429  -1658  -1708   1341       C  
ATOM    426  CD2 TRP A  53     -14.166 -10.143  33.697  1.00 49.84           C  
ANISOU  426  CD2 TRP A  53     6341   6132   6462  -1281  -1281   1352       C  
ATOM    427  CE2 TRP A  53     -14.123 -10.449  32.319  1.00 55.73           C  
ANISOU  427  CE2 TRP A  53     7170   6884   7121  -1208  -1451   1212       C  
ATOM    428  CE3 TRP A  53     -13.461  -9.020  34.166  1.00 49.36           C  
ANISOU  428  CE3 TRP A  53     6372   6030   6351  -1108  -1028   1374       C  
ATOM    429  NE1 TRP A  53     -14.894 -11.568  32.127  1.00 55.80           N  
ANISOU  429  NE1 TRP A  53     7077   6900   7226  -1433  -1723   1171       N  
ATOM    430  CZ2 TRP A  53     -13.437  -9.646  31.396  1.00 54.98           C  
ANISOU  430  CZ2 TRP A  53     7221   6806   6861   -964  -1342   1154       C  
ATOM    431  CZ3 TRP A  53     -12.739  -8.258  33.264  1.00 50.60           C  
ANISOU  431  CZ3 TRP A  53     6677   6131   6415   -902   -943   1318       C  
ATOM    432  CH2 TRP A  53     -12.737  -8.563  31.896  1.00 52.78           C  
ANISOU  432  CH2 TRP A  53     7011   6463   6580   -829  -1081   1239       C  
ATOM    433  N   ALA A  54     -12.339 -11.237  36.835  1.00 48.11           N  
ANISOU  433  N   ALA A  54     6270   5562   6447  -1628  -1139   1498       N  
ATOM    434  CA  ALA A  54     -10.888 -11.031  36.713  1.00 46.25           C  
ANISOU  434  CA  ALA A  54     6231   5133   6210  -1508  -1081   1375       C  
ATOM    435  C   ALA A  54     -10.083 -12.188  37.328  1.00 52.40           C  
ANISOU  435  C   ALA A  54     7085   5700   7124  -1651  -1219   1412       C  
ATOM    436  O   ALA A  54      -9.142 -12.659  36.691  1.00 53.77           O  
ANISOU  436  O   ALA A  54     7384   5677   7370  -1567  -1297   1276       O  
ATOM    437  CB  ALA A  54     -10.485  -9.708  37.338  1.00 45.41           C  
ANISOU  437  CB  ALA A  54     6145   5106   6001  -1381   -849   1371       C  
ATOM    438  N   ALA A  55     -10.489 -12.692  38.517  1.00 48.89           N  
ANISOU  438  N   ALA A  55     6550   5316   6710  -1848  -1250   1616       N  
ATOM    439  CA  ALA A  55      -9.840 -13.835  39.183  1.00 49.17           C  
ANISOU  439  CA  ALA A  55     6646   5146   6891  -1992  -1407   1736       C  
ATOM    440  C   ALA A  55      -9.898 -15.089  38.314  1.00 54.52           C  
ANISOU  440  C   ALA A  55     7393   5524   7799  -2063  -1666   1666       C  
ATOM    441  O   ALA A  55      -8.889 -15.785  38.190  1.00 55.88           O  
ANISOU  441  O   ALA A  55     7694   5421   8115  -2000  -1783   1596       O  
ATOM    442  CB  ALA A  55     -10.480 -14.108  40.531  1.00 51.17           C  
ANISOU  442  CB  ALA A  55     6766   5590   7088  -2206  -1383   2032       C  
ATOM    443  N   GLU A  56     -11.066 -15.355  37.692  1.00 49.87           N  
ANISOU  443  N   GLU A  56     6709   4987   7253  -2175  -1770   1655       N  
ATOM    444  CA  GLU A  56     -11.291 -16.504  36.824  1.00 50.59           C  
ANISOU  444  CA  GLU A  56     6870   4790   7561  -2272  -2055   1529       C  
ATOM    445  C   GLU A  56     -10.517 -16.363  35.517  1.00 51.59           C  
ANISOU  445  C   GLU A  56     7170   4804   7629  -1995  -2074   1170       C  
ATOM    446  O   GLU A  56      -9.914 -17.333  35.061  1.00 53.81           O  
ANISOU  446  O   GLU A  56     7601   4760   8086  -1955  -2260    999       O  
ATOM    447  CB  GLU A  56     -12.782 -16.689  36.564  1.00 53.90           C  
ANISOU  447  CB  GLU A  56     7096   5368   8016  -2493  -2168   1616       C  
ATOM    448  CG  GLU A  56     -13.102 -17.931  35.751  1.00 65.55           C  
ANISOU  448  CG  GLU A  56     8638   6509   9759  -2676  -2521   1488       C  
ATOM    449  CD  GLU A  56     -14.570 -18.268  35.604  1.00 83.48           C  
ANISOU  449  CD  GLU A  56    10673   8929  12117  -2969  -2685   1602       C  
ATOM    450  OE1 GLU A  56     -15.432 -17.417  35.933  1.00 73.80           O  
ANISOU  450  OE1 GLU A  56     9198   8126  10715  -2979  -2501   1772       O  
ATOM    451  OE2 GLU A  56     -14.855 -19.409  35.175  1.00 81.72           O1-
ANISOU  451  OE2 GLU A  56    10503   8384  12163  -3187  -3014   1509       O1-
ATOM    452  N   ALA A  57     -10.518 -15.162  34.928  1.00 43.45           N  
ANISOU  452  N   ALA A  57     6117   4042   6351  -1790  -1873   1069       N  
ATOM    453  CA  ALA A  57      -9.781 -14.901  33.705  1.00 42.63           C  
ANISOU  453  CA  ALA A  57     6145   3931   6120  -1527  -1836    793       C  
ATOM    454  C   ALA A  57      -8.286 -15.140  33.965  1.00 49.39           C  
ANISOU  454  C   ALA A  57     7117   4601   7049  -1380  -1768    724       C  
ATOM    455  O   ALA A  57      -7.669 -15.923  33.241  1.00 53.53           O  
ANISOU  455  O   ALA A  57     7760   4942   7637  -1248  -1882    488       O  
ATOM    456  CB  ALA A  57     -10.042 -13.478  33.220  1.00 41.18           C  
ANISOU  456  CB  ALA A  57     5901   4062   5685  -1366  -1615    818       C  
ATOM    457  N   ILE A  58      -7.745 -14.566  35.057  1.00 43.29           N  
ANISOU  457  N   ILE A  58     6294   3881   6273  -1403  -1607    914       N  
ATOM    458  CA  ILE A  58      -6.343 -14.738  35.460  1.00 43.21           C  
ANISOU  458  CA  ILE A  58     6331   3746   6341  -1288  -1559    897       C  
ATOM    459  C   ILE A  58      -5.982 -16.198  35.822  1.00 52.04           C  
ANISOU  459  C   ILE A  58     7517   4528   7729  -1344  -1802    908       C  
ATOM    460  O   ILE A  58      -4.951 -16.685  35.358  1.00 54.38           O  
ANISOU  460  O   ILE A  58     7879   4666   8116  -1143  -1837    736       O  
ATOM    461  CB  ILE A  58      -5.925 -13.693  36.532  1.00 43.23           C  
ANISOU  461  CB  ILE A  58     6257   3918   6250  -1325  -1368   1070       C  
ATOM    462  CG1 ILE A  58      -5.955 -12.263  35.915  1.00 41.02           C  
ANISOU  462  CG1 ILE A  58     5957   3851   5779  -1207  -1141   1013       C  
ATOM    463  CG2 ILE A  58      -4.532 -14.011  37.129  1.00 41.85           C  
ANISOU  463  CG2 ILE A  58     6085   3637   6181  -1258  -1384   1094       C  
ATOM    464  CD1 ILE A  58      -6.164 -11.165  36.932  1.00 46.38           C  
ANISOU  464  CD1 ILE A  58     6578   4674   6372  -1284   -993   1140       C  
ATOM    465  N   SER A  59      -6.827 -16.886  36.622  1.00 49.73           N  
ANISOU  465  N   SER A  59     7192   4127   7575  -1602  -1963   1127       N  
ATOM    466  CA  SER A  59      -6.599 -18.280  37.026  1.00 52.67           C  
ANISOU  466  CA  SER A  59     7638   4120   8254  -1691  -2220   1212       C  
ATOM    467  C   SER A  59      -6.576 -19.235  35.829  1.00 60.15           C  
ANISOU  467  C   SER A  59     8729   4747   9380  -1580  -2430    887       C  
ATOM    468  O   SER A  59      -5.683 -20.078  35.763  1.00 62.98           O  
ANISOU  468  O   SER A  59     9189   4780   9959  -1426  -2561    788       O  
ATOM    469  CB  SER A  59      -7.636 -18.749  38.044  1.00 56.26           C  
ANISOU  469  CB  SER A  59     8007   4565   8805  -2034  -2330   1570       C  
ATOM    470  OG  SER A  59      -7.558 -17.989  39.238  1.00 66.19           O  
ANISOU  470  OG  SER A  59     9155   6121   9872  -2103  -2152   1840       O  
ATOM    471  N   ASP A  60      -7.538 -19.098  34.886  1.00 55.58           N  
ANISOU  471  N   ASP A  60     8153   4268   8696  -1631  -2477    698       N  
ATOM    472  CA  ASP A  60      -7.601 -19.936  33.691  1.00 57.97           C  
ANISOU  472  CA  ASP A  60     8605   4320   9102  -1530  -2696    318       C  
ATOM    473  C   ASP A  60      -6.358 -19.749  32.814  1.00 62.32           C  
ANISOU  473  C   ASP A  60     9251   4916   9513  -1126  -2560    -19       C  
ATOM    474  O   ASP A  60      -5.780 -20.753  32.377  1.00 66.43           O  
ANISOU  474  O   ASP A  60     9915   5097  10229   -955  -2729   -290       O  
ATOM    475  CB  ASP A  60      -8.883 -19.672  32.875  1.00 60.43           C  
ANISOU  475  CB  ASP A  60     8863   4833   9264  -1678  -2782    205       C  
ATOM    476  CG  ASP A  60     -10.181 -20.139  33.514  1.00 76.05           C  
ANISOU  476  CG  ASP A  60    10717   6735  11444  -2091  -2975    483       C  
ATOM    477  OD1 ASP A  60     -10.140 -21.096  34.330  1.00 81.01           O  
ANISOU  477  OD1 ASP A  60    11380   6996  12406  -2286  -3151    681       O  
ATOM    478  OD2 ASP A  60     -11.240 -19.583  33.167  1.00 79.89           O1-
ANISOU  478  OD2 ASP A  60    11054   7533  11769  -2218  -2959    526       O1-
ATOM    479  N   ALA A  61      -5.925 -18.480  32.586  1.00 53.27           N  
ANISOU  479  N   ALA A  61     8014   4176   8051   -969  -2251     11       N  
ATOM    480  CA  ALA A  61      -4.735 -18.183  31.774  1.00 53.14           C  
ANISOU  480  CA  ALA A  61     8024   4295   7870   -616  -2067   -228       C  
ATOM    481  C   ALA A  61      -3.452 -18.750  32.393  1.00 58.69           C  
ANISOU  481  C   ALA A  61     8719   4775   8807   -455  -2064   -199       C  
ATOM    482  O   ALA A  61      -2.630 -19.327  31.672  1.00 62.09           O  
ANISOU  482  O   ALA A  61     9212   5107   9272   -155  -2075   -499       O  
ATOM    483  CB  ALA A  61      -4.596 -16.686  31.543  1.00 50.90           C  
ANISOU  483  CB  ALA A  61     7626   4444   7271   -565  -1755    -97       C  
ATOM    484  N   ARG A  62      -3.313 -18.634  33.729  1.00 51.60           N  
ANISOU  484  N   ARG A  62     7734   3819   8055   -633  -2065    152       N  
ATOM    485  CA  ARG A  62      -2.164 -19.124  34.485  1.00 51.89           C  
ANISOU  485  CA  ARG A  62     7728   3678   8310   -510  -2102    261       C  
ATOM    486  C   ARG A  62      -2.049 -20.644  34.359  1.00 58.24           C  
ANISOU  486  C   ARG A  62     8678   3984   9467   -417  -2400    114       C  
ATOM    487  O   ARG A  62      -0.975 -21.170  34.072  1.00 59.91           O  
ANISOU  487  O   ARG A  62     8895   4050   9818   -100  -2413    -62       O  
ATOM    488  CB  ARG A  62      -2.308 -18.717  35.951  1.00 52.57           C  
ANISOU  488  CB  ARG A  62     7711   3850   8412   -765  -2088    673       C  
ATOM    489  CG  ARG A  62      -0.994 -18.730  36.737  1.00 65.35           C  
ANISOU  489  CG  ARG A  62     9221   5478  10129   -632  -2065    816       C  
ATOM    490  CD  ARG A  62      -1.038 -19.624  37.962  1.00 78.59           C  
ANISOU  490  CD  ARG A  62    10919   6893  12050   -777  -2307   1134       C  
ATOM    491  NE  ARG A  62      -2.263 -19.441  38.739  1.00 88.28           N  
ANISOU  491  NE  ARG A  62    12152   8208  13182  -1133  -2339   1415       N  
ATOM    492  CZ  ARG A  62      -3.176 -20.384  38.933  1.00106.73           C  
ANISOU  492  CZ  ARG A  62    14577  10270  15707  -1340  -2546   1549       C  
ATOM    493  NH1 ARG A  62      -3.002 -21.600  38.432  1.00100.09           N1+
ANISOU  493  NH1 ARG A  62    13869   8971  15191  -1235  -2777   1402       N1+
ATOM    494  NH2 ARG A  62      -4.267 -20.121  39.631  1.00 92.62           N  
ANISOU  494  NH2 ARG A  62    12733   8660  13797  -1654  -2524   1823       N  
ATOM    495  N   GLU A  63      -3.176 -21.339  34.546  1.00 55.64           N  
ANISOU  495  N   GLU A  63     8453   3384   9303   -691  -2642    183       N  
ATOM    496  CA  GLU A  63      -3.310 -22.782  34.449  1.00 59.06           C  
ANISOU  496  CA  GLU A  63     9057   3254  10130   -695  -2978     66       C  
ATOM    497  C   GLU A  63      -2.907 -23.267  33.044  1.00 66.55           C  
ANISOU  497  C   GLU A  63    10150   4069  11068   -336  -3022   -503       C  
ATOM    498  O   GLU A  63      -2.195 -24.272  32.926  1.00 70.98           O  
ANISOU  498  O   GLU A  63    10821   4211  11937    -83  -3185   -689       O  
ATOM    499  CB  GLU A  63      -4.765 -23.144  34.777  1.00 60.90           C  
ANISOU  499  CB  GLU A  63     9319   3350  10470  -1132  -3181    254       C  
ATOM    500  CG  GLU A  63      -5.148 -24.610  34.678  1.00 68.07           C  
ANISOU  500  CG  GLU A  63    10403   3618  11844  -1261  -3571    197       C  
ATOM    501  CD  GLU A  63      -6.647 -24.783  34.525  1.00 89.96           C  
ANISOU  501  CD  GLU A  63    13165   6351  14665  -1682  -3754    254       C  
ATOM    502  OE1 GLU A  63      -7.065 -25.694  33.774  1.00 82.35           O  
ANISOU  502  OE1 GLU A  63    12369   4970  13951  -1726  -4053    -71       O  
ATOM    503  OE2 GLU A  63      -7.408 -23.994  35.133  1.00 86.48           O1-
ANISOU  503  OE2 GLU A  63    12536   6309  14015  -1961  -3604    599       O1-
ATOM    504  N   ASN A  64      -3.348 -22.544  31.994  1.00 61.61           N  
ANISOU  504  N   ASN A  64     9522   3818  10070   -285  -2873   -774       N  
ATOM    505  CA  ASN A  64      -3.060 -22.875  30.595  1.00 65.27           C  
ANISOU  505  CA  ASN A  64    10116   4294  10391     53  -2884  -1328       C  
ATOM    506  C   ASN A  64      -1.604 -22.642  30.188  1.00 69.60           C  
ANISOU  506  C   ASN A  64    10582   5053  10811    512  -2620  -1503       C  
ATOM    507  O   ASN A  64      -1.043 -23.446  29.431  1.00 72.95           O  
ANISOU  507  O   ASN A  64    11125   5279  11313    867  -2694  -1940       O  
ATOM    508  CB  ASN A  64      -4.034 -22.169  29.650  1.00 68.30           C  
ANISOU  508  CB  ASN A  64    10508   5065  10378    -57  -2832  -1491       C  
ATOM    509  CG  ASN A  64      -5.354 -22.892  29.522  1.00 90.83           C  
ANISOU  509  CG  ASN A  64    13479   7622  13410   -384  -3194  -1580       C  
ATOM    510  ND2 ASN A  64      -6.358 -22.454  30.271  1.00 73.71           N  
ANISOU  510  ND2 ASN A  64    11183   5546  11279   -787  -3224  -1169       N  
ATOM    511  OD1 ASN A  64      -5.475 -23.876  28.782  1.00 99.63           O  
ANISOU  511  OD1 ASN A  64    14789   8416  14649   -283  -3459  -2028       O  
ATOM    512  N   ILE A  65      -0.996 -21.555  30.693  1.00 63.65           N  
ANISOU  512  N   ILE A  65     9611   4703   9871    506  -2316  -1182       N  
ATOM    513  CA  ILE A  65       0.400 -21.222  30.419  1.00 64.64           C  
ANISOU  513  CA  ILE A  65     9578   5092   9892    876  -2048  -1261       C  
ATOM    514  C   ILE A  65       1.329 -22.265  31.078  1.00 72.33           C  
ANISOU  514  C   ILE A  65    10537   5657  11287   1104  -2202  -1257       C  
ATOM    515  O   ILE A  65       2.214 -22.811  30.404  1.00 74.71           O  
ANISOU  515  O   ILE A  65    10823   5943  11619   1535  -2140  -1597       O  
ATOM    516  CB  ILE A  65       0.747 -19.725  30.695  1.00 63.90           C  
ANISOU  516  CB  ILE A  65     9255   5509   9515    759  -1715   -931       C  
ATOM    517  CG1 ILE A  65       2.065 -19.300  30.022  1.00 66.00           C  
ANISOU  517  CG1 ILE A  65     9335   6150   9591   1117  -1406  -1067       C  
ATOM    518  CG2 ILE A  65       0.740 -19.362  32.181  1.00 61.87           C  
ANISOU  518  CG2 ILE A  65     8887   5177   9444    472  -1758   -476       C  
ATOM    519  CD1 ILE A  65       2.214 -17.771  29.849  1.00 70.50           C  
ANISOU  519  CD1 ILE A  65     9731   7222   9835    982  -1083   -820       C  
ATOM    520  N   GLN A  66       1.026 -22.633  32.351  1.00 69.27           N  
ANISOU  520  N   GLN A  66    10165   4935  11220    833  -2421   -882       N  
ATOM    521  CA  GLN A  66       1.764 -23.654  33.122  1.00 72.36           C  
ANISOU  521  CA  GLN A  66    10554   4894  12044   1005  -2625   -770       C  
ATOM    522  C   GLN A  66       1.690 -25.016  32.420  1.00 79.94           C  
ANISOU  522  C   GLN A  66    11760   5300  13313   1264  -2893  -1202       C  
ATOM    523  O   GLN A  66       2.697 -25.723  32.329  1.00 82.20           O  
ANISOU  523  O   GLN A  66    12023   5365  13845   1683  -2934  -1377       O  
ATOM    524  CB  GLN A  66       1.247 -23.752  34.577  1.00 72.28           C  
ANISOU  524  CB  GLN A  66    10532   4696  12236    607  -2810   -228       C  
ATOM    525  CG  GLN A  66       1.671 -22.585  35.500  1.00 78.10           C  
ANISOU  525  CG  GLN A  66    11025   5907  12741    447  -2594    162       C  
ATOM    526  CD  GLN A  66       1.384 -22.888  36.963  1.00 94.65           C  
ANISOU  526  CD  GLN A  66    13113   7836  15015    149  -2793    661       C  
ATOM    527  NE2 GLN A  66       2.271 -23.641  37.615  1.00 92.89           N  
ANISOU  527  NE2 GLN A  66    12828   7389  15078    341  -2953    843       N  
ATOM    528  OE1 GLN A  66       0.355 -22.489  37.519  1.00 82.68           O  
ANISOU  528  OE1 GLN A  66    11632   6410  13373   -235  -2809    901       O  
ATOM    529  N   ARG A  67       0.508 -25.345  31.876  1.00 76.97           N  
ANISOU  529  N   ARG A  67    11605   4713  12926   1029  -3080  -1405       N  
ATOM    530  CA  ARG A  67       0.267 -26.583  31.142  1.00 82.36           C  
ANISOU  530  CA  ARG A  67    12562   4835  13895   1201  -3381  -1879       C  
ATOM    531  C   ARG A  67       1.161 -26.693  29.895  1.00 90.09           C  
ANISOU  531  C   ARG A  67    13564   5996  14669   1771  -3210  -2494       C  
ATOM    532  O   ARG A  67       1.749 -27.755  29.665  1.00 95.75           O  
ANISOU  532  O   ARG A  67    14421   6233  15726   2142  -3389  -2838       O  
ATOM    533  CB  ARG A  67      -1.216 -26.710  30.762  1.00 80.94           C  
ANISOU  533  CB  ARG A  67    12555   4529  13670    774  -3600  -1966       C  
ATOM    534  CG  ARG A  67      -1.616 -28.136  30.396  1.00 92.51           C  
ANISOU  534  CG  ARG A  67    14321   5247  15583    794  -4028  -2343       C  
ATOM    535  CD  ARG A  67      -3.011 -28.224  29.813  1.00 97.58           C  
ANISOU  535  CD  ARG A  67    15093   5847  16135    394  -4250  -2521       C  
ATOM    536  NE  ARG A  67      -4.040 -28.176  30.852  1.00 99.93           N  
ANISOU  536  NE  ARG A  67    15308   6025  16637   -192  -4396  -1928       N  
ATOM    537  CZ  ARG A  67      -4.803 -27.121  31.108  1.00103.29           C  
ANISOU  537  CZ  ARG A  67    15536   6998  16713   -522  -4207  -1589       C  
ATOM    538  NH1 ARG A  67      -4.682 -26.015  30.385  1.00 89.54           N1+
ANISOU  538  NH1 ARG A  67    13684   5906  14431   -351  -3893  -1759       N1+
ATOM    539  NH2 ARG A  67      -5.714 -27.174  32.066  1.00 84.30           N  
ANISOU  539  NH2 ARG A  67    13037   4495  14499  -1015  -4328  -1073       N  
ATOM    540  N   PHE A  68       1.272 -25.599  29.109  1.00 83.23           N  
ANISOU  540  N   PHE A  68    12554   5821  13249   1854  -2858  -2612       N  
ATOM    541  CA  PHE A  68       2.086 -25.555  27.890  1.00 85.63           C  
ANISOU  541  CA  PHE A  68    12832   6462  13240   2372  -2624  -3137       C  
ATOM    542  C   PHE A  68       3.584 -25.777  28.154  1.00 91.50           C  
ANISOU  542  C   PHE A  68    13362   7242  14163   2848  -2448  -3133       C  
ATOM    543  O   PHE A  68       4.249 -26.455  27.368  1.00 95.36           O  
ANISOU  543  O   PHE A  68    13911   7642  14678   3360  -2428  -3650       O  
ATOM    544  CB  PHE A  68       1.851 -24.238  27.107  1.00 83.32           C  
ANISOU  544  CB  PHE A  68    12408   6934  12316   2288  -2278  -3111       C  
ATOM    545  CG  PHE A  68       2.786 -24.032  25.931  1.00 86.92           C  
ANISOU  545  CG  PHE A  68    12765   7888  12374   2799  -1953  -3519       C  
ATOM    546  CD1 PHE A  68       2.527 -24.628  24.701  1.00 93.38           C  
ANISOU  546  CD1 PHE A  68    13809   8721  12950   3078  -2037  -4156       C  
ATOM    547  CD2 PHE A  68       3.951 -23.283  26.071  1.00 86.52           C  
ANISOU  547  CD2 PHE A  68    12378   8311  12184   2998  -1571  -3273       C  
ATOM    548  CE1 PHE A  68       3.407 -24.463  23.628  1.00 97.28           C  
ANISOU  548  CE1 PHE A  68    14196   9745  13021   3577  -1707  -4528       C  
ATOM    549  CE2 PHE A  68       4.831 -23.122  24.998  1.00 92.05           C  
ANISOU  549  CE2 PHE A  68    12940   9521  12513   3465  -1241  -3606       C  
ATOM    550  CZ  PHE A  68       4.548 -23.704  23.783  1.00 94.79           C  
ANISOU  550  CZ  PHE A  68    13516   9926  12573   3765  -1292  -4224       C  
ATOM    551  N   PHE A  69       4.112 -25.176  29.229  1.00 85.93           N  
ANISOU  551  N   PHE A  69    12387   6708  13552   2697  -2320  -2580       N  
ATOM    552  CA  PHE A  69       5.532 -25.266  29.558  1.00 88.26           C  
ANISOU  552  CA  PHE A  69    12403   7124  14009   3100  -2162  -2501       C  
ATOM    553  C   PHE A  69       6.037 -26.570  30.186  1.00100.26           C  
ANISOU  553  C   PHE A  69    13997   7975  16123   3377  -2475  -2519       C  
ATOM    554  O   PHE A  69       7.208 -26.904  29.996  1.00104.37           O  
ANISOU  554  O   PHE A  69    14323   8571  16761   3892  -2356  -2690       O  
ATOM    555  CB  PHE A  69       6.044 -23.997  30.257  1.00 84.53           C  
ANISOU  555  CB  PHE A  69    11579   7200  13339   2871  -1886  -1984       C  
ATOM    556  CG  PHE A  69       6.121 -22.798  29.337  1.00 82.95           C  
ANISOU  556  CG  PHE A  69    11231   7693  12594   2847  -1492  -2054       C  
ATOM    557  CD1 PHE A  69       7.121 -22.700  28.375  1.00 89.39           C  
ANISOU  557  CD1 PHE A  69    11856   8930  13177   3311  -1186  -2369       C  
ATOM    558  CD2 PHE A  69       5.199 -21.767  29.434  1.00 78.75           C  
ANISOU  558  CD2 PHE A  69    10732   7402  11786   2376  -1419  -1774       C  
ATOM    559  CE1 PHE A  69       7.186 -21.595  27.520  1.00 88.40           C  
ANISOU  559  CE1 PHE A  69    11592   9454  12544   3263   -820  -2356       C  
ATOM    560  CE2 PHE A  69       5.275 -20.657  28.587  1.00 79.66           C  
ANISOU  560  CE2 PHE A  69    10723   8109  11436   2357  -1076  -1780       C  
ATOM    561  CZ  PHE A  69       6.268 -20.577  27.639  1.00 81.41           C  
ANISOU  561  CZ  PHE A  69    10766   8740  11425   2780   -781  -2044       C  
ATOM    562  N   GLY A  70       5.164 -27.307  30.878  1.00 99.58           N  
ANISOU  562  N   GLY A  70    14169   7253  16413   3055  -2865  -2329       N  
ATOM    563  CA  GLY A  70       5.530 -28.597  31.457  1.00105.87           C  
ANISOU  563  CA  GLY A  70    15083   7326  17819   3288  -3207  -2295       C  
ATOM    564  C   GLY A  70       4.971 -28.950  32.822  1.00111.66           C  
ANISOU  564  C   GLY A  70    15890   7616  18922   2838  -3525  -1678       C  
ATOM    565  O   GLY A  70       5.476 -29.883  33.457  1.00115.46           O  
ANISOU  565  O   GLY A  70    16399   7574  19897   3047  -3778  -1503       O  
ATOM    566  N   HIS A  71       3.923 -28.235  33.277  1.00105.25           N  
ANISOU  566  N   HIS A  71    15101   7018  17870   2243  -3513  -1329       N  
ATOM    567  CA  HIS A  71       3.272 -28.477  34.566  1.00105.20           C  
ANISOU  567  CA  HIS A  71    15143   6714  18114   1773  -3765   -716       C  
ATOM    568  C   HIS A  71       2.394 -29.730  34.494  1.00114.28           C  
ANISOU  568  C   HIS A  71    16634   7056  19730   1611  -4177   -809       C  
ATOM    569  O   HIS A  71       1.539 -29.834  33.607  1.00114.46           O  
ANISOU  569  O   HIS A  71    16853   6978  19659   1490  -4235  -1225       O  
ATOM    570  CB  HIS A  71       2.446 -27.253  34.975  1.00100.34           C  
ANISOU  570  CB  HIS A  71    14414   6657  17054   1254  -3568   -386       C  
ATOM    571  CG  HIS A  71       1.980 -27.242  36.395  1.00102.86           C  
ANISOU  571  CG  HIS A  71    14691   6907  17485    821  -3717    273       C  
ATOM    572  CD2 HIS A  71       0.720 -27.191  36.885  1.00103.73           C  
ANISOU  572  CD2 HIS A  71    14897   6927  17587    308  -3840    570       C  
ATOM    573  ND1 HIS A  71       2.874 -27.185  37.452  1.00104.68           N  
ANISOU  573  ND1 HIS A  71    14722   7274  17778    906  -3717    696       N  
ATOM    574  CE1 HIS A  71       2.132 -27.147  38.547  1.00103.10           C  
ANISOU  574  CE1 HIS A  71    14539   7052  17584    458  -3844   1223       C  
ATOM    575  NE2 HIS A  71       0.829 -27.148  38.255  1.00102.84           N  
ANISOU  575  NE2 HIS A  71    14667   6892  17515     90  -3902   1176       N  
ATOM    576  N   GLY A  72       2.639 -30.664  35.421  1.00115.22           N  
ANISOU  576  N   GLY A  72    16813   6611  20355   1606  -4477   -408       N  
ATOM    577  CA  GLY A  72       1.943 -31.944  35.539  1.00120.88           C  
ANISOU  577  CA  GLY A  72    17840   6452  21635   1431  -4911   -374       C  
ATOM    578  C   GLY A  72       0.435 -31.827  35.628  1.00123.71           C  
ANISOU  578  C   GLY A  72    18318   6767  21917    777  -5026   -213       C  
ATOM    579  O   GLY A  72      -0.079 -30.884  36.238  1.00118.08           O  
ANISOU  579  O   GLY A  72    17421   6627  20819    379  -4829    192       O  
ATOM    580  N   ALA A  73      -0.276 -32.775  34.994  1.00126.06           N  
ANISOU  580  N   ALA A  73    18913   6390  22592    677  -5352   -564       N  
ATOM    581  CA  ALA A  73      -1.742 -32.824  34.934  1.00126.17           C  
ANISOU  581  CA  ALA A  73    19027   6292  22618     58  -5523   -476       C  
ATOM    582  C   ALA A  73      -2.407 -32.818  36.318  1.00130.00           C  
ANISOU  582  C   ALA A  73    19395   6761  23237   -515  -5616    394       C  
ATOM    583  O   ALA A  73      -3.271 -31.968  36.565  1.00124.52           O  
ANISOU  583  O   ALA A  73    18540   6606  22166   -954  -5450    642       O  
ATOM    584  CB  ALA A  73      -2.196 -34.030  34.122  1.00134.17           C  
ANISOU  584  CB  ALA A  73    20386   6464  24130     82  -5933  -1005       C  
ATOM    585  N   GLU A  74      -1.972 -33.737  37.223  1.00131.82           N  
ANISOU  585  N   GLU A  74    19690   6420  23976   -473  -5864    872       N  
ATOM    586  CA  GLU A  74      -2.463 -33.873  38.602  1.00131.99           C  
ANISOU  586  CA  GLU A  74    19607   6419  24125   -965  -5963   1759       C  
ATOM    587  C   GLU A  74      -2.171 -32.597  39.419  1.00129.56           C  
ANISOU  587  C   GLU A  74    18979   7052  23196  -1016  -5573   2169       C  
ATOM    588  O   GLU A  74      -3.005 -32.187  40.231  1.00127.53           O  
ANISOU  588  O   GLU A  74    18583   7144  22728  -1515  -5503   2705       O  
ATOM    589  CB  GLU A  74      -1.835 -35.107  39.271  1.00140.36           C  
ANISOU  589  CB  GLU A  74    20821   6660  25851   -791  -6317   2143       C  
ATOM    590  CG  GLU A  74      -2.590 -35.617  40.489  1.00154.47           C  
ANISOU  590  CG  GLU A  74    22582   8211  27900  -1371  -6526   3050       C  
ATOM    591  CD  GLU A  74      -3.837 -36.427  40.192  1.00178.89           C  
ANISOU  591  CD  GLU A  74    25873  10963  31134  -1868  -6457   2995       C  
ATOM    592  OE1 GLU A  74      -4.941 -35.839  40.200  1.00177.58           O  
ANISOU  592  OE1 GLU A  74    25533  11142  30797  -2412  -6534   3179       O  
ATOM    593  OE2 GLU A  74      -3.715 -37.654  39.973  1.00180.23           O1-
ANISOU  593  OE2 GLU A  74    26367  10577  31535  -1711  -6244   2766       O1-
ATOM    594  N   ASP A  75      -1.002 -31.965  39.174  1.00122.74           N  
ANISOU  594  N   ASP A  75    17988   6605  22042   -502  -5321   1889       N  
ATOM    595  CA  ASP A  75      -0.556 -30.733  39.826  1.00116.60           C  
ANISOU  595  CA  ASP A  75    16925   6670  20709   -495  -4977   2157       C  
ATOM    596  C   ASP A  75      -1.463 -29.551  39.486  1.00114.47           C  
ANISOU  596  C   ASP A  75    16539   7058  19896   -816  -4680   2012       C  
ATOM    597  O   ASP A  75      -1.657 -28.680  40.333  1.00109.58           O  
ANISOU  597  O   ASP A  75    15730   7012  18895  -1054  -4481   2405       O  
ATOM    598  CB  ASP A  75       0.897 -30.411  39.436  1.00117.75           C  
ANISOU  598  CB  ASP A  75    16951   7038  20751    118  -4807   1810       C  
ATOM    599  CG  ASP A  75       1.938 -31.415  39.904  1.00131.89           C  
ANISOU  599  CG  ASP A  75    18776   8305  23033    516  -5065   2001       C  
ATOM    600  OD1 ASP A  75       1.717 -32.637  39.720  1.00137.81           O  
ANISOU  600  OD1 ASP A  75    19773   8243  24346    523  -5411   2020       O  
ATOM    601  OD2 ASP A  75       3.005 -30.977  40.388  1.00136.31           O1-
ANISOU  601  OD2 ASP A  75    19109   9242  23442    841  -4934   2101       O1-
ATOM    602  N   SER A  76      -2.021 -29.527  38.252  1.00111.50           N  
ANISOU  602  N   SER A  76    16284   6600  19482   -797  -4666   1437       N  
ATOM    603  CA  SER A  76      -2.935 -28.484  37.769  1.00106.63           C  
ANISOU  603  CA  SER A  76    15572   6544  18399  -1052  -4427   1262       C  
ATOM    604  C   SER A  76      -4.301 -28.583  38.449  1.00110.20           C  
ANISOU  604  C   SER A  76    15978   7008  18886  -1653  -4530   1729       C  
ATOM    605  O   SER A  76      -4.914 -27.557  38.726  1.00105.05           O  
ANISOU  605  O   SER A  76    15145   6958  17809  -1881  -4281   1880       O  
ATOM    606  CB  SER A  76      -3.109 -28.571  36.255  1.00111.94           C  
ANISOU  606  CB  SER A  76    16396   7100  19037   -844  -4448    543       C  
ATOM    607  OG  SER A  76      -1.888 -28.374  35.561  1.00123.77           O  
ANISOU  607  OG  SER A  76    17915   8625  20488   -271  -4327    101       O  
ATOM    608  N   LEU A  77      -4.779 -29.817  38.708  1.00112.75           N  
ANISOU  608  N   LEU A  77    16449   6656  19736  -1902  -4894   1963       N  
ATOM    609  CA  LEU A  77      -6.070 -30.086  39.354  1.00114.13           C  
ANISOU  609  CA  LEU A  77    16552   6785  20028  -2505  -5021   2464       C  
ATOM    610  C   LEU A  77      -6.151 -29.514  40.770  1.00114.81           C  
ANISOU  610  C   LEU A  77    16415   7383  19826  -2732  -4827   3168       C  
ATOM    611  O   LEU A  77      -7.200 -28.988  41.160  1.00112.57           O  
ANISOU  611  O   LEU A  77    15951   7525  19295  -3135  -4696   3455       O  
ATOM    612  CB  LEU A  77      -6.376 -31.595  39.359  1.00121.80           C  
ANISOU  612  CB  LEU A  77    17743   6835  21701  -2709  -5478   2589       C  
ATOM    613  CG  LEU A  77      -6.548 -32.251  37.991  1.00130.04           C  
ANISOU  613  CG  LEU A  77    19035   7324  23051  -2568  -5733   1857       C  
ATOM    614  CD1 LEU A  77      -6.677 -33.754  38.114  1.00138.02           C  
ANISOU  614  CD1 LEU A  77    20292   7326  24824  -2729  -6209   1990       C  
ATOM    615  CD2 LEU A  77      -7.722 -31.654  37.246  1.00131.01           C  
ANISOU  615  CD2 LEU A  77    19057   7840  22880  -2879  -5668   1564       C  
ATOM    616  N   ALA A  78      -5.033 -29.612  41.524  1.00110.74           N  
ANISOU  616  N   ALA A  78    15895   6862  19320  -2447  -4813   3424       N  
ATOM    617  CA  ALA A  78      -4.890 -29.088  42.884  1.00108.36           C  
ANISOU  617  CA  ALA A  78    15405   7074  18693  -2586  -4655   4036       C  
ATOM    618  C   ALA A  78      -4.940 -27.555  42.852  1.00104.11           C  
ANISOU  618  C   ALA A  78    14673   7374  17509  -2534  -4251   3829       C  
ATOM    619  O   ALA A  78      -5.590 -26.943  43.699  1.00102.83           O  
ANISOU  619  O   ALA A  78    14344   7726  17001  -2822  -4082   4218       O  
ATOM    620  CB  ALA A  78      -3.579 -29.572  43.495  1.00111.30           C  
ANISOU  620  CB  ALA A  78    15821   7225  19242  -2232  -4786   4257       C  
ATOM    621  N   ASP A  79      -4.294 -26.945  41.842  1.00 95.97           N  
ANISOU  621  N   ASP A  79    13669   6470  16325  -2166  -4096   3217       N  
ATOM    622  CA  ASP A  79      -4.289 -25.498  41.629  1.00 89.78           C  
ANISOU  622  CA  ASP A  79    12735   6368  15008  -2093  -3738   2978       C  
ATOM    623  C   ASP A  79      -5.719 -25.014  41.301  1.00 90.94           C  
ANISOU  623  C   ASP A  79    12810   6770  14974  -2434  -3631   2936       C  
ATOM    624  O   ASP A  79      -6.133 -23.962  41.785  1.00 87.75           O  
ANISOU  624  O   ASP A  79    12244   6933  14163  -2554  -3376   3062       O  
ATOM    625  CB  ASP A  79      -3.327 -25.125  40.483  1.00 89.58           C  
ANISOU  625  CB  ASP A  79    12757   6352  14928  -1639  -3623   2385       C  
ATOM    626  CG  ASP A  79      -1.853 -25.447  40.707  1.00100.56           C  
ANISOU  626  CG  ASP A  79    14149   7576  16483  -1245  -3690   2370       C  
ATOM    627  OD1 ASP A  79      -1.494 -25.872  41.831  1.00103.62           O  
ANISOU  627  OD1 ASP A  79    14501   7880  16991  -1303  -3832   2842       O  
ATOM    628  OD2 ASP A  79      -1.054 -25.247  39.767  1.00104.85           O1-
ANISOU  628  OD2 ASP A  79    14701   8125  17010   -870  -3591   1910       O1-
ATOM    629  N   GLN A  80      -6.473 -25.816  40.521  1.00 88.46           N  
ANISOU  629  N   GLN A  80    12606   6023  14980  -2582  -3851   2751       N  
ATOM    630  CA  GLN A  80      -7.851 -25.553  40.098  1.00 86.92           C  
ANISOU  630  CA  GLN A  80    12319   6010  14695  -2910  -3827   2698       C  
ATOM    631  C   GLN A  80      -8.850 -25.526  41.253  1.00 91.46           C  
ANISOU  631  C   GLN A  80    12698   6853  15200  -3359  -3786   3307       C  
ATOM    632  O   GLN A  80      -9.700 -24.630  41.307  1.00 88.44           O  
ANISOU  632  O   GLN A  80    12122   6996  14486  -3507  -3564   3336       O  
ATOM    633  CB  GLN A  80      -8.283 -26.553  39.008  1.00 91.47           C  
ANISOU  633  CB  GLN A  80    13071   6004  15679  -2972  -4149   2344       C  
ATOM    634  CG  GLN A  80      -7.729 -26.188  37.636  1.00 94.90           C  
ANISOU  634  CG  GLN A  80    13633   6453  15972  -2563  -4089   1656       C  
ATOM    635  CD  GLN A  80      -7.840 -27.278  36.614  1.00106.30           C  
ANISOU  635  CD  GLN A  80    15304   7277  17809  -2532  -4436   1230       C  
ATOM    636  NE2 GLN A  80      -6.730 -27.943  36.331  1.00 92.95           N  
ANISOU  636  NE2 GLN A  80    13810   5146  16361  -2147  -4550    962       N  
ATOM    637  OE1 GLN A  80      -8.893 -27.487  36.011  1.00107.48           O  
ANISOU  637  OE1 GLN A  80    15446   7359  18033  -2821  -4606   1090       O  
ATOM    638  N   ALA A  81      -8.732 -26.495  42.179  1.00 91.83           N  
ANISOU  638  N   ALA A  81    12782   6559  15550  -3551  -3990   3812       N  
ATOM    639  CA  ALA A  81      -9.603 -26.625  43.347  1.00 94.01           C  
ANISOU  639  CA  ALA A  81    12866   7095  15760  -3985  -3953   4475       C  
ATOM    640  C   ALA A  81      -9.376 -25.488  44.338  1.00 94.38           C  
ANISOU  640  C   ALA A  81    12742   7884  15234  -3892  -3605   4681       C  
ATOM    641  O   ALA A  81     -10.338 -24.959  44.910  1.00 94.13           O  
ANISOU  641  O   ALA A  81    12486   8367  14913  -4155  -3408   4958       O  
ATOM    642  CB  ALA A  81      -9.364 -27.968  44.022  1.00100.72           C  
ANISOU  642  CB  ALA A  81    13832   7355  17082  -4163  -4273   4983       C  
ATOM    643  N   ALA A  82      -8.093 -25.097  44.502  1.00 88.01           N  
ANISOU  643  N   ALA A  82    12031   7142  14268  -3503  -3535   4502       N  
ATOM    644  CA  ALA A  82      -7.654 -24.024  45.385  1.00 84.57           C  
ANISOU  644  CA  ALA A  82    11479   7337  13317  -3376  -3261   4594       C  
ATOM    645  C   ALA A  82      -8.231 -22.670  44.937  1.00 86.08           C  
ANISOU  645  C   ALA A  82    11545   8049  13112  -3324  -2943   4230       C  
ATOM    646  O   ALA A  82      -8.743 -21.923  45.776  1.00 85.35           O  
ANISOU  646  O   ALA A  82    11292   8510  12627  -3438  -2718   4432       O  
ATOM    647  CB  ALA A  82      -6.138 -23.978  45.416  1.00 84.01           C  
ANISOU  647  CB  ALA A  82    11519   7138  13264  -2989  -3316   4421       C  
ATOM    648  N   ASN A  83      -8.196 -22.382  43.611  1.00 81.19           N  
ANISOU  648  N   ASN A  83    11000   7257  12590  -3140  -2931   3705       N  
ATOM    649  CA  ASN A  83      -8.740 -21.150  43.014  1.00 77.51           C  
ANISOU  649  CA  ASN A  83    10436   7201  11812  -3060  -2670   3371       C  
ATOM    650  C   ASN A  83     -10.256 -21.031  43.254  1.00 82.98           C  
ANISOU  650  C   ASN A  83    10924   8185  12420  -3389  -2593   3601       C  
ATOM    651  O   ASN A  83     -10.723 -19.972  43.676  1.00 80.32           O  
ANISOU  651  O   ASN A  83    10433   8366  11718  -3369  -2323   3605       O  
ATOM    652  CB  ASN A  83      -8.462 -21.094  41.499  1.00 76.07           C  
ANISOU  652  CB  ASN A  83    10381   6755  11768  -2824  -2724   2842       C  
ATOM    653  CG  ASN A  83      -7.019 -20.950  41.085  1.00 85.03           C  
ANISOU  653  CG  ASN A  83    11649   7742  12917  -2454  -2710   2555       C  
ATOM    654  ND2 ASN A  83      -6.256 -20.115  41.754  1.00 82.28           N  
ANISOU  654  ND2 ASN A  83    11244   7720  12298  -2317  -2520   2592       N  
ATOM    655  OD1 ASN A  83      -6.578 -21.556  40.111  1.00 61.86           O  
ANISOU  655  OD1 ASN A  83     8853   4423  10228  -2279  -2864   2262       O  
ATOM    656  N   GLU A  84     -11.012 -22.128  42.998  1.00 83.70           N  
ANISOU  656  N   GLU A  84    10999   7930  12875  -3689  -2841   3788       N  
ATOM    657  CA  GLU A  84     -12.465 -22.192  43.180  1.00 85.46           C  
ANISOU  657  CA  GLU A  84    10973   8400  13097  -4053  -2812   4051       C  
ATOM    658  C   GLU A  84     -12.906 -21.927  44.619  1.00 90.45           C  
ANISOU  658  C   GLU A  84    11388   9553  13427  -4242  -2597   4566       C  
ATOM    659  O   GLU A  84     -13.867 -21.186  44.830  1.00 89.64           O  
ANISOU  659  O   GLU A  84    11035   9969  13054  -4315  -2363   4611       O  
ATOM    660  CB  GLU A  84     -13.024 -23.524  42.675  1.00 91.38           C  
ANISOU  660  CB  GLU A  84    11763   8591  14365  -4379  -3176   4171       C  
ATOM    661  CG  GLU A  84     -13.897 -23.366  41.444  1.00101.46           C  
ANISOU  661  CG  GLU A  84    12961   9849  15741  -4458  -3269   3814       C  
ATOM    662  CD  GLU A  84     -13.264 -23.795  40.136  1.00123.67           C  
ANISOU  662  CD  GLU A  84    16050  12184  18755  -4202  -3489   3238       C  
ATOM    663  OE1 GLU A  84     -13.956 -24.485  39.352  1.00117.97           O  
ANISOU  663  OE1 GLU A  84    15327  11196  18302  -4404  -3752   3055       O  
ATOM    664  OE2 GLU A  84     -12.083 -23.450  39.893  1.00118.07           O1-
ANISOU  664  OE2 GLU A  84    15540  11399  17922  -3807  -3400   2962       O1-
ATOM    665  N   TRP A  85     -12.182 -22.505  45.602  1.00 89.51           N  
ANISOU  665  N   TRP A  85    11357   9331  13322  -4282  -2673   4944       N  
ATOM    666  CA  TRP A  85     -12.462 -22.343  47.030  1.00 91.80           C  
ANISOU  666  CA  TRP A  85    11474  10143  13264  -4444  -2489   5457       C  
ATOM    667  C   TRP A  85     -12.484 -20.857  47.425  1.00 92.13           C  
ANISOU  667  C   TRP A  85    11414  10850  12742  -4190  -2121   5203       C  
ATOM    668  O   TRP A  85     -13.489 -20.380  47.965  1.00 92.36           O  
ANISOU  668  O   TRP A  85    11187  11429  12477  -4323  -1881   5392       O  
ATOM    669  CB  TRP A  85     -11.459 -23.149  47.875  1.00 93.31           C  
ANISOU  669  CB  TRP A  85    11827  10076  13552  -4446  -2680   5843       C  
ATOM    670  CG  TRP A  85     -11.668 -23.032  49.364  1.00 97.36           C  
ANISOU  670  CG  TRP A  85    12182  11161  13648  -4605  -2517   6400       C  
ATOM    671  CD1 TRP A  85     -11.160 -22.070  50.191  1.00 98.53           C  
ANISOU  671  CD1 TRP A  85    12318  11867  13252  -4384  -2295   6328       C  
ATOM    672  CD2 TRP A  85     -12.415 -23.925  50.201  1.00103.21           C  
ANISOU  672  CD2 TRP A  85    12764  11986  14467  -5026  -2579   7119       C  
ATOM    673  CE2 TRP A  85     -12.303 -23.448  51.527  1.00108.66           C  
ANISOU  673  CE2 TRP A  85    13349  13355  14583  -5009  -2363   7460       C  
ATOM    674  CE3 TRP A  85     -13.161 -25.094  49.963  1.00109.21           C  
ANISOU  674  CE3 TRP A  85    13454  12311  15731  -5440  -2806   7519       C  
ATOM    675  NE1 TRP A  85     -11.544 -22.306  51.489  1.00102.61           N  
ANISOU  675  NE1 TRP A  85    12685  12858  13444  -4610  -2206   6926       N  
ATOM    676  CZ2 TRP A  85     -12.954 -24.065  52.598  1.00113.82           C  
ANISOU  676  CZ2 TRP A  85    13813  14335  15098  -5375  -2325   8217       C  
ATOM    677  CZ3 TRP A  85     -13.783 -25.721  51.033  1.00116.38           C  
ANISOU  677  CZ3 TRP A  85    14170  13478  16573  -5837  -2786   8300       C  
ATOM    678  CH2 TRP A  85     -13.668 -25.213  52.332  1.00118.36           C  
ANISOU  678  CH2 TRP A  85    14306  14463  16202  -5793  -2534   8663       C  
ATOM    679  N   GLY A  86     -11.398 -20.147  47.107  1.00 85.81           N  
ANISOU  679  N   GLY A  86    10802   9978  11825  -3828  -2082   4769       N  
ATOM    680  CA  GLY A  86     -11.252 -18.720  47.380  1.00 82.67           C  
ANISOU  680  CA  GLY A  86    10367  10068  10975  -3574  -1785   4461       C  
ATOM    681  C   GLY A  86     -12.301 -17.872  46.695  1.00 84.43           C  
ANISOU  681  C   GLY A  86    10432  10538  11110  -3525  -1581   4190       C  
ATOM    682  O   GLY A  86     -13.029 -17.133  47.367  1.00 85.24           O  
ANISOU  682  O   GLY A  86    10348  11176  10862  -3520  -1321   4250       O  
ATOM    683  N   ARG A  87     -12.425 -18.026  45.361  1.00 78.43           N  
ANISOU  683  N   ARG A  87     9733   9407  10659  -3475  -1711   3900       N  
ATOM    684  CA  ARG A  87     -13.394 -17.307  44.522  1.00 77.12           C  
ANISOU  684  CA  ARG A  87     9421   9422  10460  -3412  -1585   3653       C  
ATOM    685  C   ARG A  87     -14.836 -17.437  45.021  1.00 82.60           C  
ANISOU  685  C   ARG A  87     9782  10519  11085  -3680  -1478   3988       C  
ATOM    686  O   ARG A  87     -15.601 -16.482  44.917  1.00 81.40           O  
ANISOU  686  O   ARG A  87     9443  10757  10730  -3552  -1255   3850       O  
ATOM    687  CB  ARG A  87     -13.300 -17.778  43.072  1.00 76.81           C  
ANISOU  687  CB  ARG A  87     9508   8918  10758  -3376  -1818   3365       C  
ATOM    688  CG  ARG A  87     -13.628 -16.692  42.066  1.00 78.79           C  
ANISOU  688  CG  ARG A  87     9749   9306  10880  -3111  -1681   2969       C  
ATOM    689  CD  ARG A  87     -13.492 -17.189  40.639  1.00 77.17           C  
ANISOU  689  CD  ARG A  87     9675   8717  10929  -3067  -1916   2683       C  
ATOM    690  NE  ARG A  87     -12.146 -17.691  40.369  1.00 81.00           N  
ANISOU  690  NE  ARG A  87    10430   8781  11566  -2934  -2061   2527       N  
ATOM    691  CZ  ARG A  87     -11.885 -18.821  39.723  1.00 92.81           C  
ANISOU  691  CZ  ARG A  87    12060   9829  13375  -3010  -2348   2435       C  
ATOM    692  NH1 ARG A  87     -12.875 -19.567  39.250  1.00 82.91           N1+
ANISOU  692  NH1 ARG A  87    10713   8463  12328  -3265  -2553   2474       N1+
ATOM    693  NH2 ARG A  87     -10.632 -19.206  39.532  1.00 74.29           N  
ANISOU  693  NH2 ARG A  87     9930   7144  11154  -2823  -2442   2281       N  
ATOM    694  N   SER A  88     -15.190 -18.593  45.602  1.00 82.64           N  
ANISOU  694  N   SER A  88     9691  10441  11267  -4041  -1627   4456       N  
ATOM    695  CA  SER A  88     -16.525 -18.829  46.158  1.00 86.68           C  
ANISOU  695  CA  SER A  88     9835  11368  11731  -4356  -1521   4866       C  
ATOM    696  C   SER A  88     -16.737 -18.161  47.544  1.00 92.37           C  
ANISOU  696  C   SER A  88    10380  12768  11947  -4298  -1176   5102       C  
ATOM    697  O   SER A  88     -17.766 -18.381  48.175  1.00 95.60           O  
ANISOU  697  O   SER A  88    10455  13616  12254  -4546  -1037   5498       O  
ATOM    698  CB  SER A  88     -16.834 -20.323  46.202  1.00 94.54           C  
ANISOU  698  CB  SER A  88    10794  11978  13149  -4805  -1825   5312       C  
ATOM    699  OG  SER A  88     -16.014 -20.995  47.143  1.00105.15           O  
ANISOU  699  OG  SER A  88    12315  13149  14489  -4878  -1915   5652       O  
ATOM    700  N   GLY A  89     -15.769 -17.357  47.992  1.00 87.49           N  
ANISOU  700  N   GLY A  89     9975  12254  11012  -3977  -1044   4843       N  
ATOM    701  CA  GLY A  89     -15.832 -16.631  49.259  1.00 89.10           C  
ANISOU  701  CA  GLY A  89    10080  13085  10690  -3862   -742   4932       C  
ATOM    702  C   GLY A  89     -15.519 -17.441  50.502  1.00 97.92           C  
ANISOU  702  C   GLY A  89    11197  14380  11629  -4093   -785   5459       C  
ATOM    703  O   GLY A  89     -15.679 -16.932  51.617  1.00 99.81           O  
ANISOU  703  O   GLY A  89    11328  15229  11368  -4028   -533   5573       O  
ATOM    704  N   LYS A  90     -15.080 -18.702  50.334  1.00 95.94           N  
ANISOU  704  N   LYS A  90    11074  13609  11770  -4345  -1109   5785       N  
ATOM    705  CA  LYS A  90     -14.722 -19.561  51.465  1.00100.09           C  
ANISOU  705  CA  LYS A  90    11620  14228  12181  -4567  -1202   6365       C  
ATOM    706  C   LYS A  90     -13.354 -19.106  52.008  1.00102.37           C  
ANISOU  706  C   LYS A  90    12184  14524  12190  -4278  -1244   6154       C  
ATOM    707  O   LYS A  90     -12.583 -18.496  51.260  1.00 97.74           O  
ANISOU  707  O   LYS A  90    11801  13613  11721  -3994  -1308   5623       O  
ATOM    708  CB  LYS A  90     -14.731 -21.046  51.063  1.00104.99           C  
ANISOU  708  CB  LYS A  90    12293  14208  13389  -4917  -1561   6783       C  
ATOM    709  CG  LYS A  90     -16.044 -21.504  50.427  1.00113.57           C  
ANISOU  709  CG  LYS A  90    13099  15249  14803  -5254  -1578   6960       C  
ATOM    710  CD  LYS A  90     -16.146 -23.015  50.295  1.00118.62           C  
ANISOU  710  CD  LYS A  90    13771  15308  15993  -5679  -1930   7477       C  
ATOM    711  CE  LYS A  90     -17.148 -23.458  49.256  1.00114.97           C  
ANISOU  711  CE  LYS A  90    13137  14541  16006  -5963  -2084   7411       C  
ATOM    712  NZ  LYS A  90     -16.564 -23.477  47.887  1.00107.19           N1+
ANISOU  712  NZ  LYS A  90    12444  12886  15396  -5736  -2345   6784       N1+
ATOM    713  N   ASP A  91     -13.084 -19.337  53.309  1.00102.22           N  
ANISOU  713  N   ASP A  91    12138  14936  11767  -4359  -1199   6577       N  
ATOM    714  CA  ASP A  91     -11.847 -18.889  53.965  1.00100.74           C  
ANISOU  714  CA  ASP A  91    12159  14874  11243  -4120  -1257   6419       C  
ATOM    715  C   ASP A  91     -10.524 -19.435  53.376  1.00100.80           C  
ANISOU  715  C   ASP A  91    12437  14180  11681  -4005  -1615   6303       C  
ATOM    716  O   ASP A  91     -10.320 -20.648  53.373  1.00101.92           O  
ANISOU  716  O   ASP A  91    12629  13899  12199  -4197  -1881   6755       O  
ATOM    717  CB  ASP A  91     -11.917 -19.075  55.492  1.00108.02           C  
ANISOU  717  CB  ASP A  91    12977  16460  11606  -4253  -1164   6952       C  
ATOM    718  CG  ASP A  91     -10.759 -18.443  56.248  1.00118.10           C  
ANISOU  718  CG  ASP A  91    14430  18015  12426  -4007  -1214   6730       C  
ATOM    719  OD1 ASP A  91     -10.439 -17.264  55.970  1.00114.28           O  
ANISOU  719  OD1 ASP A  91    14023  17659  11737  -3726  -1076   6085       O  
ATOM    720  OD2 ASP A  91     -10.192 -19.118  57.138  1.00128.04           O1-
ANISOU  720  OD2 ASP A  91    15743  19370  13538  -4109  -1407   7219       O1-
ATOM    721  N   PRO A  92      -9.612 -18.555  52.879  1.00 93.41           N  
ANISOU  721  N   PRO A  92    11664  13109  10719  -3687  -1620   5711       N  
ATOM    722  CA  PRO A  92      -8.334 -19.054  52.321  1.00 90.90           C  
ANISOU  722  CA  PRO A  92    11546  12198  10795  -3547  -1924   5594       C  
ATOM    723  C   PRO A  92      -7.397 -19.757  53.324  1.00 95.86           C  
ANISOU  723  C   PRO A  92    12239  12862  11319  -3567  -2165   6029       C  
ATOM    724  O   PRO A  92      -6.705 -20.705  52.933  1.00 95.83           O  
ANISOU  724  O   PRO A  92    12343  12301  11768  -3536  -2453   6180       O  
ATOM    725  CB  PRO A  92      -7.696 -17.801  51.715  1.00 87.70           C  
ANISOU  725  CB  PRO A  92    11228  11790  10304  -3246  -1810   4918       C  
ATOM    726  CG  PRO A  92      -8.301 -16.664  52.469  1.00 92.61           C  
ANISOU  726  CG  PRO A  92    11753  13062  10371  -3208  -1514   4752       C  
ATOM    727  CD  PRO A  92      -9.706 -17.082  52.762  1.00 91.53           C  
ANISOU  727  CD  PRO A  92    11419  13221  10139  -3444  -1353   5135       C  
ATOM    728  N   ASN A  93      -7.396 -19.324  54.613  1.00 93.14           N  
ANISOU  728  N   ASN A  93    11828  13187  10373  -3599  -2057   6232       N  
ATOM    729  CA  ASN A  93      -6.559 -19.891  55.688  1.00 96.66           C  
ANISOU  729  CA  ASN A  93    12312  13812  10600  -3616  -2286   6685       C  
ATOM    730  C   ASN A  93      -6.740 -21.403  55.892  1.00103.33           C  
ANISOU  730  C   ASN A  93    13152  14297  11812  -3853  -2528   7429       C  
ATOM    731  O   ASN A  93      -6.032 -22.016  56.686  1.00106.07           O  
ANISOU  731  O   ASN A  93    13535  14706  12059  -3860  -2762   7889       O  
ATOM    732  CB  ASN A  93      -6.765 -19.136  57.007  1.00100.43           C  
ANISOU  732  CB  ASN A  93    12709  15163  10286  -3629  -2094   6745       C  
ATOM    733  CG  ASN A  93      -6.174 -17.749  57.011  1.00112.71           C  
ANISOU  733  CG  ASN A  93    14329  16984  11510  -3377  -1985   6040       C  
ATOM    734  ND2 ASN A  93      -6.982 -16.768  57.380  1.00104.84           N  
ANISOU  734  ND2 ASN A  93    13260  16522  10054  -3349  -1660   5751       N  
ATOM    735  OD1 ASN A  93      -4.994 -17.541  56.708  1.00100.26           O  
ANISOU  735  OD1 ASN A  93    12853  15149  10094  -3207  -2194   5758       O  
ATOM    736  N   HIS A  94      -7.684 -21.988  55.144  1.00 99.32           N  
ANISOU  736  N   HIS A  94    12599  13385  11753  -4051  -2499   7542       N  
ATOM    737  CA  HIS A  94      -8.018 -23.402  55.083  1.00103.00           C  
ANISOU  737  CA  HIS A  94    13073  13348  12713  -4320  -2736   8167       C  
ATOM    738  C   HIS A  94      -6.805 -24.151  54.499  1.00107.96           C  
ANISOU  738  C   HIS A  94    13906  13217  13898  -4105  -3109   8098       C  
ATOM    739  O   HIS A  94      -6.505 -25.255  54.937  1.00113.57           O  
ANISOU  739  O   HIS A  94    14672  13602  14877  -4210  -3387   8693       O  
ATOM    740  CB  HIS A  94      -9.235 -23.558  54.164  1.00102.14           C  
ANISOU  740  CB  HIS A  94    12867  12978  12964  -4541  -2619   8055       C  
ATOM    741  CG  HIS A  94      -9.967 -24.842  54.298  1.00110.27           C  
ANISOU  741  CG  HIS A  94    13833  13668  14398  -4943  -2789   8749       C  
ATOM    742  CD2 HIS A  94      -9.719 -26.046  53.742  1.00113.86           C  
ANISOU  742  CD2 HIS A  94    14436  13280  15548  -5044  -3143   8965       C  
ATOM    743  ND1 HIS A  94     -11.127 -24.926  55.040  1.00115.93           N  
ANISOU  743  ND1 HIS A  94    14295  14932  14821  -5298  -2576   9277       N  
ATOM    744  CE1 HIS A  94     -11.542 -26.174  54.922  1.00120.00           C  
ANISOU  744  CE1 HIS A  94    14804  14913  15879  -5650  -2817   9841       C  
ATOM    745  NE2 HIS A  94     -10.735 -26.884  54.143  1.00119.43           N  
ANISOU  745  NE2 HIS A  94    14991  13961  16427  -5508  -3176   9656       N  
ATOM    746  N   PHE A  95      -6.110 -23.540  53.525  1.00 99.52           N  
ANISOU  746  N   PHE A  95    12932  11884  12996  -3790  -3105   7395       N  
ATOM    747  CA  PHE A  95      -4.933 -24.108  52.861  1.00 98.52           C  
ANISOU  747  CA  PHE A  95    12957  11114  13361  -3514  -3396   7214       C  
ATOM    748  C   PHE A  95      -3.628 -23.504  53.411  1.00 99.50           C  
ANISOU  748  C   PHE A  95    13079  11564  13164  -3223  -3459   7059       C  
ATOM    749  O   PHE A  95      -2.560 -23.696  52.810  1.00 97.86           O  
ANISOU  749  O   PHE A  95    12937  10951  13296  -2936  -3640   6805       O  
ATOM    750  CB  PHE A  95      -5.000 -23.836  51.346  1.00 95.83           C  
ANISOU  750  CB  PHE A  95    12689  10321  13402  -3357  -3334   6547       C  
ATOM    751  CG  PHE A  95      -6.198 -24.395  50.621  1.00 98.35           C  
ANISOU  751  CG  PHE A  95    13008  10287  14073  -3619  -3324   6578       C  
ATOM    752  CD1 PHE A  95      -6.222 -25.720  50.197  1.00104.57           C  
ANISOU  752  CD1 PHE A  95    13918  10333  15481  -3704  -3629   6799       C  
ATOM    753  CD2 PHE A  95      -7.278 -23.584  50.307  1.00 97.80           C  
ANISOU  753  CD2 PHE A  95    12813  10595  13751  -3762  -3035   6341       C  
ATOM    754  CE1 PHE A  95      -7.318 -26.225  49.491  1.00106.21           C  
ANISOU  754  CE1 PHE A  95    14121  10202  16032  -3979  -3663   6778       C  
ATOM    755  CE2 PHE A  95      -8.375 -24.093  49.609  1.00101.28           C  
ANISOU  755  CE2 PHE A  95    13215  10742  14524  -4016  -3060   6359       C  
ATOM    756  CZ  PHE A  95      -8.391 -25.411  49.208  1.00102.72           C  
ANISOU  756  CZ  PHE A  95    13519  10205  15307  -4147  -3383   6573       C  
ATOM    757  N   ARG A  96      -3.716 -22.761  54.533  1.00 94.29           N  
ANISOU  757  N   ARG A  96    12324  11658  11842  -3294  -3314   7184       N  
ATOM    758  CA  ARG A  96      -2.567 -22.080  55.124  1.00 92.20           C  
ANISOU  758  CA  ARG A  96    12037  11783  11212  -3076  -3390   7005       C  
ATOM    759  C   ARG A  96      -1.495 -23.027  55.679  1.00100.82           C  
ANISOU  759  C   ARG A  96    13145  12684  12479  -2957  -3771   7487       C  
ATOM    760  O   ARG A  96      -1.798 -23.840  56.560  1.00105.41           O  
ANISOU  760  O   ARG A  96    13718  13380  12953  -3138  -3904   8184       O  
ATOM    761  CB  ARG A  96      -3.004 -21.044  56.175  1.00 88.70           C  
ANISOU  761  CB  ARG A  96    11513  12193   9994  -3182  -3155   6956       C  
ATOM    762  CG  ARG A  96      -1.889 -20.111  56.613  1.00 89.85           C  
ANISOU  762  CG  ARG A  96    11643  12723   9772  -2982  -3223   6583       C  
ATOM    763  CD  ARG A  96      -2.307 -19.180  57.728  1.00 93.39           C  
ANISOU  763  CD  ARG A  96    12046  13995   9441  -3074  -3030   6512       C  
ATOM    764  NE  ARG A  96      -1.237 -18.233  58.047  1.00102.44           N  
ANISOU  764  NE  ARG A  96    13191  15444  10287  -2914  -3128   6067       N  
ATOM    765  CZ  ARG A  96      -1.058 -17.060  57.448  1.00108.49           C  
ANISOU  765  CZ  ARG A  96    13980  16190  11053  -2810  -2966   5373       C  
ATOM    766  NH1 ARG A  96      -1.895 -16.657  56.498  1.00 94.34           N1+
ANISOU  766  NH1 ARG A  96    12217  14122   9505  -2812  -2688   5050       N1+
ATOM    767  NH2 ARG A  96      -0.049 -16.275  57.801  1.00 92.12           N  
ANISOU  767  NH2 ARG A  96    11891  14365   8745  -2719  -3103   5020       N  
ATOM    768  N   PRO A  97      -0.229 -22.910  55.193  1.00 96.19           N  
ANISOU  768  N   PRO A  97    12553  11849  12144  -2647  -3944   7156       N  
ATOM    769  CA  PRO A  97       0.846 -23.742  55.761  1.00100.50           C  
ANISOU  769  CA  PRO A  97    13072  12269  12846  -2480  -4318   7605       C  
ATOM    770  C   PRO A  97       1.190 -23.234  57.169  1.00108.51           C  
ANISOU  770  C   PRO A  97    13994  14083  13151  -2550  -4389   7880       C  
ATOM    771  O   PRO A  97       1.216 -22.020  57.391  1.00105.73           O  
ANISOU  771  O   PRO A  97    13594  14277  12302  -2577  -4194   7430       O  
ATOM    772  CB  PRO A  97       2.001 -23.588  54.761  1.00 99.42           C  
ANISOU  772  CB  PRO A  97    12893  11761  13123  -2124  -4406   7082       C  
ATOM    773  CG  PRO A  97       1.472 -22.704  53.615  1.00 98.07           C  
ANISOU  773  CG  PRO A  97    12762  11460  13040  -2135  -4076   6408       C  
ATOM    774  CD  PRO A  97       0.295 -21.974  54.170  1.00 92.33           C  
ANISOU  774  CD  PRO A  97    12047  11247  11787  -2433  -3801   6407       C  
ATOM    775  N   ALA A  98       1.389 -24.163  58.128  1.00111.01           N  
ANISOU  775  N   ALA A  98    14302  14464  13412  -2587  -4677   8625       N  
ATOM    776  CA  ALA A  98       1.650 -23.890  59.549  1.00115.71           C  
ANISOU  776  CA  ALA A  98    14822  15850  13294  -2664  -4795   9015       C  
ATOM    777  C   ALA A  98       2.716 -22.844  59.923  1.00119.28           C  
ANISOU  777  C   ALA A  98    15161  16843  13318  -2495  -4880   8542       C  
ATOM    778  O   ALA A  98       2.523 -22.118  60.903  1.00120.82           O  
ANISOU  778  O   ALA A  98    15328  17809  12770  -2624  -4813   8534       O  
ATOM    779  CB  ALA A  98       1.888 -25.190  60.307  1.00123.46           C  
ANISOU  779  CB  ALA A  98    15813  16668  14428  -2670  -5151   9926       C  
ATOM    780  N   GLY A  99       3.815 -22.783  59.172  1.00113.90           N  
ANISOU  780  N   GLY A  99    14402  15782  13091  -2218  -5030   8153       N  
ATOM    781  CA  GLY A  99       4.903 -21.846  59.446  1.00113.23           C  
ANISOU  781  CA  GLY A  99    14168  16144  12711  -2091  -5150   7724       C  
ATOM    782  C   GLY A  99       4.961 -20.591  58.589  1.00111.20           C  
ANISOU  782  C   GLY A  99    13893  15873  12484  -2080  -4868   6877       C  
ATOM    783  O   GLY A  99       6.031 -19.982  58.480  1.00110.80           O  
ANISOU  783  O   GLY A  99    13689  15960  12449  -1953  -4998   6513       O  
ATOM    784  N   LEU A 100       3.822 -20.182  57.990  1.00102.75           N  
ANISOU  784  N   LEU A 100    12957  14651  11432  -2223  -4495   6592       N  
ATOM    785  CA  LEU A 100       3.745 -18.989  57.142  1.00 97.31           C  
ANISOU  785  CA  LEU A 100    12276  13912  10787  -2217  -4211   5849       C  
ATOM    786  C   LEU A 100       3.525 -17.708  57.972  1.00104.03           C  
ANISOU  786  C   LEU A 100    13137  15444  10947  -2365  -4093   5500       C  
ATOM    787  O   LEU A 100       2.571 -17.659  58.756  1.00106.46           O  
ANISOU  787  O   LEU A 100    13523  16166  10762  -2526  -3968   5715       O  
ATOM    788  CB  LEU A 100       2.647 -19.148  56.073  1.00 92.95           C  
ANISOU  788  CB  LEU A 100    11850  12893  10574  -2274  -3902   5711       C  
ATOM    789  CG  LEU A 100       2.567 -18.076  54.978  1.00 91.08           C  
ANISOU  789  CG  LEU A 100    11628  12468  10512  -2221  -3629   5024       C  
ATOM    790  CD1 LEU A 100       3.612 -18.309  53.892  1.00 89.44           C  
ANISOU  790  CD1 LEU A 100    11337  11770  10878  -1978  -3729   4819       C  
ATOM    791  CD2 LEU A 100       1.192 -18.048  54.359  1.00 87.27           C  
ANISOU  791  CD2 LEU A 100    11261  11802  10094  -2343  -3324   4945       C  
ATOM    792  N   PRO A 101       4.381 -16.664  57.795  1.00 99.95           N  
ANISOU  792  N   PRO A 101    12535  15044  10398  -2315  -4125   4953       N  
ATOM    793  CA  PRO A 101       4.219 -15.418  58.578  1.00101.20           C  
ANISOU  793  CA  PRO A 101    12732  15778   9940  -2449  -4051   4548       C  
ATOM    794  C   PRO A 101       2.860 -14.729  58.456  1.00104.35           C  
ANISOU  794  C   PRO A 101    13292  16270  10087  -2552  -3651   4270       C  
ATOM    795  O   PRO A 101       2.229 -14.776  57.402  1.00100.12           O  
ANISOU  795  O   PRO A 101    12810  15281   9950  -2523  -3400   4160       O  
ATOM    796  CB  PRO A 101       5.361 -14.528  58.079  1.00101.29           C  
ANISOU  796  CB  PRO A 101    12617  15683  10184  -2399  -4154   4027       C  
ATOM    797  CG  PRO A 101       6.372 -15.482  57.530  1.00105.90           C  
ANISOU  797  CG  PRO A 101    13025  15889  11325  -2218  -4385   4320       C  
ATOM    798  CD  PRO A 101       5.567 -16.588  56.916  1.00 99.69           C  
ANISOU  798  CD  PRO A 101    12349  14640  10887  -2143  -4240   4691       C  
ATOM    799  N   GLU A 102       2.432 -14.086  59.560  1.00105.45           N  
ANISOU  799  N   GLU A 102    13494  17037   9537  -2649  -3605   4144       N  
ATOM    800  CA  GLU A 102       1.155 -13.395  59.769  1.00105.40           C  
ANISOU  800  CA  GLU A 102    13606  17290   9150  -2706  -3239   3893       C  
ATOM    801  C   GLU A 102       0.744 -12.393  58.700  1.00105.04           C  
ANISOU  801  C   GLU A 102    13628  16849   9434  -2657  -2945   3302       C  
ATOM    802  O   GLU A 102      -0.457 -12.242  58.450  1.00104.03           O  
ANISOU  802  O   GLU A 102    13554  16709   9261  -2659  -2623   3272       O  
ATOM    803  CB  GLU A 102       1.125 -12.739  61.158  1.00112.17           C  
ANISOU  803  CB  GLU A 102    14508  18924   9187  -2758  -3297   3729       C  
ATOM    804  CG  GLU A 102      -0.112 -13.076  61.974  1.00128.13           C  
ANISOU  804  CG  GLU A 102    16563  21462  10658  -2815  -3051   4071       C  
ATOM    805  CD  GLU A 102      -0.129 -14.467  62.579  1.00155.51           C  
ANISOU  805  CD  GLU A 102    19955  25114  14020  -2893  -3224   4939       C  
ATOM    806  OE1 GLU A 102       0.436 -14.643  63.683  1.00152.31           O  
ANISOU  806  OE1 GLU A 102    19524  25259  13089  -2917  -3494   5184       O  
ATOM    807  OE2 GLU A 102      -0.708 -15.382  61.949  1.00150.74           O1-
ANISOU  807  OE2 GLU A 102    19319  24093  13862  -2940  -3110   5382       O1-
ATOM    808  N   LYS A 103       1.728 -11.703  58.078  1.00 98.53           N  
ANISOU  808  N   LYS A 103    12774  15723   8940  -2618  -3057   2874       N  
ATOM    809  CA  LYS A 103       1.476 -10.713  57.032  1.00 93.29           C  
ANISOU  809  CA  LYS A 103    12173  14662   8609  -2576  -2808   2362       C  
ATOM    810  C   LYS A 103       0.762 -11.294  55.818  1.00 92.26           C  
ANISOU  810  C   LYS A 103    12048  14040   8965  -2512  -2586   2542       C  
ATOM    811  O   LYS A 103      -0.104 -10.624  55.257  1.00 90.57           O  
ANISOU  811  O   LYS A 103    11912  13696   8805  -2480  -2298   2266       O  
ATOM    812  CB  LYS A 103       2.774 -10.011  56.606  1.00 94.82           C  
ANISOU  812  CB  LYS A 103    12292  14635   9098  -2590  -2996   1996       C  
ATOM    813  CG  LYS A 103       3.266  -8.968  57.576  1.00118.22           C  
ANISOU  813  CG  LYS A 103    15290  18003  11627  -2686  -3171   1590       C  
ATOM    814  CD  LYS A 103       4.454  -8.207  56.989  1.00129.99           C  
ANISOU  814  CD  LYS A 103    16677  19203  13512  -2753  -3326   1238       C  
ATOM    815  CE  LYS A 103       5.217  -7.400  58.023  1.00146.16           C  
ANISOU  815  CE  LYS A 103    18723  21626  15184  -2896  -3611    861       C  
ATOM    816  NZ  LYS A 103       6.400  -6.711  57.435  1.00153.02           N1+
ANISOU  816  NZ  LYS A 103    19447  22197  16496  -3016  -3770    565       N1+
ATOM    817  N   TYR A 104       1.108 -12.538  55.423  1.00 86.31           N  
ANISOU  817  N   TYR A 104    11215  13015   8563  -2480  -2737   2991       N  
ATOM    818  CA  TYR A 104       0.520 -13.232  54.274  1.00 81.79           C  
ANISOU  818  CA  TYR A 104    10656  11960   8459  -2427  -2593   3149       C  
ATOM    819  C   TYR A 104      -0.872 -13.814  54.561  1.00 86.85           C  
ANISOU  819  C   TYR A 104    11340  12735   8924  -2516  -2421   3477       C  
ATOM    820  O   TYR A 104      -1.258 -13.926  55.746  1.00 88.68           O  
ANISOU  820  O   TYR A 104    11565  13456   8672  -2608  -2448   3736       O  
ATOM    821  CB  TYR A 104       1.461 -14.333  53.750  1.00 82.59           C  
ANISOU  821  CB  TYR A 104    10671  11687   9022  -2329  -2839   3442       C  
ATOM    822  CG  TYR A 104       2.887 -13.883  53.520  1.00 83.37           C  
ANISOU  822  CG  TYR A 104    10649  11731   9298  -2243  -3014   3197       C  
ATOM    823  CD1 TYR A 104       3.195 -12.953  52.531  1.00 81.78           C  
ANISOU  823  CD1 TYR A 104    10428  11280   9366  -2192  -2858   2764       C  
ATOM    824  CD2 TYR A 104       3.934 -14.408  54.271  1.00 87.45           C  
ANISOU  824  CD2 TYR A 104    11040  12465   9722  -2221  -3343   3442       C  
ATOM    825  CE1 TYR A 104       4.504 -12.529  52.320  1.00 82.67           C  
ANISOU  825  CE1 TYR A 104    10379  11375   9658  -2151  -3003   2580       C  
ATOM    826  CE2 TYR A 104       5.249 -13.995  54.065  1.00 88.33           C  
ANISOU  826  CE2 TYR A 104    10978  12569  10016  -2158  -3513   3234       C  
ATOM    827  CZ  TYR A 104       5.530 -13.059  53.086  1.00 90.64           C  
ANISOU  827  CZ  TYR A 104    11232  12619  10587  -2138  -3330   2804       C  
ATOM    828  OH  TYR A 104       6.821 -12.647  52.876  1.00 91.07           O  
ANISOU  828  OH  TYR A 104    11069  12696  10837  -2113  -3481   2639       O  
ATOM    829  OXT TYR A 104      -1.551 -14.220  53.591  1.00 93.23           O1-
ANISOU  829  OXT TYR A 104    12166  13185  10073  -2504  -2272   3504       O1-
TER   
END


A second structure was input as follows:


CRYST1   93.850   93.850  130.520  90.00  90.00 120.00 H 3 2         3
ATOM      1  N   ARG A   1     -23.982   2.835  35.374  1.00 89.90           N  
ANISOU    1  N   ARG A   1     9443  12653  12061   2685    280   2074       N  
ATOM      2  CA  ARG A   1     -22.979   3.037  36.425  1.00 87.93           C  
ANISOU    2  CA  ARG A   1     9547  12069  11792   2567    474   1772       C  
ATOM      3  C   ARG A   1     -22.425   1.704  36.958  1.00 87.82           C  
ANISOU    3  C   ARG A   1     9564  12232  11572   2025    445   1709       C  
ATOM      4  O   ARG A   1     -21.281   1.656  37.427  1.00 84.59           O  
ANISOU    4  O   ARG A   1     9510  11502  11129   1816    490   1542       O  
ATOM      5  CB  ARG A   1     -23.534   3.902  37.574  1.00 93.04           C  
ANISOU    5  CB  ARG A   1    10092  12759  12500   2975    752   1509       C  
ATOM      6  CG  ARG A   1     -22.450   4.492  38.480  1.00103.00           C  
ANISOU    6  CG  ARG A   1    11796  13549  13789   2964    901   1165       C  
ATOM      7  CD  ARG A   1     -23.033   5.130  39.722  1.00115.91           C  
ANISOU    7  CD  ARG A   1    13320  15335  15388   3324   1175    826       C  
ATOM      8  NE  ARG A   1     -23.478   6.501  39.476  1.00125.28           N  
ANISOU    8  NE  ARG A   1    14536  16206  16857   3918   1236    748       N  
ATOM      9  CZ  ARG A   1     -23.522   7.455  40.400  1.00138.70           C  
ANISOU    9  CZ  ARG A   1    16347  17731  18622   4309   1445    350       C  
ATOM     10  NH1 ARG A   1     -23.141   7.200  41.647  1.00120.85           N1+
ANISOU   10  NH1 ARG A   1    14174  15638  16104   4157   1616    -10       N1+
ATOM     11  NH2 ARG A   1     -23.935   8.673  40.083  1.00130.56           N  
ANISOU   11  NH2 ARG A   1    15355  16344  17908   4870   1469    299       N  
ATOM     12  N   SER A   2     -23.225   0.621  36.872  1.00 84.29           N  
ANISOU   12  N   SER A   2     8735  12275  11017   1790    348   1862       N  
ATOM     13  CA  SER A   2     -22.784  -0.713  37.298  1.00 81.24           C  
ANISOU   13  CA  SER A   2     8360  12021  10487   1277    283   1860       C  
ATOM     14  C   SER A   2     -21.631  -1.252  36.426  1.00 81.10           C  
ANISOU   14  C   SER A   2     8699  11656  10461    975     66   1889       C  
ATOM     15  O   SER A   2     -20.791  -2.007  36.930  1.00 79.67           O  
ANISOU   15  O   SER A   2     8703  11361  10207    643     60   1806       O  
ATOM     16  CB  SER A   2     -23.954  -1.696  37.423  1.00 86.38           C  
ANISOU   16  CB  SER A   2     8507  13224  11089   1077    211   2046       C  
ATOM     17  OG  SER A   2     -24.724  -1.891  36.248  1.00 95.99           O  
ANISOU   17  OG  SER A   2     9482  14613  12377   1104    -43   2248       O  
ATOM     18  N   PHE A   3     -21.536  -0.761  35.162  1.00 75.92           N  
ANISOU   18  N   PHE A   3     8142  10839   9864   1135    -91   2009       N  
ATOM     19  CA  PHE A   3     -20.478  -1.116  34.211  1.00 72.77           C  
ANISOU   19  CA  PHE A   3     8060  10170   9420    935   -260   2038       C  
ATOM     20  C   PHE A   3     -19.092  -0.618  34.643  1.00 71.76           C  
ANISOU   20  C   PHE A   3     8339   9596   9330    898   -117   1885       C  
ATOM     21  O   PHE A   3     -18.125  -1.373  34.510  1.00 69.47           O  
ANISOU   21  O   PHE A   3     8243   9176   8975    605   -191   1833       O  
ATOM     22  CB  PHE A   3     -20.800  -0.641  32.779  1.00 76.97           C  
ANISOU   22  CB  PHE A   3     8574  10725   9947   1158   -433   2241       C  
ATOM     23  CG  PHE A   3     -22.167  -0.969  32.208  1.00 82.66           C  
ANISOU   23  CG  PHE A   3     8883  11897  10628   1207   -635   2403       C  
ATOM     24  CD1 PHE A   3     -22.784  -2.188  32.480  1.00 86.75           C  
ANISOU   24  CD1 PHE A   3     9136  12732  11093    861   -775   2378       C  
ATOM     25  CD2 PHE A   3     -22.812  -0.083  31.349  1.00 88.51           C  
ANISOU   25  CD2 PHE A   3     9495  12735  11399   1574   -722   2608       C  
ATOM     26  CE1 PHE A   3     -24.044  -2.490  31.949  1.00 91.21           C  
ANISOU   26  CE1 PHE A   3     9288  13721  11646    859   -996   2525       C  
ATOM     27  CE2 PHE A   3     -24.062  -0.395  30.800  1.00 94.77           C  
ANISOU   27  CE2 PHE A   3     9874  13987  12148   1609   -949   2761       C  
ATOM     28  CZ  PHE A   3     -24.671  -1.595  31.106  1.00 93.14           C  
ANISOU   28  CZ  PHE A   3     9385  14108  11897   1236  -1087   2704       C  
ATOM     29  N   PHE A   4     -18.987   0.635  35.157  1.00 67.19           N  
ANISOU   29  N   PHE A   4     7878   8775   8879   1198     69   1798       N  
ATOM     30  CA  PHE A   4     -17.704   1.192  35.612  1.00 64.92           C  
ANISOU   30  CA  PHE A   4     7948   8053   8664   1143    179   1638       C  
ATOM     31  C   PHE A   4     -17.228   0.557  36.894  1.00 63.39           C  
ANISOU   31  C   PHE A   4     7792   7923   8372    888    266   1421       C  
ATOM     32  O   PHE A   4     -16.024   0.387  37.070  1.00 59.74           O  
ANISOU   32  O   PHE A   4     7574   7219   7906    668    252   1336       O  
ATOM     33  CB  PHE A   4     -17.752   2.710  35.776  1.00 70.42           C  
ANISOU   33  CB  PHE A   4     8771   8420   9567   1521    311   1579       C  
ATOM     34  CG  PHE A   4     -17.978   3.444  34.485  1.00 74.92           C  
ANISOU   34  CG  PHE A   4     9390   8817  10258   1755    217   1858       C  
ATOM     35  CD1 PHE A   4     -16.916   3.722  33.629  1.00 77.46           C  
ANISOU   35  CD1 PHE A   4     9991   8810  10629   1626    166   1998       C  
ATOM     36  CD2 PHE A   4     -19.254   3.869  34.121  1.00 81.05           C  
ANISOU   36  CD2 PHE A   4     9908   9797  11091   2114    182   2018       C  
ATOM     37  CE1 PHE A   4     -17.129   4.418  32.433  1.00 80.90           C  
ANISOU   37  CE1 PHE A   4    10473   9124  11141   1840     88   2320       C  
ATOM     38  CE2 PHE A   4     -19.466   4.556  32.919  1.00 85.69           C  
ANISOU   38  CE2 PHE A   4    10544  10245  11771   2345     73   2328       C  
ATOM     39  CZ  PHE A   4     -18.405   4.823  32.084  1.00 82.78           C  
ANISOU   39  CZ  PHE A   4    10479   9551  11422   2200     30   2489       C  
ATOM     40  N   SER A   5     -18.171   0.221  37.801  1.00 59.89           N  
ANISOU   40  N   SER A   5     7079   7841   7835    923    357   1358       N  
ATOM     41  CA  SER A   5     -17.863  -0.461  39.052  1.00 57.48           C  
ANISOU   41  CA  SER A   5     6768   7695   7377    684    438   1218       C  
ATOM     42  C   SER A   5     -17.280  -1.799  38.676  1.00 56.98           C  
ANISOU   42  C   SER A   5     6739   7660   7253    281    256   1341       C  
ATOM     43  O   SER A   5     -16.186  -2.127  39.129  1.00 54.32           O  
ANISOU   43  O   SER A   5     6612   7152   6876     73    243   1247       O  
ATOM     44  CB  SER A   5     -19.118  -0.668  39.888  1.00 62.84           C  
ANISOU   44  CB  SER A   5     7085   8853   7938    789    576   1224       C  
ATOM     45  OG  SER A   5     -19.535   0.559  40.459  1.00 78.16           O  
ANISOU   45  OG  SER A   5     9011  10760   9926   1212    770   1035       O  
ATOM     46  N   PHE A   6     -17.944  -2.506  37.741  1.00 52.39           N  
ANISOU   46  N   PHE A   6     5966   7255   6685    195     88   1532       N  
ATOM     47  CA  PHE A   6     -17.489  -3.809  37.273  1.00 49.75           C  
ANISOU   47  CA  PHE A   6     5668   6909   6326   -151   -116   1611       C  
ATOM     48  C   PHE A   6     -16.025  -3.773  36.782  1.00 51.66           C  
ANISOU   48  C   PHE A   6     6254   6778   6595   -230   -169   1531       C  
ATOM     49  O   PHE A   6     -15.240  -4.667  37.121  1.00 49.25           O  
ANISOU   49  O   PHE A   6     6052   6393   6270   -483   -236   1496       O  
ATOM     50  CB  PHE A   6     -18.426  -4.342  36.178  1.00 52.30           C  
ANISOU   50  CB  PHE A   6     5766   7438   6668   -177   -319   1764       C  
ATOM     51  CG  PHE A   6     -18.195  -5.797  35.853  1.00 52.66           C  
ANISOU   51  CG  PHE A   6     5807   7489   6713   -542   -546   1799       C  
ATOM     52  CD1 PHE A   6     -18.889  -6.797  36.530  1.00 56.58           C  
ANISOU   52  CD1 PHE A   6     6050   8221   7229   -807   -601   1901       C  
ATOM     53  CD2 PHE A   6     -17.272  -6.173  34.882  1.00 53.19           C  
ANISOU   53  CD2 PHE A   6     6121   7318   6771   -615   -701   1732       C  
ATOM     54  CE1 PHE A   6     -18.680  -8.143  36.229  1.00 57.30           C  
ANISOU   54  CE1 PHE A   6     6163   8226   7383  -1148   -841   1930       C  
ATOM     55  CE2 PHE A   6     -17.043  -7.527  34.605  1.00 55.73           C  
ANISOU   55  CE2 PHE A   6     6465   7589   7122   -911   -921   1707       C  
ATOM     56  CZ  PHE A   6     -17.760  -8.499  35.265  1.00 55.10           C  
ANISOU   56  CZ  PHE A   6     6160   7662   7113  -1180  -1008   1803       C  
ATOM     57  N   LEU A   7     -15.661  -2.730  36.012  1.00 48.62           N  
ANISOU   57  N   LEU A   7     6023   6179   6270     -9   -133   1535       N  
ATOM     58  CA  LEU A   7     -14.298  -2.572  35.504  1.00 46.93           C  
ANISOU   58  CA  LEU A   7     6083   5664   6086    -77   -146   1501       C  
ATOM     59  C   LEU A   7     -13.294  -2.217  36.583  1.00 48.66           C  
ANISOU   59  C   LEU A   7     6470   5673   6347   -157    -27   1345       C  
ATOM     60  O   LEU A   7     -12.199  -2.774  36.583  1.00 47.90           O  
ANISOU   60  O   LEU A   7     6498   5456   6247   -345    -77   1307       O  
ATOM     61  CB  LEU A   7     -14.227  -1.588  34.333  1.00 48.28           C  
ANISOU   61  CB  LEU A   7     6344   5700   6298    144   -142   1629       C  
ATOM     62  CG  LEU A   7     -14.800  -2.079  33.007  1.00 54.91           C  
ANISOU   62  CG  LEU A   7     7080   6756   7026    177   -316   1775       C  
ATOM     63  CD1 LEU A   7     -14.312  -1.213  31.898  1.00 56.28           C  
ANISOU   63  CD1 LEU A   7     7401   6797   7187    345   -296   1936       C  
ATOM     64  CD2 LEU A   7     -14.387  -3.547  32.694  1.00 56.77           C  
ANISOU   64  CD2 LEU A   7     7330   7084   7158    -92   -478   1693       C  
ATOM     65  N   GLY A   8     -13.683  -1.327  37.493  1.00 44.93           N  
ANISOU   65  N   GLY A   8     5983   5183   5904      0    113   1234       N  
ATOM     66  CA  GLY A   8     -12.872  -0.955  38.644  1.00 45.10           C  
ANISOU   66  CA  GLY A   8     6152   5058   5925    -73    198   1032       C  
ATOM     67  C   GLY A   8     -12.646  -2.168  39.545  1.00 46.93           C  
ANISOU   67  C   GLY A   8     6318   5507   6007   -335    144   1009       C  
ATOM     68  O   GLY A   8     -11.517  -2.426  39.949  1.00 46.41           O  
ANISOU   68  O   GLY A   8     6388   5312   5935   -508    102    935       O  
ATOM     69  N   GLU A   9     -13.701  -2.959  39.799  1.00 42.07           N  
ANISOU   69  N   GLU A   9     5472   5223   5289   -380    126   1117       N  
ATOM     70  CA  GLU A   9     -13.634  -4.209  40.576  1.00 42.37           C  
ANISOU   70  CA  GLU A   9     5423   5465   5210   -648     58   1192       C  
ATOM     71  C   GLU A   9     -12.662  -5.192  39.878  1.00 47.08           C  
ANISOU   71  C   GLU A   9     6134   5867   5888   -859   -128   1266       C  
ATOM     72  O   GLU A   9     -11.897  -5.873  40.557  1.00 44.94           O  
ANISOU   72  O   GLU A   9     5923   5575   5578  -1044   -190   1273       O  
ATOM     73  CB  GLU A   9     -15.019  -4.887  40.686  1.00 44.64           C  
ANISOU   73  CB  GLU A   9     5405   6115   5439   -689     56   1362       C  
ATOM     74  CG  GLU A   9     -16.067  -4.142  41.503  1.00 52.13           C  
ANISOU   74  CG  GLU A   9     6165   7373   6267   -479    267   1304       C  
ATOM     75  CD  GLU A   9     -17.517  -4.572  41.318  1.00 74.44           C  
ANISOU   75  CD  GLU A   9     8622  10573   9089   -460    282   1493       C  
ATOM     76  OE1 GLU A   9     -17.803  -5.390  40.416  1.00 62.53           O  
ANISOU   76  OE1 GLU A   9     7012   9056   7691   -624     90   1659       O  
ATOM     77  OE2 GLU A   9     -18.379  -4.063  42.070  1.00 79.68           O1-
ANISOU   77  OE2 GLU A   9     9080  11558   9635   -271    483   1453       O1-
ATOM     78  N   ALA A  10     -12.684  -5.232  38.522  1.00 44.23           N  
ANISOU   78  N   ALA A  10     5798   5388   5621   -799   -216   1314       N  
ATOM     79  CA  ALA A  10     -11.828  -6.104  37.728  1.00 43.04           C  
ANISOU   79  CA  ALA A  10     5748   5079   5525   -926   -369   1331       C  
ATOM     80  C   ALA A  10     -10.342  -5.737  37.867  1.00 50.30           C  
ANISOU   80  C   ALA A  10     6853   5771   6486   -941   -329   1238       C  
ATOM     81  O   ALA A  10      -9.550  -6.614  38.227  1.00 49.22           O  
ANISOU   81  O   ALA A  10     6756   5575   6370  -1091   -423   1234       O  
ATOM     82  CB  ALA A  10     -12.273  -6.103  36.270  1.00 43.43           C  
ANISOU   82  CB  ALA A  10     5775   5141   5585   -818   -452   1375       C  
ATOM     83  N   PHE A  11      -9.975  -4.439  37.666  1.00 49.03           N  
ANISOU   83  N   PHE A  11     6787   5473   6368   -797   -203   1181       N  
ATOM     84  CA  PHE A  11      -8.596  -3.969  37.822  1.00 49.74           C  
ANISOU   84  CA  PHE A  11     7010   5358   6532   -850   -167   1109       C  
ATOM     85  C   PHE A  11      -8.082  -4.214  39.238  1.00 48.92           C  
ANISOU   85  C   PHE A  11     6918   5290   6381   -992   -188   1011       C  
ATOM     86  O   PHE A  11      -6.949  -4.660  39.411  1.00 47.03           O  
ANISOU   86  O   PHE A  11     6712   4980   6179  -1114   -258    997       O  
ATOM     87  CB  PHE A  11      -8.453  -2.488  37.429  1.00 55.16           C  
ANISOU   87  CB  PHE A  11     7788   5850   7320   -706    -46   1100       C  
ATOM     88  CG  PHE A  11      -8.423  -2.235  35.943  1.00 60.15           C  
ANISOU   88  CG  PHE A  11     8440   6433   7980   -602    -34   1254       C  
ATOM     89  CD1 PHE A  11      -7.261  -2.455  35.207  1.00 65.19           C  
ANISOU   89  CD1 PHE A  11     9120   7006   8644   -679    -34   1309       C  
ATOM     90  CD2 PHE A  11      -9.553  -1.771  35.274  1.00 66.36           C  
ANISOU   90  CD2 PHE A  11     9182   7289   8742   -408    -17   1361       C  
ATOM     91  CE1 PHE A  11      -7.235  -2.222  33.822  1.00 68.00           C  
ANISOU   91  CE1 PHE A  11     9490   7394   8953   -573     -1   1470       C  
ATOM     92  CE2 PHE A  11      -9.522  -1.522  33.890  1.00 70.94           C  
ANISOU   92  CE2 PHE A  11     9785   7879   9290   -306    -19   1534       C  
ATOM     93  CZ  PHE A  11      -8.363  -1.749  33.175  1.00 68.78           C  
ANISOU   93  CZ  PHE A  11     9572   7567   8996   -393     -2   1588       C  
ATOM     94  N   ASP A  12      -8.942  -3.975  40.240  1.00 44.69           N  
ANISOU   94  N   ASP A  12     6328   4917   5734   -959   -129    955       N  
ATOM     95  CA  ASP A  12      -8.645  -4.204  41.652  1.00 44.69           C  
ANISOU   95  CA  ASP A  12     6331   5051   5598  -1077   -145    874       C  
ATOM     96  C   ASP A  12      -8.460  -5.699  41.935  1.00 48.95           C  
ANISOU   96  C   ASP A  12     6796   5714   6088  -1262   -288   1039       C  
ATOM     97  O   ASP A  12      -7.557  -6.064  42.686  1.00 47.47           O  
ANISOU   97  O   ASP A  12     6646   5535   5855  -1385   -373   1031       O  
ATOM     98  CB  ASP A  12      -9.725  -3.585  42.550  1.00 47.38           C  
ANISOU   98  CB  ASP A  12     6612   5608   5782   -952    -11    774       C  
ATOM     99  CG  ASP A  12      -9.660  -2.074  42.683  1.00 54.30           C  
ANISOU   99  CG  ASP A  12     7611   6296   6725   -765    104    539       C  
ATOM    100  OD1 ASP A  12      -8.661  -1.466  42.218  1.00 55.07           O  
ANISOU  100  OD1 ASP A  12     7848   6083   6993   -803     65    470       O  
ATOM    101  OD2 ASP A  12     -10.587  -1.501  43.254  1.00 62.07           O1-
ANISOU  101  OD2 ASP A  12     8542   7432   7610   -583    232    427       O1-
ATOM    102  N   GLY A  13      -9.292  -6.534  41.303  1.00 46.79           N  
ANISOU  102  N   GLY A  13     6419   5510   5848  -1280   -340   1190       N  
ATOM    103  CA  GLY A  13      -9.211  -7.989  41.389  1.00 46.46           C  
ANISOU  103  CA  GLY A  13     6327   5485   5840  -1456   -504   1356       C  
ATOM    104  C   GLY A  13      -7.895  -8.481  40.807  1.00 49.14           C  
ANISOU  104  C   GLY A  13     6768   5583   6319  -1478   -624   1325       C  
ATOM    105  O   GLY A  13      -7.217  -9.326  41.405  1.00 48.00           O  
ANISOU  105  O   GLY A  13     6633   5404   6199  -1591   -749   1407       O  
ATOM    106  N   ALA A  14      -7.498  -7.872  39.668  1.00 45.60           N  
ANISOU  106  N   ALA A  14     6381   4992   5951  -1347   -571   1226       N  
ATOM    107  CA  ALA A  14      -6.238  -8.100  38.952  1.00 44.53           C  
ANISOU  107  CA  ALA A  14     6305   4691   5923  -1317   -619   1179       C  
ATOM    108  C   ALA A  14      -5.047  -7.756  39.839  1.00 45.58           C  
ANISOU  108  C   ALA A  14     6455   4794   6069  -1381   -619   1137       C  
ATOM    109  O   ALA A  14      -4.100  -8.529  39.895  1.00 45.85           O  
ANISOU  109  O   ALA A  14     6471   4766   6183  -1410   -725   1160       O  
ATOM    110  CB  ALA A  14      -6.201  -7.270  37.671  1.00 45.26           C  
ANISOU  110  CB  ALA A  14     6434   4728   6034  -1171   -511   1133       C  
ATOM    111  N   ARG A  15      -5.124  -6.638  40.581  1.00 42.14           N  
ANISOU  111  N   ARG A  15     6045   4406   5560  -1392   -524   1057       N  
ATOM    112  CA  ARG A  15      -4.061  -6.211  41.511  1.00 42.84           C  
ANISOU  112  CA  ARG A  15     6148   4492   5638  -1483   -561    975       C  
ATOM    113  C   ARG A  15      -3.932  -7.196  42.695  1.00 47.56           C  
ANISOU  113  C   ARG A  15     6703   5248   6119  -1598   -707   1067       C  
ATOM    114  O   ARG A  15      -2.809  -7.545  43.046  1.00 47.53           O  
ANISOU  114  O   ARG A  15     6665   5230   6162  -1661   -826   1087       O  
ATOM    115  CB  ARG A  15      -4.329  -4.800  42.030  1.00 42.26           C  
ANISOU  115  CB  ARG A  15     6145   4401   5512  -1458   -450    809       C  
ATOM    116  CG  ARG A  15      -4.214  -3.711  40.975  1.00 53.18           C  
ANISOU  116  CG  ARG A  15     7582   5562   7061  -1375   -334    770       C  
ATOM    117  CD  ARG A  15      -4.920  -2.448  41.425  1.00 55.79           C  
ANISOU  117  CD  ARG A  15     8004   5817   7378  -1288   -230    615       C  
ATOM    118  NE  ARG A  15      -4.329  -1.880  42.638  1.00 48.15           N  
ANISOU  118  NE  ARG A  15     7094   4844   6356  -1393   -288    402       N  
ATOM    119  CZ  ARG A  15      -5.023  -1.507  43.709  1.00 62.81           C  
ANISOU  119  CZ  ARG A  15     8998   6843   8024  -1336   -257    221       C  
ATOM    120  NH1 ARG A  15      -6.343  -1.643  43.732  1.00 52.27           N1+
ANISOU  120  NH1 ARG A  15     7620   5676   6564  -1175   -148    261       N1+
ATOM    121  NH2 ARG A  15      -4.405  -0.970  44.756  1.00 43.94           N  
ANISOU  121  NH2 ARG A  15     6680   4462   5554  -1434   -336    -18       N  
ATOM    122  N   ASP A  16      -5.082  -7.649  43.285  1.00 44.44           N  
ANISOU  122  N   ASP A  16     6282   5027   5574  -1626   -698   1165       N  
ATOM    123  CA  ASP A  16      -5.144  -8.636  44.382  1.00 46.44           C  
ANISOU  123  CA  ASP A  16     6490   5460   5695  -1750   -822   1344       C  
ATOM    124  C   ASP A  16      -4.592  -9.995  43.933  1.00 51.77           C  
ANISOU  124  C   ASP A  16     7142   5967   6561  -1787  -1001   1521       C  
ATOM    125  O   ASP A  16      -3.955 -10.664  44.728  1.00 53.45           O  
ANISOU  125  O   ASP A  16     7335   6231   6744  -1862  -1150   1662       O  
ATOM    126  CB  ASP A  16      -6.582  -8.846  44.871  1.00 49.06           C  
ANISOU  126  CB  ASP A  16     6756   6027   5858  -1783   -737   1463       C  
ATOM    127  CG  ASP A  16      -7.264  -7.629  45.435  1.00 57.20           C  
ANISOU  127  CG  ASP A  16     7792   7264   6679  -1693   -550   1276       C  
ATOM    128  OD1 ASP A  16      -6.632  -6.913  46.235  1.00 60.17           O  
ANISOU  128  OD1 ASP A  16     8237   7715   6910  -1691   -548   1100       O  
ATOM    129  OD2 ASP A  16      -8.453  -7.435  45.135  1.00 62.54           O1-
ANISOU  129  OD2 ASP A  16     8391   8040   7332  -1618   -422   1293       O1-
ATOM    130  N   MET A  17      -4.861 -10.407  42.668  1.00 46.58           N  
ANISOU  130  N   MET A  17     6494   5114   6090  -1712  -1001   1505       N  
ATOM    131  CA  MET A  17      -4.296 -11.623  42.086  1.00 45.60           C  
ANISOU  131  CA  MET A  17     6377   4776   6174  -1690  -1165   1579       C  
ATOM    132  C   MET A  17      -2.763 -11.426  41.956  1.00 50.79           C  
ANISOU  132  C   MET A  17     7016   5357   6923  -1603  -1199   1490       C  
ATOM    133  O   MET A  17      -1.996 -12.303  42.345  1.00 50.80           O  
ANISOU  133  O   MET A  17     6989   5286   7028  -1600  -1363   1600       O  
ATOM    134  CB  MET A  17      -4.915 -11.924  40.709  1.00 46.17           C  
ANISOU  134  CB  MET A  17     6477   4704   6362  -1609  -1152   1494       C  
ATOM    135  CG  MET A  17      -6.323 -12.532  40.785  1.00 49.06           C  
ANISOU  135  CG  MET A  17     6809   5109   6722  -1735  -1208   1627       C  
ATOM    136  SD  MET A  17      -6.457 -14.108  41.683  1.00 53.56           S  
ANISOU  136  SD  MET A  17     7363   5561   7426  -1932  -1446   1923       S  
ATOM    137  CE  MET A  17      -5.586 -15.218  40.588  1.00 50.19           C  
ANISOU  137  CE  MET A  17     7038   4731   7301  -1797  -1639   1784       C  
ATOM    138  N   TRP A  18      -2.323 -10.250  41.464  1.00 46.64           N  
ANISOU  138  N   TRP A  18     6487   4854   6379  -1541  -1049   1323       N  
ATOM    139  CA  TRP A  18      -0.892  -9.952  41.352  1.00 46.50           C  
ANISOU  139  CA  TRP A  18     6395   4814   6459  -1501  -1061   1262       C  
ATOM    140  C   TRP A  18      -0.203  -9.993  42.723  1.00 51.92           C  
ANISOU  140  C   TRP A  18     7025   5631   7072  -1614  -1202   1330       C  
ATOM    141  O   TRP A  18       0.895 -10.551  42.844  1.00 53.85           O  
ANISOU  141  O   TRP A  18     7167   5861   7433  -1576  -1331   1387       O  
ATOM    142  CB  TRP A  18      -0.641  -8.583  40.669  1.00 43.62           C  
ANISOU  142  CB  TRP A  18     6030   4440   6102  -1480   -875   1130       C  
ATOM    143  CG  TRP A  18       0.818  -8.298  40.507  1.00 45.11           C  
ANISOU  143  CG  TRP A  18     6089   4631   6418  -1482   -879   1106       C  
ATOM    144  CD1 TRP A  18       1.675  -7.819  41.453  1.00 48.58           C  
ANISOU  144  CD1 TRP A  18     6446   5149   6865  -1612   -966   1085       C  
ATOM    145  CD2 TRP A  18       1.608  -8.560  39.344  1.00 45.94           C  
ANISOU  145  CD2 TRP A  18     6096   4708   6651  -1348   -805   1103       C  
ATOM    146  CE2 TRP A  18       2.938  -8.202  39.653  1.00 50.08           C  
ANISOU  146  CE2 TRP A  18     6442   5303   7282  -1412   -832   1114       C  
ATOM    147  CE3 TRP A  18       1.320  -9.069  38.061  1.00 47.29           C  
ANISOU  147  CE3 TRP A  18     6300   4840   6828  -1173   -719   1077       C  
ATOM    148  NE1 TRP A  18       2.951  -7.766  40.953  1.00 48.53           N  
ANISOU  148  NE1 TRP A  18     6263   5156   7019  -1588   -956   1098       N  
ATOM    149  CZ2 TRP A  18       3.981  -8.345  38.735  1.00 50.95           C  
ANISOU  149  CZ2 TRP A  18     6375   5469   7515  -1298   -740   1129       C  
ATOM    150  CZ3 TRP A  18       2.355  -9.187  37.145  1.00 49.90           C  
ANISOU  150  CZ3 TRP A  18     6493   5230   7236  -1040   -625   1057       C  
ATOM    151  CH2 TRP A  18       3.665  -8.821  37.482  1.00 51.53           C  
ANISOU  151  CH2 TRP A  18     6493   5529   7558  -1098   -617   1099       C  
ATOM    152  N   ARG A  19      -0.854  -9.393  43.738  1.00 47.81           N  
ANISOU  152  N   ARG A  19     6557   5272   6335  -1727  -1180   1314       N  
ATOM    153  CA  ARG A  19      -0.364  -9.284  45.108  1.00 49.25           C  
ANISOU  153  CA  ARG A  19     6711   5658   6345  -1840  -1313   1345       C  
ATOM    154  C   ARG A  19      -0.133 -10.661  45.730  1.00 54.16           C  
ANISOU  154  C   ARG A  19     7284   6322   6971  -1854  -1521   1615       C  
ATOM    155  O   ARG A  19       0.866 -10.860  46.427  1.00 57.13           O  
ANISOU  155  O   ARG A  19     7577   6802   7327  -1884  -1694   1681       O  
ATOM    156  CB  ARG A  19      -1.325  -8.414  45.935  1.00 50.59           C  
ANISOU  156  CB  ARG A  19     6966   6019   6237  -1904  -1208   1235       C  
ATOM    157  CG  ARG A  19      -0.823  -8.007  47.328  1.00 59.80           C  
ANISOU  157  CG  ARG A  19     8130   7444   7149  -2011  -1328   1160       C  
ATOM    158  CD  ARG A  19      -1.692  -6.927  47.965  1.00 58.81           C  
ANISOU  158  CD  ARG A  19     8105   7475   6764  -2012  -1185    925       C  
ATOM    159  NE  ARG A  19      -3.130  -7.153  47.773  1.00 69.62           N  
ANISOU  159  NE  ARG A  19     9497   8915   8042  -1940  -1012   1015       N  
ATOM    160  CZ  ARG A  19      -3.894  -7.866  48.591  1.00 86.29           C  
ANISOU  160  CZ  ARG A  19    11571  11320   9895  -1983  -1013   1219       C  
ATOM    161  NH1 ARG A  19      -5.190  -8.011  48.342  1.00 80.24           N1+
ANISOU  161  NH1 ARG A  19    10771  10630   9085  -1937   -850   1307       N1+
ATOM    162  NH2 ARG A  19      -3.369  -8.437  49.668  1.00 74.24           N  
ANISOU  162  NH2 ARG A  19    10018  10043   8148  -2083  -1183   1372       N  
ATOM    163  N   ALA A  20      -1.016 -11.614  45.428  1.00 49.62           N  
ANISOU  163  N   ALA A  20     6753   5642   6457  -1838  -1529   1785       N  
ATOM    164  CA  ALA A  20      -0.929 -12.989  45.911  1.00 51.75           C  
ANISOU  164  CA  ALA A  20     7005   5853   6806  -1861  -1735   2085       C  
ATOM    165  C   ALA A  20       0.353 -13.659  45.393  1.00 57.13           C  
ANISOU  165  C   ALA A  20     7614   6325   7770  -1711  -1883   2095       C  
ATOM    166  O   ALA A  20       1.077 -14.268  46.178  1.00 57.14           O  
ANISOU  166  O   ALA A  20     7549   6378   7783  -1708  -2085   2296       O  
ATOM    167  CB  ALA A  20      -2.156 -13.773  45.477  1.00 52.04           C  
ANISOU  167  CB  ALA A  20     7100   5743   6931  -1905  -1714   2220       C  
ATOM    168  N   TYR A  21       0.651 -13.509  44.078  1.00 53.71           N  
ANISOU  168  N   TYR A  21     7170   5699   7536  -1563  -1774   1884       N  
ATOM    169  CA  TYR A  21       1.858 -14.100  43.497  1.00 55.49           C  
ANISOU  169  CA  TYR A  21     7293   5775   8015  -1369  -1864   1853       C  
ATOM    170  C   TYR A  21       3.128 -13.381  43.897  1.00 57.87           C  
ANISOU  170  C   TYR A  21     7421   6274   8294  -1367  -1886   1800       C  
ATOM    171  O   TYR A  21       4.149 -14.033  44.104  1.00 58.39           O  
ANISOU  171  O   TYR A  21     7347   6321   8518  -1243  -2048   1897       O  
ATOM    172  CB  TYR A  21       1.734 -14.378  41.987  1.00 56.95           C  
ANISOU  172  CB  TYR A  21     7520   5747   8372  -1190  -1743   1658       C  
ATOM    173  CG  TYR A  21       0.553 -15.277  41.702  1.00 61.46           C  
ANISOU  173  CG  TYR A  21     8244   6100   9007  -1219  -1807   1711       C  
ATOM    174  CD1 TYR A  21       0.487 -16.562  42.234  1.00 65.96           C  
ANISOU  174  CD1 TYR A  21     8858   6452   9753  -1222  -2042   1926       C  
ATOM    175  CD2 TYR A  21      -0.543 -14.811  40.980  1.00 61.16           C  
ANISOU  175  CD2 TYR A  21     8295   6072   8872  -1272  -1659   1580       C  
ATOM    176  CE1 TYR A  21      -0.633 -17.363  42.053  1.00 68.32           C  
ANISOU  176  CE1 TYR A  21     9283   6527  10148  -1318  -2127   1998       C  
ATOM    177  CE2 TYR A  21      -1.675 -15.599  40.802  1.00 62.85           C  
ANISOU  177  CE2 TYR A  21     8609   6118   9152  -1351  -1748   1637       C  
ATOM    178  CZ  TYR A  21      -1.713 -16.883  41.332  1.00 72.60           C  
ANISOU  178  CZ  TYR A  21     9884   7115  10585  -1394  -1984   1840       C  
ATOM    179  OH  TYR A  21      -2.803 -17.702  41.148  1.00 69.40           O  
ANISOU  179  OH  TYR A  21     9564   6506  10299  -1523  -2099   1910       O  
ATOM    180  N   SER A  22       3.049 -12.049  44.067  1.00 52.73           N  
ANISOU  180  N   SER A  22     6768   5798   7469  -1509  -1751   1651       N  
ATOM    181  CA  SER A  22       4.152 -11.227  44.547  1.00 52.89           C  
ANISOU  181  CA  SER A  22     6626   5999   7469  -1589  -1800   1579       C  
ATOM    182  C   SER A  22       4.526 -11.696  45.969  1.00 57.61           C  
ANISOU  182  C   SER A  22     7170   6793   7925  -1670  -2067   1764       C  
ATOM    183  O   SER A  22       5.694 -11.965  46.228  1.00 57.57           O  
ANISOU  183  O   SER A  22     6965   6879   8031  -1622  -2234   1832       O  
ATOM    184  CB  SER A  22       3.757  -9.753  44.522  1.00 54.02           C  
ANISOU  184  CB  SER A  22     6844   6200   7482  -1743  -1629   1373       C  
ATOM    185  OG  SER A  22       4.818  -8.943  45.002  1.00 59.12           O  
ANISOU  185  OG  SER A  22     7337   6977   8151  -1869  -1708   1284       O  
ATOM    186  N   ASP A  23       3.505 -11.911  46.836  1.00 56.51           N  
ANISOU  186  N   ASP A  23     7186   6750   7536  -1773  -2105   1883       N  
ATOM    187  CA  ASP A  23       3.656 -12.416  48.207  1.00 59.96           C  
ANISOU  187  CA  ASP A  23     7602   7428   7752  -1854  -2342   2117       C  
ATOM    188  C   ASP A  23       4.189 -13.858  48.245  1.00 67.41           C  
ANISOU  188  C   ASP A  23     8467   8227   8918  -1705  -2562   2436       C  
ATOM    189  O   ASP A  23       5.012 -14.181  49.105  1.00 68.86           O  
ANISOU  189  O   ASP A  23     8528   8596   9038  -1703  -2807   2620       O  
ATOM    190  CB  ASP A  23       2.323 -12.316  48.978  1.00 61.77           C  
ANISOU  190  CB  ASP A  23     7998   7831   7642  -1986  -2262   2192       C  
ATOM    191  CG  ASP A  23       1.976 -10.924  49.495  1.00 65.88           C  
ANISOU  191  CG  ASP A  23     8584   8585   7860  -2107  -2133   1890       C  
ATOM    192  OD1 ASP A  23       2.847 -10.018  49.410  1.00 65.03           O  
ANISOU  192  OD1 ASP A  23     8408   8495   7807  -2143  -2160   1642       O  
ATOM    193  OD2 ASP A  23       0.847 -10.748  50.020  1.00 66.40           O1-
ANISOU  193  OD2 ASP A  23     8760   8819   7649  -2165  -2013   1901       O1-
ATOM    194  N   MET A  24       3.727 -14.712  47.308  1.00 65.56           N  
ANISOU  194  N   MET A  24     8308   7649   8954  -1570  -2497   2486       N  
ATOM    195  CA  MET A  24       4.156 -16.109  47.158  1.00 69.07           C  
ANISOU  195  CA  MET A  24     8719   7827   9696  -1387  -2697   2732       C  
ATOM    196  C   MET A  24       5.676 -16.177  46.925  1.00 74.78           C  
ANISOU  196  C   MET A  24     9204   8574  10637  -1182  -2810   2675       C  
ATOM    197  O   MET A  24       6.352 -17.015  47.528  1.00 78.57           O  
ANISOU  197  O   MET A  24     9583   9042  11230  -1067  -3068   2943       O  
ATOM    198  CB  MET A  24       3.394 -16.782  46.001  1.00 70.91           C  
ANISOU  198  CB  MET A  24     9094   7667  10181  -1287  -2590   2649       C  
ATOM    199  CG  MET A  24       3.610 -18.283  45.906  1.00 78.75           C  
ANISOU  199  CG  MET A  24    10119   8292  11512  -1114  -2817   2878       C  
ATOM    200  SD  MET A  24       2.466 -19.050  44.729  1.00 83.01           S  
ANISOU  200  SD  MET A  24    10866   8373  12301  -1080  -2746   2742       S  
ATOM    201  CE  MET A  24       3.453 -20.417  44.203  1.00 83.82           C  
ANISOU  201  CE  MET A  24    10946   8024  12878   -720  -2979   2770       C  
ATOM    202  N   ARG A  25       6.206 -15.267  46.082  1.00 67.80           N  
ANISOU  202  N   ARG A  25     8205   7748   9809  -1142  -2616   2365       N  
ATOM    203  CA  ARG A  25       7.631 -15.147  45.774  1.00 68.39           C  
ANISOU  203  CA  ARG A  25     7987   7920  10077   -981  -2661   2294       C  
ATOM    204  C   ARG A  25       8.406 -14.667  46.994  1.00 74.27           C  
ANISOU  204  C   ARG A  25     8547   9021  10650  -1133  -2881   2404       C  
ATOM    205  O   ARG A  25       9.507 -15.159  47.232  1.00 78.48           O  
ANISOU  205  O   ARG A  25     8824   9643  11352   -975  -3077   2532       O  
ATOM    206  CB  ARG A  25       7.864 -14.174  44.602  1.00 65.10           C  
ANISOU  206  CB  ARG A  25     7496   7522   9718   -976  -2365   1991       C  
ATOM    207  CG  ARG A  25       7.502 -14.743  43.243  1.00 76.13           C  
ANISOU  207  CG  ARG A  25     8974   8646  11307   -730  -2188   1859       C  
ATOM    208  CD  ARG A  25       7.866 -13.793  42.115  1.00 85.73           C  
ANISOU  208  CD  ARG A  25    10076   9960  12538   -712  -1899   1633       C  
ATOM    209  NE  ARG A  25       6.674 -13.126  41.599  1.00 89.37           N  
ANISOU  209  NE  ARG A  25    10787  10342  12829   -856  -1701   1511       N  
ATOM    210  CZ  ARG A  25       6.388 -11.847  41.779  1.00 99.59           C  
ANISOU  210  CZ  ARG A  25    12114  11757  13967  -1095  -1579   1443       C  
ATOM    211  NH1 ARG A  25       7.196 -11.075  42.493  1.00 93.51           N1+
ANISOU  211  NH1 ARG A  25    11162  11180  13186  -1263  -1646   1456       N1+
ATOM    212  NH2 ARG A  25       5.273 -11.334  41.279  1.00 82.05           N  
ANISOU  212  NH2 ARG A  25    10107   9448  11620  -1166  -1414   1355       N  
ATOM    213  N   GLU A  26       7.837 -13.706  47.755  1.00 68.39           N  
ANISOU  213  N   GLU A  26     7924   8496   9566  -1419  -2860   2326       N  
ATOM    214  CA  GLU A  26       8.442 -13.114  48.946  1.00 70.62           C  
ANISOU  214  CA  GLU A  26     8079   9146   9607  -1604  -3081   2347       C  
ATOM    215  C   GLU A  26       8.593 -14.151  50.066  1.00 79.95           C  
ANISOU  215  C   GLU A  26     9244  10473  10660  -1551  -3403   2724       C  
ATOM    216  O   GLU A  26       9.697 -14.337  50.572  1.00 82.70           O  
ANISOU  216  O   GLU A  26     9340  11040  11042  -1507  -3667   2844       O  
ATOM    217  CB  GLU A  26       7.626 -11.895  49.415  1.00 70.24           C  
ANISOU  217  CB  GLU A  26     8224   9244   9220  -1873  -2951   2102       C  
ATOM    218  CG  GLU A  26       8.365 -10.979  50.388  1.00 79.43           C  
ANISOU  218  CG  GLU A  26     9262  10753  10166  -2084  -3155   1962       C  
ATOM    219  CD  GLU A  26       7.520  -9.868  50.988  1.00 87.00           C  
ANISOU  219  CD  GLU A  26    10450  11841  10765  -2300  -3061   1689       C  
ATOM    220  OE1 GLU A  26       7.800  -8.684  50.693  1.00 86.63           O  
ANISOU  220  OE1 GLU A  26    10385  11743  10789  -2447  -2977   1370       O  
ATOM    221  OE2 GLU A  26       6.571 -10.179  51.743  1.00 68.65           O1-
ANISOU  221  OE2 GLU A  26     8320   9663   8102  -2315  -3065   1800       O1-
ATOM    222  N   ALA A  27       7.484 -14.831  50.421  1.00 77.95           N  
ANISOU  222  N   ALA A  27     9234  10112  10272  -1564  -3388   2946       N  
ATOM    223  CA  ALA A  27       7.389 -15.869  51.447  1.00 81.87           C  
ANISOU  223  CA  ALA A  27     9761  10710  10635  -1541  -3661   3392       C  
ATOM    224  C   ALA A  27       8.419 -16.984  51.241  1.00 92.72           C  
ANISOU  224  C   ALA A  27    10942  11887  12401  -1252  -3901   3659       C  
ATOM    225  O   ALA A  27       9.094 -17.375  52.206  1.00 96.71           O  
ANISOU  225  O   ALA A  27    11310  12638  12798  -1221  -4215   3962       O  
ATOM    226  CB  ALA A  27       5.985 -16.461  51.463  1.00 81.10           C  
ANISOU  226  CB  ALA A  27     9929  10439  10446  -1619  -3536   3587       C  
ATOM    227  N   ASN A  28       8.543 -17.483  49.983  1.00 89.64           N  
ANISOU  227  N   ASN A  28    10539  11074  12447  -1015  -3758   3529       N  
ATOM    228  CA  ASN A  28       9.432 -18.578  49.565  1.00 93.02           C  
ANISOU  228  CA  ASN A  28    10804  11230  13312   -658  -3928   3692       C  
ATOM    229  C   ASN A  28       9.184 -19.878  50.373  1.00101.75           C  
ANISOU  229  C   ASN A  28    12022  12151  14490   -577  -4223   4207       C  
ATOM    230  O   ASN A  28      10.084 -20.697  50.559  1.00105.62           O  
ANISOU  230  O   ASN A  28    12335  12546  15248   -301  -4483   4452       O  
ATOM    231  CB  ASN A  28      10.914 -18.134  49.539  1.00 96.04           C  
ANISOU  231  CB  ASN A  28    10790  11897  13802   -525  -4036   3587       C  
ATOM    232  CG  ASN A  28      11.861 -19.051  48.787  1.00113.27           C  
ANISOU  232  CG  ASN A  28    12751  13819  16467    -91  -4085   3600       C  
ATOM    233  ND2 ASN A  28      11.395 -19.669  47.707  1.00100.08           N  
ANISOU  233  ND2 ASN A  28    11245  11716  15064    110  -3879   3423       N  
ATOM    234  OD1 ASN A  28      13.021 -19.226  49.175  1.00110.14           O  
ANISOU  234  OD1 ASN A  28    12021  13629  16198     88  -4316   3749       O  
ATOM    235  N   TYR A  29       7.932 -20.049  50.837  1.00 98.40           N  
ANISOU  235  N   TYR A  29    11873  11672  13841   -818  -4174   4396       N  
ATOM    236  CA  TYR A  29       7.454 -21.196  51.603  1.00102.53           C  
ANISOU  236  CA  TYR A  29    12534  12018  14406   -835  -4411   4943       C  
ATOM    237  C   TYR A  29       7.029 -22.304  50.644  1.00108.96           C  
ANISOU  237  C   TYR A  29    13510  12150  15739   -648  -4396   4966       C  
ATOM    238  O   TYR A  29       6.238 -22.069  49.731  1.00105.60           O  
ANISOU  238  O   TYR A  29    13230  11502  15389   -716  -4139   4635       O  
ATOM    239  CB  TYR A  29       6.278 -20.794  52.517  1.00103.08           C  
ANISOU  239  CB  TYR A  29    12779  12420  13968  -1208  -4330   5141       C  
ATOM    240  CG  TYR A  29       6.186 -21.636  53.766  1.00110.55           C  
ANISOU  240  CG  TYR A  29    13749  13511  14743  -1277  -4626   5793       C  
ATOM    241  CD1 TYR A  29       6.794 -21.230  54.950  1.00115.83           C  
ANISOU  241  CD1 TYR A  29    14278  14772  14958  -1344  -4827   5978       C  
ATOM    242  CD2 TYR A  29       5.516 -22.856  53.761  1.00114.01           C  
ANISOU  242  CD2 TYR A  29    14349  13494  15476  -1286  -4731   6246       C  
ATOM    243  CE1 TYR A  29       6.755 -22.025  56.095  1.00122.28           C  
ANISOU  243  CE1 TYR A  29    15112  15775  15573  -1393  -5111   6631       C  
ATOM    244  CE2 TYR A  29       5.466 -23.658  54.901  1.00120.57           C  
ANISOU  244  CE2 TYR A  29    15197  14447  16168  -1357  -5009   6930       C  
ATOM    245  CZ  TYR A  29       6.070 -23.229  56.073  1.00131.65           C  
ANISOU  245  CZ  TYR A  29    16458  16500  17064  -1403  -5187   7138       C  
ATOM    246  OH  TYR A  29       6.017 -24.011  57.204  1.00139.18           O  
ANISOU  246  OH  TYR A  29    17427  17633  17822  -1469  -5463   7858       O  
ATOM    247  N   ILE A  30       7.572 -23.506  50.839  1.00111.70           N  
ANISOU  247  N   ILE A  30    13835  12151  16453   -402  -4696   5344       N  
ATOM    248  CA  ILE A  30       7.267 -24.661  49.991  1.00113.34           C  
ANISOU  248  CA  ILE A  30    14217  11636  17211   -197  -4750   5351       C  
ATOM    249  C   ILE A  30       5.873 -25.204  50.334  1.00116.42           C  
ANISOU  249  C   ILE A  30    14882  11787  17564   -537  -4757   5686       C  
ATOM    250  O   ILE A  30       5.525 -25.312  51.509  1.00118.22           O  
ANISOU  250  O   ILE A  30    15129  12289  17501   -775  -4892   6205       O  
ATOM    251  CB  ILE A  30       8.373 -25.759  50.048  1.00122.58           C  
ANISOU  251  CB  ILE A  30    15266  12452  18858    239  -5081   5612       C  
ATOM    252  CG1 ILE A  30       9.786 -25.180  50.349  1.00124.06           C  
ANISOU  252  CG1 ILE A  30    15077  13120  18941    480  -5158   5521       C  
ATOM    253  CG2 ILE A  30       8.385 -26.576  48.754  1.00124.79           C  
ANISOU  253  CG2 ILE A  30    15680  12014  19722    569  -5054   5298       C  
ATOM    254  CD1 ILE A  30      10.245 -25.302  51.808  1.00136.27           C  
ANISOU  254  CD1 ILE A  30    16479  15092  20207    399  -5485   6087       C  
ATOM    255  N   GLY A  31       4.928 -25.539  49.397  1.00110.61           N  
ANISOU  255  N   GLY A  31    14334  10590  17101   -566  -4614   5397       N  
ATOM    256  CA  GLY A  31       3.414 -25.757  49.608  1.00111.16           C  
ANISOU  256  CA  GLY A  31    14623  10409  17202   -915  -4611   5666       C  
ATOM    257  C   GLY A  31       2.218 -24.681  49.472  1.00111.28           C  
ANISOU  257  C   GLY A  31    14646  10946  16692  -1294  -4311   5543       C  
ATOM    258  O   GLY A  31       0.836 -24.674  49.508  1.00111.43           O  
ANISOU  258  O   GLY A  31    14772  10926  16642  -1624  -4285   5837       O  
ATOM    259  N   SER A  32       2.807 -23.560  49.237  1.00103.94           N  
ANISOU  259  N   SER A  32    13583  10494  15416  -1244  -4081   5112       N  
ATOM    260  CA  SER A  32       2.102 -22.378  49.254  1.00 99.38           C  
ANISOU  260  CA  SER A  32    13005  10395  14359  -1525  -3789   4916       C  
ATOM    261  C   SER A  32       1.326 -22.350  48.112  1.00 98.88           C  
ANISOU  261  C   SER A  32    13057  10073  14441  -1586  -3571   4533       C  
ATOM    262  O   SER A  32       0.428 -21.743  48.120  1.00 96.52           O  
ANISOU  262  O   SER A  32    12784  10043  13844  -1844  -3370   4500       O  
ATOM    263  CB  SER A  32       3.125 -21.363  49.241  1.00100.40           C  
ANISOU  263  CB  SER A  32    12969  11029  14149  -1448  -3672   4600       C  
ATOM    264  OG  SER A  32       4.149 -21.861  48.477  1.00108.37           O  
ANISOU  264  OG  SER A  32    13890  11845  15440  -1156  -3616   4183       O  
ATOM    265  N   ASP A  33       1.643 -23.074  47.121  1.00 94.80           N  
ANISOU  265  N   ASP A  33    12594   9066  14360  -1322  -3614   4230       N  
ATOM    266  CA  ASP A  33       0.996 -22.737  45.989  1.00 91.94           C  
ANISOU  266  CA  ASP A  33    12342   8435  14154  -1313  -3459   3815       C  
ATOM    267  C   ASP A  33      -0.307 -22.718  46.203  1.00 91.73           C  
ANISOU  267  C   ASP A  33    12396   8492  13967  -1678  -3348   3921       C  
ATOM    268  O   ASP A  33      -0.811 -21.813  45.900  1.00 88.39           O  
ANISOU  268  O   ASP A  33    11945   8360  13279  -1750  -3093   3619       O  
ATOM    269  CB  ASP A  33       1.037 -23.700  44.943  1.00 97.47           C  
ANISOU  269  CB  ASP A  33    13157   8486  15391  -1041  -3653   3675       C  
ATOM    270  CG  ASP A  33       2.248 -23.863  44.524  1.00111.95           C  
ANISOU  270  CG  ASP A  33    14872  10299  17366   -607  -3641   3363       C  
ATOM    271  OD1 ASP A  33       3.023 -23.665  45.384  1.00116.33           O  
ANISOU  271  OD1 ASP A  33    15302  10896  18002   -439  -3814   3628       O  
ATOM    272  OD2 ASP A  33       2.453 -24.187  43.427  1.00114.84           O1-
ANISOU  272  OD2 ASP A  33    15245  10637  17750   -427  -3460   2877       O1-
ATOM    273  N   LYS A  34      -0.935 -23.647  46.800  1.00 88.55           N  
ANISOU  273  N   LYS A  34    12062   7859  13723  -1911  -3537   4394       N  
ATOM    274  CA  LYS A  34      -2.341 -23.525  46.996  1.00 86.91           C  
ANISOU  274  CA  LYS A  34    11871   7737  13412  -2290  -3458   4597       C  
ATOM    275  C   LYS A  34      -2.769 -22.542  47.891  1.00 86.05           C  
ANISOU  275  C   LYS A  34    11633   8329  12732  -2477  -3197   4672       C  
ATOM    276  O   LYS A  34      -3.632 -21.926  47.626  1.00 83.85           O  
ANISOU  276  O   LYS A  34    11324   8234  12302  -2613  -2990   4469       O  
ATOM    277  CB  LYS A  34      -2.931 -24.832  47.378  1.00 93.92           C  
ANISOU  277  CB  LYS A  34    12829   8226  14628  -2516  -3735   5173       C  
ATOM    278  CG  LYS A  34      -2.754 -25.820  46.353  1.00 96.50           C  
ANISOU  278  CG  LYS A  34    13327   7764  15575  -2412  -3984   5010       C  
ATOM    279  CD  LYS A  34      -3.031 -27.138  46.896  1.00101.56           C  
ANISOU  279  CD  LYS A  34    14054   7916  16617  -2626  -4301   5629       C  
ATOM    280  CE  LYS A  34      -4.360 -27.315  47.467  1.00 97.06           C  
ANISOU  280  CE  LYS A  34    13473   7271  16135  -3110  -4308   5909       C  
ATOM    281  NZ  LYS A  34      -4.261 -28.664  47.316  1.00108.95           N1+
ANISOU  281  NZ  LYS A  34    15108   8077  18211  -3298  -4667   6406       N1+
ATOM    282  N   TYR A  35      -2.164 -22.349  48.985  1.00 81.77           N  
ANISOU  282  N   TYR A  35    11014   8187  11867  -2461  -3217   4931       N  
ATOM    283  CA  TYR A  35      -2.903 -21.326  49.708  1.00 79.62           C  
ANISOU  283  CA  TYR A  35    10643   8587  11024  -2600  -2985   4943       C  
ATOM    284  C   TYR A  35      -3.021 -20.087  48.855  1.00 80.07           C  
ANISOU  284  C   TYR A  35    10678   8844  10901  -2480  -2714   4352       C  
ATOM    285  O   TYR A  35      -3.818 -19.236  49.122  1.00 78.61           O  
ANISOU  285  O   TYR A  35    10449   8974  10444  -2618  -2486   4267       O  
ATOM    286  CB  TYR A  35      -2.235 -20.976  51.034  1.00 82.11           C  
ANISOU  286  CB  TYR A  35    10896   9291  11009  -2563  -3104   5233       C  
ATOM    287  CG  TYR A  35      -2.538 -19.743  51.767  1.00 81.49           C  
ANISOU  287  CG  TYR A  35    10745   9897  10321  -2649  -2874   5098       C  
ATOM    288  CD1 TYR A  35      -3.499 -19.634  52.498  1.00 85.28           C  
ANISOU  288  CD1 TYR A  35    11177  10785  10439  -2895  -2725   5395       C  
ATOM    289  CD2 TYR A  35      -1.764 -18.710  51.732  1.00 79.17           C  
ANISOU  289  CD2 TYR A  35    10422   9826   9833  -2483  -2789   4635       C  
ATOM    290  CE1 TYR A  35      -3.703 -18.605  53.083  1.00 85.06           C  
ANISOU  290  CE1 TYR A  35    11095  11376   9847  -2921  -2496   5190       C  
ATOM    291  CE2 TYR A  35      -2.042 -17.681  52.339  1.00 79.06           C  
ANISOU  291  CE2 TYR A  35    10376  10359   9302  -2549  -2592   4431       C  
ATOM    292  CZ  TYR A  35      -3.011 -17.659  52.978  1.00 86.70           C  
ANISOU  292  CZ  TYR A  35    11318  11729   9894  -2741  -2444   4685       C  
ATOM    293  OH  TYR A  35      -3.339 -16.624  53.609  1.00 85.51           O  
ANISOU  293  OH  TYR A  35    11148  12119   9225  -2755  -2243   4429       O  
ATOM    294  N   PHE A  36      -2.074 -19.842  47.976  1.00 74.88           N  
ANISOU  294  N   PHE A  36    10029   8022  10399  -2214  -2734   3982       N  
ATOM    295  CA  PHE A  36      -2.090 -18.507  47.373  1.00 71.15           C  
ANISOU  295  CA  PHE A  36     9539   7698   9798  -2105  -2495   3484       C  
ATOM    296  C   PHE A  36      -2.814 -18.399  46.210  1.00 70.99           C  
ANISOU  296  C   PHE A  36     9576   7447   9951  -2117  -2368   3244       C  
ATOM    297  O   PHE A  36      -3.334 -17.474  46.004  1.00 67.81           O  
ANISOU  297  O   PHE A  36     9154   7264   9345  -2131  -2142   2991       O  
ATOM    298  CB  PHE A  36      -0.729 -17.956  46.952  1.00 72.38           C  
ANISOU  298  CB  PHE A  36     9637   7816  10049  -1862  -2540   3233       C  
ATOM    299  CG  PHE A  36       0.067 -17.371  48.018  1.00 75.40           C  
ANISOU  299  CG  PHE A  36     9926   8584  10139  -1886  -2621   3349       C  
ATOM    300  CD1 PHE A  36      -0.382 -16.480  48.745  1.00 77.59           C  
ANISOU  300  CD1 PHE A  36    10182   9276  10020  -1995  -2454   3166       C  
ATOM    301  CD2 PHE A  36       1.239 -17.747  48.244  1.00 81.25           C  
ANISOU  301  CD2 PHE A  36    10600   9268  11002  -1788  -2889   3623       C  
ATOM    302  CE1 PHE A  36       0.335 -16.022  49.603  1.00 80.67           C  
ANISOU  302  CE1 PHE A  36    10500  10035  10117  -2033  -2566   3219       C  
ATOM    303  CE2 PHE A  36       1.838 -17.258  49.130  1.00 86.43           C  
ANISOU  303  CE2 PHE A  36    11155  10331  11356  -1822  -3004   3725       C  
ATOM    304  CZ  PHE A  36       1.389 -16.411  49.784  1.00 83.21           C  
ANISOU  304  CZ  PHE A  36    10740  10348  10529  -1959  -2847   3503       C  
ATOM    305  N   HIS A  37      -2.891 -19.463  45.515  1.00 68.45           N  
ANISOU  305  N   HIS A  37     9329   6675  10003  -2118  -2538   3334       N  
ATOM    306  CA  HIS A  37      -3.724 -19.502  44.490  1.00 66.90           C  
ANISOU  306  CA  HIS A  37     9187   6266   9966  -2165  -2485   3125       C  
ATOM    307  C   HIS A  37      -4.993 -19.307  45.113  1.00 70.92           C  
ANISOU  307  C   HIS A  37     9618   7080  10247  -2451  -2357   3325       C  
ATOM    308  O   HIS A  37      -5.791 -19.083  44.485  1.00 68.61           O  
ANISOU  308  O   HIS A  37     9294   6917   9857  -2459  -2188   3083       O  
ATOM    309  CB  HIS A  37      -3.737 -20.748  43.927  1.00 70.36           C  
ANISOU  309  CB  HIS A  37     9737   6132  10863  -2134  -2751   3174       C  
ATOM    310  CG  HIS A  37      -2.614 -21.017  43.076  1.00 73.40           C  
ANISOU  310  CG  HIS A  37    10185   6224  11481  -1785  -2822   2848       C  
ATOM    311  CD2 HIS A  37      -1.942 -20.263  42.266  1.00 71.86           C  
ANISOU  311  CD2 HIS A  37     9962   6162  11180  -1541  -2646   2443       C  
ATOM    312  ND1 HIS A  37      -2.092 -22.232  42.916  1.00 78.79           N  
ANISOU  312  ND1 HIS A  37    10952   6427  12556  -1653  -3090   2953       N  
ATOM    313  CE1 HIS A  37      -1.114 -22.234  42.077  1.00 77.25           C  
ANISOU  313  CE1 HIS A  37    10761   6132  12457  -1304  -3050   2576       C  
ATOM    314  NE2 HIS A  37      -1.017 -21.039  41.650  1.00 73.63           N  
ANISOU  314  NE2 HIS A  37    10226   6053  11694  -1246  -2778   2282       N  
ATOM    315  N   ALA A  38      -5.240 -19.404  46.371  1.00 69.32           N  
ANISOU  315  N   ALA A  38     9358   7060   9920  -2660  -2418   3785       N  
ATOM    316  CA  ALA A  38      -6.582 -19.142  46.830  1.00 69.65           C  
ANISOU  316  CA  ALA A  38     9273   7482   9707  -2926  -2275   4052       C  
ATOM    317  C   ALA A  38      -6.880 -17.977  47.569  1.00 71.36           C  
ANISOU  317  C   ALA A  38     9407   8270   9437  -2861  -1992   3877       C  
ATOM    318  O   ALA A  38      -7.856 -17.716  47.729  1.00 70.92           O  
ANISOU  318  O   ALA A  38     9242   8490   9215  -2951  -1798   3841       O  
ATOM    319  CB  ALA A  38      -7.039 -20.296  47.591  1.00 74.65           C  
ANISOU  319  CB  ALA A  38     9874   8117  10372  -3165  -2441   4652       C  
ATOM    320  N   ARG A  39      -5.975 -17.322  48.114  1.00 67.70           N  
ANISOU  320  N   ARG A  39     8981   7978   8764  -2704  -1985   3761       N  
ATOM    321  CA  ARG A  39      -6.033 -15.985  48.731  1.00 66.82           C  
ANISOU  321  CA  ARG A  39     8828   8348   8215  -2642  -1759   3542       C  
ATOM    322  C   ARG A  39      -6.303 -14.871  47.705  1.00 67.79           C  
ANISOU  322  C   ARG A  39     8967   8425   8364  -2490  -1561   3076       C  
ATOM    323  O   ARG A  39      -7.149 -14.000  47.941  1.00 67.32           O  
ANISOU  323  O   ARG A  39     8847   8684   8049  -2487  -1342   2954       O  
ATOM    324  CB  ARG A  39      -4.759 -15.691  49.550  1.00 67.21           C  
ANISOU  324  CB  ARG A  39     8910   8560   8068  -2553  -1866   3524       C  
ATOM    325  CG  ARG A  39      -4.946 -14.596  50.605  1.00 67.49           C  
ANISOU  325  CG  ARG A  39     8915   9136   7593  -2557  -1694   3384       C  
ATOM    326  CD  ARG A  39      -3.630 -13.932  50.972  1.00 70.41           C  
ANISOU  326  CD  ARG A  39     9324   9582   7846  -2445  -1796   3142       C  
ATOM    327  NE  ARG A  39      -3.207 -12.940  49.978  1.00 63.78           N  
ANISOU  327  NE  ARG A  39     8524   8516   7193  -2304  -1695   2681       N  
ATOM    328  CZ  ARG A  39      -2.076 -12.244  50.030  1.00 76.64           C  
ANISOU  328  CZ  ARG A  39    10157  10134   8828  -2233  -1772   2435       C  
ATOM    329  NH1 ARG A  39      -1.227 -12.413  51.040  1.00 71.48           N1+
ANISOU  329  NH1 ARG A  39     9468   9702   7991  -2272  -1975   2563       N1+
ATOM    330  NH2 ARG A  39      -1.784 -11.372  49.074  1.00 66.56           N  
ANISOU  330  NH2 ARG A  39     8903   8644   7741  -2139  -1658   2089       N  
ATOM    331  N   GLY A  40      -5.603 -14.922  46.576  1.00 62.41           N  
ANISOU  331  N   GLY A  40     8361   7368   7986  -2344  -1634   2840       N  
ATOM    332  CA  GLY A  40      -5.778 -13.961  45.492  1.00 58.75           C  
ANISOU  332  CA  GLY A  40     7920   6835   7567  -2200  -1471   2468       C  
ATOM    333  C   GLY A  40      -7.177 -14.017  44.925  1.00 61.72           C  
ANISOU  333  C   GLY A  40     8236   7236   7977  -2270  -1377   2482       C  
ATOM    334  O   GLY A  40      -7.776 -12.975  44.651  1.00 60.41           O  
ANISOU  334  O   GLY A  40     8037   7237   7677  -2187  -1183   2285       O  
ATOM    335  N   ASN A  41      -7.703 -15.250  44.741  1.00 59.59           N  
ANISOU  335  N   ASN A  41     7941   6778   7921  -2428  -1537   2726       N  
ATOM    336  CA  ASN A  41      -9.056 -15.495  44.244  1.00 59.28           C  
ANISOU  336  CA  ASN A  41     7800   6770   7955  -2555  -1508   2784       C  
ATOM    337  C   ASN A  41     -10.099 -15.004  45.242  1.00 65.19           C  
ANISOU  337  C   ASN A  41     8373   7992   8403  -2672  -1315   2973       C  
ATOM    338  O   ASN A  41     -11.106 -14.448  44.823  1.00 64.78           O  
ANISOU  338  O   ASN A  41     8200   8116   8299  -2651  -1176   2879       O  
ATOM    339  CB  ASN A  41      -9.256 -16.963  43.887  1.00 57.55           C  
ANISOU  339  CB  ASN A  41     7604   6181   8080  -2735  -1770   2989       C  
ATOM    340  CG  ASN A  41      -8.790 -17.304  42.491  1.00 65.13           C  
ANISOU  340  CG  ASN A  41     8698   6736   9310  -2583  -1906   2673       C  
ATOM    341  ND2 ASN A  41      -7.545 -17.690  42.382  1.00 53.09           N  
ANISOU  341  ND2 ASN A  41     7305   4956   7913  -2418  -2011   2579       N  
ATOM    342  OD1 ASN A  41      -9.531 -17.227  41.495  1.00 55.61           O  
ANISOU  342  OD1 ASN A  41     7466   5488   8176  -2591  -1918   2503       O  
ATOM    343  N   TYR A  42      -9.823 -15.123  46.550  1.00 65.20           N  
ANISOU  343  N   TYR A  42     8351   8248   8175  -2758  -1295   3221       N  
ATOM    344  CA  TYR A  42     -10.732 -14.682  47.614  1.00 68.33           C  
ANISOU  344  CA  TYR A  42     8577   9176   8210  -2840  -1085   3394       C  
ATOM    345  C   TYR A  42     -10.804 -13.164  47.670  1.00 71.36           C  
ANISOU  345  C   TYR A  42     8968   9827   8319  -2594   -836   3005       C  
ATOM    346  O   TYR A  42     -11.907 -12.612  47.676  1.00 72.81           O  
ANISOU  346  O   TYR A  42     8990  10301   8375  -2555   -636   2963       O  
ATOM    347  CB  TYR A  42     -10.353 -15.299  48.988  1.00 72.70           C  
ANISOU  347  CB  TYR A  42     9124   9957   8542  -2990  -1155   3781       C  
ATOM    348  CG  TYR A  42     -11.152 -14.761  50.162  1.00 77.51           C  
ANISOU  348  CG  TYR A  42     9563  11209   8677  -3035   -906   3929       C  
ATOM    349  CD1 TYR A  42     -12.381 -15.316  50.509  1.00 83.19           C  
ANISOU  349  CD1 TYR A  42    10042  12204   9361  -3265   -813   4317       C  
ATOM    350  CD2 TYR A  42     -10.677 -13.696  50.929  1.00 77.73           C  
ANISOU  350  CD2 TYR A  42     9656  11591   8288  -2852   -763   3666       C  
ATOM    351  CE1 TYR A  42     -13.121 -14.822  51.587  1.00 87.54           C  
ANISOU  351  CE1 TYR A  42    10403  13423   9435  -3274   -543   4451       C  
ATOM    352  CE2 TYR A  42     -11.415 -13.185  51.998  1.00 81.52           C  
ANISOU  352  CE2 TYR A  42     9989  12698   8285  -2846   -518   3736       C  
ATOM    353  CZ  TYR A  42     -12.628 -13.762  52.333  1.00 91.72           C  
ANISOU  353  CZ  TYR A  42    11026  14312   9513  -3041   -389   4139       C  
ATOM    354  OH  TYR A  42     -13.349 -13.267  53.391  1.00 96.55           O  
ANISOU  354  OH  TYR A  42    11460  15612   9611  -3005   -110   4210       O  
ATOM    355  N   ASP A  43      -9.635 -12.502  47.713  1.00 65.93           N  
ANISOU  355  N   ASP A  43     8451   9025   7575  -2430   -862   2728       N  
ATOM    356  CA  ASP A  43      -9.522 -11.045  47.750  1.00 64.75           C  
ANISOU  356  CA  ASP A  43     8356   9010   7238  -2215   -674   2338       C  
ATOM    357  C   ASP A  43     -10.178 -10.415  46.524  1.00 66.82           C  
ANISOU  357  C   ASP A  43     8595   9103   7692  -2069   -568   2120       C  
ATOM    358  O   ASP A  43     -10.964  -9.478  46.683  1.00 68.81           O  
ANISOU  358  O   ASP A  43     8779   9580   7785  -1927   -363   1956       O  
ATOM    359  CB  ASP A  43      -8.049 -10.605  47.855  1.00 65.24           C  
ANISOU  359  CB  ASP A  43     8585   8900   7304  -2138   -783   2126       C  
ATOM    360  CG  ASP A  43      -7.327 -11.005  49.125  1.00 74.39           C  
ANISOU  360  CG  ASP A  43     9762  10291   8213  -2242   -905   2302       C  
ATOM    361  OD1 ASP A  43      -7.934 -11.696  49.959  1.00 77.10           O  
ANISOU  361  OD1 ASP A  43    10006  10936   8352  -2379   -894   2632       O  
ATOM    362  OD2 ASP A  43      -6.141 -10.643  49.270  1.00 80.44           O1-
ANISOU  362  OD2 ASP A  43    10620  10960   8984  -2198  -1022   2141       O1-
ATOM    363  N   ALA A  44      -9.872 -10.937  45.309  1.00 58.98           N  
ANISOU  363  N   ALA A  44     7653   7735   7022  -2079   -713   2116       N  
ATOM    364  CA  ALA A  44     -10.441 -10.444  44.047  1.00 55.69           C  
ANISOU  364  CA  ALA A  44     7219   7180   6762  -1948   -657   1951       C  
ATOM    365  C   ALA A  44     -11.966 -10.584  44.055  1.00 59.16           C  
ANISOU  365  C   ALA A  44     7437   7882   7160  -2004   -570   2098       C  
ATOM    366  O   ALA A  44     -12.648  -9.609  43.779  1.00 58.54           O  
ANISOU  366  O   ALA A  44     7288   7932   7022  -1825   -411   1950       O  
ATOM    367  CB  ALA A  44      -9.850 -11.197  42.865  1.00 54.76           C  
ANISOU  367  CB  ALA A  44     7195   6688   6923  -1961   -847   1927       C  
ATOM    368  N   ALA A  45     -12.499 -11.764  44.455  1.00 56.92           N  
ANISOU  368  N   ALA A  45     7021   7686   6920  -2255   -675   2418       N  
ATOM    369  CA  ALA A  45     -13.943 -12.006  44.524  1.00 58.37           C  
ANISOU  369  CA  ALA A  45     6930   8161   7089  -2372   -606   2618       C  
ATOM    370  C   ALA A  45     -14.651 -11.046  45.479  1.00 62.54           C  
ANISOU  370  C   ALA A  45     7292   9180   7289  -2237   -316   2590       C  
ATOM    371  O   ALA A  45     -15.798 -10.667  45.214  1.00 62.32           O  
ANISOU  371  O   ALA A  45     7031   9399   7250  -2165   -190   2599       O  
ATOM    372  CB  ALA A  45     -14.219 -13.443  44.920  1.00 61.51           C  
ANISOU  372  CB  ALA A  45     7230   8522   7621  -2717   -783   3010       C  
ATOM    373  N   LYS A  46     -13.945 -10.620  46.563  1.00 59.57           N  
ANISOU  373  N   LYS A  46     7034   8960   6639  -2174   -219   2524       N  
ATOM    374  CA  LYS A  46     -14.459  -9.707  47.594  1.00 61.68           C  
ANISOU  374  CA  LYS A  46     7198   9699   6538  -2009     53   2416       C  
ATOM    375  C   LYS A  46     -14.725  -8.288  47.044  1.00 63.17           C  
ANISOU  375  C   LYS A  46     7426   9835   6742  -1661    216   2022       C  
ATOM    376  O   LYS A  46     -15.571  -7.573  47.580  1.00 65.27           O  
ANISOU  376  O   LYS A  46     7527  10476   6797  -1475    453   1928       O  
ATOM    377  CB  LYS A  46     -13.528  -9.697  48.824  1.00 65.17           C  
ANISOU  377  CB  LYS A  46     7798  10287   6676  -2044     45   2400       C  
ATOM    378  CG  LYS A  46     -14.160  -9.109  50.091  1.00 89.01           C  
ANISOU  378  CG  LYS A  46    10686  13906   9227  -1935    310   2356       C  
ATOM    379  CD  LYS A  46     -13.358  -9.417  51.362  1.00101.04           C  
ANISOU  379  CD  LYS A  46    12311  15681  10400  -2063    248   2490       C  
ATOM    380  CE  LYS A  46     -14.147  -9.056  52.599  1.00112.99           C  
ANISOU  380  CE  LYS A  46    13660  17887  11383  -1970    526   2490       C  
ATOM    381  NZ  LYS A  46     -13.666  -9.784  53.800  1.00122.60           N1+
ANISOU  381  NZ  LYS A  46    14889  19464  12231  -2177    452   2828       N1+
ATOM    382  N   ARG A  47     -14.026  -7.906  45.967  1.00 56.25           N  
ANISOU  382  N   ARG A  47     6751   8499   6122  -1561     94   1818       N  
ATOM    383  CA  ARG A  47     -14.156  -6.606  45.301  1.00 55.63           C  
ANISOU  383  CA  ARG A  47     6743   8270   6125  -1255    205   1515       C  
ATOM    384  C   ARG A  47     -15.538  -6.445  44.666  1.00 62.28           C  
ANISOU  384  C   ARG A  47     7319   9290   7053  -1136    290   1602       C  
ATOM    385  O   ARG A  47     -16.030  -5.316  44.543  1.00 63.20           O  
ANISOU  385  O   ARG A  47     7401   9460   7151   -832    452   1405       O  
ATOM    386  CB  ARG A  47     -13.079  -6.435  44.207  1.00 51.46           C  
ANISOU  386  CB  ARG A  47     6455   7250   5846  -1233     49   1389       C  
ATOM    387  CG  ARG A  47     -11.632  -6.462  44.693  1.00 58.64           C  
ANISOU  387  CG  ARG A  47     7585   7975   6720  -1329    -48   1289       C  
ATOM    388  CD  ARG A  47     -11.284  -5.287  45.578  1.00 61.65           C  
ANISOU  388  CD  ARG A  47     8087   8407   6930  -1177     78    993       C  
ATOM    389  NE  ARG A  47      -9.847  -5.212  45.809  1.00 63.53           N  
ANISOU  389  NE  ARG A  47     8511   8427   7201  -1280    -58    885       N  
ATOM    390  CZ  ARG A  47      -9.227  -4.171  46.347  1.00 76.91           C  
ANISOU  390  CZ  ARG A  47    10352  10044   8828  -1206    -29    591       C  
ATOM    391  NH1 ARG A  47      -9.918  -3.105  46.735  1.00 62.84           N1+
ANISOU  391  NH1 ARG A  47     8589   8347   6940   -995    139    341       N1+
ATOM    392  NH2 ARG A  47      -7.913  -4.183  46.501  1.00 66.68           N  
ANISOU  392  NH2 ARG A  47     9170   8576   7589  -1336   -181    528       N  
ATOM    393  N   GLY A  48     -16.115  -7.576  44.252  1.00 58.74           N  
ANISOU  393  N   GLY A  48     6688   8903   6730  -1375    153   1890       N  
ATOM    394  CA  GLY A  48     -17.414  -7.670  43.604  1.00 60.25           C  
ANISOU  394  CA  GLY A  48     6576   9291   7026  -1344    162   2020       C  
ATOM    395  C   GLY A  48     -17.387  -8.521  42.343  1.00 61.81           C  
ANISOU  395  C   GLY A  48     6786   9211   7486  -1530   -114   2126       C  
ATOM    396  O   GLY A  48     -16.387  -9.196  42.064  1.00 59.97           O  
ANISOU  396  O   GLY A  48     6785   8647   7354  -1692   -296   2122       O  
ATOM    397  N   PRO A  49     -18.474  -8.478  41.540  1.00 57.38           N  
ANISOU  397  N   PRO A  49     5973   8795   7033  -1483   -162   2195       N  
ATOM    398  CA  PRO A  49     -18.532  -9.289  40.311  1.00 56.55           C  
ANISOU  398  CA  PRO A  49     5882   8466   7138  -1659   -456   2243       C  
ATOM    399  C   PRO A  49     -17.372  -9.136  39.322  1.00 58.52           C  
ANISOU  399  C   PRO A  49     6490   8285   7460  -1556   -588   2033       C  
ATOM    400  O   PRO A  49     -16.970 -10.120  38.701  1.00 57.30           O  
ANISOU  400  O   PRO A  49     6443   7894   7433  -1754   -825   2037       O  
ATOM    401  CB  PRO A  49     -19.864  -8.881  39.695  1.00 60.66           C  
ANISOU  401  CB  PRO A  49     6063   9287   7699  -1533   -454   2303       C  
ATOM    402  CG  PRO A  49     -20.682  -8.467  40.848  1.00 67.44           C  
ANISOU  402  CG  PRO A  49     6626  10590   8408  -1441   -177   2408       C  
ATOM    403  CD  PRO A  49     -19.742  -7.757  41.752  1.00 61.42           C  
ANISOU  403  CD  PRO A  49     6146   9721   7470  -1261     32   2224       C  
ATOM    404  N   GLY A  50     -16.849  -7.923  39.181  1.00 54.30           N  
ANISOU  404  N   GLY A  50     6126   7650   6855  -1251   -434   1854       N  
ATOM    405  CA  GLY A  50     -15.711  -7.652  38.310  1.00 52.07           C  
ANISOU  405  CA  GLY A  50     6145   7019   6619  -1152   -503   1699       C  
ATOM    406  C   GLY A  50     -14.469  -8.386  38.780  1.00 53.81           C  
ANISOU  406  C   GLY A  50     6578   7006   6862  -1333   -569   1667       C  
ATOM    407  O   GLY A  50     -13.704  -8.907  37.963  1.00 50.38           O  
ANISOU  407  O   GLY A  50     6303   6334   6507  -1375   -717   1601       O  
ATOM    408  N   GLY A  51     -14.319  -8.469  40.107  1.00 51.72           N  
ANISOU  408  N   GLY A  51     6291   6854   6506  -1422   -465   1718       N  
ATOM    409  CA  GLY A  51     -13.233  -9.179  40.772  1.00 50.51           C  
ANISOU  409  CA  GLY A  51     6291   6543   6356  -1588   -539   1742       C  
ATOM    410  C   GLY A  51     -13.320 -10.674  40.541  1.00 55.00           C  
ANISOU  410  C   GLY A  51     6825   6999   7074  -1850   -772   1907       C  
ATOM    411  O   GLY A  51     -12.293 -11.304  40.275  1.00 54.77           O  
ANISOU  411  O   GLY A  51     6969   6691   7150  -1901   -910   1864       O  
ATOM    412  N   VAL A  52     -14.551 -11.246  40.612  1.00 51.04           N  
ANISOU  412  N   VAL A  52     6083   6698   6613  -2015   -826   2092       N  
ATOM    413  CA  VAL A  52     -14.820 -12.673  40.366  1.00 52.83           C  
ANISOU  413  CA  VAL A  52     6257   6775   7042  -2311  -1080   2260       C  
ATOM    414  C   VAL A  52     -14.378 -13.017  38.925  1.00 57.49           C  
ANISOU  414  C   VAL A  52     7015   7042   7785  -2246  -1288   2041       C  
ATOM    415  O   VAL A  52     -13.652 -13.990  38.704  1.00 57.36           O  
ANISOU  415  O   VAL A  52     7158   6703   7932  -2350  -1483   2012       O  
ATOM    416  CB  VAL A  52     -16.331 -13.027  40.599  1.00 59.28           C  
ANISOU  416  CB  VAL A  52     6724   7913   7886  -2514  -1085   2500       C  
ATOM    417  CG1 VAL A  52     -16.682 -14.413  40.051  1.00 60.74           C  
ANISOU  417  CG1 VAL A  52     6864   7865   8351  -2846  -1401   2632       C  
ATOM    418  CG2 VAL A  52     -16.710 -12.916  42.073  1.00 60.72           C  
ANISOU  418  CG2 VAL A  52     6727   8472   7873  -2589   -863   2741       C  
ATOM    419  N   TRP A  53     -14.829 -12.199  37.961  1.00 53.64           N  
ANISOU  419  N   TRP A  53     6490   6665   7228  -2042  -1243   1889       N  
ATOM    420  CA  TRP A  53     -14.537 -12.319  36.539  1.00 52.11           C  
ANISOU  420  CA  TRP A  53     6432   6297   7072  -1933  -1400   1679       C  
ATOM    421  C   TRP A  53     -13.018 -12.255  36.277  1.00 52.31           C  
ANISOU  421  C   TRP A  53     6736   6054   7087  -1784  -1367   1508       C  
ATOM    422  O   TRP A  53     -12.475 -13.139  35.613  1.00 51.62           O  
ANISOU  422  O   TRP A  53     6784   5729   7099  -1814  -1552   1374       O  
ATOM    423  CB  TRP A  53     -15.309 -11.226  35.780  1.00 50.94           C  
ANISOU  423  CB  TRP A  53     6165   6397   6793  -1712  -1312   1635       C  
ATOM    424  CG  TRP A  53     -14.989 -11.130  34.323  1.00 51.43           C  
ANISOU  424  CG  TRP A  53     6372   6375   6796  -1556  -1432   1448       C  
ATOM    425  CD1 TRP A  53     -15.411 -11.965  33.334  1.00 56.15           C  
ANISOU  425  CD1 TRP A  53     6959   6947   7429  -1658  -1708   1341       C  
ATOM    426  CD2 TRP A  53     -14.166 -10.143  33.697  1.00 49.84           C  
ANISOU  426  CD2 TRP A  53     6341   6132   6462  -1281  -1281   1352       C  
ATOM    427  CE2 TRP A  53     -14.123 -10.449  32.319  1.00 55.73           C  
ANISOU  427  CE2 TRP A  53     7170   6884   7121  -1208  -1451   1212       C  
ATOM    428  CE3 TRP A  53     -13.461  -9.020  34.166  1.00 49.36           C  
ANISOU  428  CE3 TRP A  53     6372   6030   6351  -1108  -1028   1374       C  
ATOM    429  NE1 TRP A  53     -14.894 -11.568  32.127  1.00 55.80           N  
ANISOU  429  NE1 TRP A  53     7077   6900   7226  -1433  -1723   1171       N  
ATOM    430  CZ2 TRP A  53     -13.437  -9.646  31.396  1.00 54.98           C  
ANISOU  430  CZ2 TRP A  53     7221   6806   6861   -964  -1342   1154       C  
ATOM    431  CZ3 TRP A  53     -12.739  -8.258  33.264  1.00 50.60           C  
ANISOU  431  CZ3 TRP A  53     6677   6131   6415   -902   -943   1318       C  
ATOM    432  CH2 TRP A  53     -12.737  -8.563  31.896  1.00 52.78           C  
ANISOU  432  CH2 TRP A  53     7011   6463   6580   -829  -1081   1239       C  
ATOM    433  N   ALA A  54     -12.339 -11.237  36.835  1.00 48.11           N  
ANISOU  433  N   ALA A  54     6270   5562   6447  -1628  -1139   1498       N  
ATOM    434  CA  ALA A  54     -10.888 -11.031  36.713  1.00 46.25           C  
ANISOU  434  CA  ALA A  54     6231   5133   6210  -1508  -1081   1375       C  
ATOM    435  C   ALA A  54     -10.083 -12.188  37.328  1.00 52.40           C  
ANISOU  435  C   ALA A  54     7085   5700   7124  -1651  -1219   1412       C  
ATOM    436  O   ALA A  54      -9.142 -12.659  36.691  1.00 53.77           O  
ANISOU  436  O   ALA A  54     7384   5677   7370  -1567  -1297   1276       O  
ATOM    437  CB  ALA A  54     -10.485  -9.708  37.338  1.00 45.41           C  
ANISOU  437  CB  ALA A  54     6145   5106   6001  -1381   -849   1371       C  
ATOM    438  N   ALA A  55     -10.489 -12.692  38.517  1.00 48.89           N  
ANISOU  438  N   ALA A  55     6550   5316   6710  -1848  -1250   1616       N  
ATOM    439  CA  ALA A  55      -9.840 -13.835  39.183  1.00 49.17           C  
ANISOU  439  CA  ALA A  55     6646   5146   6891  -1992  -1407   1736       C  
ATOM    440  C   ALA A  55      -9.898 -15.089  38.314  1.00 54.52           C  
ANISOU  440  C   ALA A  55     7393   5524   7799  -2063  -1666   1666       C  
ATOM    441  O   ALA A  55      -8.889 -15.785  38.190  1.00 55.88           O  
ANISOU  441  O   ALA A  55     7694   5421   8115  -2000  -1783   1596       O  
ATOM    442  CB  ALA A  55     -10.480 -14.108  40.531  1.00 51.17           C  
ANISOU  442  CB  ALA A  55     6766   5590   7088  -2206  -1383   2032       C  
ATOM    443  N   GLU A  56     -11.066 -15.355  37.692  1.00 49.87           N  
ANISOU  443  N   GLU A  56     6709   4987   7253  -2175  -1770   1655       N  
ATOM    444  CA  GLU A  56     -11.291 -16.504  36.824  1.00 50.59           C  
ANISOU  444  CA  GLU A  56     6870   4790   7561  -2272  -2055   1529       C  
ATOM    445  C   GLU A  56     -10.517 -16.363  35.517  1.00 51.59           C  
ANISOU  445  C   GLU A  56     7170   4804   7629  -1995  -2074   1170       C  
ATOM    446  O   GLU A  56      -9.914 -17.333  35.061  1.00 53.81           O  
ANISOU  446  O   GLU A  56     7601   4760   8086  -1955  -2260    999       O  
ATOM    447  CB  GLU A  56     -12.782 -16.689  36.564  1.00 53.90           C  
ANISOU  447  CB  GLU A  56     7096   5368   8016  -2493  -2168   1616       C  
ATOM    448  CG  GLU A  56     -13.102 -17.931  35.751  1.00 65.55           C  
ANISOU  448  CG  GLU A  56     8638   6509   9759  -2676  -2521   1488       C  
ATOM    449  CD  GLU A  56     -14.570 -18.268  35.604  1.00 83.48           C  
ANISOU  449  CD  GLU A  56    10673   8929  12117  -2969  -2685   1602       C  
ATOM    450  OE1 GLU A  56     -15.432 -17.417  35.933  1.00 73.80           O  
ANISOU  450  OE1 GLU A  56     9198   8126  10715  -2979  -2501   1772       O  
ATOM    451  OE2 GLU A  56     -14.855 -19.409  35.175  1.00 81.72           O1-
ANISOU  451  OE2 GLU A  56    10503   8384  12163  -3187  -3014   1509       O1-
ATOM    452  N   ALA A  57     -10.518 -15.162  34.928  1.00 43.45           N  
ANISOU  452  N   ALA A  57     6117   4042   6351  -1790  -1873   1069       N  
ATOM    453  CA  ALA A  57      -9.781 -14.901  33.705  1.00 42.63           C  
ANISOU  453  CA  ALA A  57     6145   3931   6120  -1527  -1836    793       C  
ATOM    454  C   ALA A  57      -8.286 -15.140  33.965  1.00 49.39           C  
ANISOU  454  C   ALA A  57     7117   4601   7049  -1380  -1768    724       C  
ATOM    455  O   ALA A  57      -7.669 -15.923  33.241  1.00 53.53           O  
ANISOU  455  O   ALA A  57     7760   4942   7637  -1248  -1882    488       O  
ATOM    456  CB  ALA A  57     -10.042 -13.478  33.220  1.00 41.18           C  
ANISOU  456  CB  ALA A  57     5901   4062   5685  -1366  -1615    818       C  
ATOM    457  N   ILE A  58      -7.745 -14.566  35.057  1.00 43.29           N  
ANISOU  457  N   ILE A  58     6294   3881   6273  -1403  -1607    914       N  
ATOM    458  CA  ILE A  58      -6.343 -14.738  35.460  1.00 43.21           C  
ANISOU  458  CA  ILE A  58     6331   3746   6341  -1288  -1559    897       C  
ATOM    459  C   ILE A  58      -5.982 -16.198  35.822  1.00 52.04           C  
ANISOU  459  C   ILE A  58     7517   4528   7729  -1344  -1802    908       C  
ATOM    460  O   ILE A  58      -4.951 -16.685  35.358  1.00 54.38           O  
ANISOU  460  O   ILE A  58     7879   4666   8116  -1143  -1837    736       O  
ATOM    461  CB  ILE A  58      -5.925 -13.693  36.532  1.00 43.23           C  
ANISOU  461  CB  ILE A  58     6257   3918   6250  -1325  -1368   1070       C  
ATOM    462  CG1 ILE A  58      -5.955 -12.263  35.915  1.00 41.02           C  
ANISOU  462  CG1 ILE A  58     5957   3851   5779  -1207  -1141   1013       C  
ATOM    463  CG2 ILE A  58      -4.532 -14.011  37.129  1.00 41.85           C  
ANISOU  463  CG2 ILE A  58     6085   3637   6181  -1258  -1384   1094       C  
ATOM    464  CD1 ILE A  58      -6.164 -11.165  36.932  1.00 46.38           C  
ANISOU  464  CD1 ILE A  58     6578   4674   6372  -1284   -993   1140       C  
ATOM    465  N   SER A  59      -6.827 -16.886  36.622  1.00 49.73           N  
ANISOU  465  N   SER A  59     7192   4127   7575  -1602  -1963   1127       N  
ATOM    466  CA  SER A  59      -6.599 -18.280  37.026  1.00 52.67           C  
ANISOU  466  CA  SER A  59     7638   4120   8254  -1691  -2220   1212       C  
ATOM    467  C   SER A  59      -6.576 -19.235  35.829  1.00 60.15           C  
ANISOU  467  C   SER A  59     8729   4747   9380  -1580  -2430    887       C  
ATOM    468  O   SER A  59      -5.683 -20.078  35.763  1.00 62.98           O  
ANISOU  468  O   SER A  59     9189   4780   9959  -1426  -2561    788       O  
ATOM    469  CB  SER A  59      -7.636 -18.749  38.044  1.00 56.26           C  
ANISOU  469  CB  SER A  59     8007   4565   8805  -2034  -2330   1570       C  
ATOM    470  OG  SER A  59      -7.558 -17.989  39.238  1.00 66.19           O  
ANISOU  470  OG  SER A  59     9155   6121   9872  -2103  -2152   1840       O  
ATOM    471  N   ASP A  60      -7.538 -19.098  34.886  1.00 55.58           N  
ANISOU  471  N   ASP A  60     8153   4268   8696  -1631  -2477    698       N  
ATOM    472  CA  ASP A  60      -7.601 -19.936  33.691  1.00 57.97           C  
ANISOU  472  CA  ASP A  60     8605   4320   9102  -1530  -2696    318       C  
ATOM    473  C   ASP A  60      -6.358 -19.749  32.814  1.00 62.32           C  
ANISOU  473  C   ASP A  60     9251   4916   9513  -1126  -2560    -19       C  
ATOM    474  O   ASP A  60      -5.780 -20.753  32.377  1.00 66.43           O  
ANISOU  474  O   ASP A  60     9915   5097  10229   -955  -2729   -290       O  
ATOM    475  CB  ASP A  60      -8.883 -19.672  32.875  1.00 60.43           C  
ANISOU  475  CB  ASP A  60     8863   4833   9264  -1678  -2782    205       C  
ATOM    476  CG  ASP A  60     -10.181 -20.139  33.514  1.00 76.05           C  
ANISOU  476  CG  ASP A  60    10717   6735  11444  -2091  -2975    483       C  
ATOM    477  OD1 ASP A  60     -10.140 -21.096  34.330  1.00 81.01           O  
ANISOU  477  OD1 ASP A  60    11380   6996  12406  -2286  -3151    681       O  
ATOM    478  OD2 ASP A  60     -11.240 -19.583  33.167  1.00 79.89           O1-
ANISOU  478  OD2 ASP A  60    11054   7533  11769  -2218  -2959    526       O1-
ATOM    479  N   ALA A  61      -5.925 -18.480  32.586  1.00 53.27           N  
ANISOU  479  N   ALA A  61     8014   4176   8051   -969  -2251     11       N  
ATOM    480  CA  ALA A  61      -4.735 -18.183  31.774  1.00 53.14           C  
ANISOU  480  CA  ALA A  61     8024   4295   7870   -616  -2067   -228       C  
ATOM    481  C   ALA A  61      -3.452 -18.750  32.393  1.00 58.69           C  
ANISOU  481  C   ALA A  61     8719   4775   8807   -455  -2064   -199       C  
ATOM    482  O   ALA A  61      -2.630 -19.327  31.672  1.00 62.09           O  
ANISOU  482  O   ALA A  61     9212   5107   9272   -155  -2075   -499       O  
ATOM    483  CB  ALA A  61      -4.596 -16.686  31.543  1.00 50.90           C  
ANISOU  483  CB  ALA A  61     7626   4444   7271   -565  -1755    -97       C  
ATOM    484  N   ARG A  62      -3.313 -18.634  33.729  1.00 51.60           N  
ANISOU  484  N   ARG A  62     7734   3819   8055   -633  -2065    152       N  
ATOM    485  CA  ARG A  62      -2.164 -19.124  34.485  1.00 51.89           C  
ANISOU  485  CA  ARG A  62     7728   3678   8310   -510  -2102    261       C  
ATOM    486  C   ARG A  62      -2.049 -20.644  34.359  1.00 58.24           C  
ANISOU  486  C   ARG A  62     8678   3984   9467   -417  -2400    114       C  
ATOM    487  O   ARG A  62      -0.975 -21.170  34.072  1.00 59.91           O  
ANISOU  487  O   ARG A  62     8895   4050   9818   -100  -2413    -62       O  
ATOM    488  CB  ARG A  62      -2.308 -18.717  35.951  1.00 52.57           C  
ANISOU  488  CB  ARG A  62     7711   3850   8412   -765  -2088    673       C  
ATOM    489  CG  ARG A  62      -0.994 -18.730  36.737  1.00 65.35           C  
ANISOU  489  CG  ARG A  62     9221   5478  10129   -632  -2065    816       C  
ATOM    490  CD  ARG A  62      -1.038 -19.624  37.962  1.00 78.59           C  
ANISOU  490  CD  ARG A  62    10919   6893  12050   -777  -2307   1134       C  
ATOM    491  NE  ARG A  62      -2.263 -19.441  38.739  1.00 88.28           N  
ANISOU  491  NE  ARG A  62    12152   8208  13182  -1133  -2339   1415       N  
ATOM    492  CZ  ARG A  62      -3.176 -20.384  38.933  1.00106.73           C  
ANISOU  492  CZ  ARG A  62    14577  10270  15707  -1340  -2546   1549       C  
ATOM    493  NH1 ARG A  62      -3.002 -21.600  38.432  1.00100.09           N1+
ANISOU  493  NH1 ARG A  62    13869   8971  15191  -1235  -2777   1402       N1+
ATOM    494  NH2 ARG A  62      -4.267 -20.121  39.631  1.00 92.62           N  
ANISOU  494  NH2 ARG A  62    12733   8660  13797  -1654  -2524   1823       N  
ATOM    495  N   GLU A  63      -3.176 -21.339  34.546  1.00 55.64           N  
ANISOU  495  N   GLU A  63     8453   3384   9303   -691  -2642    183       N  
ATOM    496  CA  GLU A  63      -3.310 -22.782  34.449  1.00 59.06           C  
ANISOU  496  CA  GLU A  63     9057   3254  10130   -695  -2978     66       C  
ATOM    497  C   GLU A  63      -2.907 -23.267  33.044  1.00 66.55           C  
ANISOU  497  C   GLU A  63    10150   4069  11068   -336  -3022   -503       C  
ATOM    498  O   GLU A  63      -2.195 -24.272  32.926  1.00 70.98           O  
ANISOU  498  O   GLU A  63    10821   4211  11937    -83  -3185   -689       O  
ATOM    499  CB  GLU A  63      -4.765 -23.144  34.777  1.00 60.90           C  
ANISOU  499  CB  GLU A  63     9319   3350  10470  -1132  -3181    254       C  
ATOM    500  CG  GLU A  63      -5.148 -24.610  34.678  1.00 68.07           C  
ANISOU  500  CG  GLU A  63    10403   3618  11844  -1261  -3571    197       C  
ATOM    501  CD  GLU A  63      -6.647 -24.783  34.525  1.00 89.96           C  
ANISOU  501  CD  GLU A  63    13165   6351  14665  -1682  -3754    254       C  
ATOM    502  OE1 GLU A  63      -7.065 -25.694  33.774  1.00 82.35           O  
ANISOU  502  OE1 GLU A  63    12369   4970  13951  -1726  -4053    -71       O  
ATOM    503  OE2 GLU A  63      -7.408 -23.994  35.133  1.00 86.48           O1-
ANISOU  503  OE2 GLU A  63    12536   6309  14015  -1961  -3604    599       O1-
ATOM    504  N   ASN A  64      -3.348 -22.544  31.994  1.00 61.61           N  
ANISOU  504  N   ASN A  64     9522   3818  10070   -285  -2873   -774       N  
ATOM    505  CA  ASN A  64      -3.060 -22.875  30.595  1.00 65.27           C  
ANISOU  505  CA  ASN A  64    10116   4294  10391     53  -2884  -1328       C  
ATOM    506  C   ASN A  64      -1.604 -22.642  30.188  1.00 69.60           C  
ANISOU  506  C   ASN A  64    10582   5053  10811    512  -2620  -1503       C  
ATOM    507  O   ASN A  64      -1.043 -23.446  29.431  1.00 72.95           O  
ANISOU  507  O   ASN A  64    11125   5279  11313    867  -2694  -1940       O  
ATOM    508  CB  ASN A  64      -4.034 -22.169  29.650  1.00 68.30           C  
ANISOU  508  CB  ASN A  64    10508   5065  10378    -57  -2832  -1491       C  
ATOM    509  CG  ASN A  64      -5.354 -22.892  29.522  1.00 90.83           C  
ANISOU  509  CG  ASN A  64    13479   7622  13410   -384  -3194  -1580       C  
ATOM    510  ND2 ASN A  64      -6.358 -22.454  30.271  1.00 73.71           N  
ANISOU  510  ND2 ASN A  64    11183   5546  11279   -787  -3224  -1169       N  
ATOM    511  OD1 ASN A  64      -5.475 -23.876  28.782  1.00 99.63           O  
ANISOU  511  OD1 ASN A  64    14789   8416  14649   -283  -3459  -2028       O  
ATOM    512  N   ILE A  65      -0.996 -21.555  30.693  1.00 63.65           N  
ANISOU  512  N   ILE A  65     9611   4703   9871    506  -2316  -1182       N  
ATOM    513  CA  ILE A  65       0.400 -21.222  30.419  1.00 64.64           C  
ANISOU  513  CA  ILE A  65     9578   5092   9892    876  -2048  -1261       C  
ATOM    514  C   ILE A  65       1.329 -22.265  31.078  1.00 72.33           C  
ANISOU  514  C   ILE A  65    10537   5657  11287   1104  -2202  -1257       C  
ATOM    515  O   ILE A  65       2.214 -22.811  30.404  1.00 74.71           O  
ANISOU  515  O   ILE A  65    10823   5943  11619   1535  -2140  -1597       O  
ATOM    516  CB  ILE A  65       0.747 -19.725  30.695  1.00 63.90           C  
ANISOU  516  CB  ILE A  65     9255   5509   9515    759  -1715   -931       C  
ATOM    517  CG1 ILE A  65       2.065 -19.300  30.022  1.00 66.00           C  
ANISOU  517  CG1 ILE A  65     9335   6150   9591   1117  -1406  -1067       C  
ATOM    518  CG2 ILE A  65       0.740 -19.362  32.181  1.00 61.87           C  
ANISOU  518  CG2 ILE A  65     8887   5177   9444    472  -1758   -476       C  
ATOM    519  CD1 ILE A  65       2.214 -17.771  29.849  1.00 70.50           C  
ANISOU  519  CD1 ILE A  65     9731   7222   9835    982  -1083   -820       C  
ATOM    520  N   GLN A  66       1.026 -22.633  32.351  1.00 69.27           N  
ANISOU  520  N   GLN A  66    10165   4935  11220    833  -2421   -882       N  
ATOM    521  CA  GLN A  66       1.764 -23.654  33.122  1.00 72.36           C  
ANISOU  521  CA  GLN A  66    10554   4894  12044   1005  -2625   -770       C  
ATOM    522  C   GLN A  66       1.690 -25.016  32.420  1.00 79.94           C  
ANISOU  522  C   GLN A  66    11760   5300  13313   1264  -2893  -1202       C  
ATOM    523  O   GLN A  66       2.697 -25.723  32.329  1.00 82.20           O  
ANISOU  523  O   GLN A  66    12023   5365  13845   1683  -2934  -1377       O  
ATOM    524  CB  GLN A  66       1.247 -23.752  34.577  1.00 72.28           C  
ANISOU  524  CB  GLN A  66    10532   4696  12236    607  -2810   -228       C  
ATOM    525  CG  GLN A  66       1.671 -22.585  35.500  1.00 78.10           C  
ANISOU  525  CG  GLN A  66    11025   5907  12741    447  -2594    162       C  
ATOM    526  CD  GLN A  66       1.384 -22.888  36.963  1.00 94.65           C  
ANISOU  526  CD  GLN A  66    13113   7836  15015    149  -2793    661       C  
ATOM    527  NE2 GLN A  66       2.271 -23.641  37.615  1.00 92.89           N  
ANISOU  527  NE2 GLN A  66    12828   7389  15078    341  -2953    843       N  
ATOM    528  OE1 GLN A  66       0.355 -22.489  37.519  1.00 82.68           O  
ANISOU  528  OE1 GLN A  66    11632   6410  13373   -235  -2809    901       O  
ATOM    529  N   ARG A  67       0.508 -25.345  31.876  1.00 76.97           N  
ANISOU  529  N   ARG A  67    11605   4713  12926   1029  -3080  -1405       N  
ATOM    530  CA  ARG A  67       0.267 -26.583  31.142  1.00 82.36           C  
ANISOU  530  CA  ARG A  67    12562   4835  13895   1201  -3381  -1879       C  
ATOM    531  C   ARG A  67       1.161 -26.693  29.895  1.00 90.09           C  
ANISOU  531  C   ARG A  67    13564   5996  14669   1771  -3210  -2494       C  
ATOM    532  O   ARG A  67       1.749 -27.755  29.665  1.00 95.75           O  
ANISOU  532  O   ARG A  67    14421   6233  15726   2142  -3389  -2838       O  
ATOM    533  CB  ARG A  67      -1.216 -26.710  30.762  1.00 80.94           C  
ANISOU  533  CB  ARG A  67    12555   4529  13670    774  -3600  -1966       C  
ATOM    534  CG  ARG A  67      -1.616 -28.136  30.396  1.00 92.51           C  
ANISOU  534  CG  ARG A  67    14321   5247  15583    794  -4028  -2343       C  
ATOM    535  CD  ARG A  67      -3.011 -28.224  29.813  1.00 97.58           C  
ANISOU  535  CD  ARG A  67    15093   5847  16135    394  -4250  -2521       C  
ATOM    536  NE  ARG A  67      -4.040 -28.176  30.852  1.00 99.93           N  
ANISOU  536  NE  ARG A  67    15308   6025  16637   -192  -4396  -1928       N  
ATOM    537  CZ  ARG A  67      -4.803 -27.121  31.108  1.00103.29           C  
ANISOU  537  CZ  ARG A  67    15536   6998  16713   -522  -4207  -1589       C  
ATOM    538  NH1 ARG A  67      -4.682 -26.015  30.385  1.00 89.54           N1+
ANISOU  538  NH1 ARG A  67    13684   5906  14431   -351  -3893  -1759       N1+
ATOM    539  NH2 ARG A  67      -5.714 -27.174  32.066  1.00 84.30           N  
ANISOU  539  NH2 ARG A  67    13037   4495  14499  -1015  -4328  -1073       N  
ATOM    540  N   PHE A  68       1.272 -25.599  29.109  1.00 83.23           N  
ANISOU  540  N   PHE A  68    12554   5821  13249   1854  -2858  -2612       N  
ATOM    541  CA  PHE A  68       2.086 -25.555  27.890  1.00 85.63           C  
ANISOU  541  CA  PHE A  68    12832   6462  13240   2372  -2624  -3137       C  
ATOM    542  C   PHE A  68       3.584 -25.777  28.154  1.00 91.50           C  
ANISOU  542  C   PHE A  68    13362   7242  14163   2848  -2448  -3133       C  
ATOM    543  O   PHE A  68       4.249 -26.455  27.368  1.00 95.36           O  
ANISOU  543  O   PHE A  68    13911   7642  14678   3360  -2428  -3650       O  
ATOM    544  CB  PHE A  68       1.851 -24.238  27.107  1.00 83.32           C  
ANISOU  544  CB  PHE A  68    12408   6934  12316   2288  -2278  -3111       C  
ATOM    545  CG  PHE A  68       2.786 -24.032  25.931  1.00 86.92           C  
ANISOU  545  CG  PHE A  68    12765   7888  12374   2799  -1953  -3519       C  
ATOM    546  CD1 PHE A  68       2.527 -24.628  24.701  1.00 93.38           C  
ANISOU  546  CD1 PHE A  68    13809   8721  12950   3078  -2037  -4156       C  
ATOM    547  CD2 PHE A  68       3.951 -23.283  26.071  1.00 86.52           C  
ANISOU  547  CD2 PHE A  68    12378   8311  12184   2998  -1571  -3273       C  
ATOM    548  CE1 PHE A  68       3.407 -24.463  23.628  1.00 97.28           C  
ANISOU  548  CE1 PHE A  68    14196   9745  13021   3577  -1707  -4528       C  
ATOM    549  CE2 PHE A  68       4.831 -23.122  24.998  1.00 92.05           C  
ANISOU  549  CE2 PHE A  68    12940   9521  12513   3465  -1241  -3606       C  
ATOM    550  CZ  PHE A  68       4.548 -23.704  23.783  1.00 94.79           C  
ANISOU  550  CZ  PHE A  68    13516   9926  12573   3765  -1292  -4224       C  
ATOM    551  N   PHE A  69       4.112 -25.176  29.229  1.00 85.93           N  
ANISOU  551  N   PHE A  69    12387   6708  13552   2697  -2320  -2580       N  
ATOM    552  CA  PHE A  69       5.532 -25.266  29.558  1.00 88.26           C  
ANISOU  552  CA  PHE A  69    12403   7124  14009   3100  -2162  -2501       C  
ATOM    553  C   PHE A  69       6.037 -26.570  30.186  1.00100.26           C  
ANISOU  553  C   PHE A  69    13997   7975  16123   3377  -2475  -2519       C  
ATOM    554  O   PHE A  69       7.208 -26.904  29.996  1.00104.37           O  
ANISOU  554  O   PHE A  69    14323   8571  16761   3892  -2356  -2690       O  
ATOM    555  CB  PHE A  69       6.044 -23.997  30.257  1.00 84.53           C  
ANISOU  555  CB  PHE A  69    11579   7200  13339   2871  -1886  -1984       C  
ATOM    556  CG  PHE A  69       6.121 -22.798  29.337  1.00 82.95           C  
ANISOU  556  CG  PHE A  69    11231   7693  12594   2847  -1492  -2054       C  
ATOM    557  CD1 PHE A  69       7.121 -22.700  28.375  1.00 89.39           C  
ANISOU  557  CD1 PHE A  69    11856   8930  13177   3311  -1186  -2369       C  
ATOM    558  CD2 PHE A  69       5.199 -21.767  29.434  1.00 78.75           C  
ANISOU  558  CD2 PHE A  69    10732   7402  11786   2376  -1419  -1774       C  
ATOM    559  CE1 PHE A  69       7.186 -21.595  27.520  1.00 88.40           C  
ANISOU  559  CE1 PHE A  69    11592   9454  12544   3263   -820  -2356       C  
ATOM    560  CE2 PHE A  69       5.275 -20.657  28.587  1.00 79.66           C  
ANISOU  560  CE2 PHE A  69    10723   8109  11436   2357  -1076  -1780       C  
ATOM    561  CZ  PHE A  69       6.268 -20.577  27.639  1.00 81.41           C  
ANISOU  561  CZ  PHE A  69    10766   8740  11425   2780   -781  -2044       C  
ATOM    562  N   GLY A  70       5.164 -27.307  30.878  1.00 99.58           N  
ANISOU  562  N   GLY A  70    14169   7253  16413   3055  -2865  -2329       N  
ATOM    563  CA  GLY A  70       5.530 -28.597  31.457  1.00105.87           C  
ANISOU  563  CA  GLY A  70    15083   7326  17819   3288  -3207  -2295       C  
ATOM    564  C   GLY A  70       4.971 -28.950  32.822  1.00111.66           C  
ANISOU  564  C   GLY A  70    15890   7616  18922   2838  -3525  -1678       C  
ATOM    565  O   GLY A  70       5.476 -29.883  33.457  1.00115.46           O  
ANISOU  565  O   GLY A  70    16399   7574  19897   3047  -3778  -1503       O  
ATOM    566  N   HIS A  71       3.923 -28.235  33.277  1.00105.25           N  
ANISOU  566  N   HIS A  71    15101   7018  17870   2243  -3513  -1329       N  
ATOM    567  CA  HIS A  71       3.272 -28.477  34.566  1.00105.20           C  
ANISOU  567  CA  HIS A  71    15143   6714  18114   1773  -3765   -716       C  
ATOM    568  C   HIS A  71       2.394 -29.730  34.494  1.00114.28           C  
ANISOU  568  C   HIS A  71    16634   7056  19730   1611  -4177   -809       C  
ATOM    569  O   HIS A  71       1.539 -29.834  33.607  1.00114.46           O  
ANISOU  569  O   HIS A  71    16853   6978  19659   1490  -4235  -1225       O  
ATOM    570  CB  HIS A  71       2.446 -27.253  34.975  1.00100.34           C  
ANISOU  570  CB  HIS A  71    14414   6657  17054   1254  -3568   -386       C  
ATOM    571  CG  HIS A  71       1.980 -27.242  36.395  1.00102.86           C  
ANISOU  571  CG  HIS A  71    14691   6907  17485    821  -3717    273       C  
ATOM    572  CD2 HIS A  71       0.720 -27.191  36.885  1.00103.73           C  
ANISOU  572  CD2 HIS A  71    14897   6927  17587    308  -3840    570       C  
ATOM    573  ND1 HIS A  71       2.874 -27.185  37.452  1.00104.68           N  
ANISOU  573  ND1 HIS A  71    14722   7274  17778    906  -3717    696       N  
ATOM    574  CE1 HIS A  71       2.132 -27.147  38.547  1.00103.10           C  
ANISOU  574  CE1 HIS A  71    14539   7052  17584    458  -3844   1223       C  
ATOM    575  NE2 HIS A  71       0.829 -27.148  38.255  1.00102.84           N  
ANISOU  575  NE2 HIS A  71    14667   6892  17515     90  -3902   1176       N  
ATOM    576  N   GLY A  72       2.639 -30.664  35.421  1.00115.22           N  
ANISOU  576  N   GLY A  72    16813   6611  20355   1606  -4477   -408       N  
ATOM    577  CA  GLY A  72       1.943 -31.944  35.539  1.00120.88           C  
ANISOU  577  CA  GLY A  72    17840   6452  21635   1431  -4911   -374       C  
ATOM    578  C   GLY A  72       0.435 -31.827  35.628  1.00123.71           C  
ANISOU  578  C   GLY A  72    18318   6767  21917    777  -5026   -213       C  
ATOM    579  O   GLY A  72      -0.079 -30.884  36.238  1.00118.08           O  
ANISOU  579  O   GLY A  72    17421   6627  20819    379  -4829    192       O  
ATOM    580  N   ALA A  73      -0.276 -32.775  34.994  1.00126.06           N  
ANISOU  580  N   ALA A  73    18913   6390  22592    677  -5352   -564       N  
ATOM    581  CA  ALA A  73      -1.742 -32.824  34.934  1.00126.17           C  
ANISOU  581  CA  ALA A  73    19027   6292  22618     58  -5523   -476       C  
ATOM    582  C   ALA A  73      -2.407 -32.818  36.318  1.00130.00           C  
ANISOU  582  C   ALA A  73    19395   6761  23237   -515  -5616    394       C  
ATOM    583  O   ALA A  73      -3.271 -31.968  36.565  1.00124.52           O  
ANISOU  583  O   ALA A  73    18540   6606  22166   -954  -5450    642       O  
ATOM    584  CB  ALA A  73      -2.196 -34.030  34.122  1.00134.17           C  
ANISOU  584  CB  ALA A  73    20386   6464  24130     82  -5933  -1005       C  
ATOM    585  N   GLU A  74      -1.972 -33.737  37.223  1.00131.82           N  
ANISOU  585  N   GLU A  74    19690   6420  23976   -473  -5864    872       N  
ATOM    586  CA  GLU A  74      -2.463 -33.873  38.602  1.00131.99           C  
ANISOU  586  CA  GLU A  74    19607   6419  24125   -965  -5963   1759       C  
ATOM    587  C   GLU A  74      -2.171 -32.597  39.419  1.00129.56           C  
ANISOU  587  C   GLU A  74    18979   7052  23196  -1016  -5573   2169       C  
ATOM    588  O   GLU A  74      -3.005 -32.187  40.231  1.00127.53           O  
ANISOU  588  O   GLU A  74    18583   7144  22728  -1515  -5503   2705       O  
ATOM    589  CB  GLU A  74      -1.835 -35.107  39.271  1.00140.36           C  
ANISOU  589  CB  GLU A  74    20821   6660  25851   -791  -6317   2143       C  
ATOM    590  CG  GLU A  74      -2.590 -35.617  40.489  1.00154.47           C  
ANISOU  590  CG  GLU A  74    22582   8211  27900  -1371  -6526   3050       C  
ATOM    591  CD  GLU A  74      -3.837 -36.427  40.192  1.00178.89           C  
ANISOU  591  CD  GLU A  74    25873  10963  31134  -1868  -6457   2995       C  
ATOM    592  OE1 GLU A  74      -4.941 -35.839  40.200  1.00177.58           O  
ANISOU  592  OE1 GLU A  74    25533  11142  30797  -2412  -6534   3179       O  
ATOM    593  OE2 GLU A  74      -3.715 -37.654  39.973  1.00180.23           O1-
ANISOU  593  OE2 GLU A  74    26367  10577  31535  -1711  -6244   2766       O1-
ATOM    594  N   ASP A  75      -1.002 -31.965  39.174  1.00122.74           N  
ANISOU  594  N   ASP A  75    17988   6605  22042   -502  -5321   1889       N  
ATOM    595  CA  ASP A  75      -0.556 -30.733  39.826  1.00116.60           C  
ANISOU  595  CA  ASP A  75    16925   6670  20709   -495  -4977   2157       C  
ATOM    596  C   ASP A  75      -1.463 -29.551  39.486  1.00114.47           C  
ANISOU  596  C   ASP A  75    16539   7058  19896   -816  -4680   2012       C  
ATOM    597  O   ASP A  75      -1.657 -28.680  40.333  1.00109.58           O  
ANISOU  597  O   ASP A  75    15730   7012  18895  -1054  -4481   2405       O  
ATOM    598  CB  ASP A  75       0.897 -30.411  39.436  1.00117.75           C  
ANISOU  598  CB  ASP A  75    16951   7038  20751    118  -4807   1810       C  
ATOM    599  CG  ASP A  75       1.938 -31.415  39.904  1.00131.89           C  
ANISOU  599  CG  ASP A  75    18776   8305  23033    516  -5065   2001       C  
ATOM    600  OD1 ASP A  75       1.717 -32.637  39.720  1.00137.81           O  
ANISOU  600  OD1 ASP A  75    19773   8243  24346    523  -5411   2020       O  
ATOM    601  OD2 ASP A  75       3.005 -30.977  40.388  1.00136.31           O1-
ANISOU  601  OD2 ASP A  75    19109   9242  23442    841  -4934   2101       O1-
ATOM    602  N   SER A  76      -2.021 -29.527  38.252  1.00111.50           N  
ANISOU  602  N   SER A  76    16284   6600  19482   -797  -4666   1437       N  
ATOM    603  CA  SER A  76      -2.935 -28.484  37.769  1.00106.63           C  
ANISOU  603  CA  SER A  76    15572   6544  18399  -1052  -4427   1262       C  
ATOM    604  C   SER A  76      -4.301 -28.583  38.449  1.00110.20           C  
ANISOU  604  C   SER A  76    15978   7008  18886  -1653  -4530   1729       C  
ATOM    605  O   SER A  76      -4.914 -27.557  38.726  1.00105.05           O  
ANISOU  605  O   SER A  76    15145   6958  17809  -1881  -4281   1880       O  
ATOM    606  CB  SER A  76      -3.109 -28.571  36.255  1.00111.94           C  
ANISOU  606  CB  SER A  76    16396   7100  19037   -844  -4448    543       C  
ATOM    607  OG  SER A  76      -1.888 -28.374  35.561  1.00123.77           O  
ANISOU  607  OG  SER A  76    17915   8625  20488   -271  -4327    101       O  
ATOM    608  N   LEU A  77      -4.779 -29.817  38.708  1.00112.75           N  
ANISOU  608  N   LEU A  77    16449   6656  19736  -1902  -4894   1963       N  
ATOM    609  CA  LEU A  77      -6.070 -30.086  39.354  1.00114.13           C  
ANISOU  609  CA  LEU A  77    16552   6785  20028  -2505  -5021   2464       C  
ATOM    610  C   LEU A  77      -6.151 -29.514  40.770  1.00114.81           C  
ANISOU  610  C   LEU A  77    16415   7383  19826  -2732  -4827   3168       C  
ATOM    611  O   LEU A  77      -7.200 -28.988  41.160  1.00112.57           O  
ANISOU  611  O   LEU A  77    15951   7525  19295  -3135  -4696   3455       O  
ATOM    612  CB  LEU A  77      -6.376 -31.595  39.359  1.00121.80           C  
ANISOU  612  CB  LEU A  77    17743   6835  21701  -2709  -5478   2589       C  
ATOM    613  CG  LEU A  77      -6.548 -32.251  37.991  1.00130.04           C  
ANISOU  613  CG  LEU A  77    19035   7324  23051  -2568  -5733   1857       C  
ATOM    614  CD1 LEU A  77      -6.677 -33.754  38.114  1.00138.02           C  
ANISOU  614  CD1 LEU A  77    20292   7326  24824  -2729  -6209   1990       C  
ATOM    615  CD2 LEU A  77      -7.722 -31.654  37.246  1.00131.01           C  
ANISOU  615  CD2 LEU A  77    19057   7840  22880  -2879  -5668   1564       C  
ATOM    616  N   ALA A  78      -5.033 -29.612  41.524  1.00110.74           N  
ANISOU  616  N   ALA A  78    15895   6862  19320  -2447  -4813   3424       N  
ATOM    617  CA  ALA A  78      -4.890 -29.088  42.884  1.00108.36           C  
ANISOU  617  CA  ALA A  78    15405   7074  18693  -2586  -4655   4036       C  
ATOM    618  C   ALA A  78      -4.940 -27.555  42.852  1.00104.11           C  
ANISOU  618  C   ALA A  78    14673   7374  17509  -2534  -4251   3829       C  
ATOM    619  O   ALA A  78      -5.590 -26.943  43.699  1.00102.83           O  
ANISOU  619  O   ALA A  78    14344   7726  17001  -2822  -4082   4218       O  
ATOM    620  CB  ALA A  78      -3.579 -29.572  43.495  1.00111.30           C  
ANISOU  620  CB  ALA A  78    15821   7225  19242  -2232  -4786   4257       C  
ATOM    621  N   ASP A  79      -4.294 -26.945  41.842  1.00 95.97           N  
ANISOU  621  N   ASP A  79    13669   6470  16325  -2166  -4096   3217       N  
ATOM    622  CA  ASP A  79      -4.289 -25.498  41.629  1.00 89.78           C  
ANISOU  622  CA  ASP A  79    12735   6368  15008  -2093  -3738   2978       C  
ATOM    623  C   ASP A  79      -5.719 -25.014  41.301  1.00 90.94           C  
ANISOU  623  C   ASP A  79    12810   6770  14974  -2434  -3631   2936       C  
ATOM    624  O   ASP A  79      -6.133 -23.962  41.785  1.00 87.75           O  
ANISOU  624  O   ASP A  79    12244   6933  14163  -2554  -3376   3062       O  
ATOM    625  CB  ASP A  79      -3.327 -25.125  40.483  1.00 89.58           C  
ANISOU  625  CB  ASP A  79    12757   6352  14928  -1639  -3623   2385       C  
ATOM    626  CG  ASP A  79      -1.853 -25.447  40.707  1.00100.56           C  
ANISOU  626  CG  ASP A  79    14149   7576  16483  -1245  -3690   2370       C  
ATOM    627  OD1 ASP A  79      -1.494 -25.872  41.831  1.00103.62           O  
ANISOU  627  OD1 ASP A  79    14501   7880  16991  -1303  -3832   2842       O  
ATOM    628  OD2 ASP A  79      -1.054 -25.247  39.767  1.00104.85           O1-
ANISOU  628  OD2 ASP A  79    14701   8125  17010   -870  -3591   1910       O1-
ATOM    629  N   GLN A  80      -6.473 -25.816  40.521  1.00 88.46           N  
ANISOU  629  N   GLN A  80    12606   6023  14980  -2582  -3851   2751       N  
ATOM    630  CA  GLN A  80      -7.851 -25.553  40.098  1.00 86.92           C  
ANISOU  630  CA  GLN A  80    12319   6010  14695  -2910  -3827   2698       C  
ATOM    631  C   GLN A  80      -8.850 -25.526  41.253  1.00 91.46           C  
ANISOU  631  C   GLN A  80    12698   6853  15200  -3359  -3786   3307       C  
ATOM    632  O   GLN A  80      -9.700 -24.630  41.307  1.00 88.44           O  
ANISOU  632  O   GLN A  80    12122   6996  14486  -3507  -3564   3336       O  
ATOM    633  CB  GLN A  80      -8.283 -26.553  39.008  1.00 91.47           C  
ANISOU  633  CB  GLN A  80    13071   6004  15679  -2972  -4149   2344       C  
ATOM    634  CG  GLN A  80      -7.729 -26.188  37.636  1.00 94.90           C  
ANISOU  634  CG  GLN A  80    13633   6453  15972  -2563  -4089   1656       C  
ATOM    635  CD  GLN A  80      -7.840 -27.278  36.614  1.00106.30           C  
ANISOU  635  CD  GLN A  80    15304   7277  17809  -2532  -4436   1230       C  
ATOM    636  NE2 GLN A  80      -6.730 -27.943  36.331  1.00 92.95           N  
ANISOU  636  NE2 GLN A  80    13810   5146  16361  -2147  -4550    962       N  
ATOM    637  OE1 GLN A  80      -8.893 -27.487  36.011  1.00107.48           O  
ANISOU  637  OE1 GLN A  80    15446   7359  18033  -2821  -4606   1090       O  
ATOM    638  N   ALA A  81      -8.732 -26.495  42.179  1.00 91.83           N  
ANISOU  638  N   ALA A  81    12782   6559  15550  -3551  -3990   3812       N  
ATOM    639  CA  ALA A  81      -9.603 -26.625  43.347  1.00 94.01           C  
ANISOU  639  CA  ALA A  81    12866   7095  15760  -3985  -3953   4475       C  
ATOM    640  C   ALA A  81      -9.376 -25.488  44.338  1.00 94.38           C  
ANISOU  640  C   ALA A  81    12742   7884  15234  -3892  -3605   4681       C  
ATOM    641  O   ALA A  81     -10.338 -24.959  44.910  1.00 94.13           O  
ANISOU  641  O   ALA A  81    12486   8367  14913  -4155  -3408   4958       O  
ATOM    642  CB  ALA A  81      -9.364 -27.968  44.022  1.00100.72           C  
ANISOU  642  CB  ALA A  81    13832   7355  17082  -4163  -4273   4983       C  
ATOM    643  N   ALA A  82      -8.093 -25.097  44.502  1.00 88.01           N  
ANISOU  643  N   ALA A  82    12031   7142  14268  -3503  -3535   4502       N  
ATOM    644  CA  ALA A  82      -7.654 -24.024  45.385  1.00 84.57           C  
ANISOU  644  CA  ALA A  82    11479   7337  13317  -3376  -3261   4594       C  
ATOM    645  C   ALA A  82      -8.231 -22.670  44.937  1.00 86.08           C  
ANISOU  645  C   ALA A  82    11545   8049  13112  -3324  -2943   4230       C  
ATOM    646  O   ALA A  82      -8.743 -21.923  45.776  1.00 85.35           O  
ANISOU  646  O   ALA A  82    11292   8510  12627  -3438  -2718   4432       O  
ATOM    647  CB  ALA A  82      -6.138 -23.978  45.416  1.00 84.01           C  
ANISOU  647  CB  ALA A  82    11519   7138  13264  -2989  -3316   4421       C  
ATOM    648  N   ASN A  83      -8.196 -22.382  43.611  1.00 81.19           N  
ANISOU  648  N   ASN A  83    11000   7257  12590  -3140  -2931   3705       N  
ATOM    649  CA  ASN A  83      -8.740 -21.150  43.014  1.00 77.51           C  
ANISOU  649  CA  ASN A  83    10436   7201  11812  -3060  -2670   3371       C  
ATOM    650  C   ASN A  83     -10.256 -21.031  43.254  1.00 82.98           C  
ANISOU  650  C   ASN A  83    10924   8185  12420  -3389  -2593   3601       C  
ATOM    651  O   ASN A  83     -10.723 -19.972  43.676  1.00 80.32           O  
ANISOU  651  O   ASN A  83    10433   8366  11718  -3369  -2323   3605       O  
ATOM    652  CB  ASN A  83      -8.462 -21.094  41.499  1.00 76.07           C  
ANISOU  652  CB  ASN A  83    10381   6755  11768  -2824  -2724   2842       C  
ATOM    653  CG  ASN A  83      -7.019 -20.950  41.085  1.00 85.03           C  
ANISOU  653  CG  ASN A  83    11649   7742  12917  -2454  -2710   2555       C  
ATOM    654  ND2 ASN A  83      -6.256 -20.115  41.754  1.00 82.28           N  
ANISOU  654  ND2 ASN A  83    11244   7720  12298  -2317  -2520   2592       N  
ATOM    655  OD1 ASN A  83      -6.578 -21.556  40.111  1.00 61.86           O  
ANISOU  655  OD1 ASN A  83     8853   4423  10228  -2279  -2864   2262       O  
ATOM    656  N   GLU A  84     -11.012 -22.128  42.998  1.00 83.70           N  
ANISOU  656  N   GLU A  84    10999   7930  12875  -3689  -2841   3788       N  
ATOM    657  CA  GLU A  84     -12.465 -22.192  43.180  1.00 85.46           C  
ANISOU  657  CA  GLU A  84    10973   8400  13097  -4053  -2812   4051       C  
ATOM    658  C   GLU A  84     -12.906 -21.927  44.619  1.00 90.45           C  
ANISOU  658  C   GLU A  84    11388   9553  13427  -4242  -2597   4566       C  
ATOM    659  O   GLU A  84     -13.867 -21.186  44.830  1.00 89.64           O  
ANISOU  659  O   GLU A  84    11035   9969  13054  -4315  -2363   4611       O  
ATOM    660  CB  GLU A  84     -13.024 -23.524  42.675  1.00 91.38           C  
ANISOU  660  CB  GLU A  84    11763   8591  14365  -4379  -3176   4171       C  
ATOM    661  CG  GLU A  84     -13.897 -23.366  41.444  1.00101.46           C  
ANISOU  661  CG  GLU A  84    12961   9849  15741  -4458  -3269   3814       C  
ATOM    662  CD  GLU A  84     -13.264 -23.795  40.136  1.00123.67           C  
ANISOU  662  CD  GLU A  84    16050  12184  18755  -4202  -3489   3238       C  
ATOM    663  OE1 GLU A  84     -13.956 -24.485  39.352  1.00117.97           O  
ANISOU  663  OE1 GLU A  84    15327  11196  18302  -4404  -3752   3055       O  
ATOM    664  OE2 GLU A  84     -12.083 -23.450  39.893  1.00118.07           O1-
ANISOU  664  OE2 GLU A  84    15540  11399  17922  -3807  -3400   2962       O1-
ATOM    665  N   TRP A  85     -12.182 -22.505  45.602  1.00 89.51           N  
ANISOU  665  N   TRP A  85    11357   9331  13322  -4282  -2673   4944       N  
ATOM    666  CA  TRP A  85     -12.462 -22.343  47.030  1.00 91.80           C  
ANISOU  666  CA  TRP A  85    11474  10143  13264  -4444  -2489   5457       C  
ATOM    667  C   TRP A  85     -12.484 -20.857  47.425  1.00 92.13           C  
ANISOU  667  C   TRP A  85    11414  10850  12742  -4190  -2121   5203       C  
ATOM    668  O   TRP A  85     -13.489 -20.380  47.965  1.00 92.36           O  
ANISOU  668  O   TRP A  85    11187  11429  12477  -4323  -1881   5392       O  
ATOM    669  CB  TRP A  85     -11.459 -23.149  47.875  1.00 93.31           C  
ANISOU  669  CB  TRP A  85    11827  10076  13552  -4446  -2680   5843       C  
ATOM    670  CG  TRP A  85     -11.668 -23.032  49.364  1.00 97.36           C  
ANISOU  670  CG  TRP A  85    12182  11161  13648  -4605  -2517   6400       C  
ATOM    671  CD1 TRP A  85     -11.160 -22.070  50.191  1.00 98.53           C  
ANISOU  671  CD1 TRP A  85    12318  11867  13252  -4384  -2295   6328       C  
ATOM    672  CD2 TRP A  85     -12.415 -23.925  50.201  1.00103.21           C  
ANISOU  672  CD2 TRP A  85    12764  11986  14467  -5026  -2579   7119       C  
ATOM    673  CE2 TRP A  85     -12.303 -23.448  51.527  1.00108.66           C  
ANISOU  673  CE2 TRP A  85    13349  13355  14583  -5009  -2363   7460       C  
ATOM    674  CE3 TRP A  85     -13.161 -25.094  49.963  1.00109.21           C  
ANISOU  674  CE3 TRP A  85    13454  12311  15731  -5440  -2806   7519       C  
ATOM    675  NE1 TRP A  85     -11.544 -22.306  51.489  1.00102.61           N  
ANISOU  675  NE1 TRP A  85    12685  12858  13444  -4610  -2206   6926       N  
ATOM    676  CZ2 TRP A  85     -12.954 -24.065  52.598  1.00113.82           C  
ANISOU  676  CZ2 TRP A  85    13813  14335  15098  -5375  -2325   8217       C  
ATOM    677  CZ3 TRP A  85     -13.783 -25.721  51.033  1.00116.38           C  
ANISOU  677  CZ3 TRP A  85    14170  13478  16573  -5837  -2786   8300       C  
ATOM    678  CH2 TRP A  85     -13.668 -25.213  52.332  1.00118.36           C  
ANISOU  678  CH2 TRP A  85    14306  14463  16202  -5793  -2534   8663       C  
ATOM    679  N   GLY A  86     -11.398 -20.147  47.107  1.00 85.81           N  
ANISOU  679  N   GLY A  86    10802   9978  11825  -3828  -2082   4769       N  
ATOM    680  CA  GLY A  86     -11.252 -18.720  47.380  1.00 82.67           C  
ANISOU  680  CA  GLY A  86    10367  10068  10975  -3574  -1785   4461       C  
ATOM    681  C   GLY A  86     -12.301 -17.872  46.695  1.00 84.43           C  
ANISOU  681  C   GLY A  86    10432  10538  11110  -3525  -1581   4190       C  
ATOM    682  O   GLY A  86     -13.029 -17.133  47.367  1.00 85.24           O  
ANISOU  682  O   GLY A  86    10348  11176  10862  -3520  -1321   4250       O  
ATOM    683  N   ARG A  87     -12.425 -18.026  45.361  1.00 78.43           N  
ANISOU  683  N   ARG A  87     9733   9407  10659  -3475  -1711   3900       N  
ATOM    684  CA  ARG A  87     -13.394 -17.307  44.522  1.00 77.12           C  
ANISOU  684  CA  ARG A  87     9421   9422  10460  -3412  -1585   3653       C  
ATOM    685  C   ARG A  87     -14.836 -17.437  45.021  1.00 82.60           C  
ANISOU  685  C   ARG A  87     9782  10519  11085  -3680  -1478   3988       C  
ATOM    686  O   ARG A  87     -15.601 -16.482  44.917  1.00 81.40           O  
ANISOU  686  O   ARG A  87     9443  10757  10730  -3552  -1255   3850       O  
ATOM    687  CB  ARG A  87     -13.300 -17.778  43.072  1.00 76.81           C  
ANISOU  687  CB  ARG A  87     9508   8918  10758  -3376  -1818   3365       C  
ATOM    688  CG  ARG A  87     -13.628 -16.692  42.066  1.00 78.79           C  
ANISOU  688  CG  ARG A  87     9749   9306  10880  -3111  -1681   2969       C  
ATOM    689  CD  ARG A  87     -13.492 -17.189  40.639  1.00 77.17           C  
ANISOU  689  CD  ARG A  87     9675   8717  10929  -3067  -1916   2683       C  
ATOM    690  NE  ARG A  87     -12.146 -17.691  40.369  1.00 81.00           N  
ANISOU  690  NE  ARG A  87    10430   8781  11566  -2934  -2061   2527       N  
ATOM    691  CZ  ARG A  87     -11.885 -18.821  39.723  1.00 92.81           C  
ANISOU  691  CZ  ARG A  87    12060   9829  13375  -3010  -2348   2435       C  
ATOM    692  NH1 ARG A  87     -12.875 -19.567  39.250  1.00 82.91           N1+
ANISOU  692  NH1 ARG A  87    10713   8463  12328  -3265  -2553   2474       N1+
ATOM    693  NH2 ARG A  87     -10.632 -19.206  39.532  1.00 74.29           N  
ANISOU  693  NH2 ARG A  87     9930   7144  11154  -2823  -2442   2281       N  
ATOM    694  N   SER A  88     -15.190 -18.593  45.602  1.00 82.64           N  
ANISOU  694  N   SER A  88     9691  10441  11267  -4041  -1627   4456       N  
ATOM    695  CA  SER A  88     -16.525 -18.829  46.158  1.00 86.68           C  
ANISOU  695  CA  SER A  88     9835  11368  11731  -4356  -1521   4866       C  
ATOM    696  C   SER A  88     -16.737 -18.161  47.544  1.00 92.37           C  
ANISOU  696  C   SER A  88    10380  12768  11947  -4298  -1176   5102       C  
ATOM    697  O   SER A  88     -17.766 -18.381  48.175  1.00 95.60           O  
ANISOU  697  O   SER A  88    10455  13616  12254  -4546  -1037   5498       O  
ATOM    698  CB  SER A  88     -16.834 -20.323  46.202  1.00 94.54           C  
ANISOU  698  CB  SER A  88    10794  11978  13149  -4805  -1825   5312       C  
ATOM    699  OG  SER A  88     -16.014 -20.995  47.143  1.00105.15           O  
ANISOU  699  OG  SER A  88    12315  13149  14489  -4878  -1915   5652       O  
ATOM    700  N   GLY A  89     -15.769 -17.357  47.992  1.00 87.49           N  
ANISOU  700  N   GLY A  89     9975  12254  11012  -3977  -1044   4843       N  
ATOM    701  CA  GLY A  89     -15.832 -16.631  49.259  1.00 89.10           C  
ANISOU  701  CA  GLY A  89    10080  13085  10690  -3862   -742   4932       C  
ATOM    702  C   GLY A  89     -15.519 -17.441  50.502  1.00 97.92           C  
ANISOU  702  C   GLY A  89    11197  14380  11629  -4093   -785   5459       C  
ATOM    703  O   GLY A  89     -15.679 -16.932  51.617  1.00 99.81           O  
ANISOU  703  O   GLY A  89    11328  15229  11368  -4028   -533   5573       O  
ATOM    704  N   LYS A  90     -15.080 -18.702  50.334  1.00 95.94           N  
ANISOU  704  N   LYS A  90    11074  13609  11770  -4345  -1109   5785       N  
ATOM    705  CA  LYS A  90     -14.722 -19.561  51.465  1.00100.09           C  
ANISOU  705  CA  LYS A  90    11620  14228  12181  -4567  -1202   6365       C  
ATOM    706  C   LYS A  90     -13.354 -19.106  52.008  1.00102.37           C  
ANISOU  706  C   LYS A  90    12184  14524  12190  -4278  -1244   6154       C  
ATOM    707  O   LYS A  90     -12.583 -18.496  51.260  1.00 97.74           O  
ANISOU  707  O   LYS A  90    11801  13613  11721  -3994  -1308   5623       O  
ATOM    708  CB  LYS A  90     -14.731 -21.046  51.063  1.00104.99           C  
ANISOU  708  CB  LYS A  90    12293  14208  13389  -4917  -1561   6783       C  
ATOM    709  CG  LYS A  90     -16.044 -21.504  50.427  1.00113.57           C  
ANISOU  709  CG  LYS A  90    13099  15249  14803  -5254  -1578   6960       C  
ATOM    710  CD  LYS A  90     -16.146 -23.015  50.295  1.00118.62           C  
ANISOU  710  CD  LYS A  90    13771  15308  15993  -5679  -1930   7477       C  
ATOM    711  CE  LYS A  90     -17.148 -23.458  49.256  1.00114.97           C  
ANISOU  711  CE  LYS A  90    13137  14541  16006  -5963  -2084   7411       C  
ATOM    712  NZ  LYS A  90     -16.564 -23.477  47.887  1.00107.19           N1+
ANISOU  712  NZ  LYS A  90    12444  12886  15396  -5736  -2345   6784       N1+
ATOM    713  N   ASP A  91     -13.084 -19.337  53.309  1.00102.22           N  
ANISOU  713  N   ASP A  91    12138  14936  11767  -4359  -1199   6577       N  
ATOM    714  CA  ASP A  91     -11.847 -18.889  53.965  1.00100.74           C  
ANISOU  714  CA  ASP A  91    12159  14874  11243  -4120  -1257   6419       C  
ATOM    715  C   ASP A  91     -10.524 -19.435  53.376  1.00100.80           C  
ANISOU  715  C   ASP A  91    12437  14180  11681  -4005  -1615   6303       C  
ATOM    716  O   ASP A  91     -10.320 -20.648  53.373  1.00101.92           O  
ANISOU  716  O   ASP A  91    12629  13899  12199  -4197  -1881   6755       O  
ATOM    717  CB  ASP A  91     -11.917 -19.075  55.492  1.00108.02           C  
ANISOU  717  CB  ASP A  91    12977  16460  11606  -4253  -1164   6952       C  
ATOM    718  CG  ASP A  91     -10.759 -18.443  56.248  1.00118.10           C  
ANISOU  718  CG  ASP A  91    14430  18015  12426  -4007  -1214   6730       C  
ATOM    719  OD1 ASP A  91     -10.439 -17.264  55.970  1.00114.28           O  
ANISOU  719  OD1 ASP A  91    14023  17659  11737  -3726  -1076   6085       O  
ATOM    720  OD2 ASP A  91     -10.192 -19.118  57.138  1.00128.04           O1-
ANISOU  720  OD2 ASP A  91    15743  19370  13538  -4109  -1407   7219       O1-
ATOM    721  N   PRO A  92      -9.612 -18.555  52.879  1.00 93.41           N  
ANISOU  721  N   PRO A  92    11664  13109  10719  -3687  -1620   5711       N  
ATOM    722  CA  PRO A  92      -8.334 -19.054  52.321  1.00 90.90           C  
ANISOU  722  CA  PRO A  92    11546  12198  10795  -3547  -1924   5594       C  
ATOM    723  C   PRO A  92      -7.397 -19.757  53.324  1.00 95.86           C  
ANISOU  723  C   PRO A  92    12239  12862  11319  -3567  -2165   6029       C  
ATOM    724  O   PRO A  92      -6.705 -20.705  52.933  1.00 95.83           O  
ANISOU  724  O   PRO A  92    12343  12301  11768  -3536  -2453   6180       O  
ATOM    725  CB  PRO A  92      -7.696 -17.801  51.715  1.00 87.70           C  
ANISOU  725  CB  PRO A  92    11228  11790  10304  -3246  -1810   4918       C  
ATOM    726  CG  PRO A  92      -8.301 -16.664  52.469  1.00 92.61           C  
ANISOU  726  CG  PRO A  92    11753  13062  10371  -3208  -1514   4752       C  
ATOM    727  CD  PRO A  92      -9.706 -17.082  52.762  1.00 91.53           C  
ANISOU  727  CD  PRO A  92    11419  13221  10139  -3444  -1353   5135       C  
ATOM    728  N   ASN A  93      -7.396 -19.324  54.613  1.00 93.14           N  
ANISOU  728  N   ASN A  93    11828  13187  10373  -3599  -2057   6232       N  
ATOM    729  CA  ASN A  93      -6.559 -19.891  55.688  1.00 96.66           C  
ANISOU  729  CA  ASN A  93    12312  13812  10600  -3616  -2286   6685       C  
ATOM    730  C   ASN A  93      -6.740 -21.403  55.892  1.00103.33           C  
ANISOU  730  C   ASN A  93    13152  14297  11812  -3853  -2528   7429       C  
ATOM    731  O   ASN A  93      -6.032 -22.016  56.686  1.00106.07           O  
ANISOU  731  O   ASN A  93    13535  14706  12059  -3860  -2762   7889       O  
ATOM    732  CB  ASN A  93      -6.765 -19.136  57.007  1.00100.43           C  
ANISOU  732  CB  ASN A  93    12709  15163  10286  -3629  -2094   6745       C  
ATOM    733  CG  ASN A  93      -6.174 -17.749  57.011  1.00112.71           C  
ANISOU  733  CG  ASN A  93    14329  16984  11510  -3377  -1985   6040       C  
ATOM    734  ND2 ASN A  93      -6.982 -16.768  57.380  1.00104.84           N  
ANISOU  734  ND2 ASN A  93    13260  16522  10054  -3349  -1660   5751       N  
ATOM    735  OD1 ASN A  93      -4.994 -17.541  56.708  1.00100.26           O  
ANISOU  735  OD1 ASN A  93    12853  15149  10094  -3207  -2194   5758       O  
ATOM    736  N   HIS A  94      -7.684 -21.988  55.144  1.00 99.32           N  
ANISOU  736  N   HIS A  94    12599  13385  11753  -4051  -2499   7542       N  
ATOM    737  CA  HIS A  94      -8.018 -23.402  55.083  1.00103.00           C  
ANISOU  737  CA  HIS A  94    13073  13348  12713  -4320  -2736   8167       C  
ATOM    738  C   HIS A  94      -6.805 -24.151  54.499  1.00107.96           C  
ANISOU  738  C   HIS A  94    13906  13217  13898  -4105  -3109   8098       C  
ATOM    739  O   HIS A  94      -6.505 -25.255  54.937  1.00113.57           O  
ANISOU  739  O   HIS A  94    14672  13602  14877  -4210  -3387   8693       O  
ATOM    740  CB  HIS A  94      -9.235 -23.558  54.164  1.00102.14           C  
ANISOU  740  CB  HIS A  94    12867  12978  12964  -4541  -2619   8055       C  
ATOM    741  CG  HIS A  94      -9.967 -24.842  54.298  1.00110.27           C  
ANISOU  741  CG  HIS A  94    13833  13668  14398  -4943  -2789   8749       C  
ATOM    742  CD2 HIS A  94      -9.719 -26.046  53.742  1.00113.86           C  
ANISOU  742  CD2 HIS A  94    14436  13280  15548  -5044  -3143   8965       C  
ATOM    743  ND1 HIS A  94     -11.127 -24.926  55.040  1.00115.93           N  
ANISOU  743  ND1 HIS A  94    14295  14932  14821  -5298  -2576   9277       N  
ATOM    744  CE1 HIS A  94     -11.542 -26.174  54.922  1.00120.00           C  
ANISOU  744  CE1 HIS A  94    14804  14913  15879  -5650  -2817   9841       C  
ATOM    745  NE2 HIS A  94     -10.735 -26.884  54.143  1.00119.43           N  
ANISOU  745  NE2 HIS A  94    14991  13961  16427  -5508  -3176   9656       N  
ATOM    746  N   PHE A  95      -6.110 -23.540  53.525  1.00 99.52           N  
ANISOU  746  N   PHE A  95    12932  11884  12996  -3790  -3105   7395       N  
ATOM    747  CA  PHE A  95      -4.933 -24.108  52.861  1.00 98.52           C  
ANISOU  747  CA  PHE A  95    12957  11114  13361  -3514  -3396   7214       C  
ATOM    748  C   PHE A  95      -3.628 -23.504  53.411  1.00 99.50           C  
ANISOU  748  C   PHE A  95    13079  11564  13164  -3223  -3459   7059       C  
ATOM    749  O   PHE A  95      -2.560 -23.696  52.810  1.00 97.86           O  
ANISOU  749  O   PHE A  95    12937  10951  13296  -2936  -3640   6805       O  
ATOM    750  CB  PHE A  95      -5.000 -23.836  51.346  1.00 95.83           C  
ANISOU  750  CB  PHE A  95    12689  10321  13402  -3357  -3334   6547       C  
ATOM    751  CG  PHE A  95      -6.198 -24.395  50.621  1.00 98.35           C  
ANISOU  751  CG  PHE A  95    13008  10287  14073  -3619  -3324   6578       C  
ATOM    752  CD1 PHE A  95      -6.222 -25.720  50.197  1.00104.57           C  
ANISOU  752  CD1 PHE A  95    13918  10333  15481  -3704  -3629   6799       C  
ATOM    753  CD2 PHE A  95      -7.278 -23.584  50.307  1.00 97.80           C  
ANISOU  753  CD2 PHE A  95    12813  10595  13751  -3762  -3035   6341       C  
ATOM    754  CE1 PHE A  95      -7.318 -26.225  49.491  1.00106.21           C  
ANISOU  754  CE1 PHE A  95    14121  10202  16032  -3979  -3663   6778       C  
ATOM    755  CE2 PHE A  95      -8.375 -24.093  49.609  1.00101.28           C  
ANISOU  755  CE2 PHE A  95    13215  10742  14524  -4016  -3060   6359       C  
ATOM    756  CZ  PHE A  95      -8.391 -25.411  49.208  1.00102.72           C  
ANISOU  756  CZ  PHE A  95    13519  10205  15307  -4147  -3383   6573       C  
ATOM    757  N   ARG A  96      -3.716 -22.761  54.533  1.00 94.29           N  
ANISOU  757  N   ARG A  96    12324  11658  11842  -3294  -3314   7184       N  
ATOM    758  CA  ARG A  96      -2.567 -22.080  55.124  1.00 92.20           C  
ANISOU  758  CA  ARG A  96    12037  11783  11212  -3076  -3390   7005       C  
ATOM    759  C   ARG A  96      -1.495 -23.027  55.679  1.00100.82           C  
ANISOU  759  C   ARG A  96    13145  12684  12479  -2957  -3771   7487       C  
ATOM    760  O   ARG A  96      -1.798 -23.840  56.560  1.00105.41           O  
ANISOU  760  O   ARG A  96    13718  13380  12953  -3138  -3904   8184       O  
ATOM    761  CB  ARG A  96      -3.004 -21.044  56.175  1.00 88.70           C  
ANISOU  761  CB  ARG A  96    11513  12193   9994  -3182  -3155   6956       C  
ATOM    762  CG  ARG A  96      -1.889 -20.111  56.613  1.00 89.85           C  
ANISOU  762  CG  ARG A  96    11643  12723   9772  -2982  -3223   6583       C  
ATOM    763  CD  ARG A  96      -2.307 -19.180  57.728  1.00 93.39           C  
ANISOU  763  CD  ARG A  96    12046  13995   9441  -3074  -3030   6512       C  
ATOM    764  NE  ARG A  96      -1.237 -18.233  58.047  1.00102.44           N  
ANISOU  764  NE  ARG A  96    13191  15444  10287  -2914  -3128   6067       N  
ATOM    765  CZ  ARG A  96      -1.058 -17.060  57.448  1.00108.49           C  
ANISOU  765  CZ  ARG A  96    13980  16190  11053  -2810  -2966   5373       C  
ATOM    766  NH1 ARG A  96      -1.895 -16.657  56.498  1.00 94.34           N1+
ANISOU  766  NH1 ARG A  96    12217  14122   9505  -2812  -2688   5050       N1+
ATOM    767  NH2 ARG A  96      -0.049 -16.275  57.801  1.00 92.12           N  
ANISOU  767  NH2 ARG A  96    11891  14365   8745  -2719  -3103   5020       N  
ATOM    768  N   PRO A  97      -0.229 -22.910  55.193  1.00 96.19           N  
ANISOU  768  N   PRO A  97    12553  11849  12144  -2647  -3944   7156       N  
ATOM    769  CA  PRO A  97       0.846 -23.742  55.761  1.00100.50           C  
ANISOU  769  CA  PRO A  97    13072  12269  12846  -2480  -4318   7605       C  
ATOM    770  C   PRO A  97       1.190 -23.234  57.169  1.00108.51           C  
ANISOU  770  C   PRO A  97    13994  14083  13151  -2550  -4389   7880       C  
ATOM    771  O   PRO A  97       1.216 -22.020  57.391  1.00105.73           O  
ANISOU  771  O   PRO A  97    13594  14277  12302  -2577  -4194   7430       O  
ATOM    772  CB  PRO A  97       2.001 -23.588  54.761  1.00 99.42           C  
ANISOU  772  CB  PRO A  97    12893  11761  13123  -2124  -4406   7082       C  
ATOM    773  CG  PRO A  97       1.472 -22.704  53.615  1.00 98.07           C  
ANISOU  773  CG  PRO A  97    12762  11460  13040  -2135  -4076   6408       C  
ATOM    774  CD  PRO A  97       0.295 -21.974  54.170  1.00 92.33           C  
ANISOU  774  CD  PRO A  97    12047  11247  11787  -2433  -3801   6407       C  
ATOM    775  N   ALA A  98       1.389 -24.163  58.128  1.00111.01           N  
ANISOU  775  N   ALA A  98    14302  14464  13412  -2587  -4677   8625       N  
ATOM    776  CA  ALA A  98       1.650 -23.890  59.549  1.00115.71           C  
ANISOU  776  CA  ALA A  98    14822  15850  13294  -2664  -4795   9015       C  
ATOM    777  C   ALA A  98       2.716 -22.844  59.923  1.00119.28           C  
ANISOU  777  C   ALA A  98    15161  16843  13318  -2495  -4880   8542       C  
ATOM    778  O   ALA A  98       2.523 -22.118  60.903  1.00120.82           O  
ANISOU  778  O   ALA A  98    15328  17809  12770  -2624  -4813   8534       O  
ATOM    779  CB  ALA A  98       1.888 -25.190  60.307  1.00123.46           C  
ANISOU  779  CB  ALA A  98    15813  16668  14428  -2670  -5151   9926       C  
ATOM    780  N   GLY A  99       3.815 -22.783  59.172  1.00113.90           N  
ANISOU  780  N   GLY A  99    14402  15782  13091  -2218  -5030   8153       N  
ATOM    781  CA  GLY A  99       4.903 -21.846  59.446  1.00113.23           C  
ANISOU  781  CA  GLY A  99    14168  16144  12711  -2091  -5150   7724       C  
ATOM    782  C   GLY A  99       4.961 -20.591  58.589  1.00111.20           C  
ANISOU  782  C   GLY A  99    13893  15873  12484  -2080  -4868   6877       C  
ATOM    783  O   GLY A  99       6.031 -19.982  58.480  1.00110.80           O  
ANISOU  783  O   GLY A  99    13689  15960  12449  -1953  -4998   6513       O  
ATOM    784  N   LEU A 100       3.822 -20.182  57.990  1.00102.75           N  
ANISOU  784  N   LEU A 100    12957  14651  11432  -2223  -4495   6592       N  
ATOM    785  CA  LEU A 100       3.745 -18.989  57.142  1.00 97.31           C  
ANISOU  785  CA  LEU A 100    12276  13912  10787  -2217  -4211   5849       C  
ATOM    786  C   LEU A 100       3.525 -17.708  57.972  1.00104.03           C  
ANISOU  786  C   LEU A 100    13137  15444  10947  -2365  -4093   5500       C  
ATOM    787  O   LEU A 100       2.571 -17.659  58.756  1.00106.46           O  
ANISOU  787  O   LEU A 100    13523  16166  10762  -2526  -3968   5715       O  
ATOM    788  CB  LEU A 100       2.647 -19.148  56.073  1.00 92.95           C  
ANISOU  788  CB  LEU A 100    11850  12893  10574  -2274  -3902   5711       C  
ATOM    789  CG  LEU A 100       2.567 -18.076  54.978  1.00 91.08           C  
ANISOU  789  CG  LEU A 100    11628  12468  10512  -2221  -3629   5024       C  
ATOM    790  CD1 LEU A 100       3.612 -18.309  53.892  1.00 89.44           C  
ANISOU  790  CD1 LEU A 100    11337  11770  10878  -1978  -3729   4819       C  
ATOM    791  CD2 LEU A 100       1.192 -18.048  54.359  1.00 87.27           C  
ANISOU  791  CD2 LEU A 100    11261  11802  10094  -2343  -3324   4945       C  
ATOM    792  N   PRO A 101       4.381 -16.664  57.795  1.00 99.95           N  
ANISOU  792  N   PRO A 101    12535  15044  10398  -2315  -4125   4953       N  
ATOM    793  CA  PRO A 101       4.219 -15.418  58.578  1.00101.20           C  
ANISOU  793  CA  PRO A 101    12732  15778   9940  -2449  -4051   4548       C  
ATOM    794  C   PRO A 101       2.860 -14.729  58.456  1.00104.35           C  
ANISOU  794  C   PRO A 101    13292  16270  10087  -2552  -3651   4270       C  
ATOM    795  O   PRO A 101       2.229 -14.776  57.402  1.00100.12           O  
ANISOU  795  O   PRO A 101    12810  15281   9950  -2523  -3400   4160       O  
ATOM    796  CB  PRO A 101       5.361 -14.528  58.079  1.00101.29           C  
ANISOU  796  CB  PRO A 101    12617  15683  10184  -2399  -4154   4027       C  
ATOM    797  CG  PRO A 101       6.372 -15.482  57.530  1.00105.90           C  
ANISOU  797  CG  PRO A 101    13025  15889  11325  -2218  -4385   4320       C  
ATOM    798  CD  PRO A 101       5.567 -16.588  56.916  1.00 99.69           C  
ANISOU  798  CD  PRO A 101    12349  14640  10887  -2143  -4240   4691       C  
ATOM    799  N   GLU A 102       2.432 -14.086  59.560  1.00105.45           N  
ANISOU  799  N   GLU A 102    13494  17037   9537  -2649  -3605   4144       N  
ATOM    800  CA  GLU A 102       1.155 -13.395  59.769  1.00105.40           C  
ANISOU  800  CA  GLU A 102    13606  17290   9150  -2706  -3239   3893       C  
ATOM    801  C   GLU A 102       0.744 -12.393  58.700  1.00105.04           C  
ANISOU  801  C   GLU A 102    13628  16849   9434  -2657  -2945   3302       C  
ATOM    802  O   GLU A 102      -0.457 -12.242  58.450  1.00104.03           O  
ANISOU  802  O   GLU A 102    13554  16709   9261  -2659  -2623   3272       O  
ATOM    803  CB  GLU A 102       1.125 -12.739  61.158  1.00112.17           C  
ANISOU  803  CB  GLU A 102    14508  18924   9187  -2758  -3297   3729       C  
ATOM    804  CG  GLU A 102      -0.112 -13.076  61.974  1.00128.13           C  
ANISOU  804  CG  GLU A 102    16563  21462  10658  -2815  -3051   4071       C  
ATOM    805  CD  GLU A 102      -0.129 -14.467  62.579  1.00155.51           C  
ANISOU  805  CD  GLU A 102    19955  25114  14020  -2893  -3224   4939       C  
ATOM    806  OE1 GLU A 102       0.436 -14.643  63.683  1.00152.31           O  
ANISOU  806  OE1 GLU A 102    19524  25259  13089  -2917  -3494   5184       O  
ATOM    807  OE2 GLU A 102      -0.708 -15.382  61.949  1.00150.74           O1-
ANISOU  807  OE2 GLU A 102    19319  24093  13862  -2940  -3110   5382       O1-
ATOM    808  N   LYS A 103       1.728 -11.703  58.078  1.00 98.53           N  
ANISOU  808  N   LYS A 103    12774  15723   8940  -2618  -3057   2874       N  
ATOM    809  CA  LYS A 103       1.476 -10.713  57.032  1.00 93.29           C  
ANISOU  809  CA  LYS A 103    12173  14662   8609  -2576  -2808   2362       C  
ATOM    810  C   LYS A 103       0.762 -11.294  55.818  1.00 92.26           C  
ANISOU  810  C   LYS A 103    12048  14040   8965  -2512  -2586   2542       C  
ATOM    811  O   LYS A 103      -0.104 -10.624  55.257  1.00 90.57           O  
ANISOU  811  O   LYS A 103    11912  13696   8805  -2480  -2298   2266       O  
ATOM    812  CB  LYS A 103       2.774 -10.011  56.606  1.00 94.82           C  
ANISOU  812  CB  LYS A 103    12292  14635   9098  -2590  -2996   1996       C  
ATOM    813  CG  LYS A 103       3.266  -8.968  57.576  1.00118.22           C  
ANISOU  813  CG  LYS A 103    15290  18003  11627  -2686  -3171   1590       C  
ATOM    814  CD  LYS A 103       4.454  -8.207  56.989  1.00129.99           C  
ANISOU  814  CD  LYS A 103    16677  19203  13512  -2753  -3326   1238       C  
ATOM    815  CE  LYS A 103       5.217  -7.400  58.023  1.00146.16           C  
ANISOU  815  CE  LYS A 103    18723  21626  15184  -2896  -3611    861       C  
ATOM    816  NZ  LYS A 103       6.400  -6.711  57.435  1.00153.02           N1+
ANISOU  816  NZ  LYS A 103    19447  22197  16496  -3016  -3770    565       N1+
ATOM    817  N   TYR A 104       1.108 -12.538  55.423  1.00 86.31           N  
ANISOU  817  N   TYR A 104    11215  13015   8563  -2480  -2737   2991       N  
ATOM    818  CA  TYR A 104       0.520 -13.232  54.274  1.00 81.79           C  
ANISOU  818  CA  TYR A 104    10656  11960   8459  -2427  -2593   3149       C  
ATOM    819  C   TYR A 104      -0.872 -13.814  54.561  1.00 86.85           C  
ANISOU  819  C   TYR A 104    11340  12735   8924  -2516  -2421   3477       C  
ATOM    820  O   TYR A 104      -1.258 -13.926  55.746  1.00 88.68           O  
ANISOU  820  O   TYR A 104    11565  13456   8672  -2608  -2448   3736       O  
ATOM    821  CB  TYR A 104       1.461 -14.333  53.750  1.00 82.59           C  
ANISOU  821  CB  TYR A 104    10671  11687   9022  -2329  -2839   3442       C  
ATOM    822  CG  TYR A 104       2.887 -13.883  53.520  1.00 83.37           C  
ANISOU  822  CG  TYR A 104    10649  11731   9298  -2243  -3014   3197       C  
ATOM    823  CD1 TYR A 104       3.195 -12.953  52.531  1.00 81.78           C  
ANISOU  823  CD1 TYR A 104    10428  11280   9366  -2192  -2858   2764       C  
ATOM    824  CD2 TYR A 104       3.934 -14.408  54.271  1.00 87.45           C  
ANISOU  824  CD2 TYR A 104    11040  12465   9722  -2221  -3343   3442       C  
ATOM    825  CE1 TYR A 104       4.504 -12.529  52.320  1.00 82.67           C  
ANISOU  825  CE1 TYR A 104    10379  11375   9658  -2151  -3003   2580       C  
ATOM    826  CE2 TYR A 104       5.249 -13.995  54.065  1.00 88.33           C  
ANISOU  826  CE2 TYR A 104    10978  12569  10016  -2158  -3513   3234       C  
ATOM    827  CZ  TYR A 104       5.530 -13.059  53.086  1.00 90.64           C  
ANISOU  827  CZ  TYR A 104    11232  12619  10587  -2138  -3330   2804       C  
ATOM    828  OH  TYR A 104       6.821 -12.647  52.876  1.00 91.07           O  
ANISOU  828  OH  TYR A 104    11069  12696  10837  -2113  -3481   2639       O  
ATOM    829  OXT TYR A 104      -1.551 -14.220  53.591  1.00 93.23           O1-
ANISOU  829  OXT TYR A 104    12166  13185  10073  -2504  -2272   3504       O1-
TER   
END



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elNémo is maintained by Yves-Henri Sanejouand.
It was developed by Karsten Suhre.
Between 2003 and 2014, it was hosted by IGS (Marseille).
Last modification: April 25th, 2023.