***  Serum Amyloid A1  ***
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.
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