Should you encounter any unexpected behaviour,
please let us know.

* *

CA strain for 22123114225973881

--- normal mode 7 ---

This graph displays the distance variation between successive pairs of CA atoms in the two extreme conformations that were computed for this mode (DQMIN/DQMAX). Large distance variations can be an indicator for residue pairs that support the important strain in that particular normal mode movement. Note that residue pairs between chain breaks or at flexible ends of the protein may also exhibit large CA-CA distance variations. If more than one residues ae grouped together into a rigid block (NRBL>1), CA-CA distance variations between CA atoms in the same block will be very low.

This feature is still experimental and will be further developped in the future.

CA i CA i+1 vari
PHE 1 ASP 2 -0.0000

ASP 2 MET 3 -0.0027

MET 3 ILE 4 0.0000

ILE 4 ARG 5 -0.0009

ARG 5 LEU 6 0.0001

LEU 6 ALA 7 -0.0021

ALA 7 THR 8 0.0003

THR 8 ASN 9 -0.0015

ASN 9 LYS 10 0.0002

LYS 10 PHE 11 0.0014

PHE 11 SER 12 -0.0004

SER 12 GLU 13 0.0001

GLU 13 ASP 14 -0.0002

ASP 14 ASN 15 -0.0009

ASN 15 LYS 16 0.0004

LYS 16 ILE 17 0.0085

ILE 17 GLY 18 0.0002

GLY 18 GLU 19 0.0231

GLU 19 GLY 20 0.0000

GLY 20 GLY 21 0.0249

GLY 21 PHE 22 -0.0003

PHE 22 GLY 23 0.0124

GLY 23 ASP 24 -0.0000

ASP 24 VAL 25 0.0093

VAL 25 TYR 26 -0.0005

TYR 26 LYS 27 0.0048

LYS 27 GLY 28 -0.0001

GLY 28 MET 29 0.0060

MET 29 PHE 30 -0.0004

PHE 30 PRO 31 0.0009

PRO 31 ASN 32 -0.0003

ASN 32 GLY 33 0.0001

GLY 33 TYR 34 -0.0000

TYR 34 GLU 35 0.0011

GLU 35 ILE 36 -0.0001

ILE 36 ALA 37 0.0062

ALA 37 VAL 38 0.0002

VAL 38 LYS 39 0.0065

LYS 39 ARG 40 0.0004

ARG 40 LEU 41 0.0092

LEU 41 ILE 42 -0.0004

ILE 42 ARG 43 -0.0006

ARG 43 ASN 44 -0.0003

ASN 44 SER 45 0.0258

SER 45 SER 46 -0.0004

SER 46 GLN 47 -0.0056

GLN 47 GLY 48 0.0003

GLY 48 ALA 49 -0.0160

ALA 49 VAL 50 -0.0001

VAL 50 GLU 51 0.0066

GLU 51 PHE 52 0.0000

PHE 52 LYS 53 0.0004

LYS 53 ASN 54 0.0002

ASN 54 GLU 55 -0.0005

GLU 55 VAL 56 -0.0001

VAL 56 LEU 57 -0.0025

LEU 57 LEU 58 -0.0004

LEU 58 ILE 59 0.0004

ILE 59 ALA 60 -0.0000

ALA 60 LYS 61 -0.0035

LYS 61 LEU 62 0.0001

LEU 62 GLN 63 0.0004

GLN 63 HIS 64 -0.0001

HIS 64 ARG 65 -0.0030

ARG 65 ASN 66 -0.0002

ASN 66 LEU 67 -0.0035

LEU 67 VAL 68 -0.0001

VAL 68 ARG 69 -0.0038

ARG 69 LEU 70 0.0003

LEU 70 LEU 71 0.0002

LEU 71 GLY 72 -0.0003

GLY 72 PHE 73 -0.0106

PHE 73 CYS 74 -0.0001

CYS 74 ILE 75 -0.0074

ILE 75 GLN 76 0.0003

GLN 76 ARG 77 -0.0039

ARG 77 ASN 78 0.0003

ASN 78 GLU 79 0.0026

GLU 79 LYS 80 0.0000

LYS 80 ILE 81 -0.0048

ILE 81 LEU 82 -0.0001

LEU 82 ILE 83 0.0003

ILE 83 TYR 84 0.0001

TYR 84 GLU 85 -0.0044

GLU 85 TYR 86 0.0003

TYR 86 MET 87 -0.0040

MET 87 HIS 88 -0.0003

HIS 88 ASN 89 -0.0057

ASN 89 LYS 90 -0.0000

LYS 90 SER 91 -0.0032

SER 91 LEU 92 0.0002

LEU 92 ASP 93 0.0008

ASP 93 TYR 94 0.0001

TYR 94 TYR 95 0.0014

TYR 95 LEU 96 0.0001

LEU 96 PHE 97 -0.0003

PHE 97 SER 98 -0.0002

SER 98 PRO 99 0.0007

PRO 99 GLU 100 -0.0002

GLU 100 ASN 101 -0.0003

ASN 101 HIS 102 -0.0000

HIS 102 ARG 103 0.0006

ARG 103 LYS 104 -0.0001

LYS 104 LEU 105 0.0001

LEU 105 THR 106 -0.0000

THR 106 TRP 107 0.0010

TRP 107 HIS 108 -0.0001

HIS 108 ALA 109 -0.0021

ALA 109 ARG 110 -0.0004

ARG 110 TYR 111 0.0012

TYR 111 LYS 112 -0.0000

LYS 112 ILE 113 0.0021

ILE 113 ILE 114 0.0002

ILE 114 ARG 115 -0.0007

ARG 115 GLY 116 -0.0002

GLY 116 ILE 117 -0.0007

ILE 117 ALA 118 0.0001

ALA 118 ARG 119 -0.0044

ARG 119 GLY 120 0.0001

GLY 120 ILE 121 0.0013

ILE 121 LEU 122 0.0002

LEU 122 TYR 123 -0.0103

TYR 123 LEU 124 0.0000

LEU 124 HIS 125 -0.0010

HIS 125 GLU 126 0.0003

GLU 126 ASP 127 -0.0018

ASP 127 SER 128 -0.0003

SER 128 HIS 129 -0.0001

HIS 129 LEU 130 -0.0003

LEU 130 LYS 131 -0.0011

LYS 131 ILE 132 -0.0001

ILE 132 ILE 133 0.0027

ILE 133 HIS 134 -0.0001

HIS 134 CYS 135 0.0097

CYS 135 ASP 136 0.0004

ASP 136 LEU 137 0.0073

LEU 137 LYS 138 -0.0002

LYS 138 PRO 139 0.0007

PRO 139 SER 140 -0.0003

SER 140 ASN 141 0.0016

ASN 141 ILE 142 -0.0002

ILE 142 LEU 143 0.0002

LEU 143 LEU 144 0.0001

LEU 144 ASP 145 0.0007

ASP 145 ASP 146 -0.0002

ASP 146 LYS 147 -0.0038

LYS 147 MET 148 -0.0001

MET 148 ASN 149 0.0010

ASN 149 ALA 150 0.0002

ALA 150 LYS 151 -0.0024

LYS 151 ILE 152 0.0001

ILE 152 SER 153 0.0058

SER 153 ASP 154 0.0001

ASP 154 PHE 155 0.0022

PHE 155 GLY 156 0.0000

GLY 156 LEU 157 0.0112

LEU 157 ALA 158 -0.0003

ALA 158 ARG 159 0.0025

ARG 159 ILE 160 -0.0002

ILE 160 VAL 161 -0.0058

VAL 161 ALA 162 0.0004

ALA 162 ILE 163 0.0004

ILE 163 ASP 164 0.0001

ASP 164 GLN 165 -0.0002

GLN 165 MET 166 -0.0000

MET 166 GLN 167 0.0034

GLN 167 GLY 168 0.0002

GLY 168 ASN 169 0.0185

ASN 169 THR 170 0.0002

THR 170 SER 171 0.0678

SER 171 ILE 172 -0.0002

ILE 172 ILE 173 -0.0113

ILE 173 ALA 174 -0.0002

ALA 174 GLY 175 0.0025

GLY 175 THR 176 -0.0003

THR 176 TYR 177 0.0317

TYR 177 GLY 178 0.0003

GLY 178 TYR 179 0.0117

TYR 179 MET 180 -0.0005

MET 180 SER 181 -0.0027

SER 181 PRO 182 -0.0002

PRO 182 GLU 183 -0.0012

GLU 183 TYR 184 -0.0004

TYR 184 ALA 185 0.0146

ALA 185 MET 186 -0.0002

MET 186 LEU 187 -0.0097

LEU 187 GLY 188 -0.0003

GLY 188 GLN 189 0.0107

GLN 189 PHE 190 0.0002

PHE 190 SER 191 0.0066

SER 191 VAL 192 0.0002

VAL 192 LYS 193 -0.0049

LYS 193 SER 194 0.0003

SER 194 ASP 195 0.0007

ASP 195 VAL 196 -0.0001

VAL 196 PHE 197 -0.0025

PHE 197 SER 198 -0.0001

SER 198 PHE 199 0.0038

PHE 199 GLY 200 0.0002

GLY 200 VAL 201 -0.0008

VAL 201 ILE 202 0.0001

ILE 202 MET 203 0.0054

MET 203 LEU 204 -0.0003

LEU 204 GLU 205 0.0008

GLU 205 ILE 206 0.0001

ILE 206 VAL 207 0.0018

VAL 207 SER 208 -0.0000

SER 208 GLY 209 0.0016

GLY 209 LYS 210 0.0000

LYS 210 ARG 211 0.0020

ARG 211 ASN 212 0.0003

ASN 212 VAL 213 0.0023

VAL 213 ASP 214 0.0001

ASP 214 TYR 215 -0.0002

TYR 215 ASN 216 0.0001

ASN 216 GLY 217 -0.0016

GLY 217 VAL 218 -0.0000

VAL 218 ASN 219 -0.0002

ASN 219 SER 220 0.0003

SER 220 ILE 221 -0.0030

ILE 221 ASP 222 0.0001

ASP 222 ASP 223 0.0042

ASP 223 LEU 224 0.0004

LEU 224 VAL 225 0.0008

VAL 225 SER 226 0.0002

SER 226 HIS 227 -0.0033

HIS 227 ALA 228 -0.0001

ALA 228 TRP 229 0.0007

TRP 229 LYS 230 -0.0003

LYS 230 LYS 231 -0.0025

LYS 231 TRP 232 -0.0001

TRP 232 THR 233 -0.0006

THR 233 GLU 234 0.0004

GLU 234 ASN 235 -0.0006

ASN 235 LYS 236 -0.0002

LYS 236 GLN 237 0.0000

GLN 237 MET 238 -0.0002

MET 238 GLU 239 -0.0016

GLU 239 LEU 240 -0.0001

LEU 240 LEU 241 -0.0039

LEU 241 ASP 242 0.0001

ASP 242 PRO 243 0.0002

PRO 243 ALA 244 -0.0000

ALA 244 LEU 245 0.0013

LEU 245 THR 246 0.0002

THR 246 TYR 247 0.0000

TYR 247 SER 248 -0.0000

SER 248 PHE 249 0.0006

PHE 249 SER 250 -0.0000

SER 250 GLU 251 -0.0011

GLU 251 THR 252 -0.0005

THR 252 GLU 253 -0.0010

GLU 253 VAL 254 0.0001

VAL 254 SER 255 -0.0017

SER 255 ARG 256 -0.0001

ARG 256 CYS 257 0.0009

CYS 257 ILE 258 -0.0002

ILE 258 GLN 259 0.0001

GLN 259 LEU 260 -0.0003

LEU 260 GLY 261 0.0012

GLY 261 LEU 262 0.0001

LEU 262 LEU 263 -0.0009

LEU 263 CYS 264 -0.0001

CYS 264 VAL 265 -0.0019

VAL 265 GLN 266 0.0003

GLN 266 GLU 267 -0.0009

GLU 267 ASN 268 -0.0002

ASN 268 PRO 269 0.0004

PRO 269 ASP 270 -0.0001

ASP 270 GLN 271 0.0029

GLN 271 ARG 272 -0.0003

ARG 272 PRO 273 -0.0067

PRO 273 THR 274 -0.0004

THR 274 MET 275 -0.0048

MET 275 ALA 276 0.0001

ALA 276 THR 277 -0.0025

THR 277 ILE 278 0.0000

ILE 278 ALA 279 -0.0006

ALA 279 LEU 280 -0.0002

LEU 280 TYR 281 -0.0014

TYR 281 PHE 282 0.0002

PHE 282 ASN 283 -0.0007

ASN 283 ILE 284 -0.0000

ILE 284 ASP 285 0.0005

ASP 285 SER 286 0.0002

SER 286 ILE 287 0.0002

ILE 287 ASP 288 0.0002

ASP 288 LEU 289 0.0003

LEU 289 PRO 290 0.0001

PRO 290 LEU 291 -0.0039

LEU 291 PRO 292 0.0005

PRO 292 GLN 293 -0.0047

GLN 293 GLN 294 -0.0001

GLN 294 PRO 295 0.0005

PRO 295 PRO 296 0.0002

PRO 296 PHE 297 -0.0048

PHE 297 TYR 298 0.0002

TYR 298 MET 299 -0.0190

MET 299 ARG 300 -0.0001

ARG 300 GLY 301 0.0125

GLY 301 LYS 302 -0.0003

LYS 302 ILE 303 0.0098

ILE 303 GLU 304 -0.0003

GLU 304 SER 305 0.0212

SER 305 LYS 306 0.0002

LYS 306 VAL 307 0.0237

VAL 307 ALA 308 0.0002

ALA 308 SER 309 0.0535

SER 309 LYS 310 -0.0004

LYS 310 LYS 311 0.0355

LYS 311 THR 312 0.0001

THR 312 MET 313 -0.1581

MET 313 SER 314 0.0001

SER 314 GLY 315 0.0008

GLY 315 ARG 316 -0.0001

ARG 316 PRO 317 0.0242

PRO 317 ARG 318 -0.0000

ARG 318 SER 319 -0.1062

SER 319 TYR 320 0.0001

TYR 320 SER 321 -0.1263

SER 321 VAL 322 0.0002

VAL 322 THR 323 -0.0019

THR 323 ARG 324 0.0003

ARG 324 PHE 325 0.0138

If you find results from this site helpful for your research, please cite one of our papers:

K. Suhre & Y.H. Sanejouand, ElNemo: a normal mode web-server for protein movement analysis and the generation of templates for molecular replacement. Nucleic Acids Research, 32, W610-W614, 2004.
K. Suhre & Y.H. Sanejouand, On the potential of normal mode analysis for solving difficult molecular replacement problems. Acta Cryst. D vol.60, p796-799, 2004 © International Union of Crystallography.

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: October 18th, 2018.

Should you encounter any unexpected behaviour, please let us know.

*** ***

CA strain for 22123114225973881

--- normal mode 7 ---

Should you encounter any unexpected behaviour,
please let us know.

* *