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

* 2V7Y copy *

CA strain for 2402070129241772454

--- normal mode 13 ---

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
MET 1 SER 2 -0.0002

SER 2 LYS 3 0.0000

LYS 3 ILE 4 -0.0000

ILE 4 ILE 5 -0.0004

ILE 5 GLY 6 0.0002

GLY 6 ILE 7 0.0014

ILE 7 ASP 8 -0.0003

ASP 8 LEU 9 0.0004

LEU 9 GLY 10 0.0020

GLY 10 THR 11 0.0002

THR 11 THR 12 -0.0002

THR 12 ASN 13 -0.0018

ASN 13 SER 14 -0.0002

SER 14 CYS 15 0.0003

CYS 15 VAL 16 -0.0016

VAL 16 ALA 17 -0.0003

ALA 17 VAL 18 0.0003

VAL 18 LEU 19 -0.0008

LEU 19 GLU 20 0.0002

GLU 20 GLY 21 0.0000

GLY 21 GLY 22 0.0004

GLY 22 GLU 23 -0.0001

GLU 23 VAL 24 0.0001

VAL 24 LYS 25 -0.0000

LYS 25 VAL 26 -0.0000

VAL 26 ILE 27 -0.0001

ILE 27 PRO 28 -0.0008

PRO 28 ASN 29 -0.0002

ASN 29 PRO 30 0.0001

PRO 30 GLU 31 -0.0021

GLU 31 GLY 32 0.0000

GLY 32 ASN 33 0.0000

ASN 33 ARG 34 0.0009

ARG 34 THR 35 -0.0000

THR 35 THR 36 0.0002

THR 36 PRO 37 -0.0024

PRO 37 SER 38 -0.0000

SER 38 VAL 39 0.0004

VAL 39 VAL 40 -0.0006

VAL 40 ALA 41 0.0001

ALA 41 PHE 42 -0.0001

PHE 42 LYS 43 -0.0005

LYS 43 ASN 44 -0.0002

ASN 44 GLY 45 -0.0002

GLY 45 GLU 46 0.0012

GLU 46 ARG 47 0.0002

ARG 47 LEU 48 -0.0002

LEU 48 VAL 49 0.0010

VAL 49 GLY 50 -0.0000

GLY 50 GLU 51 0.0001

GLU 51 VAL 52 0.0001

VAL 52 ALA 53 0.0001

ALA 53 LYS 54 0.0002

LYS 54 ARG 55 0.0026

ARG 55 GLN 56 -0.0002

GLN 56 ALA 57 0.0001

ALA 57 ILE 58 0.0030

ILE 58 THR 59 0.0001

THR 59 ASN 60 0.0003

ASN 60 PRO 61 0.0025

PRO 61 ASN 62 0.0002

ASN 62 THR 63 -0.0001

THR 63 ILE 64 0.0004

ILE 64 ILE 65 -0.0003

ILE 65 SER 66 -0.0001

SER 66 ILE 67 0.0022

ILE 67 LYS 68 0.0002

LYS 68 ARG 69 -0.0001

ARG 69 HIS 70 0.0007

HIS 70 MET 71 0.0002

MET 71 GLY 72 -0.0001

GLY 72 THR 73 -0.0003

THR 73 ASP 74 -0.0001

ASP 74 TYR 75 0.0005

TYR 75 LYS 76 -0.0010

LYS 76 VAL 77 0.0003

VAL 77 GLU 78 -0.0004

GLU 78 ILE 79 0.0001

ILE 79 GLU 80 0.0003

GLU 80 GLY 81 -0.0001

GLY 81 LYS 82 0.0004

LYS 82 GLN 83 0.0000

GLN 83 TYR 84 -0.0002

TYR 84 THR 85 0.0003

THR 85 PRO 86 -0.0001

PRO 86 GLN 87 0.0000

GLN 87 GLU 88 -0.0002

GLU 88 ILE 89 -0.0001

ILE 89 SER 90 0.0004

SER 90 ALA 91 -0.0006

ALA 91 ILE 92 -0.0003

ILE 92 ILE 93 0.0001

ILE 93 LEU 94 0.0001

LEU 94 GLN 95 0.0001

GLN 95 TYR 96 0.0002

TYR 96 LEU 97 -0.0005

LEU 97 LYS 98 0.0001

LYS 98 SER 99 0.0001

SER 99 TYR 100 0.0011

TYR 100 ALA 101 -0.0003

ALA 101 GLU 102 -0.0002

GLU 102 ASP 103 0.0005

ASP 103 TYR 104 -0.0001

TYR 104 LEU 105 -0.0004

LEU 105 GLY 106 0.0023

GLY 106 GLU 107 -0.0001

GLU 107 PRO 108 0.0003

PRO 108 VAL 109 0.0009

VAL 109 THR 110 0.0001

THR 110 ARG 111 0.0001

ARG 111 ALA 112 0.0013

ALA 112 VAL 113 0.0000

VAL 113 ILE 114 0.0000

ILE 114 THR 115 0.0011

THR 115 VAL 116 -0.0002

VAL 116 PRO 117 0.0001

PRO 117 ALA 118 -0.0014

ALA 118 TYR 119 0.0002

TYR 119 PHE 120 -0.0003

PHE 120 ASN 121 0.0004

ASN 121 ASP 122 0.0001

ASP 122 ALA 123 -0.0001

ALA 123 GLN 124 0.0004

GLN 124 ARG 125 0.0003

ARG 125 GLN 126 -0.0000

GLN 126 ALA 127 -0.0014

ALA 127 THR 128 0.0001

THR 128 LYS 129 0.0001

LYS 129 ASP 130 0.0001

ASP 130 ALA 131 0.0001

ALA 131 GLY 132 -0.0003

GLY 132 ARG 133 0.0000

ARG 133 ILE 134 -0.0003

ILE 134 ALA 135 -0.0000

ALA 135 GLY 136 -0.0013

GLY 136 LEU 137 -0.0002

LEU 137 GLU 138 0.0002

GLU 138 VAL 139 0.0003

VAL 139 GLU 140 0.0005

GLU 140 ARG 141 -0.0002

ARG 141 ILE 142 0.0111

ILE 142 ILE 143 -0.0001

ILE 143 ASN 144 -0.0002

ASN 144 GLU 145 0.0028

GLU 145 PRO 146 0.0001

PRO 146 THR 147 0.0004

THR 147 ALA 148 0.0023

ALA 148 ALA 149 0.0001

ALA 149 ALA 150 0.0001

ALA 150 LEU 151 0.0033

LEU 151 ALA 152 -0.0002

ALA 152 TYR 153 0.0001

TYR 153 GLY 154 0.0009

GLY 154 LEU 155 -0.0001

LEU 155 ASP 156 0.0001

ASP 156 LYS 157 -0.0004

LYS 157 GLU 158 -0.0002

GLU 158 GLU 159 0.0003

GLU 159 ASP 160 -0.0001

ASP 160 GLN 161 0.0001

GLN 161 THR 162 -0.0003

THR 162 ILE 163 -0.0001

ILE 163 LEU 164 0.0003

LEU 164 VAL 165 -0.0002

VAL 165 TYR 166 0.0007

TYR 166 ASP 167 -0.0004

ASP 167 LEU 168 0.0004

LEU 168 GLY 169 -0.0002

GLY 169 GLY 170 -0.0001

GLY 170 GLY 171 -0.0001

GLY 171 THR 172 0.0008

THR 172 PHE 173 -0.0001

PHE 173 ASP 174 0.0001

ASP 174 VAL 175 -0.0007

VAL 175 SER 176 0.0002

SER 176 ILE 177 -0.0002

ILE 177 LEU 178 0.0009

LEU 178 GLU 179 -0.0002

GLU 179 LEU 180 -0.0001

LEU 180 GLY 181 -0.0004

GLY 181 ASP 182 -0.0000

ASP 182 GLY 183 -0.0001

GLY 183 VAL 184 -0.0004

VAL 184 PHE 185 0.0001

PHE 185 GLU 186 0.0002

GLU 186 VAL 187 0.0001

VAL 187 LYS 188 -0.0000

LYS 188 ALA 189 0.0001

ALA 189 THR 190 -0.0011

THR 190 ALA 191 0.0002

ALA 191 GLY 192 -0.0000

GLY 192 ASP 193 0.0005

ASP 193 ASN 194 0.0000

ASN 194 HIS 195 -0.0000

HIS 195 LEU 196 0.0009

LEU 196 GLY 197 -0.0002

GLY 197 GLY 198 -0.0001

GLY 198 ASP 199 0.0009

ASP 199 ASP 200 0.0003

ASP 200 PHE 201 0.0000

PHE 201 ASP 202 -0.0003

ASP 202 GLN 203 -0.0001

GLN 203 VAL 204 -0.0004

VAL 204 ILE 205 0.0016

ILE 205 ILE 206 0.0001

ILE 206 ASP 207 0.0004

ASP 207 TYR 208 -0.0008

TYR 208 LEU 209 0.0001

LEU 209 VAL 210 -0.0000

VAL 210 ASN 211 -0.0018

ASN 211 GLN 212 -0.0001

GLN 212 PHE 213 -0.0004

PHE 213 LYS 214 -0.0012

LYS 214 GLN 215 -0.0001

GLN 215 GLU 216 0.0002

GLU 216 HIS 217 0.0006

HIS 217 GLY 218 0.0000

GLY 218 ILE 219 -0.0001

ILE 219 ASP 220 0.0002

ASP 220 LEU 221 0.0001

LEU 221 SER 222 0.0001

SER 222 LYS 223 -0.0006

LYS 223 ASP 224 0.0004

ASP 224 LYS 225 -0.0001

LYS 225 MET 226 0.0015

MET 226 ALA 227 -0.0004

ALA 227 LEU 228 0.0002

LEU 228 GLN 229 -0.0022

GLN 229 ARG 230 -0.0004

ARG 230 LEU 231 0.0000

LEU 231 LYS 232 0.0005

LYS 232 ASP 233 -0.0001

ASP 233 ALA 234 0.0001

ALA 234 ALA 235 -0.0007

ALA 235 GLU 236 0.0003

GLU 236 LYS 237 -0.0000

LYS 237 ALA 238 0.0014

ALA 238 LYS 239 -0.0000

LYS 239 LYS 240 0.0003

LYS 240 GLU 241 0.0003

GLU 241 LEU 242 -0.0001

LEU 242 SER 243 -0.0000

SER 243 GLY 244 -0.0008

GLY 244 VAL 245 0.0003

VAL 245 THR 246 0.0001

THR 246 GLN 247 -0.0014

GLN 247 THR 248 -0.0000

THR 248 GLN 249 0.0000

GLN 249 ILE 250 0.0012

ILE 250 SER 251 -0.0003

SER 251 LEU 252 0.0001

LEU 252 PRO 253 -0.0016

PRO 253 PHE 254 0.0004

PHE 254 ILE 255 -0.0000

ILE 255 SER 256 0.0005

SER 256 ALA 257 -0.0003

ALA 257 ASN 258 0.0001

ASN 258 GLU 259 0.0008

GLU 259 ASN 260 0.0001

ASN 260 GLY 261 0.0002

GLY 261 PRO 262 -0.0009

PRO 262 LEU 263 0.0004

LEU 263 HIS 264 -0.0000

HIS 264 LEU 265 -0.0001

LEU 265 GLU 266 0.0000

GLU 266 MET 267 0.0001

MET 267 THR 268 -0.0013

THR 268 LEU 269 0.0002

LEU 269 THR 270 0.0002

THR 270 ARG 271 -0.0003

ARG 271 ALA 272 0.0002

ALA 272 LYS 273 -0.0000

LYS 273 PHE 274 -0.0006

PHE 274 GLU 275 0.0001

GLU 275 GLU 276 -0.0001

GLU 276 LEU 277 -0.0009

LEU 277 SER 278 -0.0002

SER 278 ALA 279 -0.0004

ALA 279 HIS 280 0.0009

HIS 280 LEU 281 -0.0001

LEU 281 VAL 282 -0.0002

VAL 282 GLU 283 -0.0006

GLU 283 ARG 284 -0.0003

ARG 284 THR 285 0.0000

THR 285 MET 286 -0.0000

MET 286 GLY 287 -0.0003

GLY 287 PRO 288 0.0001

PRO 288 VAL 289 -0.0003

VAL 289 ARG 290 0.0002

ARG 290 GLN 291 0.0000

GLN 291 ALA 292 0.0009

ALA 292 LEU 293 0.0003

LEU 293 GLN 294 -0.0000

GLN 294 ASP 295 0.0003

ASP 295 ALA 296 0.0004

ALA 296 GLY 297 0.0003

GLY 297 LEU 298 -0.0004

LEU 298 THR 299 0.0001

THR 299 PRO 300 0.0001

PRO 300 ALA 301 -0.0002

ALA 301 ASP 302 0.0003

ASP 302 ILE 303 0.0000

ILE 303 ASP 304 0.0003

ASP 304 LYS 305 -0.0000

LYS 305 VAL 306 0.0000

VAL 306 ILE 307 0.0006

ILE 307 LEU 308 0.0001

LEU 308 VAL 309 -0.0000

VAL 309 GLY 310 0.0007

GLY 310 GLY 311 0.0002

GLY 311 SER 312 0.0002

SER 312 THR 313 0.0005

THR 313 ARG 314 -0.0001

ARG 314 ILE 315 -0.0001

ILE 315 PRO 316 -0.0002

PRO 316 ALA 317 0.0000

ALA 317 VAL 318 0.0000

VAL 318 GLN 319 -0.0002

GLN 319 GLU 320 0.0000

GLU 320 ALA 321 0.0000

ALA 321 ILE 322 0.0007

ILE 322 LYS 323 0.0002

LYS 323 ARG 324 -0.0000

ARG 324 GLU 325 -0.0002

GLU 325 LEU 326 0.0000

LEU 326 GLY 327 0.0001

GLY 327 LYS 328 0.0001

LYS 328 GLU 329 0.0002

GLU 329 PRO 330 0.0000

PRO 330 HIS 331 0.0002

HIS 331 LYS 332 0.0001

LYS 332 GLY 333 0.0001

GLY 333 VAL 334 -0.0003

VAL 334 ASN 335 0.0001

ASN 335 PRO 336 -0.0000

PRO 336 ASP 337 0.0006

ASP 337 GLU 338 -0.0001

GLU 338 VAL 339 -0.0001

VAL 339 VAL 340 -0.0004

VAL 340 ALA 341 0.0002

ALA 341 ILE 342 -0.0004

ILE 342 GLY 343 0.0014

GLY 343 ALA 344 0.0000

ALA 344 ALA 345 -0.0000

ALA 345 ILE 346 0.0003

ILE 346 GLN 347 0.0004

GLN 347 GLY 348 0.0000

GLY 348 GLY 349 -0.0077

GLY 349 VAL 350 0.0001

VAL 350 ILE 351 -0.0000

ILE 351 ALA 352 0.0185

ALA 352 GLY 353 0.0000

GLY 353 GLU 354 0.0003

GLU 354 VAL 355 0.0445

VAL 355 LYS 356 0.0001

LYS 356 ASP 357 -0.0000

ASP 357 VAL 358 -0.0132

VAL 358 VAL 359 0.0004

VAL 359 LEU 360 -0.0001

LEU 360 LEU 361 -0.0414

LEU 361 ASP 362 0.0000

ASP 362 VAL 363 -0.0001

VAL 363 THR 364 0.0113

THR 364 PRO 365 -0.0001

PRO 365 LEU 366 0.0002

LEU 366 SER 367 -0.0016

SER 367 LEU 368 0.0003

LEU 368 GLY 369 0.0000

GLY 369 ILE 370 -0.0053

ILE 370 GLU 371 0.0002

GLU 371 THR 372 0.0001

THR 372 MET 373 0.0428

MET 373 GLY 374 -0.0001

GLY 374 GLY 375 0.0001

GLY 375 VAL 376 0.0587

VAL 376 PHE 377 -0.0003

PHE 377 THR 378 0.0004

THR 378 LYS 379 0.0947

LYS 379 LEU 380 0.0003

LEU 380 ILE 381 0.0001

ILE 381 GLU 382 -0.0253

GLU 382 ARG 383 -0.0000

ARG 383 ASN 384 -0.0000

ASN 384 THR 385 -0.0098

THR 385 THR 386 0.0002

THR 386 ILE 387 0.0003

ILE 387 PRO 388 -0.0014

PRO 388 THR 389 -0.0002

THR 389 SER 390 0.0003

SER 390 LYS 391 -0.0076

LYS 391 SER 392 0.0004

SER 392 GLN 393 -0.0002

GLN 393 VAL 394 -0.0384

VAL 394 PHE 395 -0.0002

PHE 395 THR 396 0.0001

THR 396 THR 397 -0.0276

THR 397 ALA 398 -0.0001

ALA 398 ALA 399 0.0001

ALA 399 ASP 400 -0.0010

ASP 400 ASN 401 0.0000

ASN 401 GLN 402 -0.0003

GLN 402 THR 403 -0.0022

THR 403 THR 404 0.0003

THR 404 VAL 405 -0.0000

VAL 405 ASP 406 0.0279

ASP 406 ILE 407 -0.0002

ILE 407 HIS 408 0.0004

HIS 408 VAL 409 -0.0020

VAL 409 LEU 410 0.0001

LEU 410 GLN 411 -0.0001

GLN 411 GLY 412 0.0393

GLY 412 GLU 413 0.0003

GLU 413 ARG 414 -0.0002

ARG 414 PRO 415 0.0702

PRO 415 MET 416 0.0000

MET 416 ALA 417 -0.0004

ALA 417 ALA 418 0.0243

ALA 418 ASP 419 -0.0001

ASP 419 ASN 420 0.0000

ASN 420 LYS 421 -0.0047

LYS 421 SER 422 0.0001

SER 422 LEU 423 -0.0001

LEU 423 GLY 424 0.0381

GLY 424 ARG 425 0.0000

ARG 425 PHE 426 0.0001

PHE 426 GLN 427 0.0295

GLN 427 LEU 428 -0.0002

LEU 428 THR 429 0.0001

THR 429 GLY 430 0.0015

GLY 430 ILE 431 0.0005

ILE 431 PRO 432 -0.0001

PRO 432 PRO 433 -0.0005

PRO 433 ALA 434 0.0003

ALA 434 PRO 435 0.0002

PRO 435 ARG 436 -0.0008

ARG 436 GLY 437 -0.0000

GLY 437 VAL 438 -0.0001

VAL 438 PRO 439 0.0037

PRO 439 GLN 440 0.0001

GLN 440 ILE 441 0.0004

ILE 441 GLU 442 -0.0131

GLU 442 VAL 443 0.0003

VAL 443 THR 444 0.0001

THR 444 PHE 445 -0.0113

PHE 445 ASP 446 -0.0003

ASP 446 ILE 447 -0.0000

ILE 447 ASP 448 0.0071

ASP 448 ALA 449 0.0002

ALA 449 ASN 450 0.0003

ASN 450 GLY 451 -0.0060

GLY 451 ILE 452 -0.0003

ILE 452 VAL 453 0.0003

VAL 453 HIS 454 0.0031

HIS 454 VAL 455 0.0000

VAL 455 ARG 456 -0.0003

ARG 456 ALA 457 0.0082

ALA 457 LYS 458 0.0000

LYS 458 ASP 459 -0.0003

ASP 459 LEU 460 -0.0002

LEU 460 GLY 461 -0.0001

GLY 461 THR 462 -0.0001

THR 462 ASN 463 -0.0000

ASN 463 LYS 464 0.0002

LYS 464 GLU 465 0.0001

GLU 465 GLN 466 0.0053

GLN 466 SER 467 -0.0000

SER 467 ILE 468 0.0001

ILE 468 THR 469 0.0190

THR 469 ILE 470 0.0001

ILE 470 LYS 471 -0.0000

LYS 471 SER 472 0.0201

SER 472 SER 473 -0.0002

SER 473 SER 474 -0.0005

SER 474 GLY 475 -0.0074

GLY 475 LEU 476 0.0002

LEU 476 SER 477 -0.0000

SER 477 GLU 478 -0.0063

GLU 478 GLU 479 -0.0002

GLU 479 GLU 480 -0.0001

GLU 480 ILE 481 -0.0213

ILE 481 GLN 482 -0.0002

GLN 482 ARG 483 0.0002

ARG 483 MET 484 -0.0421

MET 484 ILE 485 -0.0004

ILE 485 LYS 486 -0.0003

LYS 486 GLU 487 -0.0402

GLU 487 ALA 488 -0.0002

ALA 488 GLU 489 -0.0001

GLU 489 GLU 490 -0.0436

GLU 490 ASN 491 0.0002

ASN 491 ALA 492 0.0001

ALA 492 GLU 493 0.0446

GLU 493 ALA 494 0.0001

ALA 494 ASP 495 -0.0003

ASP 495 ARG 496 -0.0013

ARG 496 LYS 497 0.0005

LYS 497 ARG 498 0.0000

ARG 498 LYS 499 0.1049

LYS 499 GLU 500 0.0002

GLU 500 ALA 501 -0.0000

ALA 501 ALA 502 0.0682

ALA 502 GLU 503 0.0001

GLU 503 LEU 504 -0.0001

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: April 25th, 2023.

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

*** 2V7Y copy ***

CA strain for 2402070129241772454

--- normal mode 13 ---

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

* 2V7Y copy *