GPCompReports

ADA1B

Gene ADRA1B Adrenoceptors Aminergic receptors UniProt P35368
745
Total Contact Pairs
82
Significant Changes
11.57
Max Increase
-7.84
Max Decrease

Interactive snake plot

GPCRdb-style topology. Click the view buttons to recolor residues by different data layers. Toggle contact links to draw significant residue-residue contacts as arcs. Click loop labels (ICL/ECL) to expand or collapse loop regions.

Color convention: blue = active-favoring, red = inactive-favoring.

ICL1 R74 12.48x48 R74 12.48x48 R H75 12.49x49 H75 12.49x49 H L76 12.50x50 L76 12.50x50 L R77 12.51x51 R77 12.51x51 R ICL1ECL1 Y110 23.49x49 Y110 23.49x49 Y W111 23.50x50 W111 23.50x50 W V112 23.51x51 V112 23.51x51 V L113 23.52x52 L113 23.52x52 L ECL1ICL2 S150 34.50x50 S150 34.50x50 S L151 34.51x51 L151 34.51x51 L Q152 34.52x52 Q152 34.52x52 Q Y153 34.53x53 Y153 34.53x53 Y P154 34.54x54 P154 34.54x54 P T155 34.55x55 T155 34.55x55 T L156 34.56x56 L156 34.56x56 L V157 34.57x57 V157 34.57x57 V ICL2ECL2 K185 K185 K E186 E186 E P187 P187 P A188 A188 A P189 P189 P N190 N190 N D191 D191 D D192 D192 D K193 K193 K E194 E194 E C195 45.50x50 C195 45.50x50 C G196 45.51x51 G196 45.51x51 G V197 45.52x52 V197 45.52x52 V T198 T198 T E199 E199 E ECL2ICL3 G240 G240 G V241 V241 V M242 M242 M K243 K243 K E244 E244 E M245 M245 M S246 S246 S N247 N247 N S248 S248 S K249 K249 K E250 E250 E L251 L251 L T252 T252 T L253 L253 L R254 R254 R I255 I255 I H256 H256 H S257 S257 S K258 K258 K N259 N259 N F260 F260 F H261 H261 H E262 E262 E D263 D263 D T264 T264 T L265 L265 L S266 S266 S S267 S267 S T268 T268 T K269 K269 K A270 A270 A K271 K271 K G272 G272 G H273 H273 H N274 N274 N P275 P275 P R276 R276 R S277 S277 S S278 S278 S I279 I279 I A280 A280 A V281 V281 V K282 K282 K ICL3ECL3 S321 S321 S T322 T322 T L323 L323 L K324 K324 K P325 P325 P ECL3N-term M1 M1 M N2 N2 N P3 P3 P D4 D4 D L5 L5 L D6 D6 D T7 T7 T G8 G8 G H9 H9 H N10 N10 N T11 T11 T S12 S12 S A13 A13 A P14 P14 P A15 A15 A H16 H16 H W17 W17 W G18 G18 G E19 E19 E L20 L20 L K21 K21 K N22 N22 N A23 A23 A N24 N24 N F25 F25 F T26 T26 T G27 G27 G P28 P28 P N29 N29 N Q30 Q30 Q T31 T31 T S32 S32 S S33 S33 S N34 N34 N S35 S35 S T36 T36 T L37 L37 L P38 P38 P N-termC-term C365 C365 C Q366 Q366 Q C367 C367 C R368 R368 R G369 G369 G R370 R370 R G371 G371 G R372 R372 R R373 R373 R R374 R374 R R375 R375 R R376 R376 R R377 R377 R R378 R378 R R379 R379 R R380 R380 R L381 L381 L G382 G382 G G383 G383 G C384 C384 C A385 A385 A Y386 Y386 Y T387 T387 T Y388 Y388 Y R389 R389 R P390 P390 P W391 W391 W T392 T392 T R393 R393 R G394 G394 G G395 G395 G S396 S396 S L397 L397 L E398 E398 E R399 R399 R S400 S400 S Q401 Q401 Q S402 S402 S R403 R403 R K404 K404 K D405 D405 D S406 S406 S L407 L407 L D408 D408 D D409 D409 D S410 S410 S G411 G411 G S412 S412 S C413 C413 C L414 L414 L S415 S415 S G416 G416 G S417 S417 S Q418 Q418 Q R419 R419 R T420 T420 T L421 L421 L P422 P422 P S423 S423 S A424 A424 A S425 S425 S P426 P426 P S427 S427 S P428 P428 P G429 G429 G Y430 Y430 Y L431 L431 L G432 G432 G R433 R433 R G434 G434 G A435 A435 A P436 P436 P P437 P437 P P438 P438 P V439 V439 V E440 E440 E L441 L441 L C442 C442 C A443 A443 A F444 F444 F P445 P445 P E446 E446 E W447 W447 W K448 K448 K A449 A449 A P450 P450 P G451 G451 G A452 A452 A L453 L453 L L454 L454 L S455 S455 S L456 L456 L P457 P457 P A458 A458 A P459 P459 P E460 E460 E P461 P461 P P462 P462 P G463 G463 G R464 R464 R R465 R465 R G466 G466 G R467 R467 R H468 H468 H D469 D469 D S470 S470 S G471 G471 G P472 P472 P L473 L473 L F474 F474 F T475 T475 T F476 F476 F K477 K477 K L478 L478 L L479 L479 L T480 T480 T E481 E481 E P482 P482 P E483 E483 E S484 S484 S P485 P485 P G486 G486 G T487 T487 T D488 D488 D G489 G489 G G490 G490 G A491 A491 A S492 S492 S N493 N493 N G494 G494 G G495 G495 G C496 C496 C E497 E497 E A498 A498 A A499 A499 A A500 A500 A D501 D501 D V502 V502 V A503 A503 A N504 N504 N G505 G505 G Q506 Q506 Q P507 P507 P G508 G508 G F509 F509 F K510 K510 K S511 S511 S N512 N512 N M513 M513 M P514 P514 P L515 L515 L A516 A516 A P517 P517 P G518 G518 G Q519 Q519 Q F520 F520 F C-term Q39 1.26x26 Q39 1.26x26 Q L40 1.27x27 L40 1.27x27 L D41 1.28x28 D41 1.28x28 D I42 1.29x29 I42 1.29x29 I T43 1.30x30 T43 1.30x30 T R44 1.31x31 R44 1.31x31 R A45 1.32x32 A45 1.32x32 A I46 1.33x33 I46 1.33x33 I S47 1.34x34 S47 1.34x34 S V48 1.35x35 V48 1.35x35 V G49 1.36x36 G49 1.36x36 G L50 1.37x37 L50 1.37x37 L V51 1.38x38 V51 1.38x38 V L52 1.39x39 L52 1.39x39 L G53 1.40x40 G53 1.40x40 G A54 1.41x41 A54 1.41x41 A F55 1.42x42 F55 1.42x42 F I56 1.43x43 I56 1.43x43 I L57 1.44x44 L57 1.44x44 L F58 1.45x45 F58 1.45x45 F A59 1.46x46 A59 1.46x46 A I60 1.47x47 I60 1.47x47 I V61 1.48x48 V61 1.48x48 V G62 1.49x49 G62 1.49x49 G N63 1.50x50 N63 1.50x50 N I64 1.51x51 I64 1.51x51 I L65 1.52x52 L65 1.52x52 L V66 1.53x53 V66 1.53x53 V I67 1.54x54 I67 1.54x54 I L68 1.55x55 L68 1.55x55 L S69 1.56x56 S69 1.56x56 S V70 1.57x57 V70 1.57x57 V A71 1.58x58 A71 1.58x58 A C72 1.59x59 C72 1.59x59 C N73 1.60x60 N73 1.60x60 N T78 2.37x37 T78 2.37x37 T P79 2.38x38 P79 2.38x38 P T80 2.39x39 T80 2.39x39 T N81 2.40x40 N81 2.40x40 N Y82 2.41x41 Y82 2.41x41 Y F83 2.42x42 F83 2.42x42 F I84 2.43x43 I84 2.43x43 I V85 2.44x44 V85 2.44x44 V N86 2.45x45 N86 2.45x45 N L87 2.46x46 L87 2.46x46 L A88 2.47x47 A88 2.47x47 A M89 2.48x48 M89 2.48x48 M A90 2.49x49 A90 2.49x49 A D91 2.50x50 D91 2.50x50 D L92 2.51x51 L92 2.51x51 L L93 2.52x52 L93 2.52x52 L L94 2.53x53 L94 2.53x53 L S95 2.54x54 S95 2.54x54 S F96 2.55x55 F96 2.55x55 F T97 2.56x551 T97 2.56x551 T V98 2.57x56 V98 2.57x56 V L99 2.58x57 L99 2.58x57 L P100 2.59x58 P100 2.59x58 P F101 2.60x59 F101 2.60x59 F S102 2.61x60 S102 2.61x60 S A103 2.62x61 A103 2.62x61 A A104 2.63x62 A104 2.63x62 A L105 2.64x63 L105 2.64x63 L E106 2.65x64 E106 2.65x64 E V107 2.66x65 V107 2.66x65 V L108 2.67x66 L108 2.67x66 L G109 2.68x67 G109 2.68x67 G G114 3.21x21 G114 3.21x21 G R115 3.22x22 R115 3.22x22 R I116 3.23x23 I116 3.23x23 I F117 3.24x24 F117 3.24x24 F C118 3.25x25 C118 3.25x25 C D119 3.26x26 D119 3.26x26 D I120 3.27x27 I120 3.27x27 I W121 3.28x28 W121 3.28x28 W A122 3.29x29 A122 3.29x29 A A123 3.30x30 A123 3.30x30 A V124 3.31x31 V124 3.31x31 V D125 3.32x32 D125 3.32x32 D V126 3.33x33 V126 3.33x33 V L127 3.34x34 L127 3.34x34 L C128 3.35x35 C128 3.35x35 C C129 3.36x36 C129 3.36x36 C T130 3.37x37 T130 3.37x37 T A131 3.38x38 A131 3.38x38 A S132 3.39x39 S132 3.39x39 S I133 3.40x40 I133 3.40x40 I L134 3.41x41 L134 3.41x41 L S135 3.42x42 S135 3.42x42 S L136 3.43x43 L136 3.43x43 L C137 3.44x44 C137 3.44x44 C A138 3.45x45 A138 3.45x45 A I139 3.46x46 I139 3.46x46 I S140 3.47x47 S140 3.47x47 S I141 3.48x48 I141 3.48x48 I D142 3.49x49 D142 3.49x49 D R143 3.50x50 R143 3.50x50 R Y144 3.51x51 Y144 3.51x51 Y I145 3.52x52 I145 3.52x52 I G146 3.53x53 G146 3.53x53 G V147 3.54x54 V147 3.54x54 V R148 3.55x55 R148 3.55x55 R Y149 3.56x56 Y149 3.56x56 Y T158 4.38x38 T158 4.38x38 T R159 4.39x39 R159 4.39x39 R R160 4.40x40 R160 4.40x40 R K161 4.41x41 K161 4.41x41 K A162 4.42x42 A162 4.42x42 A I163 4.43x43 I163 4.43x43 I L164 4.44x44 L164 4.44x44 L A165 4.45x45 A165 4.45x45 A L166 4.46x46 L166 4.46x46 L L167 4.47x47 L167 4.47x47 L S168 4.48x48 S168 4.48x48 S V169 4.49x49 V169 4.49x49 V W170 4.50x50 W170 4.50x50 W V171 4.51x51 V171 4.51x51 V L172 4.52x52 L172 4.52x52 L S173 4.53x53 S173 4.53x53 S T174 4.54x54 T174 4.54x54 T V175 4.55x55 V175 4.55x55 V I176 4.56x56 I176 4.56x56 I S177 4.57x57 S177 4.57x57 S I178 4.58x58 I178 4.58x58 I G179 4.59x59 G179 4.59x59 G P180 4.60x60 P180 4.60x60 P L181 4.61x61 L181 4.61x61 L L182 4.62x62 L182 4.62x62 L G183 4.63x63 G183 4.63x63 G W184 4.64x64 W184 4.64x64 W E200 5.35x36 E200 5.35x36 E P201 5.36x37 P201 5.36x37 P F202 5.37x38 F202 5.37x38 F Y203 5.38x39 Y203 5.38x39 Y A204 5.39x40 A204 5.39x40 A L205 5.40x41 L205 5.40x41 L F206 5.41x42 F206 5.41x42 F S207 5.42x43 S207 5.42x43 S S208 5.43x44 S208 5.43x44 S L209 5.44x45 L209 5.44x45 L G210 5.45x46 G210 5.45x46 G S211 5.46x461 S211 5.46x461 S F212 5.47x47 F212 5.47x47 F Y213 5.48x48 Y213 5.48x48 Y I214 5.49x49 I214 5.49x49 I P215 5.50x50 P215 5.50x50 P L216 5.51x51 L216 5.51x51 L A217 5.52x52 A217 5.52x52 A V218 5.53x53 V218 5.53x53 V I219 5.54x54 I219 5.54x54 I L220 5.55x55 L220 5.55x55 L V221 5.56x56 V221 5.56x56 V M222 5.57x57 M222 5.57x57 M Y223 5.58x58 Y223 5.58x58 Y C224 5.59x59 C224 5.59x59 C R225 5.60x60 R225 5.60x60 R V226 5.61x61 V226 5.61x61 V Y227 5.62x62 Y227 5.62x62 Y I228 5.63x63 I228 5.63x63 I V229 5.64x64 V229 5.64x64 V A230 5.65x65 A230 5.65x65 A K231 5.66x66 K231 5.66x66 K R232 5.67x67 R232 5.67x67 R T233 5.68x68 T233 5.68x68 T T234 5.69x69 T234 5.69x69 T K235 5.70x70 K235 5.70x70 K N236 5.71x71 N236 5.71x71 N L237 5.72x72 L237 5.72x72 L E238 5.73x73 E238 5.73x73 E A239 5.74x74 A239 5.74x74 A L283 6.24x24 L283 6.24x24 L F284 6.25x25 F284 6.25x25 F K285 6.26x26 K285 6.26x26 K F286 6.27x27 F286 6.27x27 F S287 6.28x28 S287 6.28x28 S R288 6.29x29 R288 6.29x29 R E289 6.30x30 E289 6.30x30 E K290 6.31x31 K290 6.31x31 K K291 6.32x32 K291 6.32x32 K A292 6.33x33 A292 6.33x33 A A293 6.34x34 A293 6.34x34 A K294 6.35x35 K294 6.35x35 K T295 6.36x36 T295 6.36x36 T L296 6.37x37 L296 6.37x37 L G297 6.38x38 G297 6.38x38 G I298 6.39x39 I298 6.39x39 I V299 6.40x40 V299 6.40x40 V V300 6.41x41 V300 6.41x41 V G301 6.42x42 G301 6.42x42 G M302 6.43x43 M302 6.43x43 M F303 6.44x44 F303 6.44x44 F I304 6.45x45 I304 6.45x45 I L305 6.46x46 L305 6.46x46 L C306 6.47x47 C306 6.47x47 C W307 6.48x48 W307 6.48x48 W L308 6.49x49 L308 6.49x49 L P309 6.50x50 P309 6.50x50 P F310 6.51x51 F310 6.51x51 F F311 6.52x52 F311 6.52x52 F I312 6.53x53 I312 6.53x53 I A313 6.54x54 A313 6.54x54 A L314 6.55x55 L314 6.55x55 L P315 6.56x56 P315 6.56x56 P L316 6.57x57 L316 6.57x57 L G317 6.58x58 G317 6.58x58 G S318 6.59x59 S318 6.59x59 S L319 6.60x60 L319 6.60x60 L F320 6.61x61 F320 6.61x61 F P326 7.31x30 P326 7.31x30 P D327 7.32x31 D327 7.32x31 D A328 7.33x32 A328 7.33x32 A V329 7.34x33 V329 7.34x33 V F330 7.35x34 F330 7.35x34 F K331 7.36x35 K331 7.36x35 K V332 7.37x36 V332 7.37x36 V V333 7.38x37 V333 7.38x37 V F334 7.39x38 F334 7.39x38 F W335 7.40x39 W335 7.40x39 W L336 7.41x40 L336 7.41x40 L G337 7.42x41 G337 7.42x41 G Y338 7.43x42 Y338 7.43x42 Y F339 7.44x43 F339 7.44x43 F N340 7.45x45 N340 7.45x45 N S341 7.46x46 S341 7.46x46 S C342 7.47x47 C342 7.47x47 C L343 7.48x48 L343 7.48x48 L N344 7.49x49 N344 7.49x49 N P345 7.50x50 P345 7.50x50 P I346 7.51x51 I346 7.51x51 I I347 7.52x52 I347 7.52x52 I Y348 7.53x53 Y348 7.53x53 Y P349 7.54x54 P349 7.54x54 P C350 7.55x55 C350 7.55x55 C S351 7.56x56 S351 7.56x56 S S352 8.47x47 S352 8.47x47 S K353 8.48x48 K353 8.48x48 K E354 8.49x49 E354 8.49x49 E F359 8.54x54 F359 8.54x54 F V360 8.55x55 V360 8.55x55 V R361 8.56x56 R361 8.56x56 R F355 8.50x50 F355 8.50x50 F K356 8.51x51 K356 8.51x51 K R357 8.52x52 R357 8.52x52 R A358 8.53x53 A358 8.53x53 A I362 8.57x57 I362 8.57x57 I L363 8.58x58 L363 8.58x58 L G364 8.59x59 G364 8.59x59 G

Top 100 conformational changes

Residue pairs with the largest RRCS changes between active and inactive states. GPCRdb numbering in parentheses. Highlighted rows exceed the significance threshold.

Rank Residue 1 Residue 2 Active RRCS Inactive RRCS ΔRRCS Magnitude
1 ARG467 HIS468 11.572 0.000 +11.572 HIGH
2 HIS468 ASP469 10.241 0.000 +10.241 HIGH
3 LYS243 GLU250 0.000 7.840 -7.840 HIGH
4 THR233 (5.68x68) GLU289 (6.30x30) 7.771 0.000 +7.771 HIGH
5 ARG115 (3.22x22) ASP192 1.800 9.341 -7.541 HIGH
6 ARG148 (3.55x55) TYR149 (3.56x56) 4.241 11.182 -6.941 HIGH
7 THR80 (2.39x39) ARG143 (3.50x50) 0.000 6.808 -6.808 HIGH
8 GLU186 GLU200 (5.35x36) 8.587 15.148 -6.560 HIGH
9 THR295 (6.36x36) SER351 (7.56x56) 0.851 7.049 -6.199 HIGH
10 ASN236 (5.71x71) VAL241 0.000 6.095 -6.095 HIGH
11 GLN506 PRO507 0.000 6.063 -6.063 HIGH
12 ASP91 (2.50x50) SER341 (7.46x46) 9.193 3.188 +6.006 HIGH
13 GLU238 (5.73x73) PHE286 (6.27x27) 5.960 0.000 +5.960 HIGH
14 PHE286 (6.27x27) LYS290 (6.31x31) 5.894 0.000 +5.894 HIGH
15 ASP142 (3.49x49) ARG143 (3.50x50) 0.000 5.117 -5.117 HIGH
16 THR234 (5.69x69) GLU289 (6.30x30) 5.062 0.000 +5.062 HIGH
17 PHE303 (6.44x44) ASN340 (7.45x45) 0.000 4.920 -4.920 MED
18 ASN340 (7.45x45) ASN344 (7.49x49) 4.844 0.000 +4.844 MED
19 TRP307 (6.48x48) GLY337 (7.42x41) 3.821 8.646 -4.825 MED
20 ARG361 (8.56x56) GLN366 0.000 4.778 -4.778 MED
21 ASN73 (1.60x60) HIS75 (12.49x49) 4.704 0.000 +4.704 MED
22 GLY240 ILE255 0.000 4.703 -4.703 MED
23 GLU244 SER278 4.694 0.000 +4.694 MED
24 PHE310 (6.51x51) LEU314 (6.55x55) 1.001 5.542 -4.540 MED
25 ILE133 (3.40x40) TRP307 (6.48x48) 4.522 0.000 +4.522 MED
26 PHE303 (6.44x44) TRP307 (6.48x48) 2.469 6.920 -4.451 MED
27 PRO349 (7.54x54) PHE355 (8.50x50) 5.114 0.708 +4.406 MED
28 ARG143 (3.50x50) TYR223 (5.58x58) 4.328 0.000 +4.328 MED
29 GLU250 ARG254 4.305 0.000 +4.305 MED
30 TYR223 (5.58x58) LEU296 (6.37x37) 2.317 6.549 -4.233 MED
31 TYR144 (3.51x51) ARG148 (3.55x55) 2.052 6.262 -4.211 MED
32 GLU186 GLU199 0.000 4.208 -4.208 MED
33 ILE133 (3.40x40) PHE303 (6.44x44) 1.379 5.454 -4.074 MED
34 GLU244 LYS282 6.410 2.337 +4.074 MED
35 PRO349 (7.54x54) LYS356 (8.51x51) 0.465 4.489 -4.024 MED
36 LEU136 (3.43x43) TYR348 (7.53x53) 3.958 0.000 +3.958 MED
37 SER267 THR268 0.000 3.787 -3.787 MED
38 LEU237 (5.72x72) LYS285 (6.26x26) 3.784 0.000 +3.784 MED
39 SER150 (34.50x50) PHE286 (6.27x27) 0.000 3.742 -3.742 MED
40 TYR144 (3.51x51) MET222 (5.57x57) 4.215 0.546 +3.669 MED
41 HIS75 (12.49x49) LEU76 (12.50x50) 3.536 0.000 +3.536 MED
42 GLY179 (4.59x59) TRP184 (4.64x64) 5.755 2.384 +3.371 MED
43 ILE60 (1.47x47) PHE96 (2.55x55) 0.559 3.888 -3.328 MED
44 TYR348 (7.53x53) PHE355 (8.50x50) 0.000 3.314 -3.314 MED
45 ARG77 (12.51x51) TYR82 (2.41x41) 3.341 0.102 +3.239 MED
46 ILE84 (2.43x43) TYR348 (7.53x53) 0.262 3.482 -3.220 MED
47 ILE176 (4.56x56) TYR203 (5.38x39) 3.146 0.000 +3.146 MED
48 SER402 ARG403 0.347 3.311 -2.964 MED
49 ASP409 SER410 2.958 0.000 +2.958 MED
50 TYR223 (5.58x58) GLY297 0.000 2.884 -2.884 MED
51 TRP307 (6.48x48) ASN340 (7.45x45) 6.198 3.343 +2.855 MED
52 PRO180 LYS185 2.933 0.110 +2.824 MED
53 ASN2 PRO3 0.084 2.903 -2.819 MED
54 LYS404 ASP405 0.000 2.802 -2.802 MED
55 ARG115 (3.22x22) LYS185 2.789 0.000 +2.789 MED
56 SER352 GLU354 3.474 0.717 +2.757 MED
57 TYR223 (5.58x58) VAL300 2.088 4.812 -2.724 MED
58 LEU105 TYR110 3.593 0.870 +2.723 MED
59 LYS285 (6.26x26) GLU289 (6.30x30) 2.794 0.092 +2.703 MED
60 ARG115 (3.22x22) ALA188 2.933 0.232 +2.701 MED
61 HIS75 (12.49x49) ARG361 (8.56x56) 2.694 0.000 +2.694 MED
62 ILE133 (3.40x40) PHE212 0.122 2.813 -2.691 MED
63 SER484 PRO485 0.511 3.164 -2.653 MED
64 ASN63 ASP91 (2.50x50) 4.624 1.976 +2.649 MED
65 PRO180 THR198 2.604 0.000 +2.604 MED
66 LEU40 ARG44 2.596 0.000 +2.596 MED
67 ARG115 (3.22x22) ASP119 2.582 0.000 +2.582 MED
68 PHE55 PHE339 1.421 3.996 -2.575 MED
69 GLU186 THR198 0.000 2.546 -2.546 MED
70 PHE55 TYR338 0.000 2.517 -2.517 MED
71 LEU136 (3.43x43) PHE303 (6.44x44) 1.490 3.994 -2.505 MED
72 GLU354 ARG357 0.000 2.478 -2.478 MED
73 ASN63 ALA88 5.506 3.038 +2.469 MED
74 LEU151 GLU244 0.000 2.465 -2.465 MED
75 ASP191 LYS193 2.462 0.000 +2.462 MED
76 ASN81 PHE355 (8.50x50) 3.322 0.948 +2.374 MED
77 THR234 (5.69x69) PHE286 (6.27x27) 2.374 0.000 +2.374 MED
78 ARG143 (3.50x50) LEU296 (6.37x37) 0.000 2.352 -2.352 MED
79 SER425 PRO426 2.726 0.390 +2.336 MED
80 SER417 GLN418 2.334 0.000 +2.334 MED
81 PHE55 CYS342 1.041 3.372 -2.330 MED
82 LEU237 (5.72x72) LEU283 0.000 2.290 -2.290 MED
83 PHE58 CYS342 1.891 4.167 -2.277 LOW
84 ILE219 PHE303 (6.44x44) 2.254 0.000 +2.254 LOW
85 SER150 (34.50x50) GLU289 (6.30x30) 0.000 2.208 -2.208 LOW
86 ILE228 ARG232 2.190 0.000 +2.190 LOW
87 ASP91 (2.50x50) ASN344 (7.49x49) 4.744 2.581 +2.163 LOW
88 MET242 PHE286 (6.27x27) 0.000 2.144 -2.144 LOW
89 PHE212 PHE311 14.751 16.853 -2.102 LOW
90 THR234 (5.69x69) LYS290 (6.31x31) 0.123 2.184 -2.062 LOW
91 GLU244 ILE279 2.058 0.000 +2.058 LOW
92 LEU515 ALA516 0.000 2.031 -2.031 LOW
93 CYS496 GLU497 2.029 0.000 +2.029 LOW
94 ARG143 (3.50x50) TYR348 (7.53x53) 2.025 0.000 +2.025 LOW
95 ILE362 CYS367 0.000 1.996 -1.996 LOW
96 SER511 ASN512 0.000 1.982 -1.982 LOW
97 PRO3 ASP4 0.000 1.978 -1.978 LOW
98 ASN34 THR36 1.937 0.000 +1.937 LOW
99 ARG143 (3.50x50) TYR153 0.000 1.935 -1.935 LOW
100 LEU151 LYS282 0.000 1.913 -1.913 LOW

Transmembrane domain analysis

Active-favoring residues form stronger contacts in the active state (positive ΔRRCS). Inactive-favoring residues form stronger contacts in the inactive state (negative ΔRRCS). Only residues with |ΔRRCS| ≥ 2.28 are shown (per-receptor significance threshold = max(mean(|Δ|) + σ, 0.2)).

Per-segment summary
Segment Range Active-favoring residues Count Inactive-favoring residues Count
TM1 60-73 73 (4.7) 1 60 (-3.3) 1
TM2 80-96 91 (6.0), 82 (3.2) 2 80 (-6.8), 96 (-3.3), 84 (-3.2) 3
TM3 115-149 133 (4.5), 136 (4.0) 2 115 (-7.5), 148 (-6.9), 149 (-6.9), 143 (-6.8), 142 (-5.1), 144 (-4.2) 6
TM4 176-184 179 (3.4), 184 (3.4), 176 (3.1) 3 - 0
TM5 200-238 233 (7.8), 238 (6.0), 234 (5.1), 223 (4.3), 237 (3.8), 222 (3.7), 203 (3.1) 7 200 (-6.6), 236 (-6.1) 2
TM6 285-314 289 (7.8), 286 (6.0), 290 (5.9), 285 (3.8) 4 295 (-6.2), 303 (-4.9), 307 (-4.8), 310 (-4.5), 314 (-4.5), 296 (-4.2) 6
TM7 337-351 341 (6.0), 344 (4.8), 349 (4.4), 348 (4.0) 4 351 (-6.2), 340 (-4.9), 337 (-4.8) 3
Intracellular / Extracellular loops & H8
ICL1 75-77 75 (4.7), 76 (3.5), 77 (3.2) 3 - 0
ICL2 150-150 - 0 150 (-3.7) 1
ICL3 240-282 244 (4.7), 278 (4.7), 254 (4.3), 282 (4.1) 4 243 (-7.8), 250 (-7.8), 241 (-6.1), 240 (-4.7), 255 (-4.7), 267 (-3.8), 268 (-3.8) 7
ECL1 - - 0 - 0
ECL2 186-199 - 0 192 (-7.5), 186 (-6.6), 199 (-4.2) 3
ECL3 - - 0 - 0
H8 355-361 355 (4.4) 1 361 (-4.8), 356 (-4.0) 2

Interactive visualizations

ΔRRCS distribution

Active vs inactive comparison

Residue-wise changes

TM domain breakdown

Variants of interest

89 variants mapped to contact positions, sorted by |ΔRRCS| impact.

Position Protein change DNA change Allele freq Het / Hom ΔRRCS AM score Pathogenicity Conservation dbSNP
467 p.Arg467Ser c.1399C>A 7.75e-07 1 / 0 11.57 0.115 BENIGN 0.66
468 p.His468Arg c.1403A>G 7.73e-07 1 / 0 11.57 0.047 BENIGN 0.42 rs1755891332
467 p.Arg467Leu c.1400G>T 6.61e-06 1 / 0 11.57 - nan - rs1277910780
467 p.Arg467His c.1400G>A 1.55e-06 2 / 0 11.57 - nan - rs1277910780
468 p.His468Gln c.1404C>G 7.73e-07 1 / 0 11.57 - nan - rs1283756765
469 p.Asp469Asn c.1405G>A 2.32e-06 3 / 0 10.24 0.108 BENIGN 0.76
469 p.Asp469Tyr c.1405G>T 7.73e-07 1 / 0 10.24 - nan -
469 p.Asp469Glu c.1407C>A 1.60e-05 21 / 0 10.24 - nan - rs1489591708
289 p.Glu289Lys c.865G>A 6.84e-07 1 / 0 7.77 0.990 PATHOGENIC 0.88
233 p.Thr233Ile c.698C>T 6.84e-07 1 / 0 7.77 0.707 PATHOGENIC 0.48 rs2113149926
233 p.Thr233Asn c.698C>A 6.84e-07 1 / 0 7.77 - nan -
115 p.Arg115Trp c.343C>T 2.05e-06 3 / 0 7.54 0.533 AMBIGUOUS 0.57
192 p.Asp192Val c.575A>T 6.57e-06 1 / 0 7.54 0.157 BENIGN 0.54 rs1754354319
115 p.Arg115Gln c.344G>A 1.98e-05 29 / 0 7.54 - nan - rs1273352160
149 p.Tyr149Cys c.446A>G 2.05e-06 3 / 0 6.94 0.536 AMBIGUOUS 0.49 rs1419494240
148 p.Arg148His c.443G>A 6.84e-07 1 / 0 6.94 0.280 BENIGN 0.51 rs758643818
143 p.Arg143Gly c.427C>G 6.84e-07 1 / 0 6.81 0.996 PATHOGENIC 0.98
80 p.Thr80Ile c.239C>T 2.05e-06 3 / 0 6.81 0.992 PATHOGENIC 0.85 rs760038075
143 p.Arg143His c.428G>A 7.53e-06 11 / 0 6.81 - nan - rs757479764
186 p.Glu186Lys c.556G>A 1.37e-06 2 / 0 6.56 0.543 AMBIGUOUS 0.66 rs1256293097
186 p.Glu186Gly c.557A>G 8.89e-06 11 / 1 6.56 - nan - rs751944506
186 p.Glu186Asp c.558G>C 1.37e-06 2 / 0 6.56 - nan - rs371731539
295 p.Thr295Pro c.883A>C 6.57e-06 1 / 0 6.20 0.979 PATHOGENIC 0.92 rs202097956
351 p.Ser351Thr c.1051T>A 1.53e-06 2 / 0 6.20 0.407 AMBIGUOUS 0.44 rs777674763
295 p.Thr295Met c.884C>T 8.21e-06 12 / 0 6.20 - nan - rs758073042
351 p.Ser351Pro c.1051T>C 7.66e-07 1 / 0 6.20 - nan - rs777674763
351 p.Ser351Cys c.1052C>G 7.53e-07 1 / 0 6.20 - nan - rs749273189
241 p.Val241Leu c.721G>C 1.37e-06 2 / 0 6.10 0.496 AMBIGUOUS 0.47
506 p.Gln506His c.1518G>C 7.46e-07 1 / 0 6.06 0.114 BENIGN 0.83
507 p.Pro507Ser c.1519C>T 7.46e-07 1 / 0 6.06 0.079 BENIGN 0.74 rs1755895561
507 p.Pro507Leu c.1520C>T 2.24e-06 3 / 0 6.06 - nan -
507 p.Pro507Arg c.1520C>G 1.34e-05 16 / 1 6.06 - nan - rs1458467133
91 p.Asp91Asn c.271G>A 1.37e-06 2 / 0 6.01 0.995 PATHOGENIC 1.00 rs761487660
238 p.Glu238Gly c.713A>G 6.58e-06 1 / 0 5.96 0.794 PATHOGENIC 0.49 rs756724973
290 p.Lys290Arg c.869A>G 1.37e-06 2 / 0 5.89 0.366 AMBIGUOUS 0.75
290 p.Lys290Asn c.870G>T 6.84e-07 1 / 0 5.89 - nan -
142 p.Asp142His c.424G>C 6.57e-06 1 / 0 5.12 0.996 PATHOGENIC 0.95 rs1370209486
234 p.Thr234Ala c.700A>G 6.58e-06 1 / 0 5.06 0.436 AMBIGUOUS 0.64 rs1422658619
234 p.Thr234Ile c.701C>T 6.84e-07 1 / 0 5.06 - nan -
234 p.Thr234Asn c.701C>A 1.31e-05 2 / 0 5.06 - nan - rs1429458895
303 p.Phe303Leu c.907T>C 6.85e-07 1 / 0 4.92 1.000 PATHOGENIC 0.95 rs1214605078
344 p.Asn344Asp c.1030A>G 7.60e-07 1 / 0 4.84 0.997 PATHOGENIC 0.97 rs754540841
344 p.Asn344Thr c.1031A>C 7.95e-07 1 / 0 4.84 - nan -
307 p.Trp307Arg c.919T>C 6.85e-07 1 / 0 4.83 0.999 PATHOGENIC 0.97
366 p.Gln366Leu c.1097A>T 1.16e-05 14 / 0 4.78 0.250 BENIGN 0.49
361 p.Arg361His c.1082G>A 9.13e-06 12 / 0 4.78 0.203 BENIGN 0.53 rs770336712
366 p.Gln366His c.1098G>T 1.02e-05 13 / 0 4.78 - nan - rs771591500
366 p.Gln366His c.1098G>C 7.84e-07 1 / 0 4.78 - nan - rs771591500
75 p.His75Tyr c.223C>T 2.74e-06 4 / 0 4.70 0.376 AMBIGUOUS 0.57 rs377516133
73 p.Asn73Asp c.217A>G 5.47e-06 8 / 0 4.70 0.368 AMBIGUOUS 0.52 rs1256231726
73 p.Asn73Ser c.218A>G 6.84e-07 1 / 0 4.70 - nan - rs1754336735
244 p.Glu244Lys c.730G>A 6.84e-07 1 / 0 4.69 0.914 PATHOGENIC 0.51
278 p.Ser278Phe c.833C>T 6.57e-06 1 / 0 4.69 0.710 PATHOGENIC 0.60 rs1382562383
244 p.Glu244Val c.731A>T 6.58e-06 1 / 0 4.69 - nan - rs745539683
310 p.Phe310Val c.928T>G 6.86e-07 1 / 0 4.54 0.987 PATHOGENIC 0.97
314 p.Leu314Val c.940C>G 3.45e-06 5 / 0 4.54 0.631 PATHOGENIC 0.71 rs1305758864
133 p.Ile133Thr c.398T>C 8.89e-06 13 / 0 4.52 0.993 PATHOGENIC 1.00
355 p.Phe355Leu c.1065C>A 3.02e-06 4 / 0 4.41 0.999 PATHOGENIC 0.90 rs1755877182
349 p.Pro349Thr c.1045C>A 6.59e-06 1 / 0 4.41 0.662 PATHOGENIC 0.56 rs1221135849
223 p.Tyr223His c.667T>C 6.84e-07 1 / 0 4.33 0.998 PATHOGENIC 0.99 rs909145193
223 p.Tyr223Phe c.668A>T 1.23e-05 18 / 0 4.33 - nan - rs1754357621
223 p.Tyr223Cys c.668A>G 6.84e-07 1 / 0 4.33 - nan -
296 p.Leu296Val c.886T>G 6.84e-07 1 / 0 4.23 0.543 AMBIGUOUS 0.96
296 p.Leu296Phe c.888G>C 6.84e-07 1 / 0 4.23 - nan -
144 p.Tyr144Cys c.431A>G 6.84e-07 1 / 0 4.21 0.892 PATHOGENIC 0.97
199 p.Glu199Lys c.595G>A 1.37e-06 2 / 0 4.21 0.138 BENIGN 0.66 rs1328289918
282 p.Lys282Glu c.844A>G 6.84e-07 1 / 0 4.07 0.973 PATHOGENIC 0.67 rs1190364353
356 p.Lys356Glu c.1066A>G 7.59e-07 1 / 0 4.02 0.852 PATHOGENIC 0.73
356 p.Lys356Asn c.1068G>T 7.55e-07 1 / 0 4.02 - nan -
136 p.Leu136Gln c.407T>A 6.84e-07 1 / 0 3.96 0.998 PATHOGENIC 0.99
348 p.Tyr348His c.1042T>C 6.95e-06 9 / 0 3.96 0.997 PATHOGENIC 0.97
348 p.Tyr348Asp c.1042T>G 7.72e-07 1 / 0 3.96 - nan -
268 p.Thr268Ala c.802A>G 2.05e-06 3 / 0 3.79 0.063 BENIGN 0.43 rs1157900390
150 p.Ser150Thr c.448T>A 2.74e-06 4 / 0 3.74 0.560 AMBIGUOUS 0.68 rs1164698280
150 p.Ser150Tyr c.449C>A 6.84e-07 1 / 0 3.74 - nan -
76 p.Leu76Met c.226C>A 1.09e-05 16 / 0 3.54 0.902 PATHOGENIC 0.89 rs1754337139
179 p.Gly179Arg c.535G>A 3.42e-06 5 / 0 3.37 0.996 PATHOGENIC 0.62 rs1338417647
179 p.Gly179Glu c.536G>A 6.84e-07 1 / 0 3.37 - nan - rs761926773
96 p.Phe96Leu c.286T>C 6.84e-07 1 / 0 3.33 0.457 AMBIGUOUS 0.41 rs1218611866
60 p.Ile60Val c.178A>G 2.74e-06 4 / 0 3.33 0.061 BENIGN 0.78
60 p.Ile60Thr c.179T>C 6.84e-07 1 / 0 3.33 - nan -
96 p.Phe96Ser c.287T>C 5.47e-06 8 / 0 3.33 - nan - rs750200746
77 p.Arg77Trp c.229C>T 9.51e-05 139 / 0 3.24 0.517 AMBIGUOUS 0.73 rs571519472
82 p.Tyr82Phe c.245A>T 6.84e-07 1 / 0 3.24 0.144 BENIGN 0.71
77 p.Arg77Gln c.230G>A 1.37e-06 2 / 0 3.24 - nan - rs1754337326
82 p.Tyr82Cys c.245A>G 2.74e-06 4 / 0 3.24 - nan - rs768227684
84 p.Ile84Leu c.250A>C 1.37e-06 2 / 0 3.22 0.562 AMBIGUOUS 0.86
84 p.Ile84Thr c.251T>C 6.84e-07 1 / 0 3.22 - nan -
176 p.Ile176Val c.526A>G 1.98e-05 29 / 0 3.15 0.220 BENIGN 0.90 rs759306305

Complete RRCS results

Top 1000 contact pairs by |ΔRRCS|. Significance threshold: |ΔRRCS| ≥ 2.28, computed as max(mean(|Δ|) + σ, 0.2). Highlighted rows indicate significant changes.

Res1 AA1 Res2 AA2 Active RRCS Inactive RRCS ΔRRCS |ΔRRCS|
467 ARG 468 HIS 11.572 0.000 11.572 11.572
468 HIS 469 ASP 10.241 0.000 10.241 10.241
243 LYS 250 GLU 0.000 7.840 -7.840 7.840
233 THR 289 GLU 7.771 0.000 7.771 7.771
115 ARG 192 ASP 1.800 9.341 -7.541 7.541
148 ARG 149 TYR 4.241 11.182 -6.941 6.941
80 THR 143 ARG 0.000 6.808 -6.808 6.808
186 GLU 200 GLU 8.587 15.148 -6.560 6.560
295 THR 351 SER 0.851 7.049 -6.199 6.199
236 ASN 241 VAL 0.000 6.095 -6.095 6.095
506 GLN 507 PRO 0.000 6.063 -6.063 6.063
91 ASP 341 SER 9.193 3.188 6.006 6.006
238 GLU 286 PHE 5.960 0.000 5.960 5.960
286 PHE 290 LYS 5.894 0.000 5.894 5.894
142 ASP 143 ARG 0.000 5.117 -5.117 5.117
234 THR 289 GLU 5.062 0.000 5.062 5.062
303 PHE 340 ASN 0.000 4.920 -4.920 4.920
340 ASN 344 ASN 4.844 0.000 4.844 4.844
307 TRP 337 GLY 3.821 8.646 -4.825 4.825
361 ARG 366 GLN 0.000 4.778 -4.778 4.778
73 ASN 75 HIS 4.704 0.000 4.704 4.704
240 GLY 255 ILE 0.000 4.703 -4.703 4.703
244 GLU 278 SER 4.694 0.000 4.694 4.694
310 PHE 314 LEU 1.001 5.542 -4.540 4.540
133 ILE 307 TRP 4.522 0.000 4.522 4.522
303 PHE 307 TRP 2.469 6.920 -4.451 4.451
349 PRO 355 PHE 5.114 0.708 4.406 4.406
143 ARG 223 TYR 4.328 0.000 4.328 4.328
250 GLU 254 ARG 4.305 0.000 4.305 4.305
223 TYR 296 LEU 2.317 6.549 -4.233 4.233
144 TYR 148 ARG 2.052 6.262 -4.211 4.211
186 GLU 199 GLU 0.000 4.208 -4.208 4.208
133 ILE 303 PHE 1.379 5.454 -4.074 4.074
244 GLU 282 LYS 6.410 2.337 4.074 4.074
349 PRO 356 LYS 0.465 4.489 -4.024 4.024
136 LEU 348 TYR 3.958 0.000 3.958 3.958
267 SER 268 THR 0.000 3.787 -3.787 3.787
237 LEU 285 LYS 3.784 0.000 3.784 3.784
150 SER 286 PHE 0.000 3.742 -3.742 3.742
144 TYR 222 MET 4.215 0.546 3.669 3.669
75 HIS 76 LEU 3.536 0.000 3.536 3.536
179 GLY 184 TRP 5.755 2.384 3.371 3.371
60 ILE 96 PHE 0.559 3.888 -3.328 3.328
348 TYR 355 PHE 0.000 3.314 -3.314 3.314
77 ARG 82 TYR 3.341 0.102 3.239 3.239
84 ILE 348 TYR 0.262 3.482 -3.220 3.220
176 ILE 203 TYR 3.146 0.000 3.146 3.146
402 SER 403 ARG 0.347 3.311 -2.964 2.964
409 ASP 410 SER 2.958 0.000 2.958 2.958
223 TYR 297 GLY 0.000 2.884 -2.884 2.884
307 TRP 340 ASN 6.198 3.343 2.855 2.855
180 PRO 185 LYS 2.933 0.110 2.824 2.824
2 ASN 3 PRO 0.084 2.903 -2.819 2.819
404 LYS 405 ASP 0.000 2.802 -2.802 2.802
115 ARG 185 LYS 2.789 0.000 2.789 2.789
352 SER 354 GLU 3.474 0.717 2.757 2.757
223 TYR 300 VAL 2.088 4.812 -2.724 2.724
105 LEU 110 TYR 3.593 0.870 2.723 2.723
285 LYS 289 GLU 2.794 0.092 2.703 2.703
115 ARG 188 ALA 2.933 0.232 2.701 2.701
75 HIS 361 ARG 2.694 0.000 2.694 2.694
133 ILE 212 PHE 0.122 2.813 -2.691 2.691
484 SER 485 PRO 0.511 3.164 -2.653 2.653
63 ASN 91 ASP 4.624 1.976 2.649 2.649
180 PRO 198 THR 2.604 0.000 2.604 2.604
40 LEU 44 ARG 2.596 0.000 2.596 2.596
115 ARG 119 ASP 2.582 0.000 2.582 2.582
55 PHE 339 PHE 1.421 3.996 -2.575 2.575
186 GLU 198 THR 0.000 2.546 -2.546 2.546
55 PHE 338 TYR 0.000 2.517 -2.517 2.517
136 LEU 303 PHE 1.490 3.994 -2.505 2.505
354 GLU 357 ARG 0.000 2.478 -2.478 2.478
63 ASN 88 ALA 5.506 3.038 2.469 2.469
151 LEU 244 GLU 0.000 2.465 -2.465 2.465
191 ASP 193 LYS 2.462 0.000 2.462 2.462
81 ASN 355 PHE 3.322 0.948 2.374 2.374
234 THR 286 PHE 2.374 0.000 2.374 2.374
143 ARG 296 LEU 0.000 2.352 -2.352 2.352
425 SER 426 PRO 2.726 0.390 2.336 2.336
417 SER 418 GLN 2.334 0.000 2.334 2.334
55 PHE 342 CYS 1.041 3.372 -2.330 2.330
237 LEU 283 LEU 0.000 2.290 -2.290 2.290
58 PHE 342 CYS 1.891 4.167 -2.277 2.277
219 ILE 303 PHE 2.254 0.000 2.254 2.254
150 SER 289 GLU 0.000 2.208 -2.208 2.208
228 ILE 232 ARG 2.190 0.000 2.190 2.190
91 ASP 344 ASN 4.744 2.581 2.163 2.163
242 MET 286 PHE 0.000 2.144 -2.144 2.144
212 PHE 311 PHE 14.751 16.853 -2.102 2.102
234 THR 290 LYS 0.123 2.184 -2.062 2.062
244 GLU 279 ILE 2.058 0.000 2.058 2.058
515 LEU 516 ALA 0.000 2.031 -2.031 2.031
496 CYS 497 GLU 2.029 0.000 2.029 2.029
143 ARG 348 TYR 2.025 0.000 2.025 2.025
362 ILE 367 CYS 0.000 1.996 -1.996 1.996
511 SER 512 ASN 0.000 1.982 -1.982 1.982
3 PRO 4 ASP 0.000 1.978 -1.978 1.978
34 ASN 36 THR 1.937 0.000 1.937 1.937
143 ARG 153 TYR 0.000 1.935 -1.935 1.935
151 LEU 282 LYS 0.000 1.913 -1.913 1.913
234 THR 238 GLU 0.000 1.832 -1.832 1.832
199 GLU 318 SER 1.251 3.077 -1.825 1.825
87 LEU 136 LEU 2.592 0.772 1.820 1.820
143 ARG 351 SER 1.818 0.000 1.818 1.818
472 PRO 473 LEU 1.816 0.000 1.816 1.816
67 ILE 89 MET 2.575 0.782 1.793 1.793
421 LEU 422 PRO 2.269 0.479 1.790 1.790
233 THR 286 PHE 0.000 1.787 -1.787 1.787
66 VAL 348 TYR 0.000 1.774 -1.774 1.774
144 TYR 225 ARG 5.529 3.758 1.771 1.771
75 HIS 354 GLU 0.000 1.769 -1.769 1.769
6 ASP 7 THR 0.000 1.765 -1.765 1.765
349 PRO 359 PHE 1.689 3.452 -1.763 1.763
41 ASP 44 ARG 0.000 1.757 -1.757 1.757
137 CYS 215 PRO 1.280 3.016 -1.736 1.736
51 VAL 55 PHE 1.736 0.000 1.736 1.736
501 ASP 502 VAL 0.793 2.525 -1.732 1.732
306 CYS 340 ASN 2.800 1.087 1.713 1.713
413 CYS 414 LEU 1.699 0.000 1.699 1.699
82 TYR 159 ARG 1.536 3.227 -1.691 1.691
185 LYS 198 THR 2.400 4.063 -1.662 1.662
216 LEU 303 PHE 1.654 0.000 1.654 1.654
219 ILE 300 VAL 0.093 1.736 -1.643 1.643
62 GLY 345 PRO 3.208 4.815 -1.608 1.608
241 VAL 282 LYS 1.607 0.000 1.607 1.607
106 GLU 335 TRP 2.592 1.019 1.573 1.573
9 HIS 10 ASN 3.851 2.283 1.568 1.568
4 ASP 5 LEU 0.000 1.565 -1.565 1.565
397 LEU 398 GLU 3.395 1.844 1.551 1.551
223 TYR 299 VAL 1.548 0.000 1.548 1.548
66 VAL 349 PRO 1.539 0.000 1.539 1.539
339 PHE 343 LEU 4.413 2.878 1.535 1.535
237 LEU 282 LYS 1.522 0.000 1.522 1.522
299 VAL 348 TYR 1.894 0.374 1.519 1.519
55 PHE 335 TRP 0.000 1.519 -1.519 1.519
408 ASP 409 ASP 1.755 0.270 1.486 1.486
203 TYR 207 SER 1.587 3.057 -1.470 1.470
146 GLY 289 GLU 0.000 1.459 -1.459 1.459
69 SER 355 PHE 0.783 2.240 -1.457 1.457
500 ALA 501 ASP 1.455 0.000 1.455 1.455
262 GLU 263 ASP 0.000 1.446 -1.446 1.446
419 ARG 420 THR 1.441 0.000 1.441 1.441
481 GLU 482 PRO 2.027 0.592 1.435 1.435
40 LEU 107 VAL 0.000 1.421 -1.421 1.421
310 PHE 311 PHE 1.922 0.510 1.412 1.412
69 SER 359 PHE 3.421 2.015 1.406 1.406
140 SER 222 MET 2.910 1.513 1.397 1.397
63 ASN 345 PRO 4.845 3.451 1.393 1.393
454 LEU 455 SER 1.387 0.000 1.387 1.387
198 THR 203 TYR 1.748 3.131 -1.383 1.383
87 LEU 135 SER 2.638 1.257 1.381 1.381
41 ASP 43 THR 0.000 1.374 -1.374 1.374
185 LYS 200 GLU 1.373 0.000 1.373 1.373
139 ILE 348 TYR 1.367 0.000 1.367 1.367
255 ILE 259 ASN 1.351 0.000 1.351 1.351
86 ASN 89 MET 0.000 1.338 -1.338 1.338
461 PRO 462 PRO 2.407 1.070 1.337 1.337
80 THR 142 ASP 5.744 4.424 1.321 1.321
93 LEU 97 THR 0.000 1.313 -1.313 1.313
361 ARG 367 CYS 0.000 1.308 -1.308 1.308
344 ASN 348 TYR 1.708 3.012 -1.304 1.304
335 TRP 338 TYR 2.092 0.803 1.289 1.289
137 CYS 219 ILE 2.359 3.646 -1.287 1.287
492 SER 493 ASN 2.095 3.378 -1.283 1.283
295 THR 296 LEU 0.000 1.279 -1.279 1.279
156 LEU 161 LYS 3.117 1.843 1.274 1.274
320 PHE 323 LEU 2.121 0.848 1.273 1.273
93 LEU 128 CYS 1.042 2.311 -1.270 1.270
63 ASN 341 SER 1.651 2.920 -1.269 1.269
176 ILE 210 GLY 0.156 1.421 -1.265 1.265
412 SER 413 CYS 0.021 1.276 -1.254 1.254
426 PRO 427 SER 1.253 0.000 1.253 1.253
139 ILE 143 ARG 1.448 0.196 1.252 1.252
176 ILE 207 SER 1.248 0.000 1.248 1.248
133 ILE 311 PHE 1.247 0.000 1.247 1.247
278 SER 282 LYS 1.242 0.000 1.242 1.242
240 GLY 282 LYS 1.241 0.000 1.241 1.241
469 ASP 470 SER 1.226 0.000 1.226 1.226
456 LEU 457 PRO 0.026 1.252 -1.226 1.226
86 ASN 170 TRP 5.394 4.171 1.222 1.222
222 MET 225 ARG 0.000 1.222 -1.222 1.222
102 SER 338 TYR 3.505 2.292 1.213 1.213
347 ILE 348 TYR 1.201 0.000 1.201 1.201
250 GLU 252 THR 0.000 1.200 -1.200 1.200
184 TRP 203 TYR 3.238 2.040 1.198 1.198
199 GLU 324 LYS 2.525 3.721 -1.197 1.197
510 LYS 511 SER 1.189 0.000 1.189 1.189
344 ASN 349 PRO 1.259 0.071 1.188 1.188
306 CYS 336 LEU 6.314 7.496 -1.182 1.182
65 LEU 359 PHE 4.622 3.445 1.177 1.177
240 GLY 253 LEU 0.000 1.170 -1.170 1.170
137 CYS 218 VAL 1.558 0.389 1.169 1.169
90 ALA 132 SER 0.929 2.096 -1.167 1.167
106 GLU 331 LYS 7.067 8.228 -1.161 1.161
281 VAL 285 LYS 0.000 1.147 -1.147 1.147
52 LEU 335 TRP 5.169 6.305 -1.136 1.136
263 ASP 264 THR 0.000 1.127 -1.127 1.127
302 MET 343 LEU 0.612 1.737 -1.125 1.125
111 TRP 121 TRP 4.563 3.444 1.120 1.120
73 ASN 358 ALA 1.190 2.301 -1.111 1.111
184 TRP 200 GLU 1.141 0.033 1.109 1.109
213 TYR 311 PHE 2.890 3.990 -1.100 1.100
60 ILE 92 LEU 1.138 2.225 -1.087 1.087
64 ILE 92 LEU 0.971 2.057 -1.086 1.086
212 PHE 213 TYR 1.727 0.645 1.083 1.083
334 PHE 338 TYR 7.343 8.425 -1.082 1.082
37 LEU 38 PRO 0.758 1.838 -1.080 1.080
98 VAL 338 TYR 0.693 1.766 -1.073 1.073
115 ARG 189 PRO 1.349 0.283 1.067 1.067
516 ALA 517 PRO 0.707 1.774 -1.066 1.066
127 LEU 170 TRP 1.190 0.128 1.063 1.063
430 TYR 431 LEU 1.058 0.000 1.058 1.058
226 VAL 296 LEU 1.047 0.000 1.047 1.047
424 ALA 425 SER 1.044 0.000 1.044 1.044
70 VAL 81 ASN 0.008 1.043 -1.035 1.035
149 TYR 152 GLN 1.691 0.665 1.026 1.026
147 VAL 230 ALA 0.000 1.020 -1.020 1.020
10 ASN 11 THR 1.016 0.000 1.016 1.016
237 LEU 286 PHE 1.154 0.147 1.007 1.007
110 TYR 112 VAL 1.033 2.035 -1.002 1.002
133 ILE 219 ILE 0.086 1.085 -1.000 1.000
227 TYR 293 ALA 0.993 0.000 0.993 0.993
141 ILE 218 VAL 1.007 0.022 0.985 0.985
423 SER 424 ALA 0.976 0.000 0.976 0.976
139 ILE 296 LEU 0.000 0.972 -0.972 0.972
70 VAL 355 PHE 1.821 0.851 0.970 0.970
94 LEU 99 LEU 4.178 3.210 0.968 0.968
274 ASN 275 PRO 1.146 0.181 0.965 0.965
152 GLN 156 LEU 0.962 0.000 0.962 0.962
216 LEU 304 ILE 0.628 1.584 -0.957 0.957
45 ALA 107 VAL 2.868 1.918 0.950 0.950
487 THR 488 ASP 0.000 0.938 -0.938 0.938
209 LEU 214 ILE 4.563 5.498 -0.935 0.935
68 LEU 362 ILE 1.178 2.107 -0.929 0.929
353 LYS 354 GLU 0.914 0.000 0.914 0.914
230 ALA 289 GLU 0.912 0.000 0.912 0.912
460 GLU 461 PRO 3.426 2.526 0.900 0.900
40 LEU 45 ALA 0.000 0.895 -0.895 0.895
127 LEU 177 SER 3.162 4.048 -0.886 0.886
87 LEU 91 ASP 1.445 0.564 0.880 0.880
83 PHE 142 ASP 2.607 1.732 0.876 0.876
11 THR 12 SER 0.869 0.000 0.869 0.869
76 LEU 81 ASN 5.731 6.598 -0.867 0.867
133 ILE 215 PRO 1.069 1.896 -0.827 0.827
237 LEU 289 GLU 0.814 0.000 0.814 0.814
148 ARG 229 VAL 0.086 0.897 -0.811 0.811
71 ALA 77 ARG 2.736 3.547 -0.811 0.811
307 TRP 338 TYR 0.000 0.804 -0.804 0.804
464 ARG 465 ARG 0.794 0.000 0.794 0.794
232 ARG 236 ASN 0.000 0.790 -0.790 0.790
299 VAL 347 ILE 1.092 1.881 -0.789 0.789
72 CYS 367 CYS 0.000 0.786 -0.786 0.786
21 LYS 22 ASN 0.000 0.783 -0.783 0.783
121 TRP 334 PHE 0.017 0.795 -0.778 0.778
149 TYR 156 LEU 1.218 0.445 0.774 0.774
60 ILE 95 SER 2.954 2.185 0.768 0.768
291 LYS 351 SER 0.000 0.765 -0.765 0.765
140 SER 223 TYR 3.347 4.109 -0.762 0.762
87 LEU 132 SER 2.821 3.582 -0.760 0.760
221 VAL 225 ARG 1.276 0.518 0.758 0.758
132 SER 344 ASN 0.757 0.000 0.757 0.757
177 SER 178 ILE 0.757 0.000 0.757 0.757
66 VAL 355 PHE 0.756 0.000 0.756 0.756
69 SER 362 ILE 2.735 1.981 0.754 0.754
76 LEU 355 PHE 0.043 0.795 -0.752 0.752
184 TRP 198 THR 0.752 0.000 0.752 0.752
99 LEU 338 TYR 4.717 3.971 0.746 0.746
102 SER 335 TRP 1.942 1.203 0.740 0.740
76 LEU 354 GLU 1.550 0.813 0.737 0.737
208 SER 311 PHE 1.978 1.251 0.727 0.727
144 TYR 226 VAL 2.203 2.930 -0.726 0.726
59 ALA 95 SER 2.325 1.603 0.723 0.723
90 ALA 170 TRP 1.893 1.180 0.713 0.713
111 TRP 195 CYS 5.802 6.511 -0.709 0.709
126 VAL 177 SER 2.147 1.439 0.709 0.709
201 PRO 318 SER 3.182 3.886 -0.704 0.704
306 CYS 337 GLY 2.027 2.729 -0.702 0.702
472 PRO 474 PHE 0.000 0.701 -0.701 0.701
205 LEU 209 LEU 0.571 1.268 -0.697 0.697
200 GLU 318 SER 0.000 0.696 -0.696 0.696
86 ASN 166 LEU 2.616 3.311 -0.695 0.695
307 TRP 310 PHE 0.000 0.694 -0.694 0.694
345 PRO 359 PHE 0.089 0.782 -0.692 0.692
110 TYR 193 LYS 1.778 2.469 -0.691 0.691
253 LEU 279 ILE 0.000 0.687 -0.687 0.687
97 THR 124 VAL 0.758 1.439 -0.681 0.681
111 TRP 192 ASP 1.818 1.141 0.677 0.677
84 ILE 139 ILE 0.852 0.182 0.669 0.669
237 LEU 242 MET 0.000 0.667 -0.667 0.667
502 VAL 503 ALA 0.664 0.000 0.664 0.664
94 LEU 341 SER 1.544 0.882 0.662 0.662
310 PHE 330 PHE 0.380 1.039 -0.659 0.659
314 LEU 330 PHE 0.265 0.921 -0.656 0.656
63 ASN 344 ASN 0.000 0.654 -0.654 0.654
185 LYS 196 GLY 0.000 0.652 -0.652 0.652
134 LEU 172 LEU 1.704 2.356 -0.652 0.652
102 SER 334 PHE 0.000 0.650 -0.650 0.650
322 THR 323 LEU 0.327 0.976 -0.649 0.649
159 ARG 163 ILE 0.252 0.900 -0.648 0.648
304 ILE 308 LEU 1.436 0.790 0.646 0.646
55 PHE 99 LEU 0.000 0.646 -0.646 0.646
73 ASN 361 ARG 3.582 2.940 0.642 0.642
145 ILE 153 TYR 1.385 0.755 0.630 0.630
140 SER 218 VAL 0.621 0.000 0.621 0.621
220 LEU 300 VAL 0.621 0.000 0.621 0.621
357 ARG 361 ARG 0.618 0.000 0.618 0.618
74 ARG 446 GLU 0.615 0.000 0.615 0.615
15 ALA 16 HIS 0.000 0.614 -0.614 0.614
118 CYS 195 CYS 6.613 6.000 0.613 0.613
2 ASN 4 ASP 0.611 0.000 0.611 0.611
286 PHE 289 GLU 0.000 0.611 -0.611 0.611
5 LEU 6 ASP 0.000 0.606 -0.606 0.606
136 LEU 299 VAL 0.000 0.603 -0.603 0.603
197 VAL 314 LEU 0.000 0.603 -0.603 0.603
210 GLY 215 PRO 1.693 2.285 -0.593 0.593
304 ILE 309 PRO 0.954 0.364 0.589 0.589
227 TYR 231 LYS 0.915 1.503 -0.588 0.588
358 ALA 361 ARG 0.582 0.000 0.582 0.582
87 LEU 139 ILE 0.758 0.185 0.573 0.573
265 LEU 266 SER 0.614 0.049 0.565 0.565
132 SER 340 ASN 0.561 0.000 0.561 0.561
101 PHE 121 TRP 1.575 1.014 0.561 0.561
221 VAL 222 MET 0.007 0.560 -0.553 0.553
403 ARG 404 LYS 0.000 0.551 -0.551 0.551
140 SER 219 ILE 2.838 2.287 0.551 0.551
223 TYR 348 TYR 0.550 0.000 0.550 0.550
233 THR 237 LEU 0.187 0.732 -0.546 0.546
79 PRO 157 VAL 0.452 0.997 -0.546 0.546
87 LEU 348 TYR 1.332 0.790 0.542 0.542
125 ASP 334 PHE 1.075 0.534 0.541 0.541
86 ASN 135 SER 2.650 2.110 0.541 0.541
69 SER 70 VAL 0.000 0.541 -0.541 0.541
74 ARG 77 ARG 0.539 0.000 0.539 0.539
317 GLY 324 LYS 0.714 0.182 0.532 0.532
189 PRO 194 GLU 0.543 0.014 0.529 0.529
119 ASP 185 LYS 2.196 1.668 0.528 0.528
178 ILE 182 LEU 1.373 1.901 -0.528 0.528
112 VAL 113 LEU 0.000 0.528 -0.528 0.528
105 LEU 195 CYS 0.473 1.001 -0.528 0.528
44 ARG 106 GLU 0.000 0.527 -0.527 0.527
105 LEU 111 TRP 2.435 1.912 0.523 0.523
399 ARG 400 SER 3.000 2.478 0.523 0.523
94 LEU 129 CYS 1.036 0.515 0.522 0.522
212 PHE 307 TRP 3.325 2.804 0.521 0.521
66 VAL 359 PHE 2.898 2.378 0.519 0.519
291 LYS 353 LYS 0.000 0.519 -0.519 0.519
262 GLU 264 THR 0.517 0.000 0.517 0.517
200 GLU 201 PRO 1.321 1.839 -0.517 0.517
20 LEU 21 LYS 0.514 0.000 0.514 0.514
121 TRP 125 ASP 0.511 0.000 0.511 0.511
95 SER 100 PRO 1.701 2.210 -0.509 0.509
491 ALA 492 SER 0.195 0.702 -0.507 0.507
212 PHE 308 LEU 4.117 3.612 0.506 0.506
407 LEU 408 ASP 0.771 0.266 0.505 0.505
310 PHE 333 VAL 3.442 3.947 -0.505 0.505
73 ASN 76 LEU 1.877 1.376 0.500 0.500
172 LEU 176 ILE 0.418 0.914 -0.496 0.496
96 PHE 97 THR 0.671 0.177 0.493 0.493
247 ASN 248 SER 0.000 0.492 -0.492 0.492
499 ALA 500 ALA 0.488 0.000 0.488 0.488
274 ASN 277 SER 0.486 0.000 0.486 0.486
65 LEU 362 ILE 0.703 1.184 -0.480 0.480
212 PHE 303 PHE 1.692 1.213 0.479 0.479
14 PRO 15 ALA 0.556 0.078 0.478 0.478
123 ALA 181 LEU 0.284 0.761 -0.477 0.477
147 VAL 229 VAL 1.492 1.965 -0.473 0.473
147 VAL 226 VAL 0.236 0.708 -0.472 0.472
81 ASN 84 ILE 0.350 0.820 -0.470 0.470
405 ASP 406 SER 0.000 0.466 -0.466 0.466
278 SER 279 ILE 0.000 0.462 -0.462 0.462
302 MET 347 ILE 1.115 0.657 0.458 0.458
155 THR 161 LYS 0.458 0.000 0.458 0.458
56 ILE 99 LEU 3.538 3.081 0.456 0.456
305 LEU 336 LEU 0.433 0.886 -0.453 0.453
285 LYS 288 ARG 0.000 0.453 -0.453 0.453
91 ASP 132 SER 3.012 2.559 0.453 0.453
136 LEU 344 ASN 0.453 0.000 0.453 0.453
266 SER 267 SER 0.000 0.451 -0.451 0.451
90 ALA 128 CYS 1.522 1.073 0.449 0.449
131 ALA 170 TRP 1.666 1.217 0.448 0.448
67 ILE 85 VAL 0.068 0.514 -0.446 0.446
13 ALA 14 PRO 0.284 0.730 -0.446 0.446
145 ILE 156 LEU 0.684 1.130 -0.445 0.445
257 SER 259 ASN 0.000 0.440 -0.440 0.440
136 LEU 340 ASN 0.436 0.000 0.436 0.436
82 TYR 166 LEU 1.149 0.714 0.435 0.435
204 ALA 318 SER 0.734 0.299 0.435 0.435
40 LEU 108 LEU 0.000 0.434 -0.434 0.434
218 VAL 222 MET 0.675 0.243 0.432 0.432
279 ILE 283 LEU 0.899 0.468 0.432 0.432
414 LEU 415 SER 0.565 0.142 0.423 0.423
134 LEU 169 VAL 3.424 3.004 0.420 0.420
299 VAL 344 ASN 0.000 0.417 -0.417 0.417
352 SER 355 PHE 2.874 2.460 0.414 0.414
241 VAL 253 LEU 0.000 0.406 -0.406 0.406
418 GLN 419 ARG 0.402 0.000 0.402 0.402
398 GLU 399 ARG 1.458 1.858 -0.400 0.400
98 VAL 121 TRP 4.926 4.528 0.397 0.397
186 GLU 187 PRO 1.226 0.830 0.396 0.396
92 LEU 96 PHE 0.000 0.396 -0.396 0.396
115 ARG 190 ASN 0.000 0.395 -0.395 0.395
209 LEU 215 PRO 0.223 0.616 -0.393 0.393
130 THR 211 SER 1.254 1.645 -0.392 0.392
204 ALA 314 LEU 0.392 0.000 0.392 0.392
310 PHE 334 PHE 1.870 2.261 -0.391 0.391
177 SER 203 TYR 0.380 0.000 0.380 0.380
213 TYR 312 ILE 0.878 1.258 -0.379 0.379
56 ILE 95 SER 1.014 0.637 0.377 0.377
435 ALA 436 PRO 0.000 0.376 -0.376 0.376
90 ALA 131 ALA 0.954 0.581 0.373 0.373
44 ARG 48 VAL 0.000 0.372 -0.372 0.372
174 THR 178 ILE 1.056 0.685 0.371 0.371
227 TYR 296 LEU 0.370 0.000 0.370 0.370
129 CYS 338 TYR 0.368 0.000 0.368 0.368
140 SER 141 ILE 0.367 0.000 0.367 0.367
226 VAL 293 ALA 0.000 0.364 -0.364 0.364
57 LEU 61 VAL 0.444 0.807 -0.363 0.363
94 LEU 98 VAL 1.667 2.029 -0.362 0.362
136 LEU 219 ILE 1.389 1.750 -0.360 0.360
178 ILE 181 LEU 0.357 0.000 0.357 0.357
325 PRO 330 PHE 0.399 0.043 0.356 0.356
231 LYS 234 THR 0.353 0.000 0.353 0.353
125 ASP 338 TYR 6.480 6.128 0.353 0.353
79 PRO 162 ALA 0.349 0.000 0.349 0.349
236 ASN 242 MET 0.000 0.343 -0.343 0.343
302 MET 305 LEU 0.697 0.356 0.341 0.341
49 GLY 107 VAL 1.343 1.004 0.339 0.339
295 THR 347 ILE 0.000 0.338 -0.338 0.338
229 VAL 233 THR 0.000 0.336 -0.336 0.336
63 ASN 95 SER 0.336 0.000 0.336 0.336
284 PHE 353 LYS 0.335 0.000 0.335 0.335
313 ALA 333 VAL 0.358 0.024 0.334 0.334
56 ILE 100 PRO 1.362 1.029 0.333 0.333
143 ARG 226 VAL 0.749 1.079 -0.331 0.331
274 ASN 276 ARG 0.328 0.000 0.328 0.328
220 LEU 304 ILE 0.223 0.550 -0.326 0.326
473 LEU 475 THR 0.000 0.322 -0.322 0.322
143 ARG 299 VAL 0.322 0.000 0.322 0.322
140 SER 226 VAL 0.000 0.319 -0.319 0.319
144 TYR 229 VAL 0.000 0.318 -0.318 0.318
137 CYS 141 ILE 0.318 0.000 0.318 0.318
95 SER 99 LEU 0.752 1.069 -0.317 0.317
98 VAL 125 ASP 3.903 3.589 0.314 0.314
111 TRP 117 PHE 2.129 2.439 -0.311 0.311
251 LEU 255 ILE 0.309 0.000 0.309 0.309
55 PHE 56 ILE 0.000 0.309 -0.309 0.309
98 VAL 124 VAL 1.661 1.353 0.308 0.308
513 MET 514 PRO 0.712 1.019 -0.307 0.307
354 GLU 361 ARG 0.302 0.000 0.302 0.302
111 TRP 113 LEU 1.508 1.808 -0.300 0.300
42 ILE 46 ILE 0.700 0.996 -0.296 0.296
24 ASN 26 THR 0.296 0.000 0.296 0.296
176 ILE 211 SER 0.575 0.281 0.295 0.295
264 THR 265 LEU 0.737 0.444 0.292 0.292
133 ILE 216 LEU 0.000 0.292 -0.292 0.292
308 LEU 312 ILE 2.440 2.150 0.291 0.291
48 VAL 107 VAL 0.097 0.385 -0.288 0.288
460 GLU 462 PRO 0.000 0.284 -0.284 0.284
309 PRO 333 VAL 2.967 3.251 -0.284 0.284
242 MET 251 LEU 0.000 0.283 -0.283 0.283
179 GLY 203 TYR 0.559 0.841 -0.282 0.282
392 THR 393 ARG 0.282 0.000 0.282 0.282
127 LEU 173 SER 3.892 3.611 0.281 0.281
30 GLN 31 THR 0.000 0.279 -0.279 0.279
48 VAL 106 GLU 0.042 0.320 -0.278 0.278
147 VAL 286 PHE 0.000 0.277 -0.277 0.277
212 PHE 216 LEU 1.777 1.503 0.274 0.274
79 PRO 153 TYR 0.168 0.441 -0.273 0.273
130 THR 173 SER 5.202 4.931 0.271 0.271
329 VAL 333 VAL 0.043 0.313 -0.270 0.270
353 LYS 357 ARG 0.267 0.000 0.267 0.267
130 THR 176 ILE 0.753 1.018 -0.265 0.265
153 TYR 157 VAL 4.714 4.451 0.263 0.263
84 ILE 355 PHE 0.880 0.617 0.263 0.263
70 VAL 76 LEU 2.021 1.758 0.263 0.263
458 ALA 459 PRO 1.039 0.782 0.257 0.257
126 VAL 203 TYR 0.289 0.033 0.256 0.256
141 ILE 222 MET 0.926 1.182 -0.256 0.256
185 LYS 188 ALA 0.253 0.000 0.253 0.253
316 LEU 323 LEU 0.251 0.000 0.251 0.251
31 THR 32 SER 0.251 0.000 0.251 0.251
309 PRO 336 LEU 0.272 0.520 -0.248 0.248
307 TRP 311 PHE 2.488 2.735 -0.246 0.246
198 THR 204 ALA 0.000 0.245 -0.245 0.245
332 VAL 336 LEU 0.244 0.000 0.244 0.244
66 VAL 88 ALA 1.070 0.827 0.243 0.243
468 HIS 470 SER 0.000 0.243 -0.243 0.243
118 CYS 196 GLY 0.408 0.165 0.243 0.243
69 SER 76 LEU 1.433 1.675 -0.242 0.242
108 LEU 112 VAL 0.734 0.976 -0.242 0.242
452 ALA 453 LEU 0.240 0.000 0.240 0.240
314 LEU 315 PRO 1.330 1.092 0.238 0.238
97 THR 121 TRP 0.054 0.292 -0.238 0.238
298 ILE 351 SER 0.000 0.237 -0.237 0.237
318 SER 319 LEU 0.237 0.000 0.237 0.237
300 VAL 304 ILE 0.809 0.573 0.236 0.236
207 SER 211 SER 0.308 0.072 0.236 0.236
61 VAL 65 LEU 0.617 0.383 0.234 0.234
243 LYS 247 ASN 0.232 0.000 0.232 0.232
59 ALA 341 SER 0.703 0.474 0.229 0.229
126 VAL 207 SER 0.000 0.227 -0.227 0.227
94 LEU 125 ASP 1.439 1.212 0.227 0.227
141 ILE 145 ILE 0.879 0.654 0.225 0.225
509 PHE 510 LYS 0.839 1.060 -0.221 0.221
83 PHE 138 ALA 0.987 1.208 -0.221 0.221
273 HIS 278 SER 0.219 0.000 0.219 0.219
287 SER 291 LYS 0.218 0.000 0.218 0.218
121 TRP 122 ALA 0.772 0.554 0.218 0.218
121 TRP 195 CYS 1.499 1.283 0.216 0.216
93 LEU 98 VAL 0.446 0.230 0.216 0.216
241 VAL 283 LEU 0.214 0.000 0.214 0.214
111 TRP 118 CYS 6.157 5.944 0.213 0.213
298 ILE 347 ILE 0.000 0.212 -0.212 0.212
59 ALA 92 LEU 0.000 0.210 -0.210 0.210
163 ILE 167 LEU 0.565 0.358 0.208 0.208
295 THR 299 VAL 0.205 0.000 0.205 0.205
306 CYS 343 LEU 0.595 0.800 -0.205 0.205
60 ILE 64 ILE 0.887 0.683 0.204 0.204
130 THR 134 LEU 0.759 0.963 -0.204 0.204
231 LYS 235 LYS 0.377 0.578 -0.202 0.202
101 PHE 111 TRP 0.946 1.148 -0.201 0.201
58 PHE 346 ILE 1.759 1.959 -0.200 0.200
48 VAL 52 LEU 0.950 1.148 -0.199 0.199
180 PRO 203 TYR 5.877 5.679 0.198 0.198
223 TYR 293 ALA 0.000 0.195 -0.195 0.195
401 GLN 402 SER 0.097 0.291 -0.195 0.195
145 ILE 150 SER 0.392 0.198 0.194 0.194
101 PHE 113 LEU 2.182 1.990 0.192 0.192
185 LYS 186 GLU 0.000 0.192 -0.192 0.192
144 TYR 145 ILE 0.189 0.000 0.189 0.189
129 CYS 307 TRP 2.893 2.707 0.186 0.186
142 ASP 157 VAL 1.075 1.261 -0.186 0.186
396 SER 397 LEU 1.333 1.519 -0.186 0.186
78 THR 81 ASN 3.943 3.757 0.186 0.186
87 LEU 344 ASN 2.908 2.722 0.186 0.186
108 LEU 110 TYR 0.822 0.637 0.185 0.185
205 LEU 315 PRO 0.184 0.000 0.184 0.184
312 ILE 316 LEU 0.874 1.057 -0.183 0.183
121 TRP 338 TYR 0.554 0.372 0.182 0.182
437 PRO 438 PRO 0.633 0.815 -0.182 0.182
64 ILE 68 LEU 1.122 0.940 0.182 0.182
184 TRP 202 PHE 0.542 0.723 -0.181 0.181
310 PHE 315 PRO 0.181 0.000 0.181 0.181
114 GLY 192 ASP 0.236 0.055 0.181 0.181
219 ILE 223 TYR 1.292 1.111 0.181 0.181
273 HIS 277 SER 0.180 0.000 0.180 0.180
66 VAL 344 ASN 0.000 0.180 -0.180 0.180
317 GLY 323 LEU 0.177 0.000 0.177 0.177
436 PRO 437 PRO 0.928 0.751 0.177 0.177
459 PRO 460 GLU 0.000 0.177 -0.177 0.177
70 VAL 77 ARG 1.589 1.414 0.176 0.176
503 ALA 504 ASN 0.176 0.000 0.176 0.176
355 PHE 359 PHE 0.357 0.184 0.173 0.173
83 PHE 139 ILE 2.175 2.002 0.173 0.173
44 ARG 331 LYS 0.000 0.173 -0.173 0.173
199 GLU 330 PHE 0.169 0.000 0.169 0.169
139 ILE 223 TYR 0.385 0.216 0.169 0.169
208 SER 315 PRO 0.862 0.694 0.167 0.167
498 ALA 499 ALA 0.167 0.000 0.167 0.167
211 SER 311 PHE 1.827 1.662 0.165 0.165
80 THR 153 TYR 2.556 2.392 0.164 0.164
444 PHE 445 PRO 0.392 0.556 -0.164 0.164
188 ALA 189 PRO 0.808 0.647 0.161 0.161
152 GLN 155 THR 0.459 0.616 -0.157 0.157
240 GLY 254 ARG 0.000 0.156 -0.156 0.156
320 PHE 322 THR 0.376 0.220 0.156 0.156
303 PHE 308 LEU 0.205 0.051 0.154 0.154
135 SER 169 VAL 0.992 1.145 -0.153 0.153
306 CYS 307 TRP 0.378 0.225 0.153 0.153
63 ASN 92 LEU 2.732 2.581 0.151 0.151
347 ILE 351 SER 0.000 0.151 -0.151 0.151
238 GLU 290 LYS 0.149 0.000 0.149 0.149
118 CYS 194 GLU 0.149 0.000 0.149 0.149
131 ALA 169 VAL 1.247 1.395 -0.148 0.148
427 SER 428 PRO 2.066 2.213 -0.147 0.147
155 THR 156 LEU 0.147 0.000 0.147 0.147
69 SER 358 ALA 1.335 1.188 0.146 0.146
123 ALA 177 SER 2.867 2.723 0.144 0.144
200 GLU 203 TYR 0.572 0.430 0.142 0.142
339 PHE 342 CYS 0.544 0.403 0.142 0.142
86 ASN 169 VAL 0.334 0.193 0.141 0.141
142 ASP 153 TYR 6.086 6.225 -0.139 0.139
99 LEU 335 TRP 0.075 0.213 -0.138 0.138
126 VAL 176 ILE 0.493 0.356 0.136 0.136
111 TRP 193 LYS 5.427 5.292 0.135 0.135
115 ARG 191 ASP 0.135 0.000 0.135 0.135
143 ARG 292 ALA 0.000 0.133 -0.133 0.133
344 ASN 345 PRO 0.891 1.023 -0.133 0.133
67 ILE 92 LEU 0.744 0.875 -0.131 0.131
52 LEU 103 ALA 1.532 1.661 -0.129 0.129
400 SER 401 GLN 4.415 4.286 0.129 0.129
93 LEU 170 TRP 0.944 0.820 0.124 0.124
47 SER 48 VAL 0.025 0.150 -0.124 0.124
319 LEU 320 PHE 1.318 1.193 0.124 0.124
359 PHE 364 GLY 0.124 0.000 0.124 0.124
94 LEU 338 TYR 1.051 0.928 0.123 0.123
156 LEU 157 VAL 0.137 0.015 0.122 0.122
102 SER 121 TRP 3.936 4.057 -0.121 0.121
131 ALA 173 SER 4.086 3.966 0.120 0.120
325 PRO 329 VAL 0.652 0.770 -0.118 0.118
83 PHE 165 ALA 0.646 0.529 0.117 0.117
385 ALA 387 THR 0.116 0.000 0.116 0.116
316 LEU 320 PHE 0.490 0.382 0.108 0.108
343 LEU 347 ILE 0.450 0.557 -0.106 0.106
103 ALA 335 TRP 2.206 2.312 -0.106 0.106
205 LEU 208 SER 0.094 0.198 -0.104 0.104
208 SER 213 TYR 6.082 6.185 -0.103 0.103
158 THR 161 LYS 2.227 2.124 0.103 0.103
214 ILE 215 PRO 1.454 1.352 0.101 0.101
157 VAL 162 ALA 0.099 0.000 0.099 0.099
216 LEU 308 LEU 0.126 0.028 0.098 0.098
248 SER 252 THR 0.098 0.000 0.098 0.098
298 ILE 302 MET 0.337 0.240 0.097 0.097
113 LEU 117 PHE 1.371 1.275 0.096 0.096
62 GLY 359 PHE 0.175 0.080 0.096 0.096
174 THR 177 SER 0.198 0.103 0.096 0.096
134 LEU 215 PRO 0.606 0.702 -0.095 0.095
158 THR 160 ARG 0.462 0.366 0.095 0.095
144 TYR 149 TYR 0.106 0.011 0.095 0.095
150 SER 151 LEU 0.186 0.281 -0.095 0.095
330 PHE 333 VAL 0.094 0.000 0.094 0.094
59 ALA 99 LEU 0.000 0.093 -0.093 0.093
303 PHE 304 ILE 0.127 0.035 0.092 0.092
94 LEU 128 CYS 2.867 2.956 -0.090 0.090
169 VAL 173 SER 0.203 0.293 -0.090 0.090
136 LEU 139 ILE 0.174 0.260 -0.086 0.086
346 ILE 350 CYS 0.000 0.085 -0.085 0.085
201 PRO 202 PHE 0.085 0.000 0.085 0.085
76 LEU 358 ALA 0.609 0.524 0.085 0.085
147 VAL 289 GLU 0.000 0.084 -0.084 0.084
72 CYS 73 ASN 0.231 0.147 0.084 0.084
96 PHE 101 PHE 0.000 0.084 -0.084 0.084
315 PRO 318 SER 0.083 0.000 0.083 0.083
244 GLU 251 LEU 0.000 0.083 -0.083 0.083
59 ALA 342 CYS 1.646 1.564 0.083 0.083
308 LEU 309 PRO 0.848 0.929 -0.082 0.082
207 SER 212 PHE 0.150 0.068 0.081 0.081
83 PHE 166 LEU 2.699 2.619 0.080 0.080
340 ASN 343 LEU 0.000 0.077 -0.077 0.077
120 ILE 124 VAL 0.282 0.358 -0.076 0.076
201 PRO 319 LEU 0.130 0.205 -0.075 0.075
59 ALA 63 ASN 0.151 0.077 0.074 0.074
325 PRO 326 PRO 0.688 0.614 0.074 0.074
205 LEU 319 LEU 0.074 0.000 0.074 0.074
209 LEU 213 TYR 0.954 1.027 -0.074 0.074
119 ASP 181 LEU 0.409 0.483 -0.073 0.073
134 LEU 137 CYS 0.000 0.073 -0.073 0.073
126 VAL 197 VAL 0.073 0.000 0.073 0.073
136 LEU 300 VAL 0.000 0.071 -0.071 0.071
133 ILE 211 SER 2.716 2.645 0.071 0.071
359 PHE 363 LEU 0.068 0.000 0.068 0.068
389 ARG 390 PRO 0.323 0.390 -0.066 0.066
235 LYS 238 GLU 0.145 0.080 0.066 0.066
74 ARG 444 PHE 0.000 0.065 -0.065 0.065
315 PRO 319 LEU 0.000 0.064 -0.064 0.064
165 ALA 168 SER 0.041 0.105 -0.064 0.064
134 LEU 210 GLY 0.063 0.000 0.063 0.063
145 ILE 149 TYR 0.276 0.213 0.063 0.063
326 PRO 329 VAL 1.175 1.112 0.063 0.063
83 PHE 162 ALA 1.695 1.758 -0.062 0.062
216 LEU 220 LEU 1.296 1.358 -0.062 0.062
28 PRO 29 ASN 0.420 0.359 0.061 0.061
306 CYS 333 VAL 0.187 0.247 -0.060 0.060
70 VAL 85 VAL 1.833 1.774 0.059 0.059
127 LEU 174 THR 2.515 2.458 0.057 0.057
449 ALA 450 PRO 0.559 0.505 0.054 0.054
140 SER 300 VAL 0.000 0.053 -0.053 0.053
230 ALA 233 THR 0.053 0.000 0.053 0.053
56 ILE 60 ILE 0.799 0.851 -0.053 0.053
171 VAL 175 VAL 0.057 0.005 0.051 0.051
78 THR 80 THR 0.324 0.375 -0.051 0.051
63 ASN 66 VAL 0.000 0.050 -0.050 0.050
66 VAL 345 PRO 0.996 1.044 -0.049 0.049
98 VAL 102 SER 0.637 0.685 -0.048 0.048
68 LEU 73 ASN 0.032 0.078 -0.047 0.047
199 GLU 204 ALA 0.088 0.133 -0.046 0.046
111 TRP 194 GLU 0.089 0.044 0.045 0.045
46 ILE 50 LEU 0.672 0.627 0.045 0.045
138 ALA 169 VAL 0.000 0.044 -0.044 0.044
124 VAL 128 CYS 0.539 0.496 0.044 0.044
133 ILE 134 LEU 0.000 0.043 -0.043 0.043
246 SER 247 ASN 0.041 0.000 0.041 0.041
67 ILE 88 ALA 1.118 1.078 0.040 0.040
65 LEU 363 LEU 0.482 0.442 0.040 0.040
361 ARG 370 ARG 0.000 0.040 -0.040 0.040
203 TYR 208 SER 0.094 0.055 0.039 0.039
280 ALA 284 PHE 0.000 0.039 -0.039 0.039
44 ARG 47 SER 0.039 0.000 0.039 0.039
57 LEU 62 GLY 0.000 0.039 -0.039 0.039
59 ALA 345 PRO 0.038 0.000 0.038 0.038
348 TYR 349 PRO 0.859 0.822 0.038 0.038
116 ILE 120 ILE 0.454 0.418 0.037 0.037
241 VAL 252 THR 0.000 0.037 -0.037 0.037
261 HIS 262 GLU 0.035 0.000 0.035 0.035
197 VAL 334 PHE 0.034 0.000 0.034 0.034
334 PHE 335 TRP 0.000 0.033 -0.033 0.033
56 ILE 103 ALA 0.550 0.517 0.033 0.033
164 LEU 167 LEU 0.000 0.033 -0.033 0.033
91 ASP 340 ASN 0.000 0.033 -0.033 0.033
78 THR 79 PRO 0.971 0.938 0.033 0.033
95 SER 341 SER 0.353 0.385 -0.032 0.032
197 VAL 198 THR 0.105 0.073 0.032 0.032
58 PHE 63 ASN 0.000 0.032 -0.032 0.032
313 ALA 325 PRO 0.331 0.299 0.032 0.032
347 ILE 352 SER 0.000 0.031 -0.031 0.031
104 ALA 109 GLY 0.109 0.081 0.028 0.028
317 GLY 325 PRO 0.027 0.000 0.027 0.027
126 VAL 130 THR 0.483 0.510 -0.027 0.027
243 LYS 252 THR 0.000 0.025 -0.025 0.025
99 LEU 100 PRO 0.740 0.764 -0.025 0.025
52 LEU 106 GLU 0.523 0.546 -0.023 0.023
115 ARG 118 CYS 0.023 0.000 0.023 0.023
145 ILE 157 VAL 0.678 0.656 0.023 0.023
134 LEU 173 SER 1.201 1.223 -0.022 0.022
66 VAL 84 ILE 0.593 0.615 -0.022 0.022
83 PHE 135 SER 0.021 0.000 0.021 0.021
146 GLY 153 TYR 3.003 3.023 -0.020 0.020
44 ARG 49 GLY 0.000 0.020 -0.020 0.020
306 CYS 339 PHE 0.041 0.021 0.019 0.019
80 THR 81 ASN 0.475 0.456 0.019 0.019
137 CYS 140 SER 0.019 0.000 0.019 0.019
153 TYR 154 PRO 1.312 1.329 -0.017 0.017
302 MET 340 ASN 0.005 0.020 -0.015 0.015
241 VAL 279 ILE 0.013 0.000 0.013 0.013
68 LEU 72 CYS 0.021 0.009 0.013 0.013
321 SER 322 THR 0.094 0.105 -0.010 0.010
97 THR 98 VAL 0.640 0.630 0.010 0.010
85 VAL 89 MET 0.380 0.370 0.010 0.010
249 LYS 251 LEU 0.000 0.010 -0.010 0.010
125 ASP 129 CYS 1.382 1.373 0.009 0.009
213 TYR 315 PRO 0.349 0.357 -0.008 0.008
282 LYS 286 PHE 0.000 0.007 -0.007 0.007
324 LYS 325 PRO 0.942 0.935 0.007 0.007
453 LEU 455 SER 0.000 0.007 -0.007 0.007
182 LEU 184 TRP 0.000 0.006 -0.006 0.006
104 ALA 108 LEU 0.006 0.000 0.006 0.006
211 SER 212 PHE 0.295 0.301 -0.005 0.005
356 LYS 360 VAL 0.000 0.005 -0.005 0.005
97 THR 128 CYS 0.000 0.005 -0.005 0.005
294 LYS 298 ILE 0.336 0.331 0.004 0.004
152 GLN 246 SER 0.000 0.003 -0.003 0.003
204 ALA 315 PRO 0.003 0.000 0.003 0.003
343 LEU 346 ILE 0.023 0.021 0.002 0.002
94 LEU 100 PRO 0.030 0.031 -0.001 0.001
315 PRO 320 PHE 0.000 0.001 -0.001 0.001

RRCS change distribution

0.01
Mean ΔRRCS
1.64
Std Dev
0.03
Median

Magnitude classification

16
High (|Δ| ≥ 5.0)
66
Medium (2.3 ≤ |Δ| < 5.0)
663
Low (|Δ| < 2.3)

Methods

RRCS analysis. Residue-Residue Contact Scores (RRCS) were calculated for each conformational state based on inter-atomic distances. Changes (ΔRRCS) were computed by comparing active and inactive structures predicted by AlphaFold multistate (del Alamo et al., 2022).

Significance threshold. |ΔRRCS| ≥ 2.28, computed as max(mean(|Δ|) + σ, 0.2). The 0.2 floor ensures receptors with very small overall change still surface their largest contacts.

Variant data. Population frequencies from gnomAD v4; pathogenicity predictions from AlphaMissense; conservation from ProtVar / UniProt.

Structural annotation. TM domain boundaries and generic numbering from GPCRdb.

What is RRCS?

Residue-Residue Contact Score (RRCS) measures how strongly two amino acids interact in a protein structure. When a protein changes shape (from inactive to active), these contact strengths change.

ΔRRCS (Delta RRCS) shows the difference in contact strength between states:

  • Positive ΔRRCS. Contact is stronger in the active state.
  • Negative ΔRRCS. Contact is stronger in the inactive state.
  • Large |ΔRRCS|. Significant structural rearrangement.

Residues with large RRCS changes are critical for protein function. Mutations at these positions may disrupt the protein's ability to change shape properly.

Pathogenicity predictions

AlphaMissense predicts whether a mutation harms protein function:

  • Pathogenic (score ≥ 0.564): mutation likely damages function.
  • Ambiguous (0.34–0.563): effect uncertain.
  • Benign (< 0.34): mutation likely tolerated.

Conservation & population data

Conservation score. How well-preserved a position is across species (0 = variable, 1 = conserved). High conservation suggests the position is critical for function.

Allele frequency. How often a variant appears in the population. Rare variants (low frequency) may be more likely to be harmful.

Sources: AlphaFold multistate · RRCS · gnomAD v4 · AlphaMissense · GPCRdb · UniProt / ProtVar