GPCompReports

ADRB2

Gene ADRB2 Adrenoceptors Aminergic receptors UniProt P07550
700
Total Contact Pairs
72
Significant Changes
8.84
Max Increase
-9.02
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 E62 12.48x48 E62 12.48x48 E R63 12.49x49 R63 12.49x49 R L64 12.50x50 L64 12.50x50 L Q65 12.51x51 Q65 12.51x51 Q ICL1ECL1 M98 23.49x49 M98 23.49x49 M W99 23.50x50 W99 23.50x50 W T100 23.51x51 T100 23.51x51 T F101 23.52x52 F101 23.52x52 F ECL1ICL2 P138 34.50x50 P138 34.50x50 P F139 34.51x51 F139 34.51x51 F K140 34.52x52 K140 34.52x52 K Y141 34.53x53 Y141 34.53x53 Y Q142 34.54x54 Q142 34.54x54 Q S143 34.55x55 S143 34.55x55 S L144 34.56x56 L144 34.56x56 L L145 34.57x57 L145 34.57x57 L ICL2ECL2 W173 W173 W Y174 Y174 Y R175 R175 R A176 A176 A T177 T177 T H178 H178 H Q179 Q179 Q E180 E180 E A181 A181 A I182 I182 I N183 N183 N C184 C184 C Y185 Y185 Y A186 A186 A N187 N187 N E188 E188 E T189 T189 T C190 C190 C C191 45.50x50 C191 45.50x50 C D192 45.51x51 D192 45.51x51 D F193 45.52x52 F193 45.52x52 F F194 F194 F T195 T195 T ECL2ICL3 G238 G238 G R239 R239 R F240 F240 F H241 H241 H V242 V242 V Q243 Q243 Q N244 N244 N L245 L245 L S246 S246 S Q247 Q247 Q V248 V248 V E249 E249 E Q250 Q250 Q D251 D251 D G252 G252 G R253 R253 R T254 T254 T G255 G255 G H256 H256 H G257 G257 G L258 L258 L R259 R259 R R260 R260 R S261 S261 S ICL3ECL3 D300 D300 D N301 N301 N L302 L302 L I303 I303 I ECL3N-term M1 M1 M G2 G2 G Q3 Q3 Q P4 P4 P G5 G5 G N6 N6 N G7 G7 G S8 S8 S A9 A9 A F10 F10 F L11 L11 L L12 L12 L A13 A13 A P14 P14 P N15 N15 N G16 G16 G S17 S17 S H18 H18 H A19 A19 A P20 P20 P D21 D21 D H22 H22 H D23 D23 D V24 V24 V T25 T25 T N-termC-term L342 L342 L R343 R343 R R344 R344 R S345 S345 S S346 S346 S L347 L347 L K348 K348 K A349 A349 A Y350 Y350 Y G351 G351 G N352 N352 N G353 G353 G Y354 Y354 Y S355 S355 S S356 S356 S N357 N357 N G358 G358 G N359 N359 N T360 T360 T G361 G361 G E362 E362 E Q363 Q363 Q S364 S364 S G365 G365 G Y366 Y366 Y H367 H367 H V368 V368 V E369 E369 E Q370 Q370 Q E371 E371 E K372 K372 K E373 E373 E N374 N374 N K375 K375 K L376 L376 L L377 L377 L C378 C378 C E379 E379 E D380 D380 D L381 L381 L P382 P382 P G383 G383 G T384 T384 T E385 E385 E D386 D386 D F387 F387 F V388 V388 V G389 G389 G H390 H390 H Q391 Q391 Q G392 G392 G T393 T393 T V394 V394 V P395 P395 P S396 S396 S D397 D397 D N398 N398 N I399 I399 I D400 D400 D S401 S401 S Q402 Q402 Q G403 G403 G R404 R404 R N405 N405 N C406 C406 C S407 S407 S T408 T408 T N409 N409 N D410 D410 D S411 S411 S L412 L412 L L413 L413 L C-term Q26 1.25x25 Q26 1.25x25 Q E27 1.26x26 E27 1.26x26 E R28 1.27x27 R28 1.27x27 R D29 1.28x28 D29 1.28x28 D E30 1.29x29 E30 1.29x29 E V31 1.30x30 V31 1.30x30 V W32 1.31x31 W32 1.31x31 W V33 1.32x32 V33 1.32x32 V V34 1.33x33 V34 1.33x33 V G35 1.34x34 G35 1.34x34 G M36 1.35x35 M36 1.35x35 M G37 1.36x36 G37 1.36x36 G I38 1.37x37 I38 1.37x37 I V39 1.38x38 V39 1.38x38 V M40 1.39x39 M40 1.39x39 M S41 1.40x40 S41 1.40x40 S L42 1.41x41 L42 1.41x41 L I43 1.42x42 I43 1.42x42 I V44 1.43x43 V44 1.43x43 V L45 1.44x44 L45 1.44x44 L A46 1.45x45 A46 1.45x45 A I47 1.46x46 I47 1.46x46 I V48 1.47x47 V48 1.47x47 V F49 1.48x48 F49 1.48x48 F G50 1.49x49 G50 1.49x49 G N51 1.50x50 N51 1.50x50 N V52 1.51x51 V52 1.51x51 V L53 1.52x52 L53 1.52x52 L V54 1.53x53 V54 1.53x53 V I55 1.54x54 I55 1.54x54 I T56 1.55x55 T56 1.55x55 T A57 1.56x56 A57 1.56x56 A I58 1.57x57 I58 1.57x57 I A59 1.58x58 A59 1.58x58 A K60 1.59x59 K60 1.59x59 K F61 1.60x60 F61 1.60x60 F T66 2.37x37 T66 2.37x37 T V67 2.38x38 V67 2.38x38 V T68 2.39x39 T68 2.39x39 T N69 2.40x40 N69 2.40x40 N Y70 2.41x41 Y70 2.41x41 Y F71 2.42x42 F71 2.42x42 F I72 2.43x43 I72 2.43x43 I T73 2.44x44 T73 2.44x44 T S74 2.45x45 S74 2.45x45 S L75 2.46x46 L75 2.46x46 L A76 2.47x47 A76 2.47x47 A C77 2.48x48 C77 2.48x48 C A78 2.49x49 A78 2.49x49 A D79 2.50x50 D79 2.50x50 D L80 2.51x51 L80 2.51x51 L V81 2.52x52 V81 2.52x52 V M82 2.53x53 M82 2.53x53 M G83 2.54x54 G83 2.54x54 G L84 2.55x55 L84 2.55x55 L A85 2.56x551 A85 2.56x551 A V86 2.57x56 V86 2.57x56 V V87 2.58x57 V87 2.58x57 V P88 2.59x58 P88 2.59x58 P F89 2.60x59 F89 2.60x59 F G90 2.61x60 G90 2.61x60 G A91 2.62x61 A91 2.62x61 A A92 2.63x62 A92 2.63x62 A H93 2.64x63 H93 2.64x63 H I94 2.65x64 I94 2.65x64 I L95 2.66x65 L95 2.66x65 L M96 2.67x66 M96 2.67x66 M K97 2.68x67 K97 2.68x67 K G102 3.21x21 G102 3.21x21 G N103 3.22x22 N103 3.22x22 N F104 3.23x23 F104 3.23x23 F W105 3.24x24 W105 3.24x24 W C106 3.25x25 C106 3.25x25 C E107 3.26x26 E107 3.26x26 E F108 3.27x27 F108 3.27x27 F W109 3.28x28 W109 3.28x28 W T110 3.29x29 T110 3.29x29 T S111 3.30x30 S111 3.30x30 S I112 3.31x31 I112 3.31x31 I D113 3.32x32 D113 3.32x32 D V114 3.33x33 V114 3.33x33 V L115 3.34x34 L115 3.34x34 L C116 3.35x35 C116 3.35x35 C V117 3.36x36 V117 3.36x36 V T118 3.37x37 T118 3.37x37 T A119 3.38x38 A119 3.38x38 A S120 3.39x39 S120 3.39x39 S I121 3.40x40 I121 3.40x40 I E122 3.41x41 E122 3.41x41 E T123 3.42x42 T123 3.42x42 T L124 3.43x43 L124 3.43x43 L C125 3.44x44 C125 3.44x44 C V126 3.45x45 V126 3.45x45 V I127 3.46x46 I127 3.46x46 I A128 3.47x47 A128 3.47x47 A V129 3.48x48 V129 3.48x48 V D130 3.49x49 D130 3.49x49 D R131 3.50x50 R131 3.50x50 R Y132 3.51x51 Y132 3.51x51 Y F133 3.52x52 F133 3.52x52 F A134 3.53x53 A134 3.53x53 A I135 3.54x54 I135 3.54x54 I T136 3.55x55 T136 3.55x55 T S137 3.56x56 S137 3.56x56 S T146 4.38x38 T146 4.38x38 T K147 4.39x39 K147 4.39x39 K N148 4.40x40 N148 4.40x40 N K149 4.41x41 K149 4.41x41 K A150 4.42x42 A150 4.42x42 A R151 4.43x43 R151 4.43x43 R V152 4.44x44 V152 4.44x44 V I153 4.45x45 I153 4.45x45 I I154 4.46x46 I154 4.46x46 I L155 4.47x47 L155 4.47x47 L M156 4.48x48 M156 4.48x48 M V157 4.49x49 V157 4.49x49 V W158 4.50x50 W158 4.50x50 W I159 4.51x51 I159 4.51x51 I V160 4.52x52 V160 4.52x52 V S161 4.53x53 S161 4.53x53 S G162 4.54x54 G162 4.54x54 G L163 4.55x55 L163 4.55x55 L T164 4.56x56 T164 4.56x56 T S165 4.57x57 S165 4.57x57 S F166 4.58x58 F166 4.58x58 F L167 4.59x59 L167 4.59x59 L P168 4.60x60 P168 4.60x60 P I169 4.61x61 I169 4.61x61 I Q170 4.62x62 Q170 4.62x62 Q M171 4.63x63 M171 4.63x63 M H172 4.64x64 H172 4.64x64 H N196 5.35x36 N196 5.35x36 N Q197 5.36x37 Q197 5.36x37 Q A198 5.37x38 A198 5.37x38 A Y199 5.38x39 Y199 5.38x39 Y A200 5.39x40 A200 5.39x40 A I201 5.40x41 I201 5.40x41 I A202 5.41x42 A202 5.41x42 A S203 5.42x43 S203 5.42x43 S S204 5.43x44 S204 5.43x44 S I205 5.44x45 I205 5.44x45 I V206 5.45x46 V206 5.45x46 V S207 5.46x461 S207 5.46x461 S F208 5.47x47 F208 5.47x47 F Y209 5.48x48 Y209 5.48x48 Y V210 5.49x49 V210 5.49x49 V P211 5.50x50 P211 5.50x50 P L212 5.51x51 L212 5.51x51 L V213 5.52x52 V213 5.52x52 V I214 5.53x53 I214 5.53x53 I M215 5.54x54 M215 5.54x54 M V216 5.55x55 V216 5.55x55 V F217 5.56x56 F217 5.56x56 F V218 5.57x57 V218 5.57x57 V Y219 5.58x58 Y219 5.58x58 Y S220 5.59x59 S220 5.59x59 S R221 5.60x60 R221 5.60x60 R V222 5.61x61 V222 5.61x61 V F223 5.62x62 F223 5.62x62 F Q224 5.63x63 Q224 5.63x63 Q E225 5.64x64 E225 5.64x64 E A226 5.65x65 A226 5.65x65 A K227 5.66x66 K227 5.66x66 K R228 5.67x67 R228 5.67x67 R Q229 5.68x68 Q229 5.68x68 Q L230 5.69x69 L230 5.69x69 L Q231 5.70x70 Q231 5.70x70 Q K232 5.71x71 K232 5.71x71 K I233 5.72x72 I233 5.72x72 I D234 5.73x73 D234 5.73x73 D K235 5.74x74 K235 5.74x74 K S236 5.75x75 S236 5.75x75 S E237 5.76x76 E237 5.76x76 E S262 6.24x24 S262 6.24x24 S K263 6.25x25 K263 6.25x25 K F264 6.26x26 F264 6.26x26 F C265 6.27x27 C265 6.27x27 C L266 6.28x28 L266 6.28x28 L K267 6.29x29 K267 6.29x29 K E268 6.30x30 E268 6.30x30 E H269 6.31x31 H269 6.31x31 H K270 6.32x32 K270 6.32x32 K A271 6.33x33 A271 6.33x33 A L272 6.34x34 L272 6.34x34 L K273 6.35x35 K273 6.35x35 K T274 6.36x36 T274 6.36x36 T L275 6.37x37 L275 6.37x37 L G276 6.38x38 G276 6.38x38 G I277 6.39x39 I277 6.39x39 I I278 6.40x40 I278 6.40x40 I M279 6.41x41 M279 6.41x41 M G280 6.42x42 G280 6.42x42 G T281 6.43x43 T281 6.43x43 T F282 6.44x44 F282 6.44x44 F T283 6.45x45 T283 6.45x45 T L284 6.46x46 L284 6.46x46 L C285 6.47x47 C285 6.47x47 C W286 6.48x48 W286 6.48x48 W L287 6.49x49 L287 6.49x49 L P288 6.50x50 P288 6.50x50 P F289 6.51x51 F289 6.51x51 F F290 6.52x52 F290 6.52x52 F I291 6.53x53 I291 6.53x53 I V292 6.54x54 V292 6.54x54 V N293 6.55x55 N293 6.55x55 N I294 6.56x56 I294 6.56x56 I V295 6.57x57 V295 6.57x57 V H296 6.58x58 H296 6.58x58 H V297 6.59x59 V297 6.59x59 V I298 6.60x60 I298 6.60x60 I Q299 6.61x61 Q299 6.61x61 Q R304 7.31x30 R304 7.31x30 R K305 7.32x31 K305 7.32x31 K E306 7.33x32 E306 7.33x32 E V307 7.34x33 V307 7.34x33 V Y308 7.35x34 Y308 7.35x34 Y I309 7.36x35 I309 7.36x35 I L310 7.37x36 L310 7.37x36 L L311 7.38x37 L311 7.38x37 L N312 7.39x38 N312 7.39x38 N W313 7.40x39 W313 7.40x39 W I314 7.41x40 I314 7.41x40 I G315 7.42x41 G315 7.42x41 G Y316 7.43x42 Y316 7.43x42 Y V317 7.44x43 V317 7.44x43 V N318 7.45x45 N318 7.45x45 N S319 7.46x46 S319 7.46x46 S G320 7.47x47 G320 7.47x47 G F321 7.48x48 F321 7.48x48 F N322 7.49x49 N322 7.49x49 N P323 7.50x50 P323 7.50x50 P L324 7.51x51 L324 7.51x51 L I325 7.52x52 I325 7.52x52 I Y326 7.53x53 Y326 7.53x53 Y C327 7.54x54 C327 7.54x54 C R328 7.55x55 R328 7.55x55 R S329 8.47x47 S329 8.47x47 S P330 8.48x48 P330 8.48x48 P D331 8.49x49 D331 8.49x49 D F336 8.54x54 F336 8.54x54 F Q337 8.55x55 Q337 8.55x55 Q E338 8.56x56 E338 8.56x56 E F332 8.50x50 F332 8.50x50 F R333 8.51x51 R333 8.51x51 R I334 8.52x52 I334 8.52x52 I A335 8.53x53 A335 8.53x53 A L339 8.57x57 L339 8.57x57 L L340 8.58x58 L340 8.58x58 L C341 8.59x59 C341 8.59x59 C

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 HIS390 GLN391 0.000 9.019 -9.019 HIGH
2 CYS327 (7.54x54) PHE332 (8.50x50) 8.836 0.000 +8.836 HIGH
3 PHE89 (2.60x59) TRP105 (3.24x24) 0.000 7.537 -7.537 HIGH
4 ARG259 GLU385 7.493 0.000 +7.493 HIGH
5 GLN337 (8.55x55) ARG343 8.257 1.501 +6.755 HIGH
6 GLU338 (8.56x56) ARG344 6.446 0.000 +6.446 HIGH
7 HIS241 ARG260 5.805 0.000 +5.805 HIGH
8 PHE282 (6.44x44) TRP286 (6.48x48) 0.874 6.602 -5.728 HIGH
9 ASP130 (3.49x49) ARG131 (3.50x50) 0.376 6.046 -5.670 HIGH
10 ILE72 (2.43x43) TYR326 (7.53x53) 0.566 6.119 -5.553 HIGH
11 PHE208 (5.47x47) PHE290 (6.52x52) 12.764 18.106 -5.342 HIGH
12 GLU237 (5.76x76) SER262 (6.24x24) 0.000 5.326 -5.326 HIGH
13 PHE282 (6.44x44) ASN318 (7.45x45) 1.012 6.234 -5.222 HIGH
14 TYR219 (5.58x58) GLY276 (6.38x38) 0.000 5.093 -5.093 HIGH
15 ARG63 (12.49x49) ILE334 (8.52x52) 0.000 5.040 -5.040 HIGH
16 TYR219 (5.58x58) LEU272 (6.34x34) 0.000 4.853 -4.853 MED
17 ASP410 SER411 0.000 4.583 -4.583 MED
18 TYR219 (5.58x58) MET279 (6.41x41) 1.398 5.745 -4.347 MED
19 ILE399 ASP400 4.178 0.000 +4.178 MED
20 GLU122 (3.41x41) SER161 (4.53x53) 1.248 5.101 -3.853 MED
21 ALA128 (3.47x47) TYR219 (5.58x58) 4.878 1.110 +3.768 MED
22 ILE135 (3.54x54) GLN229 (5.68x68) 0.000 3.757 -3.757 MED
23 ARG175 TYR185 6.462 10.205 -3.743 MED
24 LYS227 (5.66x66) GLU268 (6.30x30) 3.683 0.000 +3.683 MED
25 LEU230 (5.69x69) PHE264 (6.26x26) 3.496 0.000 +3.496 MED
26 LEU124 (3.43x43) TYR326 (7.53x53) 3.478 0.000 +3.478 MED
27 TRP99 (23.50x50) CYS191 (45.50x50) 4.131 7.567 -3.437 MED
28 LYS267 (6.29x29) ASP331 (8.49x49) 0.000 3.326 -3.326 MED
29 HIS93 (2.64x63) CYS191 (45.50x50) 3.174 0.092 +3.082 MED
30 GLN231 (5.70x70) PHE264 (6.26x26) 3.081 0.000 +3.081 MED
31 TRP99 (23.50x50) TRP109 1.158 4.147 -2.989 MED
32 VAL114 SER165 2.537 5.488 -2.951 MED
33 THR164 TYR199 2.943 0.000 +2.943 MED
34 ILE121 PHE282 (6.44x44) 1.786 4.690 -2.904 MED
35 TYR326 (7.53x53) PHE332 (8.50x50) 0.000 2.867 -2.867 MED
36 ASP79 SER120 3.204 0.349 +2.855 MED
37 ASN318 (7.45x45) ASN322 3.160 0.436 +2.724 MED
38 ARG63 (12.49x49) ASP331 (8.49x49) 0.000 2.607 -2.607 MED
39 VAL292 ILE303 3.642 1.041 +2.601 MED
40 ARG131 (3.50x50) TYR141 0.000 2.594 -2.594 MED
41 LEU64 PHE332 (8.50x50) 4.002 1.410 +2.592 MED
42 ASN148 ARG151 0.315 2.869 -2.554 MED
43 ILE121 PHE208 (5.47x47) 0.422 2.961 -2.539 MED
44 ILE121 TRP286 (6.48x48) 2.459 0.000 +2.459 MED
45 PHE10 LEU12 2.448 0.000 +2.448 MED
46 TRP286 (6.48x48) ASN318 (7.45x45) 3.042 0.605 +2.437 MED
47 TRP105 (3.24x24) PHE108 2.312 4.733 -2.421 MED
48 THR68 ARG131 (3.50x50) 2.882 5.287 -2.405 MED
49 GLY50 PRO323 2.294 4.696 -2.403 MED
50 MET279 (6.41x41) PHE282 (6.44x44) 2.398 0.000 +2.398 MED
51 ILE121 SER207 3.763 1.375 +2.387 MED
52 GLU338 (8.56x56) ARG343 0.715 3.095 -2.380 MED
53 ILE325 TYR326 (7.53x53) 2.367 0.000 +2.367 MED
54 LEU53 PHE336 4.567 6.905 -2.338 MED
55 PHE264 (6.26x26) GLU268 (6.30x30) 9.020 6.688 +2.332 MED
56 GLU225 GLN229 (5.68x68) 3.134 0.818 +2.316 MED
57 LEU381 PRO382 2.311 0.000 +2.311 MED
58 HIS93 (2.64x63) MET98 4.477 6.781 -2.304 MED
59 CYS125 ILE214 2.264 0.000 +2.264 MED
60 TYR70 ILE154 0.110 2.353 -2.243 MED
61 PHE289 TYR308 5.007 7.221 -2.214 MED
62 LEU230 (5.69x69) LYS267 (6.29x29) 2.206 0.000 +2.206 MED
63 THR68 ASP130 (3.49x49) 5.175 3.014 +2.161 MED
64 ALA128 (3.47x47) MET279 (6.41x41) 0.000 2.125 -2.125 MED
65 PHE223 LEU272 (6.34x34) 2.124 0.000 +2.124 MED
66 GLN65 LYS147 1.440 3.528 -2.088 MED
67 MET82 VAL86 2.375 0.289 +2.086 MED
68 LEU144 LYS149 1.778 3.844 -2.066 MED
69 GLN229 (5.68x68) LYS232 2.063 0.000 +2.063 MED
70 THR274 ILE325 0.000 2.056 -2.056 MED
71 MET215 PHE282 (6.44x44) 2.048 0.000 +2.048 MED
72 LEU230 (5.69x69) GLU268 (6.30x30) 1.983 0.000 +1.983 MED
73 GLN337 (8.55x55) LEU342 5.053 3.102 +1.951 LOW
74 GLN197 VAL297 2.984 4.928 -1.944 LOW
75 ASN103 ASN187 4.365 2.427 +1.938 LOW
76 MET40 TRP313 5.796 7.725 -1.929 LOW
77 PHE71 ASP130 (3.49x49) 3.713 1.791 +1.922 LOW
78 ARG63 (12.49x49) ALA335 0.000 1.915 -1.915 LOW
79 TYR174 TYR199 4.665 6.571 -1.906 LOW
80 VAL117 TRP286 (6.48x48) 3.438 5.336 -1.898 LOW
81 TYR132 PHE133 1.851 0.000 +1.851 LOW
82 SER356 ASN357 0.000 1.849 -1.849 LOW
83 ILE135 (3.54x54) LEU272 (6.34x34) 0.000 1.829 -1.829 LOW
84 PHE223 LEU275 1.828 0.000 +1.828 LOW
85 TYR141 LEU145 3.169 1.356 +1.813 LOW
86 PHE101 TRP105 (3.24x24) 1.175 2.984 -1.809 LOW
87 TYR219 (5.58x58) ILE278 1.806 0.000 +1.806 LOW
88 VAL54 TYR326 (7.53x53) 0.000 1.804 -1.804 LOW
89 TYR70 ARG151 5.145 3.341 +1.804 LOW
90 LEU124 (3.43x43) ASN322 1.786 0.000 +1.786 LOW
91 ILE334 (8.52x52) GLU338 (8.56x56) 0.000 1.782 -1.782 LOW
92 ALA119 TRP158 1.778 0.000 +1.778 LOW
93 THR281 ASN318 (7.45x45) 1.378 3.113 -1.734 LOW
94 LEU124 (3.43x43) PHE282 (6.44x44) 1.295 3.024 -1.728 LOW
95 ILE121 LEU212 0.000 1.726 -1.726 LOW
96 CYS327 (7.54x54) ARG333 0.000 1.722 -1.722 LOW
97 PHE289 ASN312 7.946 6.226 +1.720 LOW
98 GLN26 GLU30 1.103 2.820 -1.717 LOW
99 TYR219 (5.58x58) LEU275 1.966 3.670 -1.705 LOW
100 SER204 PHE290 (6.52x52) 3.261 1.567 +1.694 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| ≥ 1.97 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 - - 0 - 0
TM2 72-93 93 (3.1) 1 89 (-7.5), 72 (-5.6) 2
TM3 105-135 128 (3.8), 124 (3.5) 2 105 (-7.5), 130 (-5.7), 131 (-5.7), 122 (-3.9), 135 (-3.8) 5
TM4 161-161 - 0 161 (-3.9) 1
TM5 208-237 227 (3.7), 230 (3.5), 231 (3.1) 3 208 (-5.3), 237 (-5.3), 219 (-5.1), 229 (-3.8) 4
TM6 262-290 268 (3.7), 264 (3.5) 2 282 (-5.7), 286 (-5.7), 290 (-5.3), 262 (-5.3), 276 (-5.1), 272 (-4.9), 279 (-4.3), 267 (-3.3) 8
TM7 318-327 327 (8.8) 1 326 (-5.6), 318 (-5.2) 2
Intracellular / Extracellular loops & H8
ICL1 63-63 - 0 63 (-5.0) 1
ICL2 - - 0 - 0
ICL3 241-260 259 (7.5), 241 (5.8), 260 (5.8) 3 - 0
ECL1 99-99 - 0 99 (-3.4) 1
ECL2 175-191 - 0 175 (-3.7), 185 (-3.7), 191 (-3.4) 3
ECL3 - - 0 - 0
H8 331-338 332 (8.8), 337 (6.8), 338 (6.4) 3 334 (-5.0), 331 (-3.3) 2

Interactive visualizations

ΔRRCS distribution

Active vs inactive comparison

Residue-wise changes

TM domain breakdown

Variants of interest

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

Position Protein change DNA change Allele freq Het / Hom ΔRRCS AM score Pathogenicity Conservation dbSNP
391 p.Gln391Pro c.1172A>C 6.92e-07 1 / 0 9.02 0.060 BENIGN 0.48
390 p.His390Arg c.1169A>G 1.38e-06 2 / 0 9.02 0.054 BENIGN 0.40 rs1296785467
89 p.Phe89Leu c.265T>C 6.84e-07 1 / 0 7.54 0.946 PATHOGENIC 0.52 rs145233416
105 p.Trp105Ser c.314G>C 6.84e-07 1 / 0 7.54 0.481 AMBIGUOUS 0.26
89 p.Phe89Val c.265T>G 6.84e-07 1 / 0 7.54 - nan -
105 p.Trp105Cys c.315G>C 6.84e-07 1 / 0 7.54 - nan -
259 p.Arg259Cys c.775C>T 4.10e-06 6 / 0 7.49 0.195 BENIGN 0.66 rs765634337
259 p.Arg259His c.776G>A 1.09e-05 16 / 0 7.49 - nan - rs201323763
343 p.Arg343Ser c.1027C>A 1.37e-06 2 / 0 6.76 0.355 AMBIGUOUS 0.56 rs1209605702
337 p.Gln337Arg c.1010A>G 3.42e-06 5 / 0 6.76 0.090 BENIGN 0.50 rs1329127387
343 p.Arg343Cys c.1027C>T 2.05e-06 3 / 0 6.76 - nan - rs1209605702
343 p.Arg343Leu c.1028G>T 1.37e-06 2 / 0 6.76 - nan -
343 p.Arg343His c.1028G>A 2.74e-06 4 / 0 6.76 - nan - rs748580918
338 p.Glu338Asp c.1014G>C 3.42e-06 5 / 0 6.45 0.259 BENIGN 0.45
344 p.Arg344Lys c.1031G>A 6.57e-06 1 / 0 6.45 0.074 BENIGN 0.66 rs2127360047
260 p.Arg260Thr c.779G>C 2.05e-06 3 / 0 5.80 0.440 AMBIGUOUS 0.50 rs1362685333
260 p.Arg260Ser c.780A>T 6.84e-07 1 / 0 5.80 - nan -
260 p.Arg260Ser c.780A>C 1.37e-06 2 / 0 5.80 - nan -
130 p.Asp130Asn c.388G>A 6.84e-07 1 / 0 5.67 0.990 PATHOGENIC 0.99
131 p.Arg131Cys c.391C>T 2.05e-06 3 / 0 5.67 0.979 PATHOGENIC 1.00
131 p.Arg131Leu c.392G>T 6.84e-07 1 / 0 5.67 - nan -
131 p.Arg131His c.392G>A 1.37e-06 2 / 0 5.67 - nan -
326 p.Tyr326Cys c.977A>G 6.84e-07 1 / 0 5.55 0.983 PATHOGENIC 0.98
72 p.Ile72Val c.214A>G 1.37e-06 2 / 0 5.55 0.241 BENIGN 0.82
208 p.Phe208Leu c.622T>C 3.42e-06 5 / 0 5.34 0.999 PATHOGENIC 0.98
290 p.Phe290Val c.868T>G 6.57e-06 1 / 0 5.34 0.994 PATHOGENIC 0.98 rs749002771
237 p.Glu237Lys c.709G>A 2.74e-06 4 / 0 5.33 0.230 BENIGN 0.60 rs1204656662
262 p.Ser262Cys c.785C>G 6.84e-07 1 / 0 5.33 0.177 BENIGN 0.44
276 p.Gly276Ser c.826G>A 6.84e-07 1 / 0 5.09 0.855 PATHOGENIC 0.81 rs751770115
276 p.Gly276Asp c.827G>A 6.84e-07 1 / 0 5.09 - nan -
63 p.Arg63Gly c.187C>G 5.47e-06 8 / 0 5.04 0.755 PATHOGENIC 0.71
334 p.Ile334Asn c.1001T>A 2.19e-05 32 / 0 5.04 0.140 BENIGN 0.35 rs746492442
63 p.Arg63His c.188G>A 1.37e-06 2 / 0 5.04 - nan - rs1156310662
334 p.Ile334Met c.1002T>G 6.57e-06 1 / 0 5.04 - nan - rs1411817844
410 p.Asp410Ala c.1229A>C 1.40e-06 2 / 0 4.58 0.111 BENIGN 0.75 rs746434318
400 p.Asp400Ala c.1199A>C 5.58e-06 8 / 0 4.18 0.096 BENIGN 0.68 rs1186444145
161 p.Ser161Leu c.482C>T 6.84e-07 1 / 0 3.85 0.956 PATHOGENIC 0.82
122 p.Glu122Asp c.366G>C 6.84e-07 1 / 0 3.85 0.884 PATHOGENIC 0.59
128 p.Ala128Thr c.382G>A 2.05e-06 3 / 0 3.77 0.942 PATHOGENIC 0.76 rs149199162
128 p.Ala128Ser c.382G>T 5.34e-05 78 / 0 3.77 - nan - rs149199162
128 p.Ala128Val c.383C>T 6.84e-07 1 / 0 3.77 - nan -
135 p.Ile135Val c.403A>G 6.84e-07 1 / 0 3.76 0.241 BENIGN 0.89
175 p.Arg175Gly c.523C>G 6.84e-07 1 / 0 3.74 0.716 PATHOGENIC 0.70
185 p.Tyr185Cys c.554A>G 6.84e-07 1 / 0 3.74 0.622 PATHOGENIC 0.55
175 p.Arg175Trp c.523C>T 6.84e-07 1 / 0 3.74 - nan - rs1042718
227 p.Lys227Gln c.679A>C 6.84e-07 1 / 0 3.68 0.115 BENIGN 0.51
227 p.Lys227Glu c.679A>G 2.74e-06 4 / 0 3.68 - nan - rs972763826
227 p.Lys227Arg c.680A>G 2.05e-06 3 / 0 3.68 - nan -
264 p.Phe264Ser c.791T>C 6.84e-07 1 / 0 3.50 0.757 PATHOGENIC 0.55 rs1304524860
264 p.Phe264Leu c.792C>A 2.05e-06 3 / 0 3.50 - nan -
267 p.Lys267Glu c.799A>G 2.05e-06 3 / 0 3.33 0.847 PATHOGENIC 0.79
267 p.Lys267Asn c.801G>C 2.60e-05 38 / 0 3.33 - nan - rs1041227804
231 p.Gln231Arg c.692A>G 6.84e-07 1 / 0 3.08 0.066 BENIGN 0.64

Complete RRCS results

Top 1000 contact pairs by |ΔRRCS|. Significance threshold: |ΔRRCS| ≥ 1.97, computed as max(mean(|Δ|) + σ, 0.2). Highlighted rows indicate significant changes.

Res1 AA1 Res2 AA2 Active RRCS Inactive RRCS ΔRRCS |ΔRRCS|
390 HIS 391 GLN 0.000 9.019 -9.019 9.019
327 CYS 332 PHE 8.836 0.000 8.836 8.836
89 PHE 105 TRP 0.000 7.537 -7.537 7.537
259 ARG 385 GLU 7.493 0.000 7.493 7.493
337 GLN 343 ARG 8.257 1.501 6.755 6.755
338 GLU 344 ARG 6.446 0.000 6.446 6.446
241 HIS 260 ARG 5.805 0.000 5.805 5.805
282 PHE 286 TRP 0.874 6.602 -5.728 5.728
130 ASP 131 ARG 0.376 6.046 -5.670 5.670
72 ILE 326 TYR 0.566 6.119 -5.553 5.553
208 PHE 290 PHE 12.764 18.106 -5.342 5.342
237 GLU 262 SER 0.000 5.326 -5.326 5.326
282 PHE 318 ASN 1.012 6.234 -5.222 5.222
219 TYR 276 GLY 0.000 5.093 -5.093 5.093
63 ARG 334 ILE 0.000 5.040 -5.040 5.040
219 TYR 272 LEU 0.000 4.853 -4.853 4.853
410 ASP 411 SER 0.000 4.583 -4.583 4.583
219 TYR 279 MET 1.398 5.745 -4.347 4.347
399 ILE 400 ASP 4.178 0.000 4.178 4.178
122 GLU 161 SER 1.248 5.101 -3.853 3.853
128 ALA 219 TYR 4.878 1.110 3.768 3.768
135 ILE 229 GLN 0.000 3.757 -3.757 3.757
175 ARG 185 TYR 6.462 10.205 -3.743 3.743
227 LYS 268 GLU 3.683 0.000 3.683 3.683
230 LEU 264 PHE 3.496 0.000 3.496 3.496
124 LEU 326 TYR 3.478 0.000 3.478 3.478
99 TRP 191 CYS 4.131 7.567 -3.437 3.437
267 LYS 331 ASP 0.000 3.326 -3.326 3.326
93 HIS 191 CYS 3.174 0.092 3.082 3.082
231 GLN 264 PHE 3.081 0.000 3.081 3.081
99 TRP 109 TRP 1.158 4.147 -2.989 2.989
114 VAL 165 SER 2.537 5.488 -2.951 2.951
164 THR 199 TYR 2.943 0.000 2.943 2.943
121 ILE 282 PHE 1.786 4.690 -2.904 2.904
326 TYR 332 PHE 0.000 2.867 -2.867 2.867
79 ASP 120 SER 3.204 0.349 2.855 2.855
318 ASN 322 ASN 3.160 0.436 2.724 2.724
63 ARG 331 ASP 0.000 2.607 -2.607 2.607
292 VAL 303 ILE 3.642 1.041 2.601 2.601
131 ARG 141 TYR 0.000 2.594 -2.594 2.594
64 LEU 332 PHE 4.002 1.410 2.592 2.592
148 ASN 151 ARG 0.315 2.869 -2.554 2.554
121 ILE 208 PHE 0.422 2.961 -2.539 2.539
121 ILE 286 TRP 2.459 0.000 2.459 2.459
10 PHE 12 LEU 2.448 0.000 2.448 2.448
286 TRP 318 ASN 3.042 0.605 2.437 2.437
105 TRP 108 PHE 2.312 4.733 -2.421 2.421
68 THR 131 ARG 2.882 5.287 -2.405 2.405
50 GLY 323 PRO 2.294 4.696 -2.403 2.403
279 MET 282 PHE 2.398 0.000 2.398 2.398
121 ILE 207 SER 3.763 1.375 2.387 2.387
338 GLU 343 ARG 0.715 3.095 -2.380 2.380
325 ILE 326 TYR 2.367 0.000 2.367 2.367
53 LEU 336 PHE 4.567 6.905 -2.338 2.338
264 PHE 268 GLU 9.020 6.688 2.332 2.332
225 GLU 229 GLN 3.134 0.818 2.316 2.316
381 LEU 382 PRO 2.311 0.000 2.311 2.311
93 HIS 98 MET 4.477 6.781 -2.304 2.304
125 CYS 214 ILE 2.264 0.000 2.264 2.264
70 TYR 154 ILE 0.110 2.353 -2.243 2.243
289 PHE 308 TYR 5.007 7.221 -2.214 2.214
230 LEU 267 LYS 2.206 0.000 2.206 2.206
68 THR 130 ASP 5.175 3.014 2.161 2.161
128 ALA 279 MET 0.000 2.125 -2.125 2.125
223 PHE 272 LEU 2.124 0.000 2.124 2.124
65 GLN 147 LYS 1.440 3.528 -2.088 2.088
82 MET 86 VAL 2.375 0.289 2.086 2.086
144 LEU 149 LYS 1.778 3.844 -2.066 2.066
229 GLN 232 LYS 2.063 0.000 2.063 2.063
274 THR 325 ILE 0.000 2.056 -2.056 2.056
215 MET 282 PHE 2.048 0.000 2.048 2.048
230 LEU 268 GLU 1.983 0.000 1.983 1.983
337 GLN 342 LEU 5.053 3.102 1.951 1.951
197 GLN 297 VAL 2.984 4.928 -1.944 1.944
103 ASN 187 ASN 4.365 2.427 1.938 1.938
40 MET 313 TRP 5.796 7.725 -1.929 1.929
71 PHE 130 ASP 3.713 1.791 1.922 1.922
63 ARG 335 ALA 0.000 1.915 -1.915 1.915
174 TYR 199 TYR 4.665 6.571 -1.906 1.906
117 VAL 286 TRP 3.438 5.336 -1.898 1.898
132 TYR 133 PHE 1.851 0.000 1.851 1.851
356 SER 357 ASN 0.000 1.849 -1.849 1.849
135 ILE 272 LEU 0.000 1.829 -1.829 1.829
223 PHE 275 LEU 1.828 0.000 1.828 1.828
141 TYR 145 LEU 3.169 1.356 1.813 1.813
101 PHE 105 TRP 1.175 2.984 -1.809 1.809
219 TYR 278 ILE 1.806 0.000 1.806 1.806
54 VAL 326 TYR 0.000 1.804 -1.804 1.804
70 TYR 151 ARG 5.145 3.341 1.804 1.804
124 LEU 322 ASN 1.786 0.000 1.786 1.786
334 ILE 338 GLU 0.000 1.782 -1.782 1.782
119 ALA 158 TRP 1.778 0.000 1.778 1.778
281 THR 318 ASN 1.378 3.113 -1.734 1.734
124 LEU 282 PHE 1.295 3.024 -1.728 1.728
121 ILE 212 LEU 0.000 1.726 -1.726 1.726
327 CYS 333 ARG 0.000 1.722 -1.722 1.722
289 PHE 312 ASN 7.946 6.226 1.720 1.720
26 GLN 30 GLU 1.103 2.820 -1.717 1.717
219 TYR 275 LEU 1.966 3.670 -1.705 1.705
204 SER 290 PHE 3.261 1.567 1.694 1.694
131 ARG 275 LEU 0.000 1.668 -1.668 1.668
208 PHE 287 LEU 4.924 3.272 1.653 1.653
131 ARG 134 ALA 0.000 1.642 -1.642 1.642
75 LEU 123 THR 2.910 1.281 1.629 1.629
54 VAL 327 CYS 1.628 0.000 1.628 1.628
47 ILE 319 SER 1.321 2.905 -1.584 1.584
277 ILE 328 ARG 0.559 2.138 -1.579 1.579
146 THR 149 LYS 0.678 2.246 -1.568 1.568
74 SER 154 ILE 3.680 2.129 1.550 1.550
385 GLU 386 ASP 0.000 1.548 -1.548 1.548
75 LEU 124 LEU 2.159 0.622 1.537 1.537
212 LEU 283 THR 0.250 1.782 -1.532 1.532
174 TYR 193 PHE 0.109 1.637 -1.528 1.528
233 ILE 265 CYS 0.000 1.506 -1.506 1.506
277 ILE 325 ILE 0.426 1.891 -1.465 1.465
99 TRP 105 TRP 2.018 3.478 -1.460 1.460
131 ARG 222 VAL 0.000 1.448 -1.448 1.448
134 ALA 141 TYR 6.086 7.493 -1.407 1.407
165 SER 166 PHE 1.585 0.183 1.402 1.402
20 PRO 22 HIS 1.399 0.000 1.399 1.399
29 ASP 97 LYS 0.000 1.398 -1.398 1.398
124 LEU 279 MET 0.000 1.375 -1.375 1.375
215 MET 279 MET 2.295 3.661 -1.367 1.367
234 ASP 264 PHE 1.366 0.000 1.366 1.366
99 TRP 189 THR 8.084 9.449 -1.365 1.365
274 THR 328 ARG 0.000 1.356 -1.356 1.356
278 ILE 326 TYR 1.451 2.805 -1.354 1.354
213 VAL 217 PHE 1.344 0.000 1.344 1.344
89 PHE 109 TRP 3.337 1.997 1.339 1.339
13 ALA 14 PRO 0.509 1.839 -1.330 1.330
278 ILE 322 ASN 0.000 1.322 -1.322 1.322
130 ASP 141 TYR 7.932 6.613 1.319 1.319
135 ILE 222 VAL 0.894 2.212 -1.318 1.318
132 TYR 136 THR 5.136 3.829 1.307 1.307
127 ILE 279 MET 0.000 1.301 -1.301 1.301
168 PRO 199 TYR 3.165 1.865 1.300 1.300
199 TYR 203 SER 1.966 3.265 -1.298 1.298
77 CYS 158 TRP 0.130 1.424 -1.293 1.293
67 VAL 141 TYR 0.000 1.288 -1.288 1.288
132 TYR 222 VAL 1.497 2.761 -1.265 1.265
286 TRP 312 ASN 0.199 1.460 -1.261 1.261
125 CYS 211 PRO 2.159 3.407 -1.249 1.249
118 THR 207 SER 5.258 4.023 1.235 1.235
89 PHE 101 PHE 3.553 4.767 -1.214 1.214
240 PHE 243 GLN 0.000 1.213 -1.213 1.213
131 ARG 272 LEU 0.000 1.201 -1.201 1.201
221 ARG 224 GLN 2.659 1.462 1.197 1.197
359 ASN 360 THR 0.236 1.424 -1.187 1.187
238 GLY 260 ARG 1.175 0.000 1.175 1.175
285 CYS 318 ASN 3.230 2.060 1.170 1.170
115 LEU 161 SER 3.687 2.521 1.166 1.166
79 ASP 322 ASN 4.388 3.222 1.166 1.166
69 ASN 332 PHE 2.889 1.724 1.166 1.166
65 GLN 70 TYR 0.000 1.163 -1.163 1.163
215 MET 219 TYR 1.139 0.000 1.139 1.139
296 HIS 303 ILE 1.605 0.469 1.136 1.136
241 HIS 245 LEU 0.301 1.414 -1.114 1.114
279 MET 283 THR 1.111 0.000 1.111 1.111
286 TRP 316 TYR 0.897 1.997 -1.100 1.100
120 SER 282 PHE 0.000 1.086 -1.086 1.086
219 TYR 222 VAL 0.000 1.077 -1.077 1.077
185 TYR 194 PHE 4.492 5.565 -1.073 1.073
283 THR 287 LEU 1.502 0.439 1.063 1.063
107 GLU 174 TYR 1.430 2.485 -1.056 1.056
384 THR 385 GLU 0.000 1.046 -1.046 1.046
79 ASP 319 SER 12.100 11.061 1.039 1.039
164 THR 206 VAL 1.271 0.232 1.039 1.039
125 CYS 215 MET 2.612 1.574 1.038 1.038
178 HIS 194 PHE 3.571 2.541 1.029 1.029
115 LEU 165 SER 5.365 4.341 1.023 1.023
122 GLU 206 VAL 1.021 0.000 1.021 1.021
225 GLU 228 ARG 2.769 3.786 -1.017 1.017
99 TRP 101 PHE 5.387 6.400 -1.013 1.013
208 PHE 282 PHE 1.732 0.723 1.009 1.009
68 THR 141 TYR 1.311 0.308 1.004 1.004
93 HIS 99 TRP 2.657 3.653 -0.996 0.996
114 VAL 199 TYR 0.991 0.000 0.991 0.991
163 LEU 168 PRO 2.269 1.284 0.985 0.985
127 ILE 326 TYR 0.964 0.000 0.964 0.964
111 SER 166 PHE 6.481 7.444 -0.962 0.962
61 PHE 338 GLU 4.544 3.593 0.951 0.951
167 LEU 173 TRP 1.966 2.901 -0.935 0.935
208 PHE 286 TRP 3.264 2.330 0.933 0.933
32 TRP 36 MET 5.471 4.539 0.932 0.932
122 GLU 160 VAL 3.125 2.194 0.930 0.930
266 LEU 270 LYS 0.000 0.924 -0.924 0.924
71 PHE 150 ALA 2.975 2.056 0.919 0.919
217 PHE 221 ARG 0.000 0.904 -0.904 0.904
169 ILE 199 TYR 1.868 0.968 0.900 0.900
393 THR 394 VAL 0.450 1.349 -0.899 0.899
75 LEU 79 ASP 1.823 0.927 0.896 0.896
395 PRO 396 SER 0.211 1.106 -0.895 0.895
82 MET 319 SER 0.950 1.842 -0.892 0.892
259 ARG 263 LYS 0.000 0.889 -0.889 0.889
127 ILE 275 LEU 0.000 0.882 -0.882 0.882
111 SER 165 SER 1.876 0.996 0.881 0.881
212 LEU 282 PHE 0.876 0.000 0.876 0.876
99 TRP 106 CYS 5.277 6.141 -0.864 0.864
58 ILE 69 ASN 1.182 2.044 -0.862 0.862
135 ILE 225 GLU 0.403 1.258 -0.855 0.855
278 ILE 325 ILE 1.276 2.123 -0.847 0.847
118 THR 165 SER 0.000 0.828 -0.828 0.828
71 PHE 126 VAL 2.686 3.506 -0.820 0.820
215 MET 283 THR 0.000 0.818 -0.818 0.818
75 LEU 322 ASN 2.612 1.807 0.805 0.805
271 ALA 413 LEU 0.801 0.000 0.801 0.801
162 GLY 167 LEU 1.270 0.473 0.796 0.796
329 SER 332 PHE 2.601 1.812 0.789 0.789
86 VAL 113 ASP 4.779 4.011 0.768 0.768
327 CYS 336 PHE 2.110 1.345 0.765 0.765
59 ALA 65 GLN 0.967 1.730 -0.764 0.764
36 MET 40 MET 0.000 0.758 -0.758 0.758
332 PHE 336 PHE 2.674 1.928 0.745 0.745
237 GLU 258 LEU 0.000 0.743 -0.743 0.743
117 VAL 121 ILE 0.736 0.000 0.736 0.736
179 GLN 183 ASN 3.441 4.173 -0.732 0.732
192 ASP 305 LYS 5.812 5.081 0.730 0.730
61 PHE 335 ALA 6.791 6.062 0.729 0.729
129 VAL 218 VAL 0.844 1.572 -0.728 0.728
362 GLU 363 GLN 0.943 0.218 0.725 0.725
273 LYS 328 ARG 0.000 0.724 -0.724 0.724
121 ILE 290 PHE 0.723 0.000 0.723 0.723
107 GLU 169 ILE 1.246 1.968 -0.722 0.722
71 PHE 127 ILE 1.582 2.299 -0.717 0.717
208 PHE 212 LEU 1.997 1.281 0.716 0.716
286 TRP 289 PHE 0.325 1.034 -0.709 0.709
70 TYR 147 LYS 0.000 0.709 -0.709 0.709
120 SER 322 ASN 0.706 0.000 0.706 0.706
192 ASP 194 PHE 1.988 2.692 -0.704 0.704
145 LEU 150 ALA 0.024 0.728 -0.704 0.704
222 VAL 272 LEU 0.000 0.696 -0.696 0.696
398 ASN 399 ILE 0.914 0.220 0.694 0.694
84 LEU 89 PHE 0.000 0.694 -0.694 0.694
177 THR 182 ILE 1.446 2.138 -0.691 0.691
233 ILE 237 GLU 1.184 0.494 0.691 0.691
92 ALA 101 PHE 0.000 0.686 -0.686 0.686
67 VAL 130 ASP 0.000 0.686 -0.686 0.686
110 THR 193 PHE 1.624 2.308 -0.684 0.684
82 MET 316 TYR 2.657 1.977 0.680 0.680
124 LEU 278 ILE 0.000 0.680 -0.680 0.680
135 ILE 226 ALA 0.000 0.679 -0.679 0.679
226 ALA 272 LEU 0.000 0.677 -0.677 0.677
176 ALA 194 PHE 1.543 0.866 0.677 0.677
289 PHE 290 PHE 1.524 0.847 0.676 0.676
285 CYS 314 ILE 4.531 5.207 -0.676 0.676
281 THR 325 ILE 1.732 1.060 0.672 0.672
401 SER 402 GLN 0.000 0.663 -0.663 0.663
334 ILE 343 ARG 1.962 1.300 0.662 0.662
115 LEU 166 PHE 1.966 1.310 0.656 0.656
75 LEU 127 ILE 0.654 0.000 0.654 0.654
129 VAL 214 ILE 0.652 0.000 0.652 0.652
196 ASN 199 TYR 1.189 1.834 -0.645 0.645
128 ALA 222 VAL 0.000 0.645 -0.645 0.645
340 LEU 342 LEU 0.475 1.116 -0.641 0.641
212 LEU 215 MET 0.000 0.638 -0.638 0.638
240 PHE 258 LEU 0.000 0.633 -0.633 0.633
118 THR 164 THR 1.164 0.534 0.629 0.629
299 GLN 302 LEU 1.462 2.087 -0.624 0.624
209 TYR 291 ILE 1.715 2.336 -0.622 0.622
98 MET 100 THR 0.035 0.657 -0.622 0.622
219 TYR 326 TYR 0.613 0.000 0.613 0.613
103 ASN 188 GLU 6.028 5.417 0.611 0.611
117 VAL 290 PHE 0.261 0.871 -0.610 0.610
58 ILE 64 LEU 1.393 2.001 -0.609 0.609
72 ILE 127 ILE 0.941 0.332 0.608 0.608
328 ARG 333 ARG 0.597 0.000 0.597 0.597
98 MET 189 THR 2.354 2.947 -0.593 0.593
201 ILE 297 VAL 0.032 0.621 -0.589 0.589
3 GLN 4 PRO 0.979 0.390 0.589 0.589
135 ILE 412 LEU 0.588 0.000 0.588 0.588
160 VAL 206 VAL 0.588 0.000 0.588 0.588
19 ALA 20 PRO 0.587 0.000 0.587 0.587
184 CYS 190 CYS 8.554 9.133 -0.578 0.578
136 THR 137 SER 0.535 1.111 -0.576 0.576
48 VAL 83 GLY 2.160 1.586 0.574 0.574
87 VAL 313 TRP 2.461 1.888 0.573 0.573
333 ARG 337 GLN 0.000 0.569 -0.569 0.569
78 ALA 116 CYS 1.438 2.004 -0.566 0.566
409 ASN 410 ASP 0.000 0.564 -0.564 0.564
174 TYR 185 TYR 0.592 1.155 -0.564 0.564
80 LEU 84 LEU 2.133 1.572 0.561 0.561
32 TRP 94 ILE 0.000 0.559 -0.559 0.559
230 LEU 265 CYS 0.000 0.556 -0.556 0.556
40 MET 91 ALA 2.415 2.965 -0.550 0.550
295 VAL 303 ILE 0.675 0.126 0.549 0.549
283 THR 288 PRO 0.842 0.299 0.543 0.543
387 PHE 388 VAL 0.000 0.539 -0.539 0.539
117 VAL 282 PHE 0.000 0.538 -0.538 0.538
168 PRO 174 TYR 2.263 1.728 0.535 0.535
56 THR 60 LYS 1.652 1.121 0.531 0.531
165 SER 199 TYR 0.531 0.000 0.531 0.531
133 PHE 138 PRO 0.760 0.235 0.525 0.525
313 TRP 316 TYR 0.948 1.472 -0.524 0.524
292 VAL 308 TYR 0.850 0.329 0.521 0.521
174 TYR 175 ARG 1.763 2.281 -0.518 0.518
323 PRO 336 PHE 0.000 0.517 -0.517 0.517
72 ILE 327 CYS 0.516 0.000 0.516 0.516
104 PHE 105 TRP 0.512 0.000 0.512 0.512
51 ASN 80 LEU 1.919 1.414 0.506 0.506
86 VAL 109 TRP 4.870 5.375 -0.504 0.504
167 LEU 171 MET 0.000 0.503 -0.503 0.503
96 MET 100 THR 1.073 1.573 -0.500 0.500
203 SER 207 SER 0.000 0.496 -0.496 0.496
109 TRP 110 THR 1.028 1.523 -0.495 0.495
47 ILE 316 TYR 1.319 0.825 0.494 0.494
168 PRO 173 TRP 6.251 5.759 0.492 0.492
379 GLU 380 ASP 0.492 0.000 0.492 0.492
236 SER 240 PHE 0.000 0.490 -0.490 0.490
85 ALA 109 TRP 1.366 1.852 -0.487 0.487
176 ALA 196 ASN 1.646 2.132 -0.486 0.486
71 PHE 123 THR 1.451 1.930 -0.479 0.479
171 MET 173 TRP 4.219 3.740 0.479 0.479
164 THR 207 SER 0.000 0.478 -0.478 0.478
282 PHE 283 THR 0.477 0.000 0.477 0.477
140 LYS 144 LEU 0.280 0.749 -0.469 0.469
207 SER 290 PHE 0.469 0.000 0.469 0.469
193 PHE 199 TYR 0.409 0.877 -0.468 0.468
303 ILE 307 VAL 0.621 1.089 -0.468 0.468
155 LEU 159 ILE 1.277 0.810 0.467 0.467
51 ASN 76 ALA 5.542 5.077 0.465 0.465
58 ILE 65 GLN 1.771 2.235 -0.464 0.464
204 SER 293 ASN 1.884 1.421 0.463 0.463
85 ALA 112 ILE 0.162 0.621 -0.459 0.459
208 PHE 209 TYR 2.741 2.284 0.456 0.456
90 GLY 313 TRP 1.031 1.484 -0.454 0.454
114 VAL 164 THR 0.453 0.000 0.453 0.453
145 LEU 149 LYS 0.452 0.000 0.452 0.452
67 VAL 145 LEU 1.744 2.187 -0.442 0.442
164 THR 165 SER 0.000 0.439 -0.439 0.439
132 TYR 221 ARG 1.243 0.807 0.436 0.436
284 LEU 314 ILE 0.434 0.000 0.434 0.434
169 ILE 174 TYR 5.939 5.505 0.434 0.434
304 ARG 306 GLU 2.211 2.644 -0.433 0.433
200 ALA 293 ASN 1.076 0.643 0.433 0.433
78 ALA 119 ALA 0.631 0.200 0.431 0.431
60 LYS 61 PHE 0.690 0.265 0.425 0.425
109 TRP 191 CYS 0.733 1.157 -0.424 0.424
173 TRP 199 TYR 0.122 0.547 -0.424 0.424
223 PHE 269 HIS 0.000 0.424 -0.424 0.424
122 GLU 157 VAL 5.077 4.654 0.423 0.423
99 TRP 190 CYS 0.351 0.774 -0.422 0.422
124 LEU 318 ASN 0.420 0.000 0.420 0.420
286 TRP 315 GLY 9.075 9.492 -0.417 0.417
61 PHE 63 ARG 0.000 0.415 -0.415 0.415
193 PHE 308 TYR 0.833 0.419 0.414 0.414
293 ASN 308 TYR 3.308 2.896 0.411 0.411
54 VAL 336 PHE 1.491 1.902 -0.411 0.411
108 PHE 112 ILE 2.535 2.945 -0.410 0.410
133 PHE 141 TYR 2.873 2.465 0.407 0.407
48 VAL 80 LEU 1.522 1.919 -0.397 0.397
244 ASN 248 VAL 0.000 0.396 -0.396 0.396
302 LEU 303 ILE 0.586 0.981 -0.394 0.394
206 VAL 211 PRO 2.016 2.408 -0.392 0.392
121 ILE 211 PRO 1.934 2.326 -0.392 0.392
143 SER 149 LYS 0.000 0.391 -0.391 0.391
274 THR 278 ILE 0.469 0.081 0.389 0.389
100 THR 101 PHE 3.168 2.780 0.388 0.388
51 ASN 323 PRO 3.614 3.226 0.388 0.388
304 ARG 307 VAL 0.818 0.434 0.383 0.383
74 SER 123 THR 1.920 2.302 -0.382 0.382
300 ASP 301 ASN 0.247 0.629 -0.382 0.382
122 GLU 211 PRO 0.380 0.000 0.380 0.380
145 LEU 153 ILE 0.474 0.095 0.379 0.379
106 CYS 191 CYS 6.409 6.786 -0.377 0.377
172 HIS 175 ARG 14.138 14.512 -0.375 0.375
108 PHE 170 GLN 1.210 0.839 0.371 0.371
288 PRO 311 LEU 1.596 1.966 -0.370 0.370
78 ALA 120 SER 1.311 0.941 0.370 0.370
43 ILE 313 TRP 0.558 0.189 0.369 0.369
82 MET 286 TRP 0.000 0.367 -0.367 0.367
61 PHE 339 LEU 1.477 1.111 0.366 0.366
274 THR 413 LEU 0.366 0.000 0.366 0.366
82 MET 87 VAL 3.977 4.336 -0.359 0.359
91 ALA 313 TRP 3.082 3.441 -0.359 0.359
58 ILE 72 ILE 0.376 0.735 -0.358 0.358
174 TYR 195 THR 3.162 3.518 -0.356 0.356
112 ILE 166 PHE 1.583 1.229 0.354 0.354
63 ARG 338 GLU 0.000 0.352 -0.352 0.352
209 TYR 290 PHE 3.659 4.010 -0.351 0.351
326 TYR 336 PHE 0.000 0.348 -0.348 0.348
176 ALA 181 ALA 1.028 1.375 -0.347 0.347
212 LEU 279 MET 0.346 0.000 0.346 0.346
167 LEU 168 PRO 1.431 1.089 0.342 0.342
287 LEU 291 ILE 2.310 1.969 0.341 0.341
276 GLY 281 THR 0.339 0.000 0.339 0.339
75 LEU 278 ILE 0.000 0.338 -0.338 0.338
166 PHE 170 GLN 0.176 0.507 -0.332 0.332
55 ILE 73 THR 0.000 0.331 -0.331 0.331
94 ILE 313 TRP 2.786 3.116 -0.330 0.330
195 THR 199 TYR 1.486 1.813 -0.326 0.326
234 ASP 260 ARG 0.324 0.000 0.324 0.324
20 PRO 21 ASP 0.000 0.324 -0.324 0.324
109 TRP 316 TYR 0.017 0.340 -0.323 0.323
63 ARG 64 LEU 0.000 0.322 -0.322 0.322
322 ASN 326 TYR 1.002 0.684 0.319 0.319
354 TYR 355 SER 0.318 0.000 0.318 0.318
12 LEU 13 ALA 0.000 0.317 -0.317 0.317
111 SER 170 GLN 2.338 2.023 0.314 0.314
174 TYR 196 ASN 6.626 6.315 0.312 0.312
44 VAL 87 VAL 1.543 1.234 0.310 0.310
176 ALA 182 ILE 0.007 0.316 -0.309 0.309
204 SER 209 TYR 6.019 5.713 0.305 0.305
90 GLY 109 TRP 2.026 1.722 0.304 0.304
39 VAL 43 ILE 0.283 0.584 -0.301 0.301
103 ASN 190 CYS 0.661 0.364 0.297 0.297
67 VAL 71 PHE 0.163 0.455 -0.292 0.292
217 PHE 218 VAL 0.000 0.292 -0.292 0.292
187 ASN 189 THR 4.222 4.512 -0.291 0.291
67 VAL 150 ALA 0.662 0.372 0.290 0.290
226 ALA 269 HIS 0.000 0.281 -0.281 0.281
227 LYS 231 GLN 1.494 1.215 0.279 0.279
394 VAL 395 PRO 2.117 2.395 -0.278 0.278
67 VAL 147 LYS 0.807 0.531 0.276 0.276
51 ASN 79 ASP 4.674 4.949 -0.275 0.275
289 PHE 311 LEU 3.214 3.485 -0.272 0.272
52 VAL 80 LEU 1.146 0.877 0.269 0.269
68 THR 275 LEU 0.000 0.269 -0.269 0.269
181 ALA 194 PHE 3.871 3.603 0.268 0.268
203 SER 204 SER 0.266 0.000 0.266 0.266
49 PHE 340 LEU 0.741 1.006 -0.265 0.265
103 ASN 185 TYR 2.283 2.548 -0.265 0.265
132 TYR 218 VAL 1.395 1.131 0.264 0.264
275 LEU 278 ILE 0.000 0.262 -0.262 0.262
386 ASP 387 PHE 0.000 0.260 -0.260 0.260
82 MET 116 CYS 2.654 2.395 0.259 0.259
363 GLN 364 SER 0.096 0.355 -0.259 0.259
53 LEU 339 LEU 1.560 1.818 -0.258 0.258
237 GLU 260 ARG 0.256 0.000 0.256 0.256
364 SER 366 TYR 0.000 0.255 -0.255 0.255
55 ILE 80 LEU 0.782 0.529 0.253 0.253
103 ASN 186 ALA 1.056 0.809 0.247 0.247
406 CYS 408 THR 0.245 0.000 0.245 0.245
187 ASN 190 CYS 1.090 0.845 0.245 0.245
195 THR 200 ALA 1.558 1.313 0.245 0.245
209 TYR 294 ILE 2.447 2.202 0.245 0.245
317 VAL 321 PHE 2.352 2.110 0.243 0.243
193 PHE 195 THR 3.731 3.491 0.240 0.240
400 ASP 401 SER 0.104 0.343 -0.239 0.239
71 PHE 153 ILE 0.883 1.119 -0.237 0.237
262 SER 263 LYS 0.230 0.000 0.230 0.230
110 THR 169 ILE 1.417 1.646 -0.229 0.229
74 SER 158 TRP 3.193 3.416 -0.223 0.223
141 TYR 142 GLN 0.223 0.000 0.223 0.223
64 LEU 69 ASN 6.007 6.228 -0.220 0.220
305 LYS 309 ILE 1.236 1.017 0.219 0.219
275 LEU 280 GLY 0.219 0.000 0.219 0.219
203 SER 208 PHE 0.052 0.271 -0.219 0.219
107 GLU 172 HIS 5.953 5.735 0.218 0.218
128 ALA 215 MET 0.580 0.796 -0.216 0.216
325 ILE 328 ARG 0.000 0.213 -0.213 0.213
67 VAL 146 THR 0.091 0.303 -0.212 0.212
81 VAL 116 CYS 1.562 1.773 -0.211 0.211
244 ASN 247 GLN 0.000 0.207 -0.207 0.207
111 SER 169 ILE 3.865 4.069 -0.204 0.204
285 CYS 315 GLY 2.412 2.209 0.203 0.203
292 VAL 311 LEU 1.763 1.561 0.202 0.202
54 VAL 332 PHE 0.116 0.317 -0.201 0.201
81 VAL 86 VAL 1.030 0.834 0.196 0.196
179 GLN 182 ILE 0.458 0.263 0.195 0.195
47 ILE 83 GLY 1.608 1.803 -0.195 0.195
34 VAL 38 ILE 0.271 0.465 -0.194 0.194
99 TRP 188 GLU 1.522 1.715 -0.193 0.193
75 LEU 120 SER 2.936 2.743 0.193 0.193
81 VAL 112 ILE 0.550 0.741 -0.192 0.192
396 SER 397 ASP 1.114 0.925 0.190 0.190
72 ILE 275 LEU 0.000 0.189 -0.189 0.189
184 CYS 192 ASP 1.903 2.093 -0.189 0.189
185 TYR 195 THR 0.046 0.233 -0.188 0.188
43 ILE 47 ILE 0.745 0.931 -0.186 0.186
124 LEU 215 MET 1.765 1.950 -0.185 0.185
48 VAL 52 VAL 0.319 0.137 0.182 0.182
62 GLU 65 GLN 0.032 0.213 -0.181 0.181
273 LYS 277 ILE 0.524 0.343 0.181 0.181
209 TYR 287 LEU 0.000 0.180 -0.180 0.180
57 ALA 64 LEU 2.087 2.264 -0.177 0.177
40 MET 95 LEU 0.171 0.347 -0.176 0.176
82 MET 117 VAL 1.307 1.132 0.176 0.176
147 LYS 151 ARG 0.000 0.176 -0.176 0.176
176 ALA 185 TYR 4.463 4.638 -0.175 0.175
55 ILE 77 CYS 1.106 1.281 -0.175 0.175
285 CYS 321 PHE 0.530 0.702 -0.172 0.172
149 LYS 153 ILE 0.171 0.000 0.171 0.171
81 VAL 85 ALA 0.035 0.206 -0.171 0.171
305 LYS 306 GLU 0.170 0.000 0.170 0.170
123 THR 154 ILE 0.166 0.000 0.166 0.166
114 VAL 169 ILE 0.555 0.390 0.165 0.165
322 ASN 325 ILE 0.000 0.165 -0.165 0.165
136 THR 225 GLU 0.000 0.161 -0.161 0.161
40 MET 94 ILE 1.644 1.805 -0.161 0.161
184 CYS 191 CYS 0.382 0.542 -0.160 0.160
107 GLU 170 GLN 2.257 2.101 0.157 0.157
222 VAL 275 LEU 0.156 0.000 0.156 0.156
105 TRP 109 TRP 0.000 0.156 -0.156 0.156
68 THR 72 ILE 0.000 0.154 -0.154 0.154
117 VAL 316 TYR 0.153 0.000 0.153 0.153
43 ILE 317 VAL 0.830 0.983 -0.153 0.153
201 ILE 294 ILE 0.921 0.769 0.153 0.153
185 TYR 192 ASP 0.000 0.152 -0.152 0.152
33 VAL 95 LEU 1.920 1.769 0.151 0.151
180 GLU 194 PHE 1.844 1.992 -0.148 0.148
120 SER 319 SER 0.147 0.000 0.147 0.147
322 ASN 327 CYS 0.146 0.000 0.146 0.146
78 ALA 158 TRP 2.393 2.538 -0.145 0.145
107 GLU 175 ARG 3.178 3.322 -0.144 0.144
64 LEU 331 ASP 1.579 1.722 -0.143 0.143
295 VAL 302 LEU 0.747 0.606 0.141 0.141
235 LYS 239 ARG 0.000 0.140 -0.140 0.140
296 HIS 301 ASN 0.000 0.138 -0.138 0.138
57 ALA 332 PHE 0.166 0.028 0.138 0.138
66 THR 69 ASN 4.431 4.293 0.138 0.138
143 SER 144 LEU 0.006 0.143 -0.138 0.138
218 VAL 219 TYR 0.137 0.000 0.137 0.137
312 ASN 316 TYR 6.922 7.059 -0.137 0.137
115 LEU 162 GLY 1.489 1.353 0.136 0.136
71 PHE 145 LEU 0.360 0.492 -0.132 0.132
82 MET 88 PRO 0.533 0.401 0.132 0.132
285 CYS 286 TRP 0.225 0.094 0.132 0.132
124 LEU 127 ILE 0.000 0.131 -0.131 0.131
321 PHE 325 ILE 0.451 0.319 0.131 0.131
321 PHE 324 LEU 0.012 0.143 -0.131 0.131
199 TYR 204 SER 0.020 0.151 -0.131 0.131
200 ALA 294 ILE 0.311 0.441 -0.130 0.130
106 CYS 110 THR 0.350 0.222 0.128 0.128
201 ILE 205 ILE 0.856 0.728 0.128 0.128
277 ILE 281 THR 0.396 0.522 -0.126 0.126
54 VAL 76 ALA 0.766 0.892 -0.126 0.126
212 LEU 287 LEU 0.327 0.453 -0.126 0.126
57 ALA 335 ALA 0.335 0.460 -0.125 0.125
140 LYS 145 LEU 0.125 0.000 0.125 0.125
57 ALA 336 PHE 0.995 1.119 -0.124 0.124
174 TYR 194 PHE 2.090 2.213 -0.123 0.123
92 ALA 98 MET 0.000 0.123 -0.123 0.123
57 ALA 61 PHE 0.025 0.147 -0.122 0.122
216 VAL 279 MET 0.121 0.000 0.121 0.121
48 VAL 84 LEU 1.469 1.590 -0.121 0.121
86 VAL 316 TYR 1.918 2.039 -0.121 0.121
96 MET 98 MET 0.140 0.260 -0.120 0.120
178 HIS 180 GLU 0.960 0.841 0.120 0.120
307 VAL 311 LEU 0.553 0.671 -0.118 0.118
118 THR 122 GLU 1.370 1.487 -0.117 0.117
126 VAL 157 VAL 0.602 0.488 0.115 0.115
69 ASN 72 ILE 0.974 1.089 -0.115 0.115
173 TRP 196 ASN 2.701 2.587 0.114 0.114
160 VAL 164 THR 0.000 0.111 -0.111 0.111
118 THR 161 SER 5.011 4.899 0.111 0.111
411 SER 412 LEU 0.000 0.110 -0.110 0.110
54 VAL 323 PRO 1.238 1.132 0.106 0.106
281 THR 285 CYS 0.381 0.275 0.106 0.106
285 CYS 311 LEU 0.259 0.363 -0.104 0.104
346 SER 347 LEU 0.213 0.315 -0.102 0.102
152 VAL 156 MET 0.205 0.104 0.101 0.101
205 ILE 211 PRO 0.337 0.438 -0.101 0.101
130 ASP 145 LEU 1.075 1.175 -0.101 0.101
154 ILE 158 TRP 1.257 1.157 0.100 0.100
89 PHE 99 TRP 0.995 0.895 0.100 0.100
146 THR 148 ASN 0.487 0.388 0.100 0.100
45 LEU 50 GLY 0.046 0.145 -0.099 0.099
110 THR 191 CYS 0.119 0.218 -0.098 0.098
205 ILE 210 VAL 4.695 4.793 -0.098 0.098
61 PHE 64 LEU 0.806 0.903 -0.098 0.098
127 ILE 131 ARG 0.074 0.172 -0.098 0.098
303 ILE 308 TYR 0.167 0.069 0.098 0.098
159 ILE 163 LEU 0.806 0.710 0.096 0.096
286 TRP 290 PHE 2.084 1.988 0.096 0.096
47 ILE 320 GLY 1.897 1.801 0.096 0.096
37 GLY 95 LEU 1.824 1.729 0.095 0.095
93 HIS 192 ASP 0.541 0.635 -0.094 0.094
216 VAL 220 SER 0.202 0.296 -0.094 0.094
215 MET 216 VAL 0.000 0.092 -0.092 0.092
133 PHE 136 THR 0.092 0.000 0.092 0.092
47 ILE 51 ASN 0.644 0.736 -0.092 0.092
54 VAL 72 ILE 0.451 0.542 -0.091 0.091
58 ILE 332 PHE 2.085 1.997 0.089 0.089
128 ALA 218 VAL 2.680 2.593 0.087 0.087
86 VAL 112 ILE 1.452 1.539 -0.086 0.086
233 ILE 236 SER 0.050 0.135 -0.085 0.085
138 PRO 139 PHE 0.058 0.143 -0.084 0.084
103 ASN 184 CYS 0.082 0.000 0.082 0.082
281 THR 321 PHE 1.653 1.735 -0.082 0.082
169 ILE 170 GLN 0.252 0.333 -0.081 0.081
197 GLN 298 ILE 0.000 0.080 -0.080 0.080
233 ILE 262 SER 0.000 0.079 -0.079 0.079
124 LEU 219 TYR 0.077 0.000 0.077 0.077
129 VAL 133 PHE 1.473 1.398 0.074 0.074
108 PHE 166 PHE 1.110 1.184 -0.074 0.074
113 ASP 117 VAL 0.752 0.678 0.074 0.074
224 GLN 228 ARG 0.000 0.073 -0.073 0.073
190 CYS 192 ASP 0.914 0.841 0.073 0.073
140 LYS 143 SER 0.000 0.073 -0.073 0.073
121 ILE 125 CYS 0.000 0.073 -0.073 0.073
55 ILE 76 ALA 1.914 1.842 0.072 0.072
47 ILE 79 ASP 1.378 1.449 -0.071 0.071
36 MET 95 LEU 0.484 0.554 -0.070 0.070
215 MET 326 TYR 0.070 0.000 0.070 0.070
225 GLU 232 LYS 0.069 0.000 0.069 0.069
44 VAL 88 PRO 1.859 1.928 -0.069 0.069
247 GLN 248 VAL 0.069 0.000 0.069 0.069
355 SER 356 SER 0.067 0.000 0.067 0.067
366 TYR 367 HIS 0.000 0.067 -0.067 0.067
163 LEU 167 LEU 0.260 0.194 0.065 0.065
291 ILE 295 VAL 0.268 0.203 0.065 0.065
197 GLN 201 ILE 1.425 1.360 0.065 0.065
184 CYS 194 PHE 1.434 1.498 -0.064 0.064
175 ARG 194 PHE 0.238 0.175 0.063 0.063
126 VAL 153 ILE 1.177 1.241 -0.063 0.063
82 MET 113 ASP 1.162 1.099 0.062 0.062
214 ILE 218 VAL 0.440 0.379 0.062 0.062
58 ILE 73 THR 3.198 3.260 -0.061 0.061
71 PHE 154 ILE 2.380 2.441 -0.061 0.061
178 HIS 181 ALA 2.706 2.767 -0.061 0.061
73 THR 77 CYS 0.171 0.232 -0.061 0.061
218 VAL 222 VAL 0.168 0.108 0.061 0.061
329 SER 330 PRO 1.080 1.020 0.060 0.060
43 ILE 87 VAL 0.133 0.193 -0.059 0.059
298 ILE 299 GLN 0.287 0.347 -0.059 0.059
287 LEU 288 PRO 0.870 0.928 -0.058 0.058
125 CYS 129 VAL 0.057 0.000 0.057 0.057
236 SER 237 GLU 0.000 0.055 -0.055 0.055
166 PHE 171 MET 0.120 0.066 0.054 0.054
156 MET 159 ILE 0.000 0.053 -0.053 0.053
119 ALA 161 SER 4.173 4.225 -0.053 0.053
53 LEU 340 LEU 0.893 0.944 -0.051 0.051
32 TRP 33 VAL 0.400 0.451 -0.051 0.051
14 PRO 15 ASN 0.050 0.000 0.050 0.050
123 THR 127 ILE 0.390 0.440 -0.049 0.049
87 VAL 316 TYR 1.413 1.461 -0.048 0.048
311 LEU 314 ILE 0.344 0.392 -0.047 0.047
44 VAL 83 GLY 1.045 0.998 0.047 0.047
210 VAL 214 ILE 0.497 0.543 -0.046 0.046
22 HIS 25 THR 0.048 0.094 -0.046 0.046
92 ALA 96 MET 0.000 0.045 -0.045 0.045
195 THR 297 VAL 0.089 0.134 -0.045 0.045
54 VAL 58 ILE 0.534 0.490 0.045 0.045
64 LEU 335 ALA 0.656 0.612 0.044 0.044
322 ASN 323 PRO 0.889 0.932 -0.042 0.042
181 ALA 185 TYR 1.831 1.788 0.042 0.042
329 SER 331 ASP 0.537 0.578 -0.042 0.042
282 PHE 287 LEU 0.121 0.080 0.041 0.041
113 ASP 316 TYR 6.547 6.587 -0.040 0.040
27 GLU 31 VAL 0.000 0.039 -0.039 0.039
52 VAL 56 THR 0.444 0.482 -0.038 0.038
196 ASN 198 ALA 0.742 0.778 -0.036 0.036
172 HIS 174 TYR 0.069 0.104 -0.036 0.036
94 ILE 309 ILE 1.054 1.018 0.035 0.035
134 ALA 412 LEU 0.035 0.000 0.035 0.035
230 LEU 269 HIS 0.000 0.033 -0.033 0.033
112 ILE 116 CYS 0.554 0.522 0.032 0.032
83 GLY 88 PRO 2.961 2.994 -0.032 0.032
176 ALA 178 HIS 1.577 1.545 0.032 0.032
49 PHE 53 LEU 0.109 0.078 0.031 0.031
212 LEU 216 VAL 0.660 0.631 0.030 0.030
219 TYR 273 LYS 0.000 0.029 -0.029 0.029
72 ILE 332 PHE 0.266 0.237 0.029 0.029
68 THR 69 ASN 0.030 0.058 -0.029 0.029
87 VAL 88 PRO 0.885 0.913 -0.028 0.028
38 ILE 42 LEU 0.451 0.424 0.027 0.027
119 ALA 157 VAL 0.949 0.923 0.026 0.026
106 CYS 190 CYS 0.165 0.190 -0.026 0.026
132 TYR 137 SER 0.025 0.000 0.025 0.025
109 TRP 113 ASP 0.024 0.000 0.024 0.024
75 LEU 326 TYR 0.707 0.683 0.024 0.024
46 ALA 51 ASN 0.000 0.023 -0.023 0.023
114 VAL 118 THR 0.479 0.502 -0.023 0.023
57 ALA 339 LEU 1.898 1.875 0.023 0.023
24 VAL 28 ARG 0.000 0.022 -0.022 0.022
51 ASN 319 SER 2.310 2.332 -0.022 0.022
113 ASP 286 TRP 0.000 0.021 -0.021 0.021
137 SER 138 PRO 0.122 0.102 0.020 0.020
60 LYS 339 LEU 0.626 0.645 -0.019 0.019
326 TYR 333 ARG 0.000 0.018 -0.018 0.018
123 THR 157 VAL 0.924 0.941 -0.018 0.018
137 SER 140 LYS 0.602 0.585 0.017 0.017
66 THR 68 THR 0.255 0.238 0.017 0.017
200 ALA 297 VAL 1.384 1.401 -0.017 0.017
205 ILE 209 TYR 0.210 0.194 0.016 0.016
92 ALA 97 LYS 0.005 0.020 -0.015 0.015
214 ILE 219 TYR 0.000 0.015 -0.015 0.015
86 VAL 116 CYS 0.000 0.015 -0.015 0.015
102 GLY 188 GLU 2.266 2.281 -0.015 0.015
125 CYS 212 LEU 0.000 0.014 -0.014 0.014
56 THR 339 LEU 1.478 1.464 0.014 0.014
115 LEU 119 ALA 0.000 0.013 -0.013 0.013
88 PRO 89 PHE 0.000 0.012 -0.012 0.012
153 ILE 157 VAL 0.000 0.011 -0.011 0.011
240 PHE 244 ASN 0.000 0.011 -0.011 0.011
227 LYS 264 PHE 0.010 0.000 0.010 0.010
47 ILE 87 VAL 0.383 0.390 -0.008 0.008
294 ILE 298 ILE 0.781 0.773 0.008 0.008
204 SER 294 ILE 1.469 1.476 -0.007 0.007
310 LEU 314 ILE 0.148 0.141 0.007 0.007
215 MET 220 SER 0.020 0.014 0.006 0.006
309 ILE 313 TRP 1.185 1.179 0.006 0.006
175 ARG 196 ASN 4.480 4.475 0.005 0.005
68 THR 127 ILE 0.000 0.004 -0.004 0.004
115 LEU 158 TRP 0.995 0.998 -0.002 0.002
157 VAL 161 SER 0.321 0.319 0.002 0.002
113 ASP 312 ASN 0.384 0.382 0.002 0.002
176 ALA 195 THR 2.020 2.022 -0.002 0.002
210 VAL 211 PRO 1.495 1.494 0.001 0.001
44 VAL 48 VAL 0.203 0.203 -0.000 0.000

RRCS change distribution

-0.10
Mean ΔRRCS
1.41
Std Dev
-0.05
Median

Magnitude classification

15
High (|Δ| ≥ 5.0)
57
Medium (2.0 ≤ |Δ| < 5.0)
628
Low (|Δ| < 2.0)

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| ≥ 1.97, 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