Project name: wild [mutate: VA208D, VA209D, FA146D, FA288D, LA145D, LA285D, YA289D, IA223D, AA284D]

Status: done

submitted: 2019-02-14 06:11:30, status changed: 2019-02-14 09:07:19
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Chain sequence(s) A: MRSGSHHHHHHRSDITSLYKKAGSAAAPFTMENLYFQSYQGNSDCYFGNGSAYRGTHSLTESGASCLPWNSMILIGKVYTAQNPSAQALGLGKHNYCRNPDGDAKPWCHVLKNRRLTWEYCDVPSCSTCGLRQYSQPQFRIKGGLFADIASHPWQAAIFAKHRRSPGERFLCGGILISSCWILSAAHCFQERFPPHHLTVILGRTYRVVPGEEEQKFEVEKYIVHKEFDDDTYDNDIALLQLKSDSSRCAQESSVVRTVCLPPADLQLPDWTECELSGYGKHEALSPFYSERLKEAHVRLYPSSRCTSQHLLNRTVTDNMLCAGDTRSGGPQANLHDACQGDSGGPLVCLNDGRMTLVGIISWGLGCGQKDVPGVYTKVTNYLDWIRDNMRP
Distance of aggregation 10 Å
Dynamic mode Yes
Mutated residues VA208D, VA209D, FA146D, FA288D, LA145D, LA285D, YA289D, IA223D, AA284D
Energy difference between WT (input) and mutated protein (by FoldX) 2.3257 kcal/mol

CAUTION: Your mutation/s can destabilize the protein structure

Changes in protein stability upon mutation are calculated using the FoldX forcefield. Computational prediction of protein stability is used with the intention of preventing the experimental characterization of proteins bearing mutations that significantly destabilize their structure. Mutations resulting in a predicted reduction in protein stability ≥ 1 kcal/mol are considered disruptive.

Show buried residues

Minimal score value
-3.8677
Maximal score value
1.7737
Average score
-0.8706
Total score value
-341.2615

The table below lists A3D score for protein residues. Residues with A3D score > 0.0000 are marked by yellow rows.

residue index residue name chain Aggrescan3D score mutation
residue index residue name chain Aggrescan3D score
mutation
1 M A 0.0328
2 R A -1.6393
3 S A -1.1719
4 G A -1.2412
5 S A -1.0446
6 H A -1.2501
7 H A -0.7233
8 H A -0.9983
9 H A 0.0000
10 H A -0.9165
11 H A 0.0000
12 R A -0.3209
13 S A 0.1117
14 D A 0.5794
15 I A 1.7737
16 T A 0.8521
17 S A 1.2192
18 L A 1.5006
19 Y A 0.7521
20 K A -1.2190
21 K A -1.0749
22 A A -0.6649
23 G A -0.5815
24 S A -0.6172
25 A A -0.2456
26 A A -0.2456
27 A A 0.0000
28 P A -0.0909
29 F A 0.3001
30 T A -0.2883
31 M A -0.2616
32 E A -1.6922
33 N A -0.6031
34 L A 1.3930
35 Y A 1.4695
36 F A 0.2392
37 Q A -1.2688
38 S A -1.3393
39 Y A 0.0000
40 Q A -0.8363
41 G A 0.0000
42 N A 0.0000
43 S A 0.0000
44 D A 0.0000
45 C A -0.4041
46 Y A -0.4319
47 F A -0.4984
48 G A -1.1385
49 N A -1.8880
50 G A -1.4699
51 S A -0.9688
52 A A -0.8318
53 Y A -0.6229
54 R A -1.2390
55 G A 0.0000
56 T A -1.6123
57 H A -1.5015
58 S A 0.0000
59 L A 0.3736
60 T A 0.0000
61 E A -0.3057
62 S A -0.6126
63 G A -0.5058
64 A A -0.0618
65 S A 0.4062
66 C A 0.6817
67 L A 0.4877
68 P A -0.8666
69 W A -1.0072
70 N A -1.8070
71 S A -1.2465
72 M A 0.0000
73 I A 0.5003
74 L A 0.9839
75 I A 1.3800
76 G A -0.0710
77 K A -1.3231
78 V A -0.0815
79 Y A 0.4316
80 T A 0.1048
81 A A -0.1969
82 Q A -1.4090
83 N A -1.4675
84 P A -1.3380
85 S A -0.9940
86 A A 0.0000
87 Q A -1.5923
88 A A -0.6780
89 L A -0.7401
90 G A -0.9296
91 L A -1.1916
92 G A 0.0000
93 K A -2.6235
94 H A -2.3911
95 N A -1.6799
96 Y A 0.0000
97 C A 0.0000
98 R A -0.4193
99 N A 0.0000
100 P A 0.0000
101 D A -1.6116
102 G A -1.1022
103 D A -2.1088
104 A A -1.5442
105 K A 0.0000
106 P A 0.0000
107 W A 0.0000
108 C A 0.0000
109 H A 0.0000
110 V A 0.8232
111 L A -0.5933
112 K A -2.8563
113 N A -3.2864
114 R A -3.3527
115 R A -3.4510
116 L A -1.6367
117 T A -0.4630
118 W A 0.0000
119 E A -0.3947
120 Y A 0.0000
121 C A 0.0000
122 D A -0.5791
123 V A -0.2075
124 P A -0.4127
125 S A -0.3516
126 C A 0.0000
127 S A -0.3316
128 T A -0.5160
129 C A 0.0000
130 G A -0.4980
131 L A 0.0000
132 R A -1.3550
133 Q A -1.1309
134 Y A 0.0000
135 S A -1.1543
136 Q A -1.6096
137 P A -1.4889
138 Q A 0.0000
139 F A 0.0000
140 R A 0.0000
141 I A 0.0000
142 K A -1.2414
143 G A -1.1662
144 G A -1.5215
145 D A -3.3402 mutated: LA145D
146 D A -3.3046 mutated: FA146D
147 A A 0.0000
148 D A -1.3947
149 I A 1.1496
150 A A 0.3326
151 S A -0.5811
152 H A 0.0000
153 P A 0.0000
154 W A 0.0000
155 Q A 0.0000
156 A A 0.0000
157 A A 0.1796
158 I A 0.0000
159 F A -0.2589
160 A A 0.0000
161 K A -3.2203
162 H A -3.7542
163 R A -3.8516
164 R A -3.8677
165 S A 0.0000
166 P A -2.3214
167 G A 0.0000
168 E A -2.9353
169 R A -1.6976
170 F A -0.0825
171 L A 0.0000
172 C A 0.0000
173 G A 0.0000
174 G A 0.0000
175 I A 0.0000
176 L A 0.0000
177 I A 0.0000
178 S A -0.2253
179 S A -0.6440
180 C A -0.7732
181 W A 0.0000
182 I A 0.0000
183 L A 0.0000
184 S A 0.0000
185 A A -0.5490
186 A A 0.0000
187 H A -1.8171
188 C A 0.0000
189 F A 0.0000
190 Q A -2.2646
191 E A -2.1351
192 R A -2.6574
193 F A -1.5883
194 P A -1.5332
195 P A -1.4350
196 H A -2.0994
197 H A -2.0885
198 L A 0.0000
199 T A -0.8063
200 V A 0.0000
201 I A -1.1428
202 L A 0.0000
203 G A 0.0000
204 R A -1.1245
205 T A -2.0646
206 Y A -2.5273
207 R A -2.7845
208 D A -3.5264 mutated: VA208D
209 D A -3.5048 mutated: VA209D
210 P A -2.5493
211 G A -2.4912
212 E A -3.4637
213 E A -3.4280
214 E A -2.8773
215 Q A -2.0100
216 K A -2.5491
217 F A 0.0000
218 E A -2.6832
219 V A 0.0000
220 E A -3.1023
221 K A -3.2304
222 Y A -1.7982
223 D A -2.1847 mutated: IA223D
224 V A -0.8864
225 H A -1.6203
226 K A -2.3717
227 E A -1.8189
228 F A -0.7245
229 D A -2.8439
230 D A -3.5230
231 D A -3.3799
232 T A -2.5606
233 Y A -2.1219
234 D A -2.4548
235 N A -1.9273
236 D A -1.6383
237 I A 0.0000
238 A A 0.0000
239 L A 0.0000
240 L A 0.0000
241 Q A -1.9733
242 L A -2.1708
243 K A -3.0335
244 S A -2.8105
245 D A -3.0864
246 S A -2.2780
247 S A -2.0913
248 R A -3.0245
249 C A 0.0000
250 A A -1.7998
251 Q A -1.6830
252 E A -2.1739
253 S A 0.0000
254 S A -0.1082
255 V A 0.5847
256 V A 0.0000
257 R A -0.3723
258 T A 0.0000
259 V A 0.0000
260 C A 0.0733
261 L A 0.2244
262 P A -0.1802
263 P A -0.7596
264 A A -1.2497
265 D A -2.0009
266 L A -0.6296
267 Q A -0.8287
268 L A 0.4553
269 P A -0.5435
270 D A -1.2509
271 W A -0.4406
272 T A -0.7340
273 E A -0.9955
274 C A 0.0000
275 E A 0.0000
276 L A 0.0000
277 S A 0.0000
278 G A 0.0000
279 Y A 0.0000
280 G A -0.8108
281 K A -2.0835
282 H A -2.8961
283 E A -2.6821
284 D A -2.6288 mutated: AA284D
285 D A -2.5915 mutated: LA285D
286 S A -2.3329
287 P A -2.5311
288 D A -3.5987 mutated: FA288D
289 D A -3.3319 mutated: YA289D
290 S A -2.6124
291 E A 0.0000
292 R A -3.5346
293 L A 0.0000
294 K A 0.0000
295 E A -1.7450
296 A A 0.0000
297 H A -0.8198
298 V A 0.0000
299 R A -1.4109
300 L A -0.3195
301 Y A 0.6529
302 P A 0.4992
303 S A -0.0438
304 S A -0.4491
305 R A -0.6642
306 C A -0.2807
307 T A -0.6837
308 S A -1.2036
309 Q A -1.2268
310 H A -1.1387
311 L A -0.2746
312 L A 0.4755
313 N A -1.6899
314 R A -1.5862
315 T A -1.2061
316 V A 0.0000
317 T A -0.6889
318 D A -1.1228
319 N A -1.1723
320 M A -0.0768
321 L A 0.4103
322 C A 0.0000
323 A A 0.0000
324 G A -0.9251
325 D A 0.0000
326 T A -2.2570
327 R A -3.1606
328 S A -2.1878
329 G A -1.6802
330 G A -1.2525
331 P A -1.2237
332 Q A -1.6316
333 A A -1.1314
334 N A -1.1774
335 L A -0.6886
336 H A 0.0000
337 D A 0.0000
338 A A -0.5071
339 C A -0.6577
340 Q A -1.1120
341 G A -0.6924
342 D A 0.0000
343 S A -0.4450
344 G A 0.0000
345 G A 0.0000
346 P A 0.0000
347 L A 0.0000
348 V A 0.0000
349 C A -0.1574
350 L A -0.2826
351 N A -1.2798
352 D A -1.3372
353 G A 0.0000
354 R A -0.8554
355 M A 0.0000
356 T A -0.0049
357 L A 0.0000
358 V A 0.0000
359 G A 0.0000
360 I A 0.0000
361 I A 0.0000
362 S A 0.0000
363 W A -0.2400
364 G A -0.5048
365 L A 0.0919
366 G A -0.1533
367 C A -0.3731
368 G A -1.4147
369 Q A -2.4442
370 K A -3.5581
371 D A -3.2542
372 V A 0.0000
373 P A 0.0000
374 G A 0.0000
375 V A 0.0000
376 Y A 0.0000
377 T A -0.2566
378 K A 0.0000
379 V A 0.0000
380 T A 0.0000
381 N A -1.5011
382 Y A 0.0000
383 L A 0.0000
384 D A -1.0450
385 W A -0.2533
386 I A 0.0000
387 R A -1.8774
388 D A -3.0024
389 N A -2.6921
390 M A -2.1897
391 R A -3.1235
392 P A -2.0123

Above is the comparison between the input structure and the most aggregation prone model (predicted in the flexibility simulations, download both models in the PDB file format , download table with rmsd values ). The picture presents the most aggregation prone model (in blue) superimposed on the input structure (in red). The plot shows rmsd profile (distances between residues of the superimposed structures).

Dynamic mode uses CABS-flex simulations of protein structure fluctuations. The structure fluctuations may have impact on the size and extent of aggregation "hot-spots" on the protein surface. The dynamic mode uses the following pipeline: (1) based on the input structure, CABS-flex predicts a set of different models reflecting protein dynamics in solution; (2) for each of these models A3D score is calculated; (3) finally, the most aggregation prone model (the model with the highest A3D score, -0.8706 in this case) is selected and presented in A3D results.


 

Laboratory of Theory of Biopolymers 2015