Project name: wild [mutate: VA208E, VA209E, IA223E, AA284E, LA285E, YA289E, LA145E, FA288E, FA146E]

Status: done

submitted: 2019-02-14 06:17:47, status changed: 2019-02-14 09:14:28
Settings
Chain sequence(s) A: MRSGSHHHHHHRSDITSLYKKAGSAAAPFTMENLYFQSYQGNSDCYFGNGSAYRGTHSLTESGASCLPWNSMILIGKVYTAQNPSAQALGLGKHNYCRNPDGDAKPWCHVLKNRRLTWEYCDVPSCSTCGLRQYSQPQFRIKGGLFADIASHPWQAAIFAKHRRSPGERFLCGGILISSCWILSAAHCFQERFPPHHLTVILGRTYRVVPGEEEQKFEVEKYIVHKEFDDDTYDNDIALLQLKSDSSRCAQESSVVRTVCLPPADLQLPDWTECELSGYGKHEALSPFYSERLKEAHVRLYPSSRCTSQHLLNRTVTDNMLCAGDTRSGGPQANLHDACQGDSGGPLVCLNDGRMTLVGIISWGLGCGQKDVPGVYTKVTNYLDWIRDNMRP
Distance of aggregation 10 Å
Dynamic mode Yes
Mutated residues VA208E, VA209E, IA223E, AA284E, LA285E, YA289E, LA145E, FA288E, FA146E
Energy difference between WT (input) and mutated protein (by FoldX) 2.71867 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
-3.8726
Maximal score value
2.3556
Average score
-0.8548
Total score value
-335.069

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 0.1930
2 R A -1.8752
3 S A -1.3386
4 G A -0.9431
5 S A -1.0266
6 H A -2.1276
7 H A -1.5565
8 H A -1.7098
9 H A -2.1960
10 H A -2.1968
11 H A -2.2386
12 R A -2.0532
13 S A -1.3057
14 D A -1.5286
15 I A -0.1661
16 T A -0.5478
17 S A -0.7234
18 L A -0.5108
19 Y A -0.4073
20 K A -2.1181
21 K A -2.2261
22 A A -1.3684
23 G A -1.1332
24 S A -0.8153
25 A A -0.0476
26 A A 0.5813
27 A A 0.7688
28 P A 0.9508
29 F A 2.0663
30 T A 1.0051
31 M A 0.8163
32 E A -1.5319
33 N A -0.7526
34 L A 1.4936
35 Y A 1.7544
36 F A 2.1833
37 Q A 0.8366
38 S A 0.1869
39 Y A -0.2771
40 Q A -0.6351
41 G A -0.4785
42 N A -0.2078
43 S A 0.0000
44 D A -0.7813
45 C A 0.0000
46 Y A 0.8216
47 F A 1.3565
48 G A 0.6216
49 N A -0.2775
50 G A -0.4429
51 S A -0.1546
52 A A 0.0000
53 Y A 0.0000
54 R A -1.6314
55 G A 0.0000
56 T A -1.8658
57 H A -1.7576
58 S A 0.0000
59 L A -0.3281
60 T A -0.7955
61 E A -1.7701
62 S A -1.1404
63 G A -0.6388
64 A A -0.1512
65 S A 0.2313
66 C A 0.0000
67 L A 1.2765
68 P A -0.4246
69 W A 0.0000
70 N A -0.9094
71 S A -0.6165
72 M A 0.6549
73 I A 1.9284
74 L A 2.0388
75 I A 2.3556
76 G A 0.2899
77 K A -0.3528
78 V A 2.0196
79 Y A 1.4170
80 T A 1.1234
81 A A 0.0000
82 Q A -1.1703
83 N A -1.2643
84 P A -1.0817
85 S A -0.6846
86 A A 0.0000
87 Q A -1.7254
88 A A -0.8290
89 L A -0.3344
90 G A -0.9535
91 L A -1.3846
92 G A -2.0974
93 K A -2.7693
94 H A -2.4524
95 N A -1.6119
96 Y A 0.0000
97 C A 0.0000
98 R A 0.0000
99 N A 0.0000
100 P A 0.0000
101 D A -0.8869
102 G A -0.6184
103 D A 0.0000
104 A A 0.0000
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 0.5132
111 L A -0.9091
112 K A -2.9669
113 N A -3.2981
114 R A -3.7552
115 R A -3.3746
116 L A -1.2773
117 T A -0.5336
118 W A 0.0000
119 E A 0.0000
120 Y A 0.0000
121 C A 0.0000
122 D A 0.0000
123 V A -0.2331
124 P A -0.4215
125 S A -0.2273
126 C A -0.0493
127 S A -0.6286
128 T A -0.1407
129 C A 0.0000
130 G A -0.2040
131 L A -0.0154
132 R A 0.0000
133 Q A -2.2959
134 Y A -1.6619
135 S A -1.6162
136 Q A -1.7200
137 P A -1.5953
138 Q A -1.2437
139 F A 0.0000
140 R A 0.0000
141 I A 0.0000
142 K A 0.0000
143 G A -1.2838
144 G A -1.3082
145 E A -1.8094 mutated: LA145E
146 E A -2.3086 mutated: FA146E
147 A A -1.3185
148 D A -0.7890
149 I A 1.1311
150 A A 0.5462
151 S A -0.0355
152 H A 0.0000
153 P A 0.1378
154 W A 0.0000
155 Q A 0.0000
156 A A 0.0000
157 A A -0.1235
158 I A 0.0000
159 F A 0.0000
160 A A 0.0000
161 K A -2.7666
162 H A -3.1781
163 R A -3.6250
164 R A -3.3295
165 S A -2.4046
166 P A -2.2691
167 G A -2.1093
168 E A -2.3989
169 R A -1.4722
170 F A -0.4276
171 L A 0.0000
172 C A -0.0976
173 G A 0.0629
174 G A 0.0000
175 I A 0.0000
176 L A 0.1743
177 I A 0.0000
178 S A -0.1897
179 S A -0.5667
180 C A -0.3125
181 W A -0.1137
182 I A 0.0000
183 L A 0.0000
184 S A 0.0000
185 A A 0.0000
186 A A 0.0000
187 H A -0.9021
188 C A 0.0000
189 F A -0.7929
190 Q A -1.7468
191 E A -1.7016
192 R A -2.4601
193 F A 0.0000
194 P A -1.5297
195 P A -2.0405
196 H A -2.1222
197 H A -2.2688
198 L A 0.0000
199 T A -1.2822
200 V A 0.0000
201 I A 0.0000
202 L A 0.0000
203 G A -1.2014
204 R A -2.1683
205 T A -1.4554
206 Y A -2.2692
207 R A -3.5570
208 E A -2.9503 mutated: VA208E
209 E A -3.1731 mutated: VA209E
210 P A -2.4463
211 G A -2.2333
212 E A -3.1907
213 E A -2.0306
214 E A -2.2001
215 Q A -2.3735
216 K A -2.5103
217 F A 0.0000
218 E A -2.7476
219 V A 0.0000
220 E A -2.5150
221 K A -2.2298
222 Y A -1.2119
223 E A -1.8291 mutated: IA223E
224 V A -0.8285
225 H A -1.8438
226 K A -1.8824
227 E A -2.2754
228 F A -1.1070
229 D A -2.8398
230 D A -3.4174
231 D A -3.2250
232 T A -2.3714
233 Y A 0.0000
234 D A -1.9851
235 N A -1.3928
236 D A 0.0000
237 I A 0.0000
238 A A 0.0000
239 L A -0.4895
240 L A 0.0000
241 Q A -1.4287
242 L A -1.6363
243 K A -2.7879
244 S A -2.6821
245 D A -2.3279
246 S A -1.7143
247 S A -2.1132
248 R A -3.1669
249 C A 0.0000
250 A A -1.6313
251 Q A -2.4898
252 E A -2.2983
253 S A -1.2336
254 S A -0.4546
255 V A -0.1444
256 V A 0.0000
257 R A -0.5307
258 T A 0.0886
259 V A 0.3101
260 C A 0.5967
261 L A 0.4175
262 P A -0.3492
263 P A -0.8495
264 A A -1.3571
265 D A -2.0026
266 L A -1.3716
267 Q A -2.0507
268 L A -0.8174
269 P A -1.4353
270 D A -1.9615
271 W A 0.0000
272 T A -1.0519
273 E A -1.2285
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 -0.2596
280 G A 0.0000
281 K A -1.6957
282 H A -2.1242
283 E A -2.8069
284 E A -3.3693 mutated: AA284E
285 E A -3.0656 mutated: LA285E
286 S A -2.3547
287 P A -1.8773
288 E A -1.8443 mutated: FA288E
289 E A -1.9788 mutated: YA289E
290 S A 0.0000
291 E A 0.0000
292 R A -1.5924
293 L A -0.8538
294 K A 0.0000
295 E A -1.4605
296 A A 0.0000
297 H A -0.9212
298 V A 0.0000
299 R A -1.1885
300 L A 0.0000
301 Y A 0.2024
302 P A -0.1717
303 S A -0.6115
304 S A -0.7842
305 R A -1.7564
306 C A -1.0642
307 T A -1.2572
308 S A -1.2831
309 Q A -1.2122
310 H A -1.4787
311 L A 0.0000
312 L A 0.2019
313 N A -1.3399
314 R A -2.1327
315 T A -1.1689
316 V A 0.0000
317 T A -0.5222
318 D A -0.9820
319 N A -1.0687
320 M A 0.1609
321 L A 0.3183
322 C A 0.0837
323 A A 0.0000
324 G A -1.1262
325 D A 0.0000
326 T A -2.6421
327 R A -3.7712
328 S A -2.6926
329 G A -1.9929
330 G A -1.5675
331 P A -1.2857
332 Q A -1.7473
333 A A -1.4117
334 N A -2.0821
335 L A -1.5999
336 H A -1.0293
337 D A 0.0000
338 A A 0.0000
339 C A -0.5733
340 Q A -0.7577
341 G A 0.0000
342 D A 0.0000
343 S A 0.0000
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 0.0000
350 L A 0.0000
351 N A -2.7000
352 D A -3.1252
353 G A -2.4103
354 R A -2.6404
355 M A 0.0000
356 T A -0.3472
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 -0.1834
363 W A 0.0000
364 G A -0.4399
365 L A -0.0596
366 G A -0.8185
367 C A -1.1139
368 G A -2.0650
369 Q A -2.7280
370 K A -3.8726
371 D A -3.5340
372 V A 0.0000
373 P A -0.9399
374 G A 0.0000
375 V A 0.0000
376 Y A 0.0000
377 T A 0.0000
378 K A 0.0000
379 V A 0.0000
380 T A -1.0017
381 N A -1.3909
382 Y A 0.0000
383 L A 0.0000
384 D A -1.0667
385 W A -0.3319
386 I A 0.0000
387 R A -1.8222
388 D A -2.2916
389 N A -1.6834
390 M A -1.4888
391 R A -2.5610
392 P A -1.5996

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, -0.8548 in this case) is selected and presented in A3D results.


 

Laboratory of Theory of Biopolymers 2015