Project name: SH3_E129L

Status: done

submitted: 2019-03-14 19:20:20, status changed: 2019-03-14 22:29:06
Settings
Chain sequence(s) A: TLFVALYDYEARTEDDLSFHKGEEKFQQILNSSEGDWWEARRSLTTGETGYIPSNYVAPV
Distance of aggregation 10 Å
Dynamic mode No
Mutated residues EA129L
Energy difference between WT (input) and mutated protein (by FoldX) -0.2452 kcal/mol

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
-3.103
Maximal score value
1.7964
Average score
-0.7648
Total score value
-43.5927

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
85 T A 0.5173
86 L A 0.7932
87 F A 0.9242
88 V A 0.4320
89 A A 0.0000
90 L A -0.1508
91 Y A -0.5745
92 D A -2.5598
93 Y A -1.9320
94 E A -2.6459
95 A A -2.6266
96 R A -2.9855
97 T A -2.6610
98 E A -3.1030
99 D A -3.0419
100 D A 0.0000
101 L A 0.0000
102 S A -1.8060
103 F A 0.0000
104 H A -2.7278
105 K A -2.4052
106 G A -1.4570
107 E A -1.3055
108 K A -0.6415
109 F A 0.0000
110 Q A -0.5076
111 I A -0.0554
112 L A 0.1446
113 N A -0.8883
114 S A -1.1799
115 S A -1.5966
116 E A -2.5603
117 G A -2.1347
118 D A -2.4456
119 W A -1.1053
120 W A -1.0569
121 E A -1.1508
122 A A 0.0000
123 R A -0.6363
124 S A 0.0000
125 L A 0.6011
126 T A 0.0705
127 T A 0.2712
128 G A 0.2853
129 L A 1.1335 mutated: EA129L
130 T A -0.0223
131 G A -0.7270
132 Y A -0.8657
133 I A 0.0000
134 P A 0.0000
135 S A -0.9214
136 N A -1.1508
137 Y A -0.1246
138 V A 0.0000
139 A A 0.4158
140 P A 0.7757
141 V A 1.7964

 

Laboratory of Theory of Biopolymers 2015