| Chain sequence(s) |
A: MLRVFILYAENVHTPDTDISDAYCSAVFAGVKKRTKVIKNSVNPVWNEGFEWDLKGIPLDQGSELHVVVKDHETMGRNRFLGEAKVPLREVLATPSLSASFNAPLLDTKKQPTGASLVLQVSYT |
| Distance of aggregation | 10 Å |
| Dynamic mode | Yes |
| Mutated residues | VA67D |
| Energy difference between WT (input) and mutated protein (by FoldX) | 5.35139 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. |
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 | |
| 1 | M | A | 0.0645 | |
| 2 | L | A | 0.0000 | |
| 3 | R | A | -1.0047 | |
| 4 | V | A | 0.0000 | |
| 5 | F | A | 0.0013 | |
| 6 | I | A | 0.0000 | |
| 7 | L | A | 1.0763 | |
| 8 | Y | A | 1.1225 | |
| 9 | A | A | 0.0000 | |
| 10 | E | A | -1.8433 | |
| 11 | N | A | -2.2429 | |
| 12 | V | A | 0.0000 | |
| 13 | H | A | -1.2777 | |
| 14 | T | A | 0.0000 | |
| 15 | P | A | -1.4242 | |
| 16 | D | A | -2.1685 | |
| 17 | T | A | -1.1637 | |
| 18 | D | A | -0.8626 | |
| 19 | I | A | 1.1256 | |
| 20 | S | A | 0.3996 | |
| 21 | D | A | -0.0506 | |
| 22 | A | A | 0.0000 | |
| 23 | Y | A | -0.4517 | |
| 24 | C | A | 0.0000 | |
| 25 | S | A | -1.4861 | |
| 26 | A | A | 0.0000 | |
| 27 | V | A | -0.9900 | |
| 28 | F | A | 0.0000 | |
| 29 | A | A | -0.5389 | |
| 30 | G | A | -0.7605 | |
| 31 | V | A | -1.0472 | |
| 32 | K | A | -2.3813 | |
| 33 | K | A | -2.3094 | |
| 34 | R | A | -2.7389 | |
| 35 | T | A | -1.4102 | |
| 36 | K | A | -1.1028 | |
| 37 | V | A | 0.2588 | |
| 38 | I | A | 1.6496 | |
| 39 | K | A | 0.6484 | |
| 40 | N | A | -0.2448 | |
| 41 | S | A | -0.3318 | |
| 42 | V | A | -0.6371 | |
| 43 | N | A | -1.3526 | |
| 44 | P | A | 0.0000 | |
| 45 | V | A | 1.4129 | |
| 46 | W | A | 0.0000 | |
| 47 | N | A | -0.4262 | |
| 48 | E | A | 0.0000 | |
| 49 | G | A | -0.7631 | |
| 50 | F | A | -0.9418 | |
| 51 | E | A | -1.2112 | |
| 52 | W | A | -0.8588 | |
| 53 | D | A | -1.6272 | |
| 54 | L | A | -0.5142 | |
| 55 | K | A | -1.5234 | |
| 56 | G | A | -0.8890 | |
| 57 | I | A | -0.1670 | |
| 58 | P | A | -0.4608 | |
| 59 | L | A | -0.9719 | |
| 60 | D | A | -2.5466 | |
| 61 | Q | A | -2.8585 | |
| 62 | G | A | -2.4234 | |
| 63 | S | A | 0.0000 | |
| 64 | E | A | -2.1257 | |
| 65 | L | A | 0.0000 | |
| 66 | H | A | -1.0285 | |
| 67 | D | A | 0.0000 | mutated: VA67D |
| 68 | V | A | 0.0572 | |
| 69 | V | A | 0.0000 | |
| 70 | K | A | -0.9561 | |
| 71 | D | A | 0.0000 | |
| 72 | H | A | -1.1750 | |
| 73 | E | A | -0.9302 | |
| 74 | T | A | -0.4716 | |
| 75 | M | A | 0.1798 | |
| 76 | G | A | -0.8259 | |
| 77 | R | A | -1.3824 | |
| 78 | N | A | -1.7891 | |
| 79 | R | A | -1.0021 | |
| 80 | F | A | 0.0853 | |
| 81 | L | A | 0.0000 | |
| 82 | G | A | 0.0000 | |
| 83 | E | A | -0.2139 | |
| 84 | A | A | 0.0000 | |
| 85 | K | A | -1.3824 | |
| 86 | V | A | 0.0000 | |
| 87 | P | A | -1.9911 | |
| 88 | L | A | 0.0000 | |
| 89 | R | A | -3.3486 | |
| 90 | E | A | -2.7173 | |
| 91 | V | A | -1.1690 | |
| 92 | L | A | -1.0672 | |
| 93 | A | A | -1.1363 | |
| 94 | T | A | -0.7651 | |
| 95 | P | A | -0.2635 | |
| 96 | S | A | -0.1785 | |
| 97 | L | A | 0.0000 | |
| 98 | S | A | -0.3369 | |
| 99 | A | A | -0.3970 | |
| 100 | S | A | -0.4147 | |
| 101 | F | A | -0.4127 | |
| 102 | N | A | -0.9191 | |
| 103 | A | A | 0.0000 | |
| 104 | P | A | -0.4579 | |
| 105 | L | A | 0.0000 | |
| 106 | L | A | 0.4894 | |
| 107 | D | A | 0.0000 | |
| 108 | T | A | -0.8082 | |
| 109 | K | A | -1.9908 | |
| 110 | K | A | -1.6881 | |
| 111 | Q | A | -1.8289 | |
| 112 | P | A | -0.9702 | |
| 113 | T | A | 0.0000 | |
| 114 | G | A | -1.0018 | |
| 115 | A | A | 0.0000 | |
| 116 | S | A | -0.9716 | |
| 117 | L | A | 0.0000 | |
| 118 | V | A | 0.7931 | |
| 119 | L | A | 0.0000 | |
| 120 | Q | A | -0.4181 | |
| 121 | V | A | 0.0000 | |
| 122 | S | A | -0.1123 | |
| 123 | Y | A | 0.5153 | |
| 124 | T | A | 0.1372 |
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, -0.618 in this case) is selected and presented in A3D results.
ALA alanine
ARG arginine
ASN asparagine
ASP aspartic acid
CYS cysteine
GLN glutamine
GLU glutamic acid
GLY glycine
HIS histidine
ILE isoleucine
LEU leucine
LYS lysine
MET methionine
PHE phenylalanine
PRO proline
SER serine
THR threonine
TRP tryptophan
TYR tyrosine
VAL valine