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Villin headpiece subdomain with a Gln26 to beta-3-homoglutamine substitution

Analyse Villin headpiece subdomain with a Gln26 to beta-3-homoglutamine substitution in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5I1N
Type
protein
Length
280 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.3
Molecule
Villin-1; D-Villin headpiece subdomain
UniProt
P02640
Pockets
5 · best druggability 0.60

Structure

x-ray diffraction · resolution 1.3 · 2 distinct chains · 64% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DVillin-1protein3563% helix, 0% strandP02640
E, F, G, HD-Villin headpiece subdomainprotein3566% helix, 0% strand—

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13770.600.7642empty
23960.590.7555empty
31130.390.7419empty
4970.340.7319empty
5560.310.7616empty

Interfaces

16 interfaces between chains.

  • C–F · 380 Ų buried · 4 hydrogen bonds · protein-protein
  • A–H · 362 Ų buried · 3 hydrogen bonds · protein-protein
  • D–E · 329 Ų buried · 4 hydrogen bonds · protein-protein
  • B–G · 324 Ų buried · 4 hydrogen bonds · protein-protein
  • E–G · 274 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 132 d-amino, 4 modified (D-amino acid, nonstandard).

Compared structures

  • 5I1N · Villin headpiece subdomain with a GLN26 to beta-3-homoglutamine substitution · the same entry in another collection · chain F against F, TM-score 1.00
  • P02640 · AlphaFold monomer V2.0 prediction for villin-1 (P02640) · a predicted model of the same protein · chain A against A, TM-score 0.89

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