Research workbench
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).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Villin-1 | protein | 35 | 63% helix, 0% strand | P02640 |
| E, F, G, H | D-Villin headpiece subdomain | protein | 35 | 66% helix, 0% strand | — |
Pockets
5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 377 | 0.60 | 0.76 | 42 | empty |
| 2 | 396 | 0.59 | 0.75 | 55 | empty |
| 3 | 113 | 0.39 | 0.74 | 19 | empty |
| 4 | 97 | 0.34 | 0.73 | 19 | empty |
| 5 | 56 | 0.31 | 0.76 | 16 | empty |
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
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P02640
- Elsewhere: RCSB PDB 5I1N · PDBe 5I1N · UniProt P02640
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