Research workbench
HLA-B*57:01 presenting ltvqvarvy
Analyse HLA-B*57:01 presenting ltvqvarvy in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5VUF
- Type
- protein
- Length
- 382 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class I histocompatibility antigen, B-57 alpha chain; Beta-2-microglobulin; Nonamer…
- UniProt
- P18465, P61769
- Pockets
- 4 · best druggability 0.70
Structure
x-ray diffraction · 3 distinct chains · 19% helix, 41% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | HLA class I histocompatibility antigen, B-57 alpha chain | protein | 276 | 26% helix, 39% strand | P18465 |
| B | Beta-2-microglobulin | protein | 97 | 0% helix, 51% strand | P61769 |
| C | Nonamer peptide: leu-thr-val-gln-val-ala-arg-val-tyr | protein | 9 | 0% helix, 0% strand | — |
Pockets
4 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 643 | 0.70 | 0.78 | 58 | empty |
| 2 | 104 | 0.47 | 0.80 | 19 | empty |
| 3 | 154 | 0.47 | 0.77 | 29 | empty |
| 4 | 62 | 0.37 | 0.78 | 14 | empty |
Interfaces
2 interfaces between chains.
- A–B · 1223 Ų buried · 19 hydrogen bonds · protein-protein
- A–C · 862 Ų buried · 18 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 3 disulfide (disulfide).
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 P18465
- Every structure of UniProt P61769
- Elsewhere: RCSB PDB 5VUF · PDBe 5VUF · UniProt P18465 · UniProt P61769
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