Research workbench
T cell receptor-P53-HLA-A2 complex
Analyse T cell receptor-P53-HLA-A2 complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6VRM
- Type
- protein
- Length
- 809 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- MHC class I antigen; Beta-2-microglobulin; T-cell receptor 12-6, alfa chain; TCR 12-6…
- UniProt
- Q861F7, P61769, P04637
- Pockets
- 9 · best druggability 0.72
Structure
x-ray diffraction · 5 distinct chains · 11% helix, 43% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | MHC class I antigen | protein | 273 | 26% helix, 39% strand | Q861F7 |
| B | Beta-2-microglobulin | protein | 100 | 0% helix, 49% strand | P61769 |
| D | T-cell receptor 12-6, alfa chain | protein | 183 | 2% helix, 44% strand | — |
| E | TCR 12-6, beta chain | protein | 244 | 7% helix, 48% strand | — |
| P | Cellular tumor antigen P53 peptide | protein | 9 | 0% helix, 0% strand | P04637 |
Pockets
9 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1031 | 0.72 | 0.76 | 84 | empty |
| 2 | 542 | 0.66 | 0.77 | 51 | empty |
| 3 | 94 | 0.51 | 0.83 | 22 | empty |
| 4 | 170 | 0.48 | 0.77 | 30 | empty |
| 5 | 120 | 0.40 | 0.76 | 21 | empty |
Interfaces
7 interfaces between chains.
- D–E · 2076 Ų buried · 23 hydrogen bonds · protein-protein
- A–B · 1325 Ų buried · 15 hydrogen bonds · protein-protein
- A–P · 916 Ų buried · 17 hydrogen bonds · protein-protein
- A–D · 408 Ų buried · 7 hydrogen bonds · protein-protein
- A–E · 290 Ų buried · 2 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 7 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 Q861F7
- Every structure of UniProt P61769
- Every structure of UniProt P04637
- Elsewhere: RCSB PDB 6VRM · PDBe 6VRM · UniProt Q861F7 · UniProt P61769 · UniProt P04637
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