Research workbench
Crystal structure of the TK3-GLN55HIS TCR in complex with HLA- B*3501/HPVG
Analyse Crystal structure of the TK3-GLN55HIS TCR in complex with HLA- B*3501/HPVG in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3MV8
- Type
- protein
- Length
- 829 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class I histocompatibility antigen, B-35 alpha chain; Beta-2-microglobulin; Hpvg…
- UniProt
- P30685, P61769, P03211
- Ligands
- SO4
- Pockets
- 11 · best druggability 0.70
Structure
x-ray diffraction · 5 distinct chains · 11% helix, 45% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | HLA class I histocompatibility antigen, B-35 alpha chain | protein | 276 | 25% helix, 40% strand | P30685 |
| B | Beta-2-microglobulin | protein | 100 | 0% helix, 49% strand | P61769 |
| C | Hpvg peptide from epstein-barr nuclear antigen 1 | protein | 11 | 0% helix, 0% strand | P03211 |
| D | Alpha chain of the TK3 TCR | protein | 200 | 5% helix, 48% strand | — |
| E | Beta chain of the TK3 TCR | protein | 242 | 6% helix, 51% strand | — |
Ligands and binding sites
- SO4 · Sulfate ion · ion · chains E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1105 | 0.70 | 0.75 | 83 | empty |
| 2 | 613 | 0.70 | 0.78 | 61 | empty |
| 3 | 156 | 0.45 | 0.75 | 23 | empty |
| 4 | 153 | 0.45 | 0.76 | 31 | empty |
| 5 | 84 | 0.42 | 0.79 | 22 | empty |
Interfaces
7 interfaces between chains.
- D–E · 2132 Ų buried · 21 hydrogen bonds · protein-protein
- A–B · 1284 Ų buried · 22 hydrogen bonds · protein-protein
- A–C · 908 Ų buried · 16 hydrogen bonds · protein-protein
- A–D · 402 Ų buried · 1 hydrogen bond · protein-protein
- A–E · 302 Ų buried · 1 hydrogen bond · protein-protein
Modifications
Observed in the structure: 8 disulfide (disulfide).
Compared structures
- 3MV8 · Crystal Structure of the TK3-Gln55His TCR in complex with HLA-B*3501/HPVG · the same entry in another collection · chain A against A, TM-score 1.00
- P61769 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P61769) · a predicted model of the same protein · chain B against A, TM-score 0.97
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 P30685
- Every structure of UniProt P61769
- Every structure of UniProt P03211
- Elsewhere: RCSB PDB 3MV8 · PDBe 3MV8 · UniProt P30685 · UniProt P61769 · UniProt P03211
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