Research workbench
Crystal structure of the T-cell receptor NYE_S3 bound to HLA A2*01- sllmwitqv
Analyse Crystal structure of the T-cell receptor NYE_S3 bound to HLA A2*01- sllmwitqv in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6RP9
- Type
- protein
- Length
- 2,081 residues
- Chains
- 12
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class I histocompatibility antigen, a-2 alpha chain; Beta-2-microglobulin…
- UniProt
- P01892, P61769, P78358
- Pockets
- 20 · best druggability 0.73
Structure
x-ray diffraction · 8 distinct chains · 8% helix, 45% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, F | HLA class I histocompatibility antigen, a-2 alpha chain | protein | 275 | 26% helix, 38% strand | P01892 |
| B, G | Beta-2-microglobulin | protein | 100 | 0% helix, 47% strand | P61769 |
| C, H | CANCER/TESTIS antigen 1 | protein | 9 | 0% helix, 0% strand | P78358 |
| D | T-cell receptor alpha chain | protein | 197 | 2% helix, 46% strand | — |
| E, J | T-cell receptor beta chain | protein | 244 | 7% helix, 48% strand | — |
| I | T-cell receptor alpha chain | protein | 198 | 2% helix, 46% strand | — |
| K | T-cell receptor alpha chain | protein | 187 | 2% helix, 47% strand | — |
| L | T-cell receptor beta chain | protein | 243 | 7% helix, 49% strand | — |
Pockets
20 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 864 | 0.73 | 0.78 | 79 | empty |
| 2 | 1015 | 0.73 | 0.76 | 79 | empty |
| 3 | 1189 | 0.73 | 0.76 | 76 | empty |
| 4 | 622 | 0.70 | 0.79 | 57 | empty |
| 5 | 748 | 0.70 | 0.77 | 64 | empty |
Interfaces
16 interfaces between chains.
- I–J · 2093 Ų buried · 33 hydrogen bonds · protein-protein
- D–E · 2087 Ų buried · 31 hydrogen bonds · protein-protein
- K–L · 1967 Ų buried · 26 hydrogen bonds · protein-protein
- F–G · 1499 Ų buried · 26 hydrogen bonds · protein-protein
- A–B · 1461 Ų buried · 27 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 20 disulfide (disulfide).
Compared structures
- 6RP9 · Crystal structure of the T-cell receptor NYE_S3 bound to HLA A2*01-SLLMWITQV · the same entry in another collection · chain L against L, TM-score 1.00
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 P01892
- Every structure of UniProt P61769
- Every structure of UniProt P78358
- Elsewhere: RCSB PDB 6RP9 · PDBe 6RP9 · UniProt P01892 · UniProt P61769 · UniProt P78358
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