Research workbench
1E6 TCR in complex with HLA-A02 carrying aqwgpdpaaa
Analyse 1E6 TCR in complex with HLA-A02 carrying aqwgpdpaaa in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5HYJ
- Type
- protein
- Length
- 1,650 residues
- Chains
- 10
- 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
- Pockets
- 20 · best druggability 0.76
Structure
x-ray diffraction · 5 distinct chains · 12% helix, 42% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, F | HLA class I histocompatibility antigen, a-2 alpha chain | protein | 276 | 26% helix, 36% strand | P01892 |
| B, G | Beta-2-microglobulin | protein | 100 | 0% helix, 45% strand | P61769 |
| C, H | Ala-gln-TRP-gly-pro-asp-pro-ala-ala-ala | protein | 10 | 0% helix, 0% strand | — |
| D, I | Human T-cell receptor, class I, light alpha chain | protein | 193 | 3% helix, 44% strand | — |
| E, J | Human T-cell receptor, class I, heavy beta chain | protein | 246 | 8% 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 | 1035 | 0.76 | 0.78 | 92 | empty |
| 2 | 1138 | 0.72 | 0.76 | 81 | empty |
| 3 | 500 | 0.68 | 0.79 | 45 | empty |
| 4 | 575 | 0.68 | 0.78 | 54 | empty |
| 5 | 566 | 0.65 | 0.76 | 57 | empty |
Interfaces
17 interfaces between chains.
- I–J · 2412 Ų buried · 27 hydrogen bonds · protein-protein
- D–E · 2408 Ų buried · 26 hydrogen bonds · protein-protein
- A–B · 1493 Ų buried · 18 hydrogen bonds · protein-protein
- F–G · 1446 Ų buried · 15 hydrogen bonds · protein-protein
- D–I · 845 Ų buried · 20 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 16 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 P01892
- Every structure of UniProt P61769
- Elsewhere: RCSB PDB 5HYJ · PDBe 5HYJ · UniProt P01892 · UniProt P61769
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