Research workbench
TCR peptide HLA-A2 complex
Analyse TCR peptide 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
- 7N6E
- Type
- protein
- Length
- 1,636 residues
- Chains
- 10
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- MHC class I antigen; Beta-2-microglobulin; Spike protein S1; TRAV12-1 TCR-alpha; TRBV19…
- UniProt
- Q861F7, P61769, P0DTC2
- Pockets
- 18 · best druggability 0.80
Structure
x-ray diffraction · 7 distinct chains · 13% helix, 43% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | MHC class I antigen | protein | 271 | 27% helix, 39% strand | Q861F7 |
| B, E | Beta-2-microglobulin | protein | 99 | 0% helix, 49% strand | P61769 |
| C, F | Spike protein S1 | protein | 9 | 0% helix, 0% strand | P0DTC2 |
| D | MHC class I antigen | protein | 274 | 26% helix, 40% strand | Q861F7 |
| G | TRAV12-1 TCR-alpha | protein | 198 | 4% helix, 45% strand | — |
| I | TRAV12-1 TCR-alpha | protein | 199 | 4% helix, 45% strand | — |
| H, J | TRBV19 TCR beta | protein | 239 | 6% helix, 49% strand | — |
Pockets
18 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1143 | 0.80 | 0.81 | 95 | empty |
| 2 | 963 | 0.71 | 0.76 | 87 | empty |
| 3 | 641 | 0.71 | 0.78 | 52 | empty |
| 4 | 679 | 0.69 | 0.77 | 55 | empty |
| 5 | 666 | 0.69 | 0.77 | 54 | empty |
Interfaces
18 interfaces between chains.
- G–H · 2238 Ų buried · 24 hydrogen bonds · protein-protein
- I–J · 2236 Ų buried · 25 hydrogen bonds · protein-protein
- A–B · 1346 Ų buried · 24 hydrogen bonds · protein-protein
- D–E · 1315 Ų buried · 21 hydrogen bonds · protein-protein
- A–C · 906 Ų buried · 12 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 14 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 P0DTC2
- Elsewhere: RCSB PDB 7N6E · PDBe 7N6E · UniProt Q861F7 · UniProt P61769 · UniProt P0DTC2
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