Research workbench
1E6-A*0201-alwgpdpaaa complex, triclinic
Analyse 1E6-A*0201-alwgpdpaaa complex, triclinic in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3UTT
- Type
- protein
- Length
- 1,657 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; Insulin…
- UniProt
- P01892, P61769, P01308
- Pockets
- 19 · best druggability 0.75
Structure
x-ray diffraction · 6 distinct chains · 10% helix, 45% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, F | HLA class I histocompatibility antigen, a-2 alpha chain | protein | 275 | 25% helix, 38% strand | P01892 |
| B, G | Beta-2-microglobulin | protein | 100 | 0% helix, 51% strand | P61769 |
| C, H | Insulin | protein | 10 | 0% helix, 0% strand | P01308 |
| D, I | 1E6 TCR alpha chain | protein | 199 | 0% helix, 46% strand | — |
| E | 1E6 TCR beta chain | protein | 244 | 9% helix, 47% strand | — |
| J | 1E6 TCR beta chain | protein | 245 | 8% helix, 49% strand | — |
Pockets
19 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 976 | 0.75 | 0.78 | 78 | empty |
| 2 | 902 | 0.72 | 0.77 | 73 | empty |
| 3 | 956 | 0.69 | 0.74 | 93 | empty |
| 4 | 836 | 0.67 | 0.74 | 67 | empty |
| 5 | 509 | 0.66 | 0.77 | 50 | empty |
Interfaces
18 interfaces between chains.
- D–E · 2387 Ų buried · 28 hydrogen bonds · protein-protein
- I–J · 2386 Ų buried · 26 hydrogen bonds · protein-protein
- F–G · 1369 Ų buried · 29 hydrogen bonds · protein-protein
- A–B · 1343 Ų buried · 21 hydrogen bonds · protein-protein
- A–C · 742 Ų buried · 14 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
- Every structure of UniProt P01308
- Elsewhere: RCSB PDB 3UTT · PDBe 3UTT · UniProt P01892 · UniProt P61769 · UniProt P01308
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