MolNFT v2 · #51070 · protein
Large CDR3a loop alteration as a function of MHC mutation
2UWE · HLA class I histocompatibility antigen, a-2 alpha chain: “Large CDR3a loop alteration as a function of MHC mutation”. X-ray diffraction at 2.4, 20 pockets (best druggability 0.74). MolNFT v2 #51070 on GenesisL1: 3D structure…
- PDB
- 2UWE
- Type
- protein
- Length
- 1,630 residues
- Chains
- 10
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.4
- Source
- HOMO SAPIENS; MUS MUSCULUS; SYNTHETIC CONSTRUCT
- Molecule
- HLA class I histocompatibility antigen, a-2 alpha chain; Beta-2-microglobulin…
- UniProt
- P01892, P61769, Q9NPA0
- Pockets
- 20 · best druggability 0.74
Structure
x-ray diffraction · resolution 2.4 · 5 distinct chains · 12% helix, 45% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, H | HLA class I histocompatibility antigen, a-2 alpha chain | protein | 275 | 27% helix, 40% strand | P01892 |
| B, I | Beta-2-microglobulin | protein | 100 | 0% helix, 51% strand | P61769 |
| C, J | Uncharacterized protein C15ORF24 | protein | 9 | 0% helix, 0% strand | Q9NPA0 |
| E, L | Ahiii TCR alpha chain | protein | 194 | 2% helix, 41% strand | — |
| F, M | Ahiii TCR beta chain | protein | 237 | 8% helix, 52% strand | — |
Pockets
20 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1194 | 0.74 | 0.77 | 83 | empty |
| 2 | 1178 | 0.73 | 0.76 | 82 | empty |
| 3 | 758 | 0.71 | 0.77 | 70 | empty |
| 4 | 656 | 0.70 | 0.78 | 57 | empty |
| 5 | 472 | 0.64 | 0.77 | 40 | empty |
Interfaces
18 interfaces between chains.
- E–F · 2286 Ų buried · 33 hydrogen bonds · protein-protein
- L–M · 2222 Ų buried · 35 hydrogen bonds · protein-protein
- H–I · 1437 Ų buried · 26 hydrogen bonds · protein-protein
- A–B · 1378 Ų buried · 23 hydrogen bonds · protein-protein
- H–J · 864 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 P01892
- Every structure of UniProt P61769
- Every structure of UniProt Q9NPA0
- Elsewhere: RCSB PDB 2UWE · PDBe 2UWE · UniProt P01892 · UniProt P61769 · UniProt Q9NPA0
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