Research workbench
HLA-A24 in complex with HIV-1 NEF134-8(WT)
Analyse HLA-A24 in complex with HIV-1 NEF134-8(WT) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4WU5
- Type
- protein
- Length
- 762 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class I histocompatibility antigen, a-24 alpha chain; Beta-2-microglobulin; 8-mer…
- UniProt
- P05534, P61769, Q9YYU8
- Pockets
- 10 · best druggability 0.70
Structure
x-ray diffraction · 3 distinct chains · 20% helix, 42% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | HLA class I histocompatibility antigen, a-24 alpha chain | protein | 274 | 28% helix, 40% strand | P05534 |
| B, E | Beta-2-microglobulin | protein | 99 | 0% helix, 49% strand | P61769 |
| C, F | 8-mer peptide from protein nef | protein | 8 | 0% helix, 0% strand | Q9YYU8 |
Pockets
10 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 677 | 0.70 | 0.78 | 58 | empty |
| 2 | 601 | 0.68 | 0.77 | 53 | empty |
| 3 | 713 | 0.67 | 0.75 | 66 | empty |
| 4 | 164 | 0.47 | 0.77 | 26 | empty |
| 5 | 120 | 0.42 | 0.76 | 23 | empty |
Interfaces
6 interfaces between chains.
- D–E · 1321 Ų buried · 18 hydrogen bonds · protein-protein
- A–B · 1308 Ų buried · 20 hydrogen bonds · protein-protein
- D–F · 976 Ų buried · 15 hydrogen bonds · protein-protein
- A–C · 957 Ų buried · 15 hydrogen bonds · protein-protein
- A–E · 250 Ų buried · 10 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 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 P05534
- Every structure of UniProt P61769
- Every structure of UniProt Q9YYU8
- Elsewhere: RCSB PDB 4WU5 · PDBe 4WU5 · UniProt P05534 · UniProt P61769 · UniProt Q9YYU8
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