Research workbench
HIV-1 nef protein in complex with R96I mutant fyn SH3 domain
Analyse HIV-1 nef protein in complex with R96I mutant fyn SH3 domain in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1EFN
- Type
- protein
- Length
- 322 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Fyn tyrosine kinase; HIV-1 nef protein
- EC
- 2.7.1.112
- UniProt
- P06241, P03406
- Ligands
- PBM
- Pockets
- 3 · best druggability 0.55
Structure
x-ray diffraction · 2 distinct chains · 27% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Fyn tyrosine kinase (EC 2.7.1.112) | protein | 57 | 5% helix, 49% strand | P06241 |
| B, D | HIV-1 nef protein | protein | 104 | 38% helix, 14% strand | P03406 |
Ligands and binding sites
- PBM · Trimethyl lead ion · ligand · 2 copies · chains B, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 221 | 0.55 | 0.78 | 30 | PBM |
| 2 | 89 | 0.35 | 0.75 | 17 | empty |
| 3 | 82 | 0.33 | 0.74 | 14 | empty |
Interfaces
3 interfaces between chains.
- A–B · 651 Ų buried · 11 hydrogen bonds · protein-protein
- C–D · 626 Ų buried · 9 hydrogen bonds · protein-protein
- B–D · 398 Ų buried · 2 hydrogen bonds · protein-protein
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 P06241
- Every structure of UniProt P03406
- Elsewhere: RCSB PDB 1EFN · PDBe 1EFN · UniProt P06241 · UniProt P03406
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