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Crystal structure of nelfinavir (nfv) complexed with a multidrug variant (act) (V82T/I84V) of HIV-1 protease
Analyse Crystal structure of nelfinavir (nfv) complexed with a multidrug variant (act)… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3EL5
- Type
- protein
- Length
- 198 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protease
- EC
- 3.1.26.4
- UniProt
- P03369
- Ligands
- 1UN
- Pockets
- 1 · best druggability 0.75
Structure
x-ray diffraction · 1 distinct chain · 4% helix, 54% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Protease (EC 3.1.26.4) | protein | 99 | 4% helix, 54% strand | P03369 |
Ligands and binding sites
- 1UN · 2-[2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl sulfanyl-butyl]-decahydro-isoquinoline-3-carboxylic acid tert-butylamide · ligand · chains A, B
- ACT · Acetate ion · additive · 11 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 405 | 0.75 | 0.85 | 34 | 1UN |
Interfaces
1 interface between chains.
- A–B · 1823 Ų buried · 41 hydrogen bonds · protein-protein
Compared structures
- 3EL5 · Crystal structure of nelfinavir (NFV) complexed with a multidrug variant (ACT)… · the same entry in another collection · chain A against A, TM-score 1.00
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 P03369
- Elsewhere: RCSB PDB 3EL5 · PDBe 3EL5 · UniProt P03369
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