MolNFT v1 · #73686 · protein

Crystal structure of wild-type HIV-1 protease in complex with AF53

3O9G: “Crystal structure of wild-type HIV-1 protease in complex with AF53”. X-ray diffraction, 2 ligands (F53, PO4), 1 pocket (best druggability 0.70). MolNFT v1 #73686 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB: 3O9G
Type: protein
Length: 198 residues
Chains: 2
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Protease
UniProt: Q90K99
Ligands: F53, PO4
Pockets: 1 · best druggability 0.70

Structure

x-ray diffraction · 1 distinct chain · 4% helix, 54% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A, B	Protease	protein	99	4% helix, 54% strand	Q90K99

Ligands and binding sites

F53 · (3r,3as,6ar)-hexahydrofuro[2,3-b]furan-3-yl {(1S,2R)-1-benzyl-3-[(2-ethylbutyl){[4-(hydroxymethyl) phenyl]sulfonyl}amino]-2-hydroxypropyl}carbamate · ligand · chains A, B
PO4 · Phosphate ion · ion · 3 copies · chains A

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.

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	382	0.70	0.82	35	F53

Interfaces

1 interface between chains.

A–B · 1843 Å² buried · 42 hydrogen bonds · protein-protein

Compared structures

3O9G · Crystal Structure of wild-type HIV-1 Protease in complex with af53 · 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 Q90K99
Elsewhere: RCSB PDB 3O9G · PDBe 3O9G · UniProt Q90K99

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