MolNFT v1 · #115602 · protein

X-ray crystal structure of wild type HIV-1 protease in complex with grl-015

5CON: “X-ray crystal structure of wild type HIV-1 protease in complex with grl-015”. X-ray diffraction, 1 ligand (52W), 1 pocket (best druggability 0.72). MolNFT v1 #115602 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB: 5CON
Type: protein
Length: 198 residues
Chains: 2
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: HIV-1 protease
UniProt: G0X8E3
Ligands: 52W
Pockets: 1 · best druggability 0.72

Structure

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

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A, B	HIV-1 protease	protein	99	4% helix, 54% strand	G0X8E3

Ligands and binding sites

52W · (3R,3aS,4S,7aS)-3-hydroxyhexahydro-4H-furo[2,3-b]pyran-4-yl [(2S,3R)-3-hydroxy-4-{[(4-methoxyphenyl)sulfonyl](2-methylpropyl)amino}-1-phenylbutan-2-yl]carbamate · ligand · 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.

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	385	0.72	0.83	34	52W

Interfaces

1 interface between chains.

A–B · 1780 Å² buried · 35 hydrogen bonds · protein-protein

Compared structures

5CON · X-ray crystal structure of wild type HIV-1 protease in complex with GRL-015 · 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 G0X8E3
Elsewhere: RCSB PDB 5CON · PDBe 5CON · UniProt G0X8E3

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