Crystal structure of HCV NS3/4A protease in complex with NR02-60

Structure

x-ray diffraction · 1 distinct chain · 12% helix, 45% strand (DSSP).

Ligands and binding sites

• ZK4 · (1R)-1-cyclopentyl-2,2,2-trifluoroethyl {(2R,4R,6S,12Z, 13as,14ar,16as)-2-[(7-methoxy-3-methylquinoxalin-2-yl)oxy]-14A-[(1-methylcyclopropane-1-sulfonyl) carbamoyl]-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13A,14, 14A,15,16,16A-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-6-yl}carbamate · ligand · chains A
• ZN · Zinc ion · metal · chains A
• SO4 · Sulfate ion · ion · chains A
• EDO · 1,2-ethanediol · additive · 2 copies · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

Compared structures

• 7MM5 · Crystal structure of HCV NS3/4A protease in complex with NR02-60 · 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 A0A0B4WYC6
• Elsewhere: RCSB PDB 7MM5 · PDBe 7MM5 · UniProt A0A0B4WYC6