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Crystal structure of HCV NS3/4A protease in complex with NR01-127

Analyse Crystal structure of HCV NS3/4A protease in complex with NR01-127 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7MM3
Type
protein
Length
198 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NS3 protease
UniProt
A0A0B4WYC6
Ligands
ZJG, ZN, SO4
Pockets
1 · best druggability 0.32

Structure

x-ray diffraction · 1 distinct chain · 15% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANS3 proteaseprotein19815% helix, 44% strandA0A0B4WYC6

Ligands and binding sites

  • ZJG · Cyclobutyl {(2r,4s,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 · 9 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, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1620.320.7516empty

Compared structures

  • 7MM3 · Crystal structure of HCV NS3/4A protease in complex with NR01-127 · the same entry in another collection · chain A against A, TM-score 1.00

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