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Crystal structure of HCV NS3/NS4A protease complexed with bi 201335

Analyse Crystal structure of HCV NS3/NS4A protease complexed with bi 201335 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3P8N
Type
protein
Length
390 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HCV serine protease NS3; HCV non-structural protein 4A
EC
3.4.21.98
UniProt
P26662
Ligands
L4T, NA
Pockets
2 · best druggability 0.37

Structure

x-ray diffraction · 2 distinct chains · 16% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHCV serine protease NS3 (EC 3.4.21.98)protein18217% helix, 45% strandP26662
C, DHCV non-structural protein 4Aprotein130% helix, 69% strand—

Ligands and binding sites

  • L4T · N-[(cyclopentyloxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(8-bromo-7-methoxy-2-{2-[(2-methylpropanoyl)amino]-1,3-thiazol-4-yl}quinolin-4-yl)oxy]-N-[(1R,2S)-1-carboxy-2-ethenylcyclopropyl]-L-prolinamide · ligand · 2 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B

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.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1730.370.7819empty
2540.350.7917empty

Interfaces

3 interfaces between chains.

  • B–D · 1222 Ų buried · 27 hydrogen bonds · protein-protein
  • A–C · 1196 Ų buried · 29 hydrogen bonds · protein-protein
  • A–B · 442 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 3P8N · Crystal structure of HCV NS3/NS4A protease complexed with BI 201335 · the same entry in another collection · chain A against A, TM-score 1.00

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