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Hepatitis C virus RNA polymerase genotype 2A in complex with non- nucleoside analogue inhibitor

Analyse Hepatitis C virus RNA polymerase genotype 2A in complex with non- nucleoside… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1YVX
Type
protein
Length
548 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
RNA dependent RNA polymerase
UniProt
P26660
Ligands
IPC, SO4
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 47% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARNA dependent RNA polymeraseprotein54847% helix, 14% strandP26660

Ligands and binding sites

  • IPC · 3-[isopropyl(4-methylbenzoyl)amino]-5-phenylthiophene-2-carboxylic acid · ligand · chains A
  • SO4 · Sulfate ion · ion · 9 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17540.760.8191SO4
2710.430.8116empty
31290.420.7525empty
4690.400.8015empty
5740.370.7718empty

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 1YVX · Hepatitis C Virus RNA Polymerase Genotype 2a In Complex With Non- Nucleoside Analogue… · the same entry in another collection · chain A against A, TM-score 1.00

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