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Hepatitis C virus NS5B RNA polymerase in complex with a covalent inhibitor (5X)

Analyse Hepatitis C virus NS5B RNA polymerase in complex with a covalent inhibitor (5X) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2AX0
Type
protein
Length
1,111 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Genome polyprotein
EC
2.7.7.48
UniProt
P26663
Ligands
5X, SO4
Pockets
16 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 48% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGenome polyprotein (EC 2.7.7.48)protein55449% helix, 15% strandP26663
BGenome polyprotein (EC 2.7.7.48)protein55748% helix, 15% strandP26663

Ligands and binding sites

  • 5X · 5R-(2E-methyl-3-phenyl-allyl)-3-(benzenesulfonylamino)-4-oxo-2-thionothiazolidine · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 7 copies · chains A, B

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

Pockets

16 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19370.790.8177SO4, 5X
26050.780.8370SO4, 5X
33340.540.7434empty
41190.500.8017empty
51190.480.7919empty

Interfaces

1 interface between chains.

  • A–B · 515 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 2AX0 · Hepatitis C Virus NS5b RNA Polymerase in complex with a covalent inhibitor (5x) · the same entry in another collection · chain A against A, TM-score 1.00

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