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Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function

Analyse Discovery of an allosteric mechanism for the regulation of HCV NS3 protein… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4B71
Type
protein
Length
1,287 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Non-structural protein 4A, serine protease NS3
EC
3.4.21.98, 3.6.1.15, 3.6.4.13
UniProt
P26663
Ligands
DJL
Pockets
15 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 28% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANon-structural protein 4A, serine protease NS3 (EC 3.4.21.98, 3.6.1.15, 3.6.4.13)protein64528% helix, 29% strandP26663
BNon-structural protein 4A, serine protease NS3 (EC 3.4.21.98, 3.6.1.15, 3.6.4.13)protein64228% helix, 28% strandP26663

Ligands and binding sites

  • DJL · (1R)-1-(4-chloro-2-fluoro-3-phenoxyphenyl)propan-1-aminium · ligand · 2 copies · chains A, B

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

Pockets

15 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111530.800.81115DJL
26510.780.8374empty
32570.700.8537empty
44270.660.7939empty
53960.640.7847empty

Interfaces

1 interface between chains.

  • A–B · 1467 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 4B71 · Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function · the same entry in another collection · chain A against A, TM-score 1.00

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