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MolNFT v1 · #86430 · protein

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

4B6F · Non-structural protein 4A, serine protease NS3: “Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function”. X-ray diffraction, 2 ligands (20L, SO4), 14 pockets (best druggability 0.77). MolNFT v1 #86430 on…

PDB
4B6F
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
20L, SO4
Pockets
14 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 27% 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)protein64527% helix, 29% strandP26663
BNon-structural protein 4A, serine protease NS3 (EC 3.4.21.98, 3.6.1.15, 3.6.4.13)protein64227% helix, 28% strandP26663

Ligands and binding sites

  • 20L · (4-phenoxyphenyl)methylazanium · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B

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

Pockets

14 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15830.770.8469empty
26040.770.8365SO4
32260.670.8436empty
43350.630.7934empty
52100.620.833320L

Interfaces

1 interface between chains.

  • A–B · 1416 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 4B6F · 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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