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Complex HCV core-Fab 19D9D6-protein L mutant (D55A, L57H, Y64W) in space group P21212

Analyse Complex HCV core-Fab 19D9D6-protein L mutant (D55A, L57H, Y64W) in space group… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1XCT
Type
protein
Length
1,069 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Capsid protein C; Monoclonal antibody 19D9D6 light chain; Monoclonal antibody 19D9D6…
UniProt
P26661
Pockets
10 · best druggability 0.72

Structure

x-ray diffraction · 6 distinct chains · 11% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
PCapsid protein Cprotein3010% helix, 0% strandP26661
QCapsid protein Cprotein220% helix, 0% strandP26661
A, CMonoclonal antibody 19D9D6 light chainprotein2208% helix, 52% strand—
B, DMonoclonal antibody 19D9D6 heavy chainprotein2187% helix, 48% strand—
LProtein Lprotein7027% helix, 39% strand—
MProtein Lprotein7118% helix, 37% strand—

Pockets

10 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17740.720.7867empty
23630.620.7851empty
34980.590.7470empty
42260.560.7834empty
52520.520.7636empty

Interfaces

10 interfaces between chains.

  • C–D · 1885 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 1775 Ų buried · 13 hydrogen bonds · protein-protein
  • C–M · 709 Ų buried · 13 hydrogen bonds · protein-protein
  • L–M · 674 Ų buried · 6 hydrogen bonds · protein-protein
  • P–B · 611 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 1XCT · Complex HCV core-Fab 19D9D6-Protein L mutant (D55A, L57H, Y64W) in space group P21212 · the same entry in another collection · chain P against P, TM-score 1.00

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