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Structure of hepatitis C virus envelope glycoprotein E2 core from genotype 6A bound to broadly neutralizing antibody AR3D

Analyse Structure of hepatitis C virus envelope glycoprotein E2 core from genotype 6A… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6BKD
Type
protein
Length
580 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Polyprotein; Fab AR3D heavy chain; Fab AR3D light chain
UniProt
B9V0E2, S6B2A6, Q6PIL8
Ligands
NAG
Pockets
3 · best druggability 0.59

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
EPolyproteinprotein15013% helix, 34% strandB9V0E2
HFab AR3D heavy chainprotein2232% helix, 49% strandS6B2A6
LFab AR3D light chainprotein2074% helix, 47% strandQ6PIL8

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15440.590.7363empty
21210.400.7523empty
3660.340.7617empty

Interfaces

2 interfaces between chains.

  • H–L · 1702 Ų buried · 9 hydrogen bonds · protein-protein
  • E–H · 693 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 6BKD · Structure of Hepatitis C Virus Envelope Glycoprotein E2 core from genotype 6a bound to… · the same entry in another collection · chain E against E, TM-score 1.00

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