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Structure of hepatitis C virus envelope glycoprotein E2 core from genotype 6A bound to broadly neutralizing antibody RM11-43

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
7JTG
Type
protein
Length
582 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
RM11-43 Fab heavy chain; RM11-43 Fab light chain; Envelope glycoprotein E2
UniProt
B9V0E2
Ligands
NAG
Pockets
6 · best druggability 0.49

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARM11-43 Fab heavy chainprotein2247% helix, 51% strand—
BRM11-43 Fab light chainprotein2126% helix, 52% strand—
EEnvelope glycoprotein E2protein14614% helix, 34% strandB9V0E2

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 3 copies · chains E, A

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

Pockets

6 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12100.490.7531empty
2960.480.8114empty
31160.360.7325empty
4860.350.7518empty
5540.280.7416empty

Interfaces

3 interfaces between chains.

  • A–B · 1685 Ų buried · 12 hydrogen bonds · protein-protein
  • A–E · 764 Ų buried · 3 hydrogen bonds · protein-protein
  • B–E · 98 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 7JTG · Structure of Hepatitis C Virus Envelope Glycoprotein E2 core from genotype 6a bound to… · the same entry in another collection · chain A against A, TM-score 1.00

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