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Crystal structure of broadly neutralizing antibody HEPC74 in complex with hepatitis C virus envelope glycoprotein E2 ectodomain

Analyse Crystal structure of broadly neutralizing antibody HEPC74 in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6MEH
Type
protein
Length
603 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
E2 glycoprotein; Antibody HEPC74 heavy chain; Antibody HEPC74 light chain
UniProt
A0A2P0NE26
Ligands
NAG
Pockets
6 · best druggability 0.60

Structure

x-ray diffraction · 3 distinct chains · 9% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
CE2 glycoproteinprotein16514% helix, 38% strandA0A2P0NE26
HAntibody HEPC74 heavy chainprotein2258% helix, 54% strand—
LAntibody HEPC74 light chainprotein2136% helix, 52% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 7 copies · chains C, L, H

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

Pockets

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14600.600.7551empty
2960.580.8732empty
31720.490.7737empty
41180.400.7418empty
5860.390.7716empty

Interfaces

3 interfaces between chains.

  • H–L · 1964 Ų buried · 18 hydrogen bonds · protein-protein
  • C–H · 1031 Ų buried · 10 hydrogen bonds · protein-protein
  • C–L · 111 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 11 disulfide, 5 glycan (disulfide, N-glycosylation).

Compared structures

  • 6MEH · Crystal structure of broadly neutralizing antibody HEPC74 in complex with Hepatitis C… · the same entry in another collection · chain C against C, TM-score 1.00

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