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The cryo-EM structure of hav bound to a neutralizing antibody-F7

Analyse The cryo-EM structure of hav bound to a neutralizing antibody-F7 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6JHS
Type
protein
Length
1,152 residues
Chains
5
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
VP1; VP2; VP3; Fab light chain; Fab heavy chain
Pockets
12 · best druggability 0.75

Structure

electron microscopy · 5 distinct chains · 6% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVP1protein2608% helix, 31% strand—
BVP2protein2166% helix, 40% strand—
CVP3protein2469% helix, 36% strand—
DFab light chainprotein2134% helix, 46% strand—
EFab heavy chainprotein2171% helix, 48% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18110.750.8090empty
23430.590.7732empty
32250.550.7830empty
42240.460.7330empty
51190.440.7720empty

Interfaces

6 interfaces between chains.

  • A–C · 3825 Ų buried · 55 hydrogen bonds · protein-protein
  • D–E · 2024 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 1446 Ų buried · 19 hydrogen bonds · protein-protein
  • A–B · 1432 Ų buried · 12 hydrogen bonds · protein-protein
  • C–E · 782 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6JHS · The cryo-EM structure of HAV bound to a neutralizing antibody-F7 · the same entry in another collection · chain A against A, TM-score 1.00

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