GL1X · GenesisL1 explorer

Research workbench

The cryo-EM structure of hav bound to a neutralizing antibody-F6

Analyse The cryo-EM structure of hav bound to a neutralizing antibody-F6 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6JHR
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
11 · best druggability 0.65

Structure

electron microscopy · 5 distinct chains · 6% helix, 38% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AVP1protein26011% helix, 29% strand—
BVP2protein2169% helix, 38% strand—
CVP3protein2465% helix, 33% strand—
DFab light chainprotein2134% helix, 44% strand—
EFab heavy chainprotein2171% helix, 46% strand—

Pockets

11 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13830.650.7953empty
22430.590.8031empty
32580.590.7930empty
44410.560.7451empty
51310.430.7623empty

Interfaces

6 interfaces between chains.

  • A–C · 3946 Ų buried · 56 hydrogen bonds · protein-protein
  • D–E · 2076 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 1680 Ų buried · 28 hydrogen bonds · protein-protein
  • B–C · 1510 Ų buried · 20 hydrogen bonds · protein-protein
  • C–E · 896 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6JHR · The cryo-EM structure of HAV bound to a neutralizing antibody-F6 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.