GL1X · GenesisL1 explorer

Research workbench

Crystal structure of an anti-HBV E-antigen monoclonal Fab fragment (E6), unbound

Analyse Crystal structure of an anti-HBV E-antigen monoclonal Fab fragment (E6), unbound in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3V6F
Type
protein
Length
1,733 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab E6 heavy chain; Fab E6 light chain
Pockets
20 · best druggability 0.69

Structure

x-ray diffraction · 4 distinct chains · 5% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFab E6 heavy chainprotein2186% helix, 53% strand—
B, D, F, LFab E6 light chainprotein2196% helix, 54% strand—
C, EFab E6 heavy chainprotein2124% helix, 53% strand—
HFab E6 heavy chainprotein2156% helix, 51% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19250.690.7592empty
25470.610.7576empty
31840.600.8224empty
41670.570.8124empty
53640.560.7545empty

Interfaces

12 interfaces between chains.

  • C–D · 1889 Ų buried · 18 hydrogen bonds · protein-protein
  • A–B · 1882 Ų buried · 19 hydrogen bonds · protein-protein
  • E–F · 1835 Ų buried · 18 hydrogen bonds · protein-protein
  • H–L · 1830 Ų buried · 16 hydrogen bonds · protein-protein
  • A–E · 327 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide (disulfide).

Compared structures

  • 3V6F · Crystal Structure of an anti-HBV e-antigen monoclonal Fab fragment (e6), unbound · 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.