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Hepatitis B core-antigen in complex with Fab E21

Analyse Hepatitis B core-antigen in complex with Fab E21 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6CWT
Type
protein
Length
1,081 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab E21 heavy chain; Fab E21 light chain; Capsid protein
UniProt
P03147
Pockets
11 · best druggability 0.64

Structure

x-ray diffraction · 6 distinct chains · 15% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFab E21 heavy chainprotein2144% helix, 43% strand—
BFab E21 light chainprotein2145% helix, 45% strand—
CFab E21 heavy chainprotein2006% helix, 47% strand—
DFab E21 light chainprotein2083% helix, 42% strand—
ECapsid proteinprotein12448% helix, 2% strandP03147
FCapsid proteinprotein12152% helix, 0% strandP03147

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16190.640.7555empty
26530.640.7465empty
31370.510.7922empty
4550.450.8315empty
51410.440.7621empty

Interfaces

9 interfaces between chains.

  • A–B · 1896 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 1784 Ų buried · 20 hydrogen bonds · protein-protein
  • E–F · 1371 Ų buried · 17 hydrogen bonds · protein-protein
  • D–F · 648 Ų buried · 8 hydrogen bonds · protein-protein
  • B–E · 632 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 disulfide (disulfide).

Compared structures

  • 6CWT · Hepatitis B core-antigen in complex with Fab e21 · the same entry in another collection · chain A against A, TM-score 1.00

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