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Crystal structure of broadly neutralizing antibody HEPC3.4

Analyse Crystal structure of broadly neutralizing antibody HEPC3.4 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7U0C
Type
protein
Length
1,239 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HEPC3.4 Fab heavy chain; HEPC3.4 Fab light chain
Pockets
16 · best druggability 0.74

Structure

x-ray diffraction · 6 distinct chains · 6% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHEPC3.4 Fab heavy chainprotein2194% helix, 51% strand—
BHEPC3.4 Fab light chainprotein2036% helix, 42% strand—
CHEPC3.4 Fab heavy chainprotein2104% helix, 56% strand—
DHEPC3.4 Fab light chainprotein2037% helix, 45% strand—
HHEPC3.4 Fab heavy chainprotein2106% helix, 48% strand—
LHEPC3.4 Fab light chainprotein1946% helix, 42% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17480.740.80109empty
22650.670.8335empty
32900.520.7546empty
41550.500.7821empty
52520.490.7441empty

Interfaces

8 interfaces between chains.

  • C–D · 1871 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 1759 Ų buried · 17 hydrogen bonds · protein-protein
  • H–L · 1655 Ų buried · 10 hydrogen bonds · protein-protein
  • D–L · 1174 Ų buried · 19 hydrogen bonds · protein-protein
  • B–L · 282 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 15 disulfide (disulfide).

Compared structures

  • 7U0C · Crystal structure of broadly neutralizing antibody HEPC3.4 · the same entry in another collection · chain A against A, TM-score 1.00

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