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Crystal structure of broad neutralizing antibody 10E8 with long epitope bound

Analyse Crystal structure of broad neutralizing antibody 10E8 with long epitope bound in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5GHW
Type
protein
Length
465 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab 10E8 heavy chain; Fab 10E8 light chain; Endogenous retrovirus group K member 8 env…
UniProt
G3DED6
Ligands
PO4
Pockets
3 · best druggability 0.68

Structure

x-ray diffraction · 3 distinct chains · 11% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HFab 10E8 heavy chainprotein2336% helix, 51% strand—
LFab 10E8 light chainprotein2118% helix, 50% strand—
PEndogenous retrovirus group K member 8 env polyproteinprotein2181% helix, 0% strandG3DED6

Ligands and binding sites

  • PO4 · Phosphate ion · ion · 7 copies · chains H, L

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18280.680.7573empty
2890.420.7920empty
31030.400.7625empty

Interfaces

3 interfaces between chains.

  • H–L · 2204 Ų buried · 19 hydrogen bonds · protein-protein
  • H–P · 707 Ų buried · 10 hydrogen bonds · protein-protein
  • L–P · 98 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 5GHW · Crystal structure of broad neutralizing antibody 10E8 with long epitope bound · the same entry in another collection · chain H against H, TM-score 1.00

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