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Vaccine-elicited nhp fp-targeting antibody DF2F-A.01 in complex with HIV fusion peptide (residue 512-519)

Analyse Vaccine-elicited nhp fp-targeting antibody DF2F-A.01 in complex with HIV fusion… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6PEF
Type
protein
Length
875 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody DF2F-A.01 heavy chain; Antibody DF2F-A.01 light chain; HIV fusion peptide…
Pockets
10 · best druggability 0.65

Structure

x-ray diffraction · 4 distinct chains · 7% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DAntibody DF2F-A.01 heavy chainprotein2199% helix, 51% strand—
BAntibody DF2F-A.01 light chainprotein2116% helix, 51% strand—
C, FHIV fusion peptide residue 512-519protein80% helix, 0% strand—
EAntibody DF2F-A.01 light chainprotein2106% helix, 51% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15030.650.7753empty
21630.460.7628empty
31290.420.7623empty
41100.360.7416empty
5940.350.7425empty

Interfaces

9 interfaces between chains.

  • D–E · 1720 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 1707 Ų buried · 16 hydrogen bonds · protein-protein
  • E–F · 402 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 401 Ų buried · 5 hydrogen bonds · protein-protein
  • A–E · 383 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6PEF · Vaccine-elicited NHP FP-targeting antibody DF2F-a.01 in complex with HIV fusion peptide… · the same entry in another collection · chain A against A, TM-score 1.00

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