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Crystal structure of anti-HIV-1 V3 Fab TA6 in complex with a HIV-1 GP120 V3 peptide from NY5 strain

Analyse Crystal structure of anti-HIV-1 V3 Fab TA6 in complex with a HIV-1 GP120 V3… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6DB5
Type
protein
Length
906 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Human monoclonal anti-HIV-1 GP120 V3 antibody TA6 Fab heavy chain; Human monoclonal…
Pockets
9 · best druggability 0.70

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
H, IHuman monoclonal anti-HIV-1 GP120 V3 antibody TA6 Fab heavy chainprotein2285% helix, 51% strand—
L, MHuman monoclonal anti-HIV-1 GP120 V3 antibody TA6 Fab light chainprotein2118% helix, 50% strand—
P, QHIV-1 GP120 V3 peptide from NY5 strainprotein140% helix, 57% strand—

Pockets

9 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18470.700.7699empty
24640.570.7356empty
31660.460.7617empty
4710.450.8322empty
51360.440.7628empty

Interfaces

8 interfaces between chains.

  • I–M · 1944 Ų buried · 18 hydrogen bonds · protein-protein
  • H–L · 1940 Ų buried · 21 hydrogen bonds · protein-protein
  • I–Q · 455 Ų buried · 3 hydrogen bonds · protein-protein
  • H–P · 448 Ų buried · 2 hydrogen bonds · protein-protein
  • L–P · 414 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6DB5 · Crystal structure of anti-HIV-1 V3 Fab TA6 in complex with a HIV-1 gp120 V3 peptide from… · the same entry in another collection · chain H against H, TM-score 1.00

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