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Crystal structure of anti-HIV-1 V3 Fab 3074 in complex with a UR29 V3 peptide

Analyse Crystal structure of anti-HIV-1 V3 Fab 3074 in complex with a UR29 V3 peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3MLY
Type
protein
Length
912 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Human monoclonal anti-HIV-1 GP120 V3 antibody 3074 Fab light chain; Human monoclonal…
Pockets
7 · best druggability 0.78

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L, MHuman monoclonal anti-HIV-1 GP120 V3 antibody 3074 Fab light chainprotein2147% helix, 50% strand—
H, IHuman monoclonal anti-HIV-1 GP120 V3 antibody 3074 Fab heavy chainprotein2307% helix, 53% strand—
P, QHIV-1 GP120 third variable region (V3) crownprotein120% helix, 25% strand—

Pockets

7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18490.780.8298empty
210290.750.7893empty
32330.570.7937empty
42490.540.7734empty
5900.460.8025empty

Interfaces

10 interfaces between chains.

  • M–I · 1904 Ų buried · 16 hydrogen bonds · protein-protein
  • L–H · 1808 Ų buried · 18 hydrogen bonds · protein-protein
  • H–I · 812 Ų buried · 7 hydrogen bonds · protein-protein
  • H–P · 638 Ų buried · 17 hydrogen bonds · protein-protein
  • I–Q · 610 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 disulfide (disulfide).

Compared structures

  • 3MLY · Crystal structure of anti-HIV-1 V3 Fab 3074 in complex with a UR29 V3 peptide · the same entry in another collection · chain L against L, TM-score 1.00

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