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Structure of mouse vaccination-elicited HIV neutralizing antibody VFP5.01 in complex with HIV-1 fusion peptide residue 512-519

Analyse Structure of mouse vaccination-elicited HIV neutralizing antibody VFP5.01 in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TKK
Type
protein
Length
434 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HIV-1 fusion peptide residue 512-519; Mouse antibody VFP5.01 heavy chain; Mouse antibody…
Pockets
4 · best druggability 0.61

Structure

x-ray diffraction · 3 distinct chains · 7% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHIV-1 fusion peptide residue 512-519protein838% helix, 0% strand—
HMouse antibody VFP5.01 heavy chainprotein2136% helix, 55% strand—
LMouse antibody VFP5.01 light chainprotein2137% helix, 50% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14570.610.7545empty
2770.340.7516empty
3850.330.7420empty
4700.320.7518empty

Interfaces

3 interfaces between chains.

  • H–L · 1851 Ų buried · 12 hydrogen bonds · protein-protein
  • A–H · 362 Ų buried · 5 hydrogen bonds · protein-protein
  • A–L · 265 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 5TKK · Structure of mouse vaccination-elicited HIV neutralizing antibody vFP5.01 in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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