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Crystal structure of the non-neutralizing HIV antibody 13H11 Fab fragment with a GP41 mper-derived peptide in a helical conformation

Analyse Crystal structure of the non-neutralizing HIV antibody 13H11 Fab fragment with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3MNW
Type
protein
Length
439 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GP41; Anti-HIV-1 antibody 13H11 light chain; Anti-HIV-1 antibody 13H11 heavy chain
UniProt
Q8TCD0, S6B291
Ligands
NH2
Pockets
5 · best druggability 0.46

Structure

x-ray diffraction · 3 distinct chains · 11% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
PGP41protein1984% helix, 5% strand—
AAnti-HIV-1 antibody 13H11 light chainprotein2165% helix, 51% strandQ8TCD0
BAnti-HIV-1 antibody 13H11 heavy chainprotein20411% helix, 52% strandS6B291

Ligands and binding sites

  • NH2 · Amino group · ion · chains P
  • EDO · 1,2-ethanediol · additive · chains B

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

Pockets

5 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11950.460.7530empty
2660.340.7720empty
3580.300.7515empty
4760.290.7213empty
5530.280.7412empty

Interfaces

3 interfaces between chains.

  • A–B · 1558 Ų buried · 11 hydrogen bonds · protein-protein
  • P–B · 422 Ų buried · 11 hydrogen bonds · protein-protein
  • P–A · 295 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 3MNW · Crystal structure of the non-neutralizing HIV antibody 13H11 Fab fragment with a gp41… · the same entry in another collection · chain P against P, TM-score 1.00

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