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Crystal structure analysis of anti-HIV-1 V3 Fab 2219 in complex with mn peptide

Analyse Crystal structure analysis of anti-HIV-1 V3 Fab 2219 in complex with mn peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2B0S
Type
protein
Length
457 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab 2219, light chain; Fab 2219, heavy chain; Mn peptide of exterior membrane…
UniProt
P05877
Pockets
5 · best druggability 0.62

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
LFab 2219, light chainprotein2157% helix, 50% strand—
HFab 2219, heavy chainprotein2267% helix, 51% strand—
PMn peptide of exterior membrane glycoprotein GP120protein160% helix, 50% strandP05877

Ligands and binding sites

  • ACY · Acetic acid · additive · 3 copies · chains L, H
  • EDO · 1,2-ethanediol · additive · 2 copies · chains L, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15880.620.7472EDO
2930.360.7522empty
3800.310.7317empty
4680.300.7415empty
5580.300.7514empty

Interfaces

3 interfaces between chains.

  • L–H · 1764 Ų buried · 24 hydrogen bonds · protein-protein
  • H–P · 621 Ų buried · 16 hydrogen bonds · protein-protein
  • L–P · 379 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 2B0S · Crystal structure analysis of anti-HIV-1 V3 Fab 2219 in complex with MN peptide · the same entry in another collection · chain L against L, TM-score 1.00

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