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Anti-HIV-1 Fab 2G12 + Man8 re-refinement

Analyse Anti-HIV-1 Fab 2G12 + Man8 re-refinement in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6MNF
Type
protein
Length
874 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.758
Source
Homo sapiens
Molecule
Fab 2G12, light chain; Fab 2g12, heavy chain
Ligands
MAN, BMA
Pockets
10 · best druggability 0.75

Structure

x-ray diffraction · resolution 2.758 · 2 distinct chains · 6% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L, KFab 2G12, light chainprotein2136% helix, 53% strand—
H, MFab 2g12, heavy chainprotein2247% helix, 50% strand—

Ligands and binding sites

  • MAN · alpha-D-mannopyranose · sugar · 7 copies · chains K, M
  • BMA · beta-D-mannopyranose · sugar · chains M

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19530.750.78100empty
23770.620.7848empty
32720.550.7638empty
42250.520.7634empty
51340.510.8033empty

Interfaces

6 interfaces between chains.

  • K–M · 999 Ų buried · 12 hydrogen bonds · protein-protein
  • H–M · 965 Ų buried · 13 hydrogen bonds · protein-protein
  • L–H · 963 Ų buried · 11 hydrogen bonds · protein-protein
  • L–M · 958 Ų buried · 7 hydrogen bonds · protein-protein
  • H–K · 890 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6MNF · Anti-HIV-1 Fab 2G12 + MAN8 re-refinement · the same entry in another collection · chain H against H, TM-score 1.00

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