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Crystal structure of the Fab fragment of a glycosylated lymphoma antibody

Analyse Crystal structure of the Fab fragment of a glycosylated lymphoma antibody in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7ARN
Type
protein
Length
438 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody Fab fragment heavy chain; Antibody Fab fragment light chain
Ligands
NAG, BMA, MAN
Pockets
5 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 7% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HAntibody Fab fragment heavy chainprotein2228% helix, 50% strand—
LAntibody Fab fragment light chainprotein2166% helix, 50% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains H, L
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • MAN · alpha-D-mannopyranose · sugar · 2 copies · chains L
  • GOL · Glycerol · additive · 3 copies · chains H, L

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16750.660.7562empty
2540.500.8722GOL
3710.340.7620empty
4730.330.7522empty
5740.320.7417empty

Interfaces

1 interface between chains.

  • H–L · 1762 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 7ARN · Crystal Structure of the Fab Fragment of a Glycosylated Lymphoma Antibody · the same entry in another collection · chain H against H, TM-score 1.00

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