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Afamin antibody fragment, N14 Fab, L1- glycosylated, crystal form I, parsimonious model

Analyse Afamin antibody fragment, N14 Fab, L1- glycosylated, crystal form I… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5L9D
Type
protein
Length
429 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mouse antibody Fab fragment, IGG1-kappa heavy chain; Mouse antibody Fab fragment…
Ligands
NAG, K
Pockets
3 · best druggability 0.62

Structure

x-ray diffraction · 2 distinct chains · 8% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HMouse antibody Fab fragment, IGG1-kappa heavy chainprotein2158% helix, 53% strand—
LMouse antibody Fab fragment, IGG1-kappa light chainprotein2148% helix, 51% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · chains L
  • K · Potassium ion · metal · chains H
  • PEG · Di(hydroxyethyl)ether · additive · 3 copies · chains H, L
  • PG4 · Tetraethylene glycol · additive · 2 copies · chains H, L
  • PE8 · 3,6,9,12,15,18,21-heptaoxatricosane-1,23-diol · additive · chains H
  • PGE · Triethylene glycol · additive · chains H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15280.620.7556PEG
21250.400.7526empty
3710.310.7418PG4

Interfaces

1 interface between chains.

  • H–L · 1940 Ų buried · 23 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 5L9D · AFAMIN ANTIBODY FRAGMENT, N14 FAB, L1- GLYCOSYLATED, CRYSTAL FORM I, parsimonious model · the same entry in another collection · chain H against H, TM-score 1.00

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