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Heterodimeric Fc antibody azymetric variant 1

Analyse Heterodimeric Fc antibody azymetric variant 1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4BSV
Type
protein
Length
420 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heterodimeric Fc antibody azymetric variant 2
UniProt
P01857
Ligands
NAG, MAN, FUC, BMA, GAL, IOD
Pockets
3 · best druggability 0.33

Structure

x-ray diffraction · 2 distinct chains · 11% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHeterodimeric Fc antibody azymetric variant 2protein21011% helix, 48% strandP01857
BHeterodimeric Fc antibody azymetric variant 2protein21010% helix, 47% strandP01857

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 8 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 4 copies · chains A, B
  • FUC · alpha-L-fucopyranose · sugar · 2 copies · chains A, B
  • BMA · beta-D-mannopyranose · sugar · 2 copies · chains A, B
  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A, B
  • IOD · Iodide ion · ion · 3 copies · chains B
  • EDO · 1,2-ethanediol · additive · 9 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1900.330.7322empty
2520.280.7518EDO
3510.270.7515empty

Interfaces

1 interface between chains.

  • A–B · 1144 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 4BSV · Heterodimeric Fc Antibody Azymetric Variant 1 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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