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Structure of IGG2A Fab fragment (D2.3) complexed with reaction product

Analyse Structure of IGG2A Fab fragment (D2.3) complexed with reaction product in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1YEG
Type
protein
Length
441 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
IGG2A Fab fragment
UniProt
P01863
Ligands
BPN, ZN
Pockets
4 · best druggability 0.64

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
LIGG2A Fab fragmentprotein2195% helix, 51% strand—
HIGG2A Fab fragmentprotein2227% helix, 53% strandP01863

Ligands and binding sites

  • BPN · Paranitrobenzyl alcohol · ligand · chains L, H
  • ZN · Zinc ion · metal · 7 copies · chains L, H
  • ACT · Acetate ion · additive · chains L, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11500.640.8627BPN, ACT
2640.420.8219empty
31530.390.7229empty
4500.250.7313empty

Interfaces

1 interface between chains.

  • L–H · 2093 Ų buried · 23 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 1YEG · Structure of IGG2A Fab fragment (D2.3) complexed with reaction product · the same entry in another collection · chain L against L, TM-score 1.00
  • P01863 · AlphaFold monomer V2.0 prediction for ig gamma-2A chain C region, a allele (P01863) · a predicted model of the same protein · chain H against A, TM-score 0.50

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