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Crystal structure of the CO(II)-bound glyoxalase I of escherichia COLI

Analyse Crystal structure of the CO(II)-bound glyoxalase I of escherichia COLI in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1FA6
Type
protein
Length
256 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Escherichia coli
Molecule
Glyoxalase I
EC
4.4.1.5
UniProt
P0AC81
Ligands
CO
Pockets
2 · best druggability 0.48

Structure

x-ray diffraction · resolution 1.9 · 1 distinct chain · 16% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BGlyoxalase I (EC 4.4.1.5)protein12816% helix, 44% strandP0AC81

Ligands and binding sites

  • CO · Cobalt (II) ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12230.480.7428empty
21760.430.7328empty

Interfaces

1 interface between chains.

  • A–B · 1742 Ų buried · 44 hydrogen bonds · protein-protein

Compared structures

  • 1FA6 · Crystal structure of the CO(II)-bound glyoxalase I of escherichia COLI · the same entry in another collection · chain A against A, TM-score 1.00
  • P0AC81 · AlphaFold monomer V2.0 prediction for lactoylglutathione lyase (P0AC81) · a predicted model of the same protein · chain A against A, TM-score 0.90

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