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Human glyoxalase II with S-(N-hydroxy-N-bromophenylcarbamoyl) glutathione

Analyse Human glyoxalase II with S-(N-hydroxy-N-bromophenylcarbamoyl) glutathione in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1QH5
Type
protein
Length
520 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein (hydroxyacylglutathione hydrolase)
EC
3.1.2.6
UniProt
Q16775
Ligands
GSH, GBP, ZN
Pockets
4 · best druggability 0.61

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BProtein (hydroxyacylglutathione hydrolase) (EC 3.1.2.6)protein26034% helix, 25% strandQ16775

Ligands and binding sites

  • GSH · Glutathione · ligand · chains A
  • GBP · S-(N-hydroxy-N-bromophenylcarbamoyl)glutathione · ligand · chains B
  • ZN · Zinc ion · metal · 4 copies · chains A, B

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
13460.610.7828empty
2970.390.7619GSH
3930.370.7618GBP
4650.310.7520empty

Interfaces

1 interface between chains.

  • A–B · 287 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 1QH5 · Human glyoxalase II with S-(N-hydroxy-N-BROMOPHENYLCARBAMOYL)GLUTATHIONE · the same entry in another collection · chain B against B, TM-score 1.00
  • Q16775 · AlphaFold monomer V2.0 prediction for hydroxyacylglutathione hydrolase, mitochondrial… · a predicted model of the same protein · chain B against A, TM-score 1.00

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