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PMID: 10508780 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Crystal structure of human glyoxalase II and its complex with a glutathione thiolester substrate analogue.

Structure (London, England : 1993) ·Vol. 7 ·No. 9 ·1999-09-15 ·Pages 1067-78

Cameron AD, Ridderström M, Olin B, Mannervik B

Abstract

Glyoxalase II, the second of two enzymes in the glyoxalase system, is a thiolesterase that catalyses the hydrolysis of S-D-lactoylglutathione to form glutathione and D-lactic acid. The structure of human glyoxalase II was solved initially by single isomorphous replacement with anomalous scattering and refined at a resolution of 1.9 A. The enzyme consists of two domains. The first domain folds into a four-layered beta sandwich, similar to that seen in the metallo-beta-lactamases. The second domain is predominantly alpha-helical. The active site contains a binuclear zinc-binding site and a substrate-binding site extending over the domain interface. The model contains acetate and cacodylate in the active site. A second complex was derived from crystals soaked in a solution containing the slow substrate, S-(N-hydroxy-N-bromophenylcarbamoyl)glutathione. This complex was refined at a resolution of 1.45 A. It contains the added ligand in one molecule of the asymmetric unit and glutathione in the other. The arrangement of ligands around the zinc ions includes a water molecule, presumably in the form of a hydroxide ion, coordinated to both metal ions. This hydroxide ion is situated 2.9 A from the carbonyl carbon of the substrate in such a position that it could act as the nucleophile during catalysis. The reaction mechanism may also have implications for the action of metallo-beta-lactamases.

MeSH Terms
Acetates/chemistry,metabolism Amino Acid Sequence Binding Sites Cacodylic Acid/chemistry Conserved Sequence Crystallography, X-Ray Glutathione/analogs & derivatives,chemistry,metabolism Humans Hydrolysis Metals/metabolism Models, Molecular Molecular Sequence Data Protein Conformation Substrate Specificity Thiolester Hydrolases/chemistry,metabolism
Chemicals
Acetates Metals S-(N-hydroxy-N-bromophenylcarbamoyl)glutathione Cacodylic Acid Thiolester Hydrolases hydroxyacylglutathione hydrolase Glutathione
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Cameron A D
Department of Molecular Biology Uppsala University Biomedical Center Box 590, S-751 24, Uppsala, Sweden Structural Biology Laboratory Department of Chemistry University of York Heslington, York, UK YO10 5DD,. [email protected].
Ridderström M
Olin B
Mannervik B
Article Info
Journal
Structure (London, England : 1993)
Abbr.
Structure
ISSN
0969-2126
Published
1999-09-15
Pages
1067-78
Language
English
Region
United States
NLM ID
101087697
Subset
IM
Databases
PDB
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