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Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System

Glyoxalase 2 is a mitochondrial and cytoplasmic protein belonging to the metallo-β-lactamase family encoded by the hydroxyacylglutathione hydrolase (HAGH) gene. This enzyme is the second enzyme of the glyoxalase system that is responsible for detoxification of the α-ketothaldehyde methylglyoxal in c...

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Autores principales: Scirè, Andrea, Cianfruglia, Laura, Minnelli, Cristina, Romaldi, Brenda, Laudadio, Emiliano, Galeazzi, Roberta, Antognelli, Cinzia, Armeni, Tatiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686547/
https://www.ncbi.nlm.nih.gov/pubmed/36358501
http://dx.doi.org/10.3390/antiox11112131
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author Scirè, Andrea
Cianfruglia, Laura
Minnelli, Cristina
Romaldi, Brenda
Laudadio, Emiliano
Galeazzi, Roberta
Antognelli, Cinzia
Armeni, Tatiana
author_facet Scirè, Andrea
Cianfruglia, Laura
Minnelli, Cristina
Romaldi, Brenda
Laudadio, Emiliano
Galeazzi, Roberta
Antognelli, Cinzia
Armeni, Tatiana
author_sort Scirè, Andrea
collection PubMed
description Glyoxalase 2 is a mitochondrial and cytoplasmic protein belonging to the metallo-β-lactamase family encoded by the hydroxyacylglutathione hydrolase (HAGH) gene. This enzyme is the second enzyme of the glyoxalase system that is responsible for detoxification of the α-ketothaldehyde methylglyoxal in cells. The two enzymes glyoxalase 1 (Glo1) and glyoxalase 2 (Glo2) form the complete glyoxalase pathway, which utilizes glutathione as cofactor in eukaryotic cells. The importance of Glo2 is highlighted by its ubiquitous distribution in prokaryotic and eukaryotic organisms. Its function in the system has been well defined, but in recent years, additional roles are emerging, especially those related to oxidative stress. This review focuses on Glo2 by considering its genetics, molecular and structural properties, its involvement in post-translational modifications and its interaction with specific metabolic pathways. The purpose of this review is to focus attention on an enzyme that, from the most recent studies, appears to play a role in multiple regulatory pathways that may be important in certain diseases such as cancer or oxidative stress-related diseases.
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spelling pubmed-96865472022-11-25 Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System Scirè, Andrea Cianfruglia, Laura Minnelli, Cristina Romaldi, Brenda Laudadio, Emiliano Galeazzi, Roberta Antognelli, Cinzia Armeni, Tatiana Antioxidants (Basel) Review Glyoxalase 2 is a mitochondrial and cytoplasmic protein belonging to the metallo-β-lactamase family encoded by the hydroxyacylglutathione hydrolase (HAGH) gene. This enzyme is the second enzyme of the glyoxalase system that is responsible for detoxification of the α-ketothaldehyde methylglyoxal in cells. The two enzymes glyoxalase 1 (Glo1) and glyoxalase 2 (Glo2) form the complete glyoxalase pathway, which utilizes glutathione as cofactor in eukaryotic cells. The importance of Glo2 is highlighted by its ubiquitous distribution in prokaryotic and eukaryotic organisms. Its function in the system has been well defined, but in recent years, additional roles are emerging, especially those related to oxidative stress. This review focuses on Glo2 by considering its genetics, molecular and structural properties, its involvement in post-translational modifications and its interaction with specific metabolic pathways. The purpose of this review is to focus attention on an enzyme that, from the most recent studies, appears to play a role in multiple regulatory pathways that may be important in certain diseases such as cancer or oxidative stress-related diseases. MDPI 2022-10-28 /pmc/articles/PMC9686547/ /pubmed/36358501 http://dx.doi.org/10.3390/antiox11112131 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Scirè, Andrea
Cianfruglia, Laura
Minnelli, Cristina
Romaldi, Brenda
Laudadio, Emiliano
Galeazzi, Roberta
Antognelli, Cinzia
Armeni, Tatiana
Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System
title Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System
title_full Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System
title_fullStr Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System
title_full_unstemmed Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System
title_short Glyoxalase 2: Towards a Broader View of the Second Player of the Glyoxalase System
title_sort glyoxalase 2: towards a broader view of the second player of the glyoxalase system
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686547/
https://www.ncbi.nlm.nih.gov/pubmed/36358501
http://dx.doi.org/10.3390/antiox11112131
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