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 ...
AbstractGlyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a hig...
The glyoxalase system is the ubiquitous pathway for the detoxification of methylglyoxal (MG) in the ...
The glyoxalase system has been studied since 1913. The biochemical function of this enzymatic system...
Glyoxalase 2 is a mitochondrial and cytoplasmic protein belonging to the metallo-β-lactamase family ...
AbstractGlyoxalase 1 (GlxI) is the key enzyme that converts the highly reactive α-oxo-aldehydes into...
Molecular, catalytic and structural properties of glyoxalase pathway enzymes of many species are now...
Glyoxalase 2 is a β-lactamase fold-containing enzyme that appears to be involved with cellular chemi...
Abstract Glyoxalase II, the second of 2 enzymes in the glyoxalase system, is a hydroxyacylglutathio...
AbstractBackground: Glyoxalase II, the second of two enzymes in the glyoxalase system, is a thiolest...
The glyoxalase pathway is widespread in both prokaryotic and eukaryotic organisms. This system utili...
The glyoxalase enzyme system utilizes intracellular thiols such as glutathione to convert α-ketoalde...
AbstractCytosolic glyoxalase II from Arabidopsis thaliana, GLX2-2, was overexpressed and purified to...
The glyoxalase system was discovered over a hundred years ago and since then it has been claimed to ...
All biological cells produce methylglyoxal, a toxic 2-oxoaldehyde, as a by-product of primary metabo...
Glyoxalase 1 (Glo1) and glyoxalase 2 (Glo2) are ubiquitously expressed cytosolic enzymes that cataly...
AbstractGlyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a hig...
The glyoxalase system is the ubiquitous pathway for the detoxification of methylglyoxal (MG) in the ...
The glyoxalase system has been studied since 1913. The biochemical function of this enzymatic system...
Glyoxalase 2 is a mitochondrial and cytoplasmic protein belonging to the metallo-β-lactamase family ...
AbstractGlyoxalase 1 (GlxI) is the key enzyme that converts the highly reactive α-oxo-aldehydes into...
Molecular, catalytic and structural properties of glyoxalase pathway enzymes of many species are now...
Glyoxalase 2 is a β-lactamase fold-containing enzyme that appears to be involved with cellular chemi...
Abstract Glyoxalase II, the second of 2 enzymes in the glyoxalase system, is a hydroxyacylglutathio...
AbstractBackground: Glyoxalase II, the second of two enzymes in the glyoxalase system, is a thiolest...
The glyoxalase pathway is widespread in both prokaryotic and eukaryotic organisms. This system utili...
The glyoxalase enzyme system utilizes intracellular thiols such as glutathione to convert α-ketoalde...
AbstractCytosolic glyoxalase II from Arabidopsis thaliana, GLX2-2, was overexpressed and purified to...
The glyoxalase system was discovered over a hundred years ago and since then it has been claimed to ...
All biological cells produce methylglyoxal, a toxic 2-oxoaldehyde, as a by-product of primary metabo...
Glyoxalase 1 (Glo1) and glyoxalase 2 (Glo2) are ubiquitously expressed cytosolic enzymes that cataly...
AbstractGlyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a hig...
The glyoxalase system is the ubiquitous pathway for the detoxification of methylglyoxal (MG) in the ...
The glyoxalase system has been studied since 1913. The biochemical function of this enzymatic system...