Methylglyoxal-induced modification of arginine residues decreases the activity of NADPH-generating enzymes

Free Radical Biology and Medicine

Volumn 61, Issue , 2013, Pages 229-242

  Morgan, Philip E ^a,b   Sheahan, Pamela J ^a,b   Pattison, David I ^a,b   Davies, Michael J ^a,b  

^a HEART RESEARCH INSTITUTE   (Australia)

^b University of Sydney   (Australia)

Author keywords

Advanced glycation end products; Arginine; Diabetes associated atherosclerosis; Free radicals; Glycated proteins; Methylglyoxal; NADPH; Reactive aldehydes

Indexed keywords

ALDEHYDE; ARGININE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; HYDROIMIDAZOLONE; IMIDAZOLE DERIVATIVE; ISOCITRATE DEHYDROGENASE; MALATE DEHYDROGENASE (DECARBOXYLATING); METHYLGLYOXAL; OXIDIZING AGENT; PEPTIDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; UNCLASSIFIED DRUG;

ARTICLE; CELL DAMAGE; ENZYME ACTIVITY; ENZYME MODIFICATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; OXIDATION; PRIORITY JOURNAL;

ANIMALIA;

EID: 84877678371     PISSN: 08915849     EISSN: 18734596     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2013.03.025     Document Type: Article

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