2019
DOI: 10.3390/cryst9090471
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Crystal Structure of NADPH-Dependent Methylglyoxal Reductase Gre2 from Candida Albicans

Abstract: Gre2 is a key enzyme in the methylglyoxal detoxification pathway; it uses NADPH or NADH as an electron donor to reduce the cytotoxic methylglyoxal to lactaldehyde. This enzyme is a member of the short-chain dehydrogenase/reductase (SDR) superfamily whose members catalyze this type of reaction with a broad range of substrates. To elucidate the structural features, we determined the crystal structures of the NADPH-dependent methylglyoxal reductase Gre2 from Candida albicans (CaGre2) for both the apo-form and NAD… Show more

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Cited by 4 publications
(2 citation statements)
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“…Other aldehyde dehydrogenases may also catalyze this reaction in the presence of GSH. Methylglyoxal reductase relies on NADPH or NADH to reduce MG to lactaldehyde, which may then be converted to acetol. , In E. coli , MG is directly converted to acetol through the activity of an NADPH-dependent aldehyde reductase and NADH-dependent alcohol dehydrogenase . There are several receptors that mediate the degradation of MG-AGEs to counteract oxidative stress through endocytosis and removal, including AGE-specific receptors (AGER1, AGER2, and AGER3) and CD36. …”
Section: Defense Mechanisms Against Electrophiles and Repair/removal ...mentioning
confidence: 99%
“…Other aldehyde dehydrogenases may also catalyze this reaction in the presence of GSH. Methylglyoxal reductase relies on NADPH or NADH to reduce MG to lactaldehyde, which may then be converted to acetol. , In E. coli , MG is directly converted to acetol through the activity of an NADPH-dependent aldehyde reductase and NADH-dependent alcohol dehydrogenase . There are several receptors that mediate the degradation of MG-AGEs to counteract oxidative stress through endocytosis and removal, including AGE-specific receptors (AGER1, AGER2, and AGER3) and CD36. …”
Section: Defense Mechanisms Against Electrophiles and Repair/removal ...mentioning
confidence: 99%
“…Their study provided invaluable insights for the development of potent inhibitors towards pathogenic microorganisms. This group also determined the crystal structures of an NADPH-dependent methylglyoxal reductase in apo-and NADPH-complexed form [7]. As a key enzyme in the methylglyoxal detoxification pathway, it can reduce directly the level of cytotoxic methylglyoxal.…”
mentioning
confidence: 99%