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Merck

Sirtuin chemical mechanisms.

Biochimica et biophysica acta (2010-02-06)
Anthony A Sauve
ABSTRAKT

Sirtuins are ancient proteins widely distributed in all lifeforms of earth. These proteins are universally able to bind NAD(+), and activate it to effect ADP-ribosylation of cellular nucleophiles. The most commonly observed sirtuin reaction is the ADP-ribosylation of acetyllysine, which leads to NAD(+)-dependent deacetylation. Other types of ADP-ribosylation have also been observed, including protein ADP-ribosylation, NAD(+) solvolysis and ADP-ribosyltransfer to 5,6-dimethylbenzimidazole, a reaction involved in eubacterial cobalamin biosynthesis. This review broadly surveys the chemistries and chemical mechanisms of these enzymes.

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Sigma-Aldrich
Nα-Acetyl-L-lysine
Sigma-Aldrich
5,6-Dimethylbenzimidazole, ≥99%