化学
ADP核糖基化
NAD+激酶
烟酰胺腺嘌呤二核苷酸
生物化学
酶
核糖
作者
Bernhard Lüscher,Mareike Bütepage,Laura Eckei,Sarah Krieg,Patricia Verheugd,Brian H. Shilton
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2017-11-27
卷期号:118 (3): 1092-1136
被引量:223
标识
DOI:10.1021/acs.chemrev.7b00122
摘要
Posttranslational modifications (PTMs) regulate protein functions and interactions. ADP-ribosylation is a PTM, in which ADP-ribosyltransferases use nicotinamide adenine dinucleotide (NAD+) to modify target proteins with ADP-ribose. This modification can occur as mono- or poly-ADP-ribosylation. The latter involves the synthesis of long ADP-ribose chains that have specific properties due to the nature of the polymer. ADP-Ribosylation is reversed by hydrolases that cleave the glycosidic bonds either between ADP-ribose units or between the protein proximal ADP-ribose and a given amino acid side chain. Here we discuss the properties of the different enzymes associated with ADP-ribosylation and the consequences of this PTM on substrates. Furthermore, the different domains that interpret either mono- or poly-ADP-ribosylation and the implications for cellular processes are described.
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