DHHC palmitoyl transferases: substrate interactions and (patho)physiology

被引:269
作者
Greaves, Jennifer [1 ]
Chamberlain, Luke H. [1 ]
机构
[1] Univ Edinburgh, Ctr Integrat Physiol, Edinburgh EH8 9XD, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
2-STEP REACTION-MECHANISM; CYSTEINE-STRING PROTEIN; NITRIC-OXIDE SYNTHASE; SACCHAROMYCES-CEREVISIAE; MEDIATED PALMITOYLATION; MEMBRANE INTERACTIONS; MENTAL-RETARDATION; GABA(A) RECEPTORS; MAJOR SUBSTRATE; ALPHA-SUBUNITS;
D O I
10.1016/j.tibs.2011.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S-palmitoylation is a reversible post-translational modification that occurs on diverse cellular proteins. Palmitoylation can affect proteins in many different ways, including regulating membrane attachment, intracellular trafficking, and membrane micro-localisation. Intracellular palmitoylation reactions are mediated by a family of recently identified aspartate-histidine-histidine-cysteine (DHHC) palmitoyl transferases. More than 20 DHHC proteins are encoded by mammalian genomes, and there is now a major effort to identify DHHC-substrate pairings and to determine how interaction specificity is encoded. Recent studies have highlighted how DHHC proteins regulate cell function and influence physiology and pathophysiology.
引用
收藏
页码:245 / 253
页数:9
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