Emerging roles of pseudokinases

被引:431
作者
Boudeau, Jerome
Miranda-Saavedra, Diego
Barton, Geoffrey J.
Alessi, Dario R. [1 ]
机构
[1] Univ Dundee, Sch Life Sci, MRC Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland
[2] Univ Dundee, Div Biol Chem & Mol Microbiol, Dundee DD1 5EH, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/j.tcb.2006.07.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Kinases control virtually all aspects of biology. Forty-eight human proteins have a kinase-like domain that lacks at least one of the conserved catalytic residues; these proteins are therefore predicted to be inactive and have been termed pseudokinases. Here, we describe exciting work suggesting that pseudokinases, despite lacking the ability to phosphorylate substrates, are still pivotal in regulating diverse cellular processes. We review evidence that the pseudokinase STRAD controls the function of the tumour suppressor kinase LKB1 and that a single amino acid substitution within the pseudokinase domain of the tyrosine kinase JAK2 leads to several malignant myeloproliferative disorders. We also discuss the emerging functions of other pseudokinases, including HER3 (also called ErbB3), EphB6, CCK4 (also called PTK7), KSR, Trb3, GCN2, TRRAP, ILK and CASK.
引用
收藏
页码:443 / 452
页数:10
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