Dawn of the dead: protein pseudokinases signal new adventures in cell biology

被引:75
作者
Eyers, Patrick A. [1 ]
Murphy, James M. [2 ,3 ]
机构
[1] Univ Liverpool, Inst Integrat Biol, Dept Chem Biol, Liverpool L69 7ZB, Merseyside, England
[2] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Dept Med Biol, Parkville, Vic 3050, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
kinome; protein scaffold; pseudoenzyme; pseudokinase; thermal shift assay; INTEGRIN-LINKED KINASE; PSEUDOACTIVE SITE; DOMAIN; BINDING; PHOSPHORYLATION; ILK; MECHANISMS; REVEALS; ROLES; JAK2;
D O I
10.1042/BST20130115
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
Recent studies of proteins containing kinase-like domains that lack catalytic residue(s) classically required for phosphotransfer, termed pseudokinases, have uncovered important roles in cell signalling across the kingdoms of life. Additionally, mutations within pseudokinase domains are known to underlie human diseases, suggesting that these proteins may represent new and unexplored therapeutic targets. To date, few pseudokinases have been studied in intricate detail, but as described in the present article and in the subsequent papers in this issue of Biochemical Society Transactions, several new studies have provided an advanced template and an improved framework for interrogating the roles of pseudokinases in signal transduction. In the present article, we review landmarks in the establishment of this field of study, highlight some experimental challenges and propose a simple scheme for definition of these domains based on their primary sequences, rather than experimentally defined nucleotide-binding or catalytic activities.
引用
收藏
页码:969 / 974
页数:6
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