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死亡不仅仅是生命的终结:激酶和拟激酶信号中非催化功能。

There's more to death than life: Noncatalytic functions in kinase and pseudokinase signaling.

机构信息

Biochemistry Department, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.

Inflammation Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.

出版信息

J Biol Chem. 2021 Jan-Jun;296:100705. doi: 10.1016/j.jbc.2021.100705. Epub 2021 Apr 22.

Abstract

Protein kinases are present in all domains of life and play diverse roles in cellular signaling. Whereas the impact of substrate phosphorylation by protein kinases has long been appreciated, it is becoming increasingly clear that protein kinases also play other, noncatalytic, functions. Here, we review recent developments in understanding the noncatalytic functions of protein kinases. Many noncatalytic activities are best exemplified by protein kinases that are devoid of enzymatic activity altogether-known as pseudokinases. These dead proteins illustrate that, beyond conventional notions of kinase function, catalytic activity can be dispensable for biological function. Through key examples we illustrate diverse mechanisms of noncatalytic kinase activity: as allosteric modulators; protein-based switches; scaffolds for complex assembly; and as competitive inhibitors in signaling pathways. In common, these noncatalytic mechanisms exploit the nature of the protein kinase fold as a versatile protein-protein interaction module. Many examples are also intrinsically linked to the ability of the protein kinase to switch between multiple states, a function shared with catalytic protein kinases. Finally, we consider the contemporary landscape of small molecules to modulate noncatalytic functions of protein kinases, which, although challenging, has significant potential given the scope of noncatalytic protein kinase function in health and disease.

摘要

蛋白激酶存在于所有生命领域,在细胞信号转导中发挥着多样化的作用。尽管蛋白激酶对底物磷酸化的影响早已被人们所认识,但越来越明显的是,蛋白激酶还具有其他非催化功能。在这里,我们回顾了理解蛋白激酶非催化功能的最新进展。许多非催化活性最好的例证是完全缺乏酶活性的蛋白激酶,即伪激酶。这些“死”蛋白表明,除了传统的激酶功能概念之外,催化活性对于生物学功能可能是可有可无的。通过关键示例,我们阐述了非催化激酶活性的多种机制:作为别构调节剂;基于蛋白质的开关;复杂组装的支架;以及作为信号通路中的竞争性抑制剂。总的来说,这些非催化机制利用了蛋白激酶折叠作为多功能蛋白-蛋白相互作用模块的性质。许多例子也与蛋白激酶在多种状态之间切换的能力内在相关,这种功能与催化蛋白激酶共享。最后,我们考虑了调节蛋白激酶非催化功能的小分子的当代格局,尽管具有挑战性,但鉴于蛋白激酶在健康和疾病中的非催化功能的范围,这具有重要的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f57/8141879/b3fee185f3b7/gr1.jpg

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