The PAKs come of age: Celebrating 18 years of discovery.

Jeffrey Field, Ed Manser
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引用次数: 8

Abstract

Protein kinases are versatile signaling molecules that are involved in the regulation most physiological responses. The p21-activated kinases (PAKs) can be activated directly by the small GTPases Rac and Cdc42 and are among the best characterized downstream effectors of these Rho proteins. The structure, substrate specificity and functional role of PAKS are evolutionarily conserved from protozoa to mammals. Vertebrate PAKs are particularly important for cytoskeletal remodeling and focal adhesion assembly, thereby contributing to dynamic processes such as cell migration and synaptic plasticity. This issue of Cellular Logistics focuses on the PAK family of kinases, with ten reviews written by researchers currently working in the field. Here in this introductory overview we highlight some of the most interesting recent discoveries regarding PAK biochemistry and biology. The reviews in this issue cover a range of topics including the atomic structures of PAK1 and PAK4, their role in animals as assessed by knockout studies, and how PAKs are likely to contribute to cancer and neurodegenerative diseases. The promise remains that PAK inhibitors will emerge that validate current pre-clinical studies suggesting that blocking PAK activity will positively contribute to human health.

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帕克们成年了:庆祝18年的发现。
蛋白激酶是一种多用途的信号分子,参与调节大多数生理反应。p21活化激酶(PAKs)可以被小gtpase Rac和Cdc42直接激活,是这些Rho蛋白最具特征的下游效应物之一。从原生动物到哺乳动物,PAKS的结构、底物特异性和功能作用在进化上是保守的。脊椎动物PAKs对细胞骨架重塑和黏附聚集尤为重要,从而有助于细胞迁移和突触可塑性等动态过程。本期《细胞物流》聚焦于PAK激酶家族,由目前在该领域工作的研究人员撰写了十篇综述。在这里,在这个介绍性的概述,我们强调一些最有趣的最近发现有关PAK生物化学和生物学。本期综述涵盖了一系列主题,包括PAK1和PAK4的原子结构,敲除研究评估的PAK1和PAK4在动物中的作用,以及PAKs如何可能导致癌症和神经退行性疾病。希望仍然是PAK抑制剂将出现,验证目前的临床前研究表明阻断PAK活性将对人类健康有积极贡献。
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