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哺乳动物中支架蛋白对丝裂原活化蛋白激酶信号模块的调控。

Regulation of MAP kinase signaling modules by scaffold proteins in mammals.

作者信息

Morrison Deborah K, Davis Roger J

机构信息

Regulation of Cell Growth Laboratory, NCI-Frederick, P.O. Box B, Frederick, Maryland 21702, USA.

出版信息

Annu Rev Cell Dev Biol. 2003;19:91-118. doi: 10.1146/annurev.cellbio.19.111401.091942.

Abstract

The mitogen-activated protein kinase (MAPK) group of serine/threonine protein kinases mediates the response of cells to many extracellular stimuli such as cytokines and growth factors. These protein kinases include the extracellular signal-regulated protein kinases (ERK) and two stress-activated protein kinases (SAPK), the c-Jun N-terminal kinases (JNK), and the p38 MAPK. The enzymes are evolutionarily conserved and are activated by a common mechanism that involves a protein kinase cascade. Scaffold proteins have been proposed to interact with MAPK pathway components to create a functional signaling module and to control the specificity of signal transduction. Here we critically evaluate the evidence that supports a physiologically relevant role of MAPK scaffold proteins in mammals.

摘要

丝氨酸/苏氨酸蛋白激酶的丝裂原活化蛋白激酶(MAPK)组介导细胞对许多细胞外刺激(如细胞因子和生长因子)的反应。这些蛋白激酶包括细胞外信号调节蛋白激酶(ERK)和两种应激激活蛋白激酶(SAPK),即c-Jun氨基末端激酶(JNK)和p38 MAPK。这些酶在进化上是保守的,并通过涉及蛋白激酶级联反应的共同机制被激活。有人提出支架蛋白与MAPK途径成分相互作用,以创建一个功能性信号模块并控制信号转导的特异性。在这里,我们批判性地评估了支持MAPK支架蛋白在哺乳动物中具有生理相关作用的证据。

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