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首页> 外文期刊>Molecular pharmacology. >Adenylyl cyclase--A-kinase anchoring protein complexes: the next dimension in cAMP signaling.
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Adenylyl cyclase--A-kinase anchoring protein complexes: the next dimension in cAMP signaling.

机译:腺苷酸环化酶-A激酶锚定蛋白复合物:cAMP信号传导的下一维度。

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摘要

The formation of multiprotein complexes is a repeated theme in biology ranging from the regulation of the extracellular signal-regulated kinase and cAMP signaling pathways to the formation of postsynaptic density complexes or tight junctions. A-kinase anchoring proteins (AKAPs) are well known for their ability to scaffold protein kinase A and components upstream and downstream of cAMP production, including G protein-coupled receptors, cAMP-dependent Rap-exchange factors, and phosphodiesterases. Specific adenylyl cyclase (AC) isoforms have also been identified as components of AKAP complexes, namely AKAP79, Yotiao, and mAKAP. In this review, we summarize recent evidence for AC-AKAP complexes and requirements for compartmentalization of cAMP signaling. The ability of AKAPs to assemble intricate feedback loops to control spatiotemporal aspects of cAMP signaling adds yet another dimension to the classic cAMP pathway.
机译:多蛋白复合物的形成是生物学中的重复主题,其范围从细胞外信号调节激酶和cAMP信号通路的调节到突触后密度复合物或紧密连接的形成。 A激酶锚定蛋白(AKAP)能够支撑蛋白激酶A和cAMP产生的上游和下游成分,包括G蛋白偶联受体,依赖cAMP的Rap交换因子和磷酸二酯酶。特定的腺苷酸环化酶(AC)亚型也已被确定为AKAP复合物的组成部分,即AKAP79,Yotiao和mAKAP。在这篇综述中,我们总结了AC-AKAP复合物的最新证据以及对cAMP信号传导间隔的要求。 AKAP组装复杂的反馈回路以控制cAMP信号的时空方面的能力为经典的cAMP途径增加了另一个维度。

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