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肌球蛋白磷酸酶:亚基与相互作用

Myosin phosphatase: subunits and interactions.

作者信息

Hartshorne D J

机构信息

Muscle Biology Group, University of Arizona, Tucson 85721-0038, USA.

出版信息

Acta Physiol Scand. 1998 Dec;164(4):483-93. doi: 10.1046/j.1365-201X.1998.00447.x.

Abstract

Myosin phosphorylation is an important mechanism in regulating contractile activity of smooth muscle. The level of myosin phosphorylation depends on the balance of two enzymes, myosin light chain kinase and myosin phosphatase. Recently it has been discovered that myosin phosphatase can be regulated and this renewed interest in characterization of the phosphatase. It is suggested that the myosin phosphatase is composed of three subunits: a catalytic subunit of type 1 phosphatase (delta isoform; PP1c delta); and two non-catalytic subunits, large and small (M20). The large subunit is thought to be a targeting subunit and is termed myosin phosphatase target subunit (MYPT). There are several isoforms of MYPT and two genes have been identified on human chromosomes 1 and 12. A dominant feature of MYPT is a series of ankyrin repeats at the N-terminal end of the molecule and these may be involved in binding to the catalytic subunit and to substrate, phosphorylated myosin. In addition, at the N-terminal fringe of the ankyrin motifs is a consensus PP1c binding motif. The function of the M20 subunit is not established but is known to bind to the C-terminal end of MYPT. Various interactions between subunits that might be relevant for the regulation of phosphatase activity are discussed.

摘要

肌球蛋白磷酸化是调节平滑肌收缩活性的重要机制。肌球蛋白磷酸化水平取决于两种酶——肌球蛋白轻链激酶和肌球蛋白磷酸酶之间的平衡。最近发现肌球蛋白磷酸酶可被调节,这重新引发了对该磷酸酶特性研究的兴趣。有人提出肌球蛋白磷酸酶由三个亚基组成:1型磷酸酶的催化亚基(δ亚型;PP1cδ);以及两个非催化亚基,大亚基和小亚基(M20)。大亚基被认为是一个靶向亚基,称为肌球蛋白磷酸酶靶向亚基(MYPT)。MYPT有几种亚型,在人类1号和12号染色体上已鉴定出两个基因。MYPT的一个主要特征是在分子的N末端有一系列锚蛋白重复序列,这些序列可能参与与催化亚基和底物——磷酸化肌球蛋白的结合。此外,在锚蛋白基序的N末端边缘是一个共有PP1c结合基序。M20亚基的功能尚未明确,但已知它与MYPT的C末端结合。文中讨论了亚基之间可能与磷酸酶活性调节相关的各种相互作用。

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