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Regulation of Cellular Protein Phosphatase-1 (PP1) by Phosphorylation of the CPI-17 Family, C-kinase-activated PP1 Inhibitors
被引:117
|作者:
Eto, Masumi
[1
,2
]
机构:
[1] Thomas Jefferson Univ, Dept Mol Physiol & Biophys, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
基金:
美国国家卫生研究院;
关键词:
LIGHT-CHAIN PHOSPHATASE;
ARTERIAL SMOOTH-MUSCLE;
INTEGRIN-LINKED KINASE;
MYOSIN PHOSPHATASE;
CA2+ SENSITIZATION;
PHOSPHOPROTEIN INHIBITOR;
MEDIATED ACTIVATION;
INDUCED CONTRACTION;
STRUCTURAL BASIS;
UP-REGULATION;
D O I:
10.1074/jbc.R109.059972
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The regulatory circuit controlling cellular protein phosphatase-1 (PP1), an abundant group of Ser/Thr phosphatases, involves phosphorylation of PP1-specific inhibitor proteins. Malfunctions of these inhibitor proteins have been linked to a variety of diseases, including cardiovascular disease and cancer. Upon phosphorylation at Thr(38), the 17-kDa PP1 inhibitor protein, CPI-17, selectively inhibits a specific form of PP1, myosin light chain phosphatase, which transduces multiple kinase signals into the phosphorylation of myosin II and other proteins. Here, the mechanisms underlying PP1 inhibition and the kinase/PP1 cross-talk mediated by CPI-17 and its related proteins, PHI, KEPI, and GBPI, are discussed.
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页码:35273 / 35277
页数:5
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