期刊
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
卷 640, 期 -, 页码 83-92出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2018.01.001
关键词
Binding protein; Cell signaling; Disorder; Metastasis; microRNA; Negative regulation
资金
- JSPS KAKENHI [15K01824, 15K07842, 25850244]
- Grants-in-Aid for Scientific Research [15K01824, 15K07842, 25850244] Funding Source: KAKEN
Intracellular signal transduction is built on the basis of the subtle balance between phosphorylation and dephosphorylation. Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F/POPX2) and CaMKP-N (PPM1E/POPX1) are Ser/Thr phosphatases that belong to the PPM (protein phosphatase, Mg2+/Mn2+-dependent) family. The former was discovered in rat brain as a novel protein phosphatase regulating Ca2+/calmodulin-dependent protein kinases (CaMKs), whereas the latter was first identified in human cDNA databases using the rat CaMKP sequence. Subsequent studies have revealed that they are involved in various cellular functions through regulation of not only CaMKs but also other protein kinases such as AMP-activated protein kinase. Furthermore, accumulating evidence shows possible involvement of CaMKP and CaMKP-N in the pathogenesis of various diseases including cancer. Therefore, the biochemistry of CaMKP and CaMKP-N largely contributes to molecular medicine targeting these phosphatases. In this review, we summarized recent progress in the enzymology and biology of CaMKP and CaMKP-N. We also focused on etiology studies in which CaMKP and CaMKP-N are involved. Based on the emerging evidence, future perspectives of studies on these phosphatases and related issues to be elucidated are discussed.
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