生物
酪蛋白激酶1
基因亚型
激酶
计算生物学
磷酸化
遗传学
细胞生物学
蛋白激酶A
基因
作者
Pengfei Xu,Chiara Ianes,Fabian Gärtner,Congxing Liu,Timo Burster,В. А. Бакулев,Najma Rachidi,Uwe Knippschild,Joachim Bischof
出处
期刊:Gene
[Elsevier]
日期:2019-10-01
卷期号:715: 144005-144005
被引量:47
标识
DOI:10.1016/j.gene.2019.144005
摘要
Members of the highly conserved pleiotropic CK1 family of serine/threonine-specific kinases are tightly regulated in the cell and play crucial regulatory roles in multiple cellular processes from protozoa to human. Since their dysregulation as well as mutations within their coding regions contribute to the development of various different pathologies, including cancer and neurodegenerative diseases, they have become interesting new drug targets within the last decade. However, to develop optimized CK1 isoform-specific therapeutics in personalized therapy concepts, a detailed knowledge of the regulation and functions of the different CK1 isoforms, their various splice variants and orthologs is mandatory. In this review we will focus on the stress-induced CK1 isoform delta (CK1δ), thereby addressing its regulation, physiological functions, the consequences of its deregulation for the development and progression of diseases, and its potential as therapeutic drug target.
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