蛋白质精氨酸甲基转移酶5
胍
药物开发
甲基转移酶
精氨酸
药物发现
疾病
激酶
药物靶点
计算生物学
生物
生物化学
药品
化学
癌症研究
药理学
医学
甲基化
氨基酸
基因
病理
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2017-10-27
卷期号:9 (17): 2081-2098
被引量:36
标识
DOI:10.4155/fmc-2017-0089
摘要
PRMT5 catalyzes the mono- and symmetric dimethylation of the arginine N-guanidine group of a wide variety of target proteins including histones, transcriptional elongation factors, kinases and tumor suppressors by utilizing the essential co-factor S-adenosylmethionine as methyl source. PRMT5 overexpression has been linked to the progression of various diseases, including cancer, and is oftentimes associated with a poor prognosis. Therefore, PRMT5 is promoted as a valuable target for drug discovery approaches and was a subject matter in recent endeavors aiming for the development of specific PRMT5 inhibitors. This review will embrace the significance of PRMT5 as therapeutic target with respect to its molecular interdependencies in disease states as well as its implication in drug development approaches.
科研通智能强力驱动
Strongly Powered by AbleSci AI