化学
药物发现
药品
药物靶点
计算生物学
虚拟筛选
瓜氨酸
中性粒细胞胞外陷阱
生物化学
药理学
精氨酸
炎症
免疫学
医学
生物
氨基酸
作者
Chao Yang,Zhenzhen Dong,Zhang Jing,Dehong Teng,Xinzhi Luo,Dan Li,Yingtang Zhou
标识
DOI:10.1016/j.ejmech.2021.113840
摘要
Peptidylarginine deaminase 4 (PAD4) is a crucial post-translational modifying enzyme catalyzing the conversion of arginine into citrulline residues, and mediating the formation of neutrophil extracellular traps (NETs). PAD4 plays a vital role in the occurrence and development of cardiovascular diseases, autoimmune diseases, and various tumors. Therefore, PAD4 is considered as a promising drug target for disease diagnosis and treatment. More and more efforts are devoted to developing highly efficient and selective PAD4 inhibitors via high-throughput screening, structure-based drug design and structure-activity relationship study. This article outlined the physiological and pathological functions of PAD4, and corresponding representative small molecule inhibitors reported in recent years.
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