可药性
计算生物学
药物发现
蛋白质组
药物开发
蛋白质-蛋白质相互作用
生物
人类蛋白质组计划
药物靶点
细胞生物学
血浆蛋白结合
体系结构域
小分子
蛋白质结构域
生物信息学
药品
遗传学
生物化学
蛋白质组学
药理学
计算机科学
基因
企业架构框架
软件体系结构
程序设计语言
软件
作者
Matthieu Schapira,Mike Tyers,Maricel Torrent,C.H. Arrowsmith
摘要
Antagonism of protein-protein interactions (PPIs) with small molecules is becoming more feasible as a therapeutic approach. Successful PPI inhibitors tend to target proteins containing deep peptide-binding grooves or pockets rather than the more common large, flat protein interaction surfaces. Here, we review one of the most abundant PPI domains in the human proteome, the WD40 repeat (WDR) domain, which has a central peptide-binding pocket and is a member of the β-propeller domain-containing protein family. Recently, two WDR domain-containing proteins, WDR5 and EED, as well as other β-propeller domains have been successfully targeted by potent, specific, cell-active, drug-like chemical probes. Could WDR domains be a novel target class for drug discovery? Although the research is at an early stage and therefore not clinically validated, cautious optimism is justified, as WDR domain-containing proteins are involved in multiple disease-associated pathways. The druggability and structural diversity of WDR domain binding pockets suggest that understanding how to target this prevalent domain class will open up areas of disease biology that have so far resisted drug discovery efforts.
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