4.5 Review

High-throughput structural biology in drug discovery: Protein kinases

期刊

CURRENT PHARMACEUTICAL DESIGN
卷 10, 期 10, 页码 1069-1082

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1381612043452695

关键词

crystallography; lead optimization; protein structure

向作者/读者索取更多资源

Structural biology is an invaluable tool in modern drug discovery, providing key insights into the interactions of small-molecule drugs with their protein targets. As in many aspects of the drug discovery process, significant synergies can be realized in structural biology by the contemporaneous pursuit of many target proteins from a single structural and functional class. We will review some of those synergies here using the example of the protein kinases - an important class of drug targets that has recently been the subject of intensive study. We conclude by discussing some of the technical advances in X-ray crystallography that have enabled implementation of high-throughput structural biology as applied to drug lead optimization.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据