4.5 Article

Immucillins in custom catalytic-site cavities

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 18, 期 22, 页码 5900-5903

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2008.08.047

关键词

PNP; Immucillin; ImmH; Mutant; Binding; Transition-state analogue

资金

  1. NIGMS NIH HHS [R37 GM041916-19, R37 GM041916] Funding Source: Medline

向作者/读者索取更多资源

Neighboring-group participation in the reaction catalyzed by purine nucleoside phosphorylase involves a compression mode between the 5'- and 4'-ribosyl oxygens, facilitated by His257. The His257Gly mutant opens a space in the catalytic site. Hydrophobic 5'-substituted Immucillins are transition-state analogue inhibitors of this mutant enzyme. Dissociation constants as low as 2 pM are achieved, with K-m/K-d as high as 400,000,000. (C) 2008 Elsevier Ltd. All rights reserved.

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