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嘌呤补救酶如何精确定位正确碱基。

How a purine salvage enzyme singles out the right base.

机构信息

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560064, India.

Chemistry and Physics of Materials Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560064, India.

出版信息

J Biol Chem. 2019 Aug 9;294(32):11992-11993. doi: 10.1074/jbc.H119.010025.

Abstract

Two phosphoribosyltransferases in the purine salvage pathway exhibit exquisite substrate specificity despite the chemical similarity of their distinct substrates, but the basis for this discrimination was not fully understood. Ozeir now employ a complementary biochemical, structural, and computational approach to deduce the chemical constraints governing binding and propose a distinct mechanism for catalysis in one of these enzymes, adenine phosphoribosyltransferase. These insights, built on data from an unexpected finding, finally provide direct answers to key questions regarding these enzymes and substrate recognition more generally.

摘要

嘌呤补救途径中的两种磷酸核糖基转移酶尽管其不同底物在化学上具有相似性,但表现出极高的底物特异性,但这种区分的基础尚未完全理解。Ozeir 现在采用互补的生化、结构和计算方法来推断控制结合的化学约束,并提出这些酶中的一种,即腺嘌呤磷酸核糖基转移酶,催化的独特机制。这些基于意外发现数据得出的见解,最终为这些酶以及更普遍的底物识别的关键问题提供了直接答案。

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本文引用的文献

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