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2-氨基乙胂酸作为磷酸乙醇胺的类似物。赋予磷酸乙醇胺胞苷酰转移酶CTP焦磷酸酶活性。

2-Aminoethylarsonic acid as an analogue of ethanolamine phosphate. Endowment of ethanolamine-phosphate cytidylyltransferase with CTP pyrophosphatase activity.

作者信息

Visedo-Gonzalez E, Dixon H B

机构信息

Department of Biochemistry, University of Cambridge, U.K.

出版信息

Biochem J. 1989 May 15;260(1):299-301. doi: 10.1042/bj2600299.

DOI:10.1042/bj2600299
PMID:2549956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1138663/
Abstract

2-Aminoethylarsonic acid was tested for its ability to act as a substrate for ethanolamine-phosphate cytidylytransferase as a cytidylyl acceptor in place of ethanolamine phosphate. The expected product, like all mixed anhydrides of arsonic acids, should hydrolyse spontaneously with regeneration of the substrate analogue and CMP formation; such CMP production was observed. The limiting velocity with aminoethylarsonic acid is about 90% that with ethanolamine phosphate, and the Michaelis constant is below 20 mM.

摘要

对2-氨基乙胂酸作为乙醇胺磷酸胞苷酰转移酶的底物替代乙醇胺磷酸作为胞苷酰受体的能力进行了测试。预期产物与所有胂酸的混合酸酐一样,应自发水解,使底物类似物再生并形成CMP;观察到了这种CMP的产生。氨基乙胂酸的极限速度约为乙醇胺磷酸的90%,米氏常数低于20 mM。

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本文引用的文献

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ADP-arsenate. Formation by submitochondrial particles under phosphorylating conditions.ADP-砷酸盐。在磷酸化条件下由亚线粒体颗粒形成。
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[CMP-aminoethylphosphonate: intermediary in the phosphonolipids of the rat liver].[CMP-氨乙基膦酸酯:大鼠肝脏磷脂中的中间体]
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Synthesis of 2-aminoethylarsonic acid. A new synthesis of primary.2-氨基乙磺酸的合成。一种新的伯胺合成方法。
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