INACTIVATION OF RAT LIVER GLYCOGEN SYNTHETASE BY 3'-5'-CYCLIC NUCLEOTIDES

被引：35

作者：

GLINSMANN, WH

HERN, EP

机构：

[1] Section on Physiological Controls Laboratory, Biomedical Sciences National Institute of Child Health and Human Development Bethesda

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1969年 / 36卷 / 06期

关键词：

D O I：

10.1016/0006-291X(69)90293-9

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The 3′:5′-cyclic phosphate esters of adenosine, guanosine, inosine, cytidine and uridine enhance the conversion of glycogen synthetase a to b in the perfused rat liver and in liver homogenates. This supports the possibility that these nucleotides activate a kinase which phosphorylates glycogen synthetase. © 1969.

引用

页码：931 / +

页数：1

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