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编码1型蛋白磷酸酶催化亚基的cDNA克隆的分离与序列分析:与蛋白磷酸酶2A的同源性

Isolation and sequence analysis of a cDNA clone encoding a type-1 protein phosphatase catalytic subunit: homology with protein phosphatase 2A.

作者信息

Berndt N, Campbell D G, Caudwell F B, Cohen P, da Cruz e Silva E F, da Cruz e Silva O B, Cohen P T

机构信息

Department of Biochemistry, University of Dundee, Scotland.

出版信息

FEBS Lett. 1987 Nov 2;223(2):340-6. doi: 10.1016/0014-5793(87)80316-2.

Abstract

A 1.5 kb clone containing the full-length coding sequence of a type-1 protein phosphatase catalytic subunit has been isolated from a rabbit skeletal muscle cDNA library constructed in lambda gt10. The protein sequence deduced from the cDNA contains 311 residues and has a molecular mass of 35.4 kDa. A single mRNA species at 1.6 kb was visualized by Northern blotting. The type-1 protein phosphatase was strikingly homologous to protein phosphatase 2A, 49% of the amino acids between residues 11 and 280 being identical. The first 10 and last 31 residues were dissimilar. Residues 1-101 of the type-1 protein phosphatase also showed 21% sequence identity with a region of mammalian alkaline phosphatases.

摘要

从构建于λgt10的兔骨骼肌cDNA文库中分离出一个1.5kb的克隆,其包含1型蛋白磷酸酶催化亚基的全长编码序列。从该cDNA推导的蛋白质序列含有311个残基,分子量为35.4kDa。通过Northern印迹法观察到一条1.6kb的单一mRNA条带。1型蛋白磷酸酶与2A蛋白磷酸酶显著同源,第11至280位残基间49%的氨基酸相同。前10个和后31个残基不同。1型蛋白磷酸酶的第1至101位残基与哺乳动物碱性磷酸酶的一个区域也显示出21%的序列同一性。

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