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大鼠主要急性期蛋白与激肽原之间的关系。

The relationship between rat major acute phase protein and the kininogens.

作者信息

Anderson K P, Heath E C

出版信息

J Biol Chem. 1985 Oct 5;260(22):12065-71.

PMID:2413019
Abstract

The rat major acute phase protein (alpha 1-MAP) is a cysteine protease inhibitor. The stoichiometry of the interaction between the inhibitor and enzyme was shown to be 1:2. A cDNA clone specific for rat alpha 1-MAP was isolated from a cDNA library prepared from an inflamed rat liver RNA template. The 1458-base pair insert was sequenced and positively identified by alignment with a partial amino acid sequence obtained by radiosequence analysis of the primary translation product for alpha 1-MAP. Complete sequence analysis determined the alpha 1-MAP cDNA coded for the entire protein with the exception of the first four amino acids of the signal peptide, all of which were identified by radiosequencing. The coding sequence spans 1282 nucleotides, followed by 115 base pairs of a 3' untranslated region. Two putative active sites, suggested by the enzyme-inhibitor ratio, have been identified by analysis of internal duplications of the alpha 1-MAP sequence and the alignment of these regions with the sequences of several low molecular weight cysteine protease inhibitors. A computer homology analysis of the protein sequence revealed a 59.3% overall identity between rat alpha 1-MAP and bovine low molecular weight (LMW) kininogen. The homology included the signal peptide regions. LMW kininogen is a precursor of bradykinin. alpha 1-MAP does contain a bradykinin sequence; the flanking amino acids are different, however. Evidence for the expression of the LMW and a high molecular weight kininogen from the same gene, and the high degree of homology between these proteins and the rat acute phase protein suggest that all three proteins belong to a precisely regulated gene family.

摘要

大鼠主要急性期蛋白(α1-MAP)是一种半胱氨酸蛋白酶抑制剂。该抑制剂与酶之间相互作用的化学计量比显示为1:2。从以发炎大鼠肝脏RNA模板制备的cDNA文库中分离出了大鼠α1-MAP特异的cDNA克隆。对1458个碱基对的插入片段进行了测序,并通过与通过α1-MAP初级翻译产物的放射性序列分析获得的部分氨基酸序列进行比对而得到了肯定的鉴定。完整的序列分析确定α1-MAP cDNA编码了整个蛋白质,但信号肽的前四个氨基酸除外,所有这些氨基酸均通过放射性测序得以鉴定。编码序列跨度为1282个核苷酸,随后是3'非翻译区的115个碱基对。通过对α1-MAP序列的内部重复以及这些区域与几种低分子量半胱氨酸蛋白酶抑制剂序列的比对分析,已经鉴定出由酶-抑制剂比例所提示的两个推定活性位点。对该蛋白质序列的计算机同源性分析显示,大鼠α1-MAP与牛低分子量(LMW)激肽原之间的总体一致性为59.3%。这种同源性包括信号肽区域。LMW激肽原是缓激肽的前体。α1-MAP确实包含一个缓激肽序列;然而,其侧翼氨基酸不同。来自同一基因的LMW和高分子量激肽原表达的证据,以及这些蛋白质与大鼠急性期蛋白之间的高度同源性表明,这三种蛋白质都属于一个精确调控的基因家族。

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