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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。

相似文献

1
The relationship between rat major acute phase protein and the kininogens.大鼠主要急性期蛋白与激肽原之间的关系。
J Biol Chem. 1985 Oct 5;260(22):12065-71.
2
Primary structures of the mRNAs encoding the rat precursors for bradykinin and T-kinin. Structural relationship of kininogens with major acute phase protein and alpha 1-cysteine proteinase inhibitor.
J Biol Chem. 1985 Oct 5;260(22):12054-9.
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Isolation of a human cDNA for alpha 2-thiol proteinase inhibitor and its identity with low molecular weight kininogen.人α2-巯基蛋白酶抑制剂cDNA的分离及其与低分子量激肽原的同一性
Biochemistry. 1984 Nov 20;23(24):5691-7. doi: 10.1021/bi00319a005.
4
Major acute phase alpha 1-protein of the rat is homologous to bovine kininogen and contains the sequence for bradykinin: its synthesis is regulated at the mRNA level.大鼠的主要急性期α1蛋白与牛激肽原同源,且包含缓激肽序列:其合成在mRNA水平受到调控。
FEBS Lett. 1985 Mar 11;182(1):57-61. doi: 10.1016/0014-5793(85)81153-4.
5
Structure and expression of the genes for major acute phase alpha 1-protein (thiostatin) and kininogen in the rat.大鼠主要急性期α1蛋白(硫抑素)和激肽原基因的结构与表达
J Biol Chem. 1987 Jul 5;262(19):9298-308.
6
Primary structures of bovine liver low molecular weight kininogen precursors and their two mRNAs.牛肝低分子量激肽原前体及其两种信使核糖核酸的一级结构
Proc Natl Acad Sci U S A. 1983 Jan;80(1):90-4. doi: 10.1073/pnas.80.1.90.
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Cloning and sequence analysis of cDNAs for human high molecular weight and low molecular weight prekininogens. Primary structures of two human prekininogens.
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Rat major acute-phase protein: biosynthesis and characterization of cDNA clone.
Arch Biochem Biophys. 1984 Sep;233(2):624-35. doi: 10.1016/0003-9861(84)90488-0.
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A single gene for bovine high molecular weight and low molecular weight kininogens.
Nature. 1983;305(5934):545-9. doi: 10.1038/305545a0.
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Sequence and acute phase regulation of rat alpha 1-inhibitor III messenger RNA.大鼠α1-抑制剂III信使核糖核酸的序列及急性期调控
J Biol Chem. 1988 Mar 15;263(8):3999-4012.

引用本文的文献

1
Gene expression differences of regenerating rat liver in a short interval successive partial hepatectomy.短期连续部分肝切除术后再生大鼠肝脏的基因表达差异
World J Gastroenterol. 2004 Sep 15;10(18):2680-9. doi: 10.3748/wjg.v10.i18.2680.
2
High-affinity binding of two molecules of cysteine proteinases to low-molecular-weight kininogen.两个半胱氨酸蛋白酶分子与低分子量激肽原的高亲和力结合。
Protein Sci. 1995 Sep;4(9):1874-80. doi: 10.1002/pro.5560040922.
3
Glucocorticoid and estrogen regulation of a rat T-kininogen gene.糖皮质激素和雌激素对大鼠T-激肽原基因的调控
Nucleic Acids Res. 1989 Apr 11;17(7):2835-48. doi: 10.1093/nar/17.7.2835.
4
T-kininogen gene expression is induced during aging.T-激肽原基因表达在衰老过程中被诱导。
Mol Cell Biol. 1989 Dec;9(12):5610-6. doi: 10.1128/mcb.9.12.5610-5616.1989.
5
Inhibition of chicken calpain II by proteins of the cystatin superfamily and alpha 2-macroglobulin.胱抑素超家族蛋白和α2-巨球蛋白对鸡钙蛋白酶II的抑制作用。
Biochem J. 1987 Dec 1;248(2):589-94. doi: 10.1042/bj2480589.
6
Comparison of the acute phase response of cultured Morris hepatoma 7777 cells and of rat hepatocytes.培养的莫里斯肝癌7777细胞与大鼠肝细胞急性期反应的比较。
Br J Exp Pathol. 1987 Aug;68(4):485-92.
7
Identification of a protein increasing in serum of Nagase analbuminemic rats bearing intestinal tumors as an isotype of T-kininogen.鉴定作为T-激肽原同种型的、在患有肠道肿瘤的长谷川无白蛋白血症大鼠血清中含量增加的一种蛋白质。
Jpn J Cancer Res. 1990 Jan;81(1):63-8. doi: 10.1111/j.1349-7006.1990.tb02508.x.
8
Comparative study of asparagine-linked glycans of plasma T-kininogen in normal rats and during acute inflammation.正常大鼠及急性炎症期间血浆T-激肽原天冬酰胺连接聚糖的比较研究。
Biochem J. 1992 Apr 15;283 ( Pt 2)(Pt 2):531-5. doi: 10.1042/bj2830531.
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Inhibition of cell adhesion by high molecular weight kininogen.高分子量激肽原对细胞黏附的抑制作用。
J Cell Biol. 1992 Jan;116(2):465-76. doi: 10.1083/jcb.116.2.465.