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从布氏锥虫中鉴定出一种新的EF手超家族成员。

Identification of a new EF-hand superfamily member from Trypanosoma brucei.

作者信息

Wong S, Kretsinger R H, Campbell D A

机构信息

Department of Microbiology and Immunology, University of California, Los Angeles 90024.

出版信息

Mol Gen Genet. 1992 May;233(1-2):225-30. doi: 10.1007/BF00587583.

Abstract

We identified several open reading frames between the regions encoding calmodulin and ubiquitin-EP52/1 in the genome of Trypanosoma brucei. One of these, EFH5, encodes a protein 192 amino acids long. The EFH5 transcript is present in poly(A)+ mRNA and is present at similar levels in the mammalian bloodstream form and the insect procyclic form. EFH5 contains four EF-hand homolog domains, two of which are inferred to bind Ca2+ ions. We expressed EFH5 as a fusion protein in Escherichia coli and demonstrated calcium-binding activity of the fusion protein using the 45Ca-overlay technique. The function of EFH5 remains unknown; however, as the fourth EF-hand homolog identified in trypanosomes, it attests to the broad range of functions assumed by calcium functioning as a second messenger. EFH5, which is most closely related to LAV1-2 from Physarum, represents a distinct subfamily among the EF-hand-containing proteins.

摘要

我们在布氏锥虫基因组中编码钙调蛋白和泛素-EP52/1的区域之间鉴定出了几个开放阅读框。其中一个名为EFH5,编码一个长度为192个氨基酸的蛋白质。EFH5转录本存在于多聚腺苷酸化(poly(A)+)的mRNA中,并且在哺乳动物血液型和昆虫前循环型中以相似水平存在。EFH5包含四个EF手型同源结构域,其中两个被推断可结合钙离子。我们在大肠杆菌中表达了EFH5融合蛋白,并使用45Ca覆盖技术证明了该融合蛋白的钙结合活性。EFH5的功能仍然未知;然而,作为在锥虫中鉴定出的第四个EF手型同源物,它证明了钙作为第二信使所具有的广泛功能。与黏菌的LAV1-2关系最为密切的EFH5,在含EF手型的蛋白质中代表一个独特的亚家族。

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