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FKBP23的分子克隆、特性鉴定及染色体定位,一种具有Ca2+结合能力的新型FK506结合蛋白

Molecular cloning, characterization, and chromosomal localization of FKBP23, a novel FK506-binding protein with Ca2+-binding ability.

作者信息

Nakamura T, Yabe D, Kanazawa N, Tashiro K, Sasayama S, Honjo T

机构信息

Faculty of Medicine, Kyoto University, Sakyo-ku, Kyoto, 606, Japan.

出版信息

Genomics. 1998 Nov 15;54(1):89-98. doi: 10.1006/geno.1998.5571.

Abstract

We have identified and characterized a cDNA encoding a novel FK506-binding protein (FKBP), named FKBP23, from mouse heart by the signal sequence trap method. The deduced amino acid sequence has significant homology to other FKBP family members around the peptidylprolyl cis-trans-isomerase motifs. FKBP23 also has two Ca2+-binding (EF-hand) motifs, and purified FKBP23 protein was shown to have Ca2+-binding ability. This is the first report of a Ca2+-binding FKBP. FKBP23 is a glycoprotein retained in the endoplasmic reticulum by its carboxyl-terminal tetrapeptide His-Asp-Glu-Leu, as demonstrated by immunostaining, retention, and deglycosylation assays. FKBP23 mRNA is expressed most strongly in heart, lung, and testis, beginning at day 8.5 of embryonic development. The FKBP23 gene was mapped to mouse chromosome 2.

摘要

我们通过信号序列捕获法从小鼠心脏中鉴定并表征了一种编码新型FK506结合蛋白(FKBP)的cDNA,该蛋白命名为FKBP23。推导的氨基酸序列在肽基脯氨酰顺反异构酶基序周围与其他FKBP家族成员具有显著同源性。FKBP23还具有两个Ca2+结合(EF手)基序,并且纯化的FKBP23蛋白显示具有Ca2+结合能力。这是关于一种Ca2+结合FKBP的首次报道。如免疫染色、滞留和去糖基化分析所示,FKBP23是一种通过其羧基末端四肽His-Asp-Glu-Leu保留在内质网中的糖蛋白。FKBP23 mRNA在胚胎发育第8.5天开始在心脏、肺和睾丸中表达最强。FKBP23基因定位于小鼠2号染色体。

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