4.3 Article

An extracellular calcium-binding domain in bacteria with a distant relationship to EF-hands

期刊

FEMS MICROBIOLOGY LETTERS
卷 221, 期 1, 页码 103-110

出版社

OXFORD UNIV PRESS
DOI: 10.1016/S0378-1097(03)00160-5

关键词

genome analysis; calcium-binding site; protein domain; cell envelope; S-layer; nuclease; calmodulin; evolution

向作者/读者索取更多资源

Extracellular Ca2+-dependent nuclease YokF from Bacillus subtilis and several other surface-exposed proteins from diverse bacteria are encoded in the genomes in two paralogous forms that differ by a similar to45 amino acid fragment, which comprises a novel conserved domain. Sequence analysis of this domain revealed a conserved DxDxDGxxCE motif, which is strikingly similar to the Ca2+-binding loop of the calmodulin-like EF-hand domains, suggesting an evolutionary relationship between them. Functions of many of the other proteins in which the novel domain, named Excalibur (extracellular calcium-binding region), is found, as well as a structural model of its conserved motif are consistent with the notion that the Excalibur domain binds calcium. This domain is but one more example of the diversity of structural contexts surrounding the EF-hand-like calcium-binding loop in bacteria. This loop is thus more widespread than hitherto recognized and the evolution of EF-hand-like domains is probably more complex than previously appreciated. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据