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

被引:33
|
作者
Rigden, DJ
Jedrzejas, MJ
Galperin, MY [1 ]
机构
[1] Natl Lib Med, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA
[2] EMBRAPA, Cenargen, Natl Ctr Genet Resources & Biotechnol, BR-70770900 Brasilia, DF, Brazil
[3] Childrens Hosp Oakland, Res Inst, Oakland, CA 94609 USA
关键词
genome analysis; calcium-binding site; protein domain; cell envelope; S-layer; nuclease; calmodulin; evolution;
D O I
10.1016/S0378-1097(03)00160-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:103 / 110
页数:8
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