Evolutionary comparisons of RecA-like proteins across all major kingdoms of living organisms

被引:109
作者
Brendel, V [1 ]
Brocchieri, L [1 ]
Sandler, SJ [1 ]
Clark, AJ [1 ]
Karlin, S [1 ]
机构
[1] UNIV CALIF BERKELEY, DEPT MOL & CELL BIOL, DIV GENET, BERKELEY, CA 94720 USA
关键词
protein domains; RecA-like proteins; multiple sequence alignment; SAPS program; SSPA program;
D O I
10.1007/PL00006177
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein sequences with similarities to Escherichia coli RecA were compared across the major kingdoms of eubacteria, archaebacteria, and eukaryotes. The archaeal sequences branch monophyletically and are most closely related to the eukaryotic paralogous Rad51 and Dmc1 groups. A multiple alignment of the sequences suggests a modular structure of RecA-like proteins consisting of distinct segments, some of which are conserved only within subgroups of sequences. The eukaryotic and archaeal sequences share an N-terminal domain which may play a role in interactions with other factors and nucleic acids. Several positions in the alignment blocks are highly conserved within the eubacteria as one group and within the eukaryotes and archaebacteria as a second group, but compared between the groups these positions display nonconservative amino acid substitutions. Conservation within the RecA-like core domain identifies possible key residues involved in ATP-induced conformational changes. We propose that RecA-like proteins derive evolutionarily from an assortment of independent domains and that the functional homologs of RecA in noneubacteria comprise an array of RecA-like proteins acting in series or cooperatively.
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页码:528 / 541
页数:14
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