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PMID: 7592482 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Bacterial classifications derived from recA protein sequence comparisons.

Journal of bacteriology ·Vol. 177 ·No. 23 ·1995-12-00 ·Pages 6881-93

Karlin S, Weinstock GM, Brendel V

Abstract

RecA protein sequences from 62 eubacterial sources were compared with one another and relative to one archaebacterial RecA-like and a number of eukaryotic RecA-like sequences. Pairwise similarity scores were determined by a novel method based on significant segment pair alignment. The sequences of different species were grouped on the basis of mutually high similarity scores within groups and consistency of score ranges in comparison to other groups. Following this protocol, the gamma-proteobacteria can be subclassified into two major groups, those of mostly vertebrate hosts and those of mostly soil habitat. The alpha-proteobacterial sequences also divide into two distinct groups, whereas classification of the beta-proteobacteria is more complex. The gram-positive bacterial sequences split into three groups of low and three groups of high G+C genome content. However, neither the combined low-G+C-content nor the combined high-G+C-content group nor the aggregate of all gram-positive bacteria form homogeneous groups. The mycoplasma sequences score best with the Bacillus subtilis sequence, consistent with their presumed origin from a gram-positive ancestor. The eukaryotic RAD proteins generally show a single high-scoring segment pair with the proteobacterial RecA sequences around the ATP-binding domain. The bacteriophage T4 UvsX protein aligns best with RecA sequences on two segments disjoint from the ATP-binding domain. The distribution of the most highly conserved regions shared between RecA and noneubacterial RecA-like sequences suggests a mosaic character and evolution of RecA. The discussion considers some questions on the validity and consistency of bacterial classifications derived from RecA sequence comparisons.

MeSH Terms
Amino Acid Sequence Bacteria/classification,enzymology,genetics Bacterial Typing Techniques Databases, Factual Gram-Negative Bacteria/classification,enzymology,genetics Gram-Positive Bacteria/classification,enzymology,genetics Molecular Sequence Data Rec A Recombinases/chemistry,genetics Sequence Alignment Sequence Homology, Amino Acid
Chemicals
Rec A Recombinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Karlin S
Department of Mathematics, Stanford University, California 94305-2125, USA.
Weinstock G M
Brendel V
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34 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1995-12-00
Pages
6881-93
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC177557
Subset
IM
Grants
NIGMS NIH HHS · 2R01GM10452-31 · United States
NHGRI NIH HHS · 5R01HG00335-07 · United States
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