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Pseudomonas: Biology and Diversity |
Centre for Functional and Applied Genomics, Institute for Molecular Bioscience1 and Department of Biochemistry2, University of Queensland, Brisbane, QLD 4072, Australia
Author for correspondence: John S. Mattick. Tel: +61 7 3365 4446. Fax: +61 7 3365 4388. e-mail: j.mattick{at}imb.uq.edu.au
Using the complete genome sequence of Pseudomonas aeruginosa PAO1, sequenced by the Pseudomonas Genome Project (ftp://ftp.pseudomonas.com/data/pacontigs.121599), a genome database (http://pseudomonas.bit.uq.edu.au/) has been developed containing information on more than 95% of all ORFs in Pseudomonas aeruginosa. The database is searchable by a variety of means, including gene name, position, keyword, sequence similarity and Pfam domain. Automated and manual annotation, nucleotide and peptide sequences, Pfam and SMART domains (where available), Medline and GenBank links and a scrollable, graphical representation of the surrounding genomic landscape are available for each ORF. Using the database has revealed, among other things, that P. aeruginosa contains four chemotaxis systems, two novel general secretion pathways, at least three loci encoding F17-like thin fimbriae, six novel filamentous haemagglutinin-like genes, a number of unusual composite genetic loci related to vgr/Rhs elements in Escherichia coli, a number of fix-like genes encoding a micro-oxic respiration system, novel biosynthetic pathways and 38 genes containing domains of unknown function (DUF1/DUF2). It is anticipated that this database will be a useful bioinformatic tool for the Pseudomonas community that will continue to evolve.
Keywords: proteome, gene families, regulators, adhesins, type II secretion
Abbreviations: FHA, filamentous haemagglutinin; MCP, methyl-accepting chemotaxis protein
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