Comparison of the Small Molecule Metabolic Enzymes of Escherichia coli and Saccharomyces cerevisiae

  1. Oliver Jardine1,
  2. Julian Gough2,
  3. Cyrus Chothia2, and
  4. Sarah A. Teichmann3,4,5
  1. 1Department of Crystallography, Birkbeck College, London WC1E 7HX, United Kingdom; 2MRC Laboratory of Molecular Biology, Cambridge CB2 2QH, United Kingdom; 3Department of Biochemistry and Molecular Biology, University College London, Darwin Building, London WC1E 6BT, United Kingdom

Abstract

The comparison of the small molecule metabolism pathways inEscherichia coli and Saccharomyces cerevisiae (yeast) shows that 271 enzymes are common to both organisms. These common enzymes involve 384 gene products in E. coli and 390 in yeast, which are between one half and two thirds of the gene products of small molecule metabolism in E. coli and yeast, respectively. The arrangement and family membership of the domains that form all or part of 374 E. coli sequences and 343 yeast sequences was determined. Of these, 70% consist entirely of homologous domains, and 20% have homologous domains linked to other domains that are unique toE. coli, yeast, or both. Over two thirds of the enzymes common to the two organisms have sequence identities between 30% and 50%. The remaining groups include 13 clear cases of nonorthologous displacement. Our calculations show that at most one half to two thirds of the gene products involved in small molecule metabolism are common to E. coli and yeast. We have shown that the common core of 271 enzymes has been largely conserved since the separation of prokaryotes and eukaryotes, including modifications for regulatory purposes, such as gene fusion and changes in the number of isozymes in one of the two organisms. Only one fifth of the common enzymes have nonhomologous domains between the two organisms. Around the common core very different extensions have been made to small molecule metabolism in the two organisms.

[Online supplementary material available a http://www.genome.org.]

Footnotes

  • 5 Present address: MRC Laboratory of Molecular Biology, Cambridge CB2 2QH, UK.

  • 4 Corresponding author.

  • E-MAIL sat{at}mrc-lmb.cam.ac.uk; FAX +44-(0)1223-213556.

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.228002.

    • Received December 18, 2001.
    • Accepted March 28, 2002.
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