• DocumentCode
    2767735
  • Title

    The functional make up of proteomes is remarkably conserved

  • Author

    Nasir, A. ; Naeem, A. ; Khan, M.J. ; Lopez-Nicora, H.D. ; Caetano-Anolles, G.

  • Author_Institution
    Dept. of Crop Sci., Univ. of Illinois at Urbana-Champaign, Urbana, IL, USA
  • fYear
    2011
  • fDate
    12-15 Nov. 2011
  • Firstpage
    1023
  • Lastpage
    1025
  • Abstract
    Here we analyze the functional annotation of protein domains in almost a thousand sequenced genomes. Our results yield fundamental insights into the structural and functional diversity of proteomes. We find that the functional makeup of proteomes is remarkably conserved across cellular superkingdoms. In general, most of the proteome repertoire is spent for functions related to metabolic processes but there are significant differences in the usage of protein domains both between and within superkingdoms. Our results provide support to the hypotheses that the proteomes of the eukaryal superkingdom evolved via genome expansion mechanisms while those of microbial superkingdoms evolved by reductive evolutionary processes. We also identify few genomic outlier groups in each superkingdom that deviate significantly from the conserved functional design. These genomes are reduced and belong to parasitic organisms.
  • Keywords
    cellular biophysics; microorganisms; proteins; proteomics; cellular superkingdoms; eukaryal superkingdom; functional diversity; genome expansion mechanisms; microbial superkingdoms; protein domains annotation; proteomes; reductive evolutionary processes; sequenced genomes; structural diversity; Bioinformatics; Genomics; Microorganisms; Protein engineering; Proteins; SCOP; fold superfamily; functional annotation; molecular function; protein domain; structure; superkingdom;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedicine Workshops (BIBMW), 2011 IEEE International Conference on
  • Conference_Location
    Atlanta, GA
  • Print_ISBN
    978-1-4577-1612-6
  • Type

    conf

  • DOI
    10.1109/BIBMW.2011.6112546
  • Filename
    6112546