Data in Brief (Mar 2016)

Proteome-wide dataset supporting the study of ancient metazoan macromolecular complexes

  • Sadhna Phanse,
  • Cuihong Wan,
  • Blake Borgeson,
  • Fan Tu,
  • Kevin Drew,
  • Greg Clark,
  • Xuejian Xiong,
  • Olga Kagan,
  • Julian Kwan,
  • Alexandr Bezginov,
  • Kyle Chessman,
  • Swati Pal,
  • Graham Cromar,
  • Ophelia Papoulas,
  • Zuyao Ni,
  • Daniel R. Boutz,
  • Snejana Stoilova,
  • Pierre C. Havugimana,
  • Xinghua Guo,
  • Ramy H. Malty,
  • Mihail Sarov,
  • Jack Greenblatt,
  • Mohan Babu,
  • W. Brent Derry,
  • Elisabeth R. Tillier,
  • John B. Wallingford,
  • John Parkinson,
  • Edward M. Marcotte,
  • Andrew Emili

Journal volume & issue
Vol. 6
pp. 715 – 721

Abstract

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Our analysis examines the conservation of multiprotein complexes among metazoa through use of high resolution biochemical fractionation and precision mass spectrometry applied to soluble cell extracts from 5 representative model organisms Caenorhabditis elegans, Drosophila melanogaster, Mus musculus, Strongylocentrotus purpuratus, and Homo sapiens. The interaction network obtained from the data was validated globally in 4 distant species (Xenopus laevis, Nematostella vectensis, Dictyostelium discoideum, Saccharomyces cerevisiae) and locally by targeted affinity-purification experiments. Here we provide details of our massive set of supporting biochemical fractionation data available via ProteomeXchange (http://www.ebi.ac.uk/pride/archive/projects/PXD002319-http://www.ebi.ac.uk/pride/archive/projects/PXD002328), PPIs via BioGRID (185267); and interaction network projections via (http://metazoa.med.utoronto.ca) made fully accessible to allow further exploration. The datasets here are related to the research article on metazoan macromolecular complexes in Nature [1]. Keywords: Proteomics, Metazoa, Protein complexes, Biochemical, Fractionation