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

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...

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Veröffentlicht in:Data in brief 2016-03, Vol.6, p.715-721
Hauptverfasser: Phanse, Sadhna, Wan, Cuihong, Borgeson, Blake, Tu, Fan, Drew, Kevin, Clark, Greg, Xiong, Xuejian, Kagan, Olga, Kwan, Julian, Bezginov, Alexandr, Chessman, Kyle, Pal, Swati, Cromar, Graham, Papoulas, Ophelia, Ni, Zuyao, Boutz, Daniel R., Stoilova, Snejana, Havugimana, Pierre C., Guo, Xinghua, Malty, Ramy H., Sarov, Mihail, Greenblatt, Jack, Babu, Mohan, Derry, W. Brent, Tillier, Elisabeth R., Wallingford, John B., Parkinson, John, Marcotte, Edward M., Emili, Andrew
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Sprache:eng
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Zusammenfassung: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].
ISSN:2352-3409
2352-3409
DOI:10.1016/j.dib.2015.11.062