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Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors.

Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors. Research Abstract Details 

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  • Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors. Abstract Text:

    andrew c paolettiAndrew C Paoletti,tari j parmelyTari J Parmely,chieri tomomori-satoChieri Tomomori-Sato,shigeo satoShigeo Sato,dongxiao zhuDongxiao Zhu,ronald c conawayRonald C Conaway,joan weliky conawayJoan Weliky Conaway,laurence florensLaurence Florens,michael p washburnMichael P Washburn,

    Components of multiprotein complexes are routinely determined by using proteomic approaches. However, this information lacks functional content except when new complex members are identified. To analyze quantitatively the abundance of proteins in human Mediator we used normalized spectral abundance factors generated from shotgun proteomics data sets. With this approach we define a common core of mammalian Mediator subunits shared by alternative forms that variably associate with the kinase module and RNA polymerase (pol) II. Although each version of affinity-purified Mediator contained some kinase module and RNA pol II, Mediator purified through F-Med26 contained the most RNA pol II and the least kinase module as demonstrated by the normalized spectral abundance factor approach. The distinct forms of Mediator were functionally characterized by using a transcriptional activity assay, where F-Med26 Mediator/RNA pol II was the most active. This method of protein complex visualization has important implications for the analysis of multiprotein complexes and assembly of protein interaction networks.

    Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors. Publishing Authors By Initials

    ac paolettiAC Paoletti,tj parmelyTJ Parmely,c tomomori-satoC Tomomori-Sato,s satoS Sato,d zhuD Zhu,rc conawayRC Conaway,jw conawayJW Conaway,l florensL Florens,mp washburnMP Washburn,

    For similar enzymes and coenzymes: enzymes: transferases: phosphotransferases: nucleotidyltransferases: rna nucleotidyltransferases: dna-directed rna polymerases: rna polymerase ii research abstracts see: enzymes and coenzymes: enzymes: transferases: phosphotransferases: nucleotidyltransferases: rna nucleotidyltransferases: dna-directed rna polymerases: rna polymerase ii research

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    Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Proceedings of the National Academy of Sciences of

    VOLUME: 103

    Page Numbers: 18928-33

    Journal Abbreviation: Proc. Natl. Acad. Sci. U.S.A.

    ISSN: 0027-8424

    DAY: 30

    MONTH: 11

    YEAR: 2006

    Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7505876

    Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors. Keywords Mesh Terms:

    KEYWORDS: RNA Polymerase II

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors. Information

    Substance Name: RNA Polymerase II

    Registry Number: EC 2.7.7.-

    Grant and Affiliation Information for Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors.

    AFFILIATION: Stowers Institute for Medical Research, 1000 East 50th Street, Kansas City, MO 64110, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: R37 GM 41628

    ACRONYM: GM

    MEDLINETA: Proc Natl Acad Sci U S A

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