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Role of Intrinsic Protein Disorder in the Function and Interactions of the Transcriptional Coactivators CREB-binding Protein (CBP) and p300

期刊

JOURNAL OF BIOLOGICAL CHEMISTRY
卷 291, 期 13, 页码 6714-6722

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.R115.692020

关键词

cAMP response element-binding protein (CREB); hypoxia-inducible factor (HIF); intrinsically disordered protein; protein-protein interaction; STAT transcription factor; structure-function; transcriptional coactivator; coupled folding and binding; intrinsically disordered region; viral oncoprotein; IDP; IDR; transcriptional activation

资金

  1. National Institutes of Health [GM113251, CA096865]

向作者/读者索取更多资源

The transcriptional coactivators CREB-binding protein (CBP) and p300 undergo a particularly rich set of interactions with disordered and partly ordered partners, as a part of their ubiquitous role in facilitating transcription of genes. CBP and p300 contain a number of small structured domains that provide scaffolds for the interaction of disordered transactivation domains from a wide variety of partners, including p53, hypoxia-inducible factor 1 (HIF-1), NF-B, and STAT proteins, and are the targets for the interactions of disordered viral proteins that compete with cellular factors to disrupt signaling and subvert the cell cycle. The functional diversity of the CBP/p300 interactome provides an excellent example of the power of intrinsic disorder to facilitate the complexity of living systems.

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