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http://purl.uniprot.org/citations/14736873http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/14736873http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/14736873http://www.w3.org/2000/01/rdf-schema#comment"Receptor interacting protein (RIP) 140 is a corepressor that can be recruited to nuclear receptors by means of LXXLL motifs. We have characterized four distinct autonomous repression domains in RIP140, termed RD1-4, that are highly conserved in mammals and birds. RD1 at the N terminus represses transcription in the presence of trichostatin A, suggesting that it functions by a histone deacetylase (HDAC)-independent mechanism. The repressive activity of RD2 is dependent upon carboxyl-terminal binding protein recruitment to two specific binding sites. Use of specific inhibitors indicates that RD2, RD3, and RD4 are capable of functioning by HDAC-dependent and HDAC-independent mechanisms, depending upon cell type."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.org/dc/terms/identifier"doi:10.1074/jbc.m313906200"xsd:string
http://purl.uniprot.org/citations/14736873http://purl.org/dc/terms/identifier"doi:10.1074/jbc.m313906200"xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/author"Christian M."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/author"Christian M."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/author"Parker M.G."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/author"Parker M.G."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/author"Tullet J.M.A."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/author"Tullet J.M.A."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/name"J. Biol. Chem."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/name"J. Biol. Chem."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/pages"15645-15651"xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/pages"15645-15651"xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/title"Characterization of four autonomous repression domains in the corepressor receptor interacting protein 140."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/title"Characterization of four autonomous repression domains in the corepressor receptor interacting protein 140."xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/volume"279"xsd:string
http://purl.uniprot.org/citations/14736873http://purl.uniprot.org/core/volume"279"xsd:string
http://purl.uniprot.org/citations/14736873http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/14736873
http://purl.uniprot.org/citations/14736873http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/14736873
http://purl.uniprot.org/citations/14736873http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/14736873
http://purl.uniprot.org/citations/14736873http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/14736873