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http://purl.uniprot.org/citations/12896805http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12896805http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12896805http://www.w3.org/2000/01/rdf-schema#comment"The hydrophobic estradiol-derivative RU49953 inhibits the energy-dependent interaction of yeast multidrug-transporter Pdr5p with its fluorescent drug-substrate rhodamine 6G. The potent inhibition is competitive towards drug binding (Ki=23+/-6 nM), whereas nucleoside-triphosphate hydrolysis is two-orders-of-magnitude less sensitive. RU49953 constitutes the most efficient inhibitor of drug binding to a yeast multidrug ABC exporter reported so far."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.org/dc/terms/identifier"doi:10.1016/s0005-2736(03)00193-7"xsd:string
http://purl.uniprot.org/citations/12896805http://purl.org/dc/terms/identifier"doi:10.1016/s0005-2736(03)00193-7"xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Goffeau A."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Goffeau A."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Di Pietro A."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Di Pietro A."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Conseil G."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Conseil G."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Perez-Victoria J.M."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Perez-Victoria J.M."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Renoir J.M."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/author"Renoir J.M."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/name"Biochim. Biophys. Acta"xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/name"Biochim. Biophys. Acta"xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/pages"131-134"xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/pages"131-134"xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/title"Potent competitive inhibition of drug binding to the Saccharomyces cerevisiae ABC exporter Pdr5p by the hydrophobic estradiol-derivative RU49953."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/title"Potent competitive inhibition of drug binding to the Saccharomyces cerevisiae ABC exporter Pdr5p by the hydrophobic estradiol-derivative RU49953."xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/volume"1614"xsd:string
http://purl.uniprot.org/citations/12896805http://purl.uniprot.org/core/volume"1614"xsd:string