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http://purl.uniprot.org/citations/15689149http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15689149http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15689149http://www.w3.org/2000/01/rdf-schema#comment"Human cytidine deaminase (CDA) is an enzyme prominent for its role in catalyzing metabolic processing of nucleoside-type anticancer and antiviral agents. It is thus a promising target for the development of small molecule therapeutic adjuvants. We report the first crystal structure of human CDA as a complex with a tight-binding inhibitor, diazepinone riboside 1. The structure reveals that inhibitor 1 is able to establish a canonical pi/pi-interaction with a key active site residue, Phe 137."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.org/dc/terms/identifier"doi:10.1021/jm0496279"xsd:string
http://purl.uniprot.org/citations/15689149http://purl.org/dc/terms/identifier"doi:10.1021/jm0496279"xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/author"Chung S.J."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/author"Chung S.J."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/author"Verdine G.L."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/author"Verdine G.L."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/author"Fromme J.C."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/author"Fromme J.C."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/name"J. Med. Chem."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/name"J. Med. Chem."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/pages"658-660"xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/pages"658-660"xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/title"Structure of human cytidine deaminase bound to a potent inhibitor."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/title"Structure of human cytidine deaminase bound to a potent inhibitor."xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/volume"48"xsd:string
http://purl.uniprot.org/citations/15689149http://purl.uniprot.org/core/volume"48"xsd:string
http://purl.uniprot.org/citations/15689149http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/15689149
http://purl.uniprot.org/citations/15689149http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/15689149
http://purl.uniprot.org/citations/15689149http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/15689149
http://purl.uniprot.org/citations/15689149http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/15689149