http://purl.uniprot.org/citations/16891113 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/16891113 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/16891113 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Citation |
http://purl.uniprot.org/citations/16891113 | http://www.w3.org/2000/01/rdf-schema#comment | "In a steroid degradation gene cluster of Comamonas testosteroni TA441 consisting of ORF18, 17 and tesIHA2A1DEFG, ORF18 was implicated in encoding a CoA-transferase by database searches, but the matching substrate was not clear. In this study, ORF18 was shown to be necessary for conversion of 9,17-dioxo-1,2,3,4,10,19-hexanorandrostan-5-oic acid, a product of hydrolysis of 4,5-9,10-diseco-3-hydroxy-5,9,17-trioxoandrosta-1(10),2-dien-4-oic acid in steroid degradation by TA441. The ORF18-disrupted mutant accumulates 7-hydroxy-9,17-dioxo-1,2,3,4,10,19-hexanorandrostan-5-oic acid and 7,12-dihydroxy-9,17-dioxo-1,2,3,4,10,19-hexanorandrostan-5-oic acid when incubated with chenodeoxycholic acid and cholic acid, respectively."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.org/dc/terms/identifier | "doi:10.1016/j.jsbmb.2006.06.006"xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.org/dc/terms/identifier | "doi:10.1016/j.jsbmb.2006.06.006"xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Hayashi T."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Hayashi T."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Horinouchi M."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Horinouchi M."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Koshino H."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Koshino H."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Kudo T."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/author | "Kudo T."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/date | "2006"xsd:gYear |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/date | "2006"xsd:gYear |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/name | "J. Steroid Biochem. Mol. Biol."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/name | "J. Steroid Biochem. Mol. Biol."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/pages | "78-84"xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/pages | "78-84"xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/title | "ORF18-disrupted mutant of Comamonas testosteroni TA441 accumulates significant amounts of 9,17-dioxo-1,2,3,4,10,19-hexanorandrostan-5-oic acid and its derivatives after incubation with steroids."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/title | "ORF18-disrupted mutant of Comamonas testosteroni TA441 accumulates significant amounts of 9,17-dioxo-1,2,3,4,10,19-hexanorandrostan-5-oic acid and its derivatives after incubation with steroids."xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/volume | "101"xsd:string |
http://purl.uniprot.org/citations/16891113 | http://purl.uniprot.org/core/volume | "101"xsd:string |
http://purl.uniprot.org/citations/16891113 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/16891113 |