| http://purl.uniprot.org/citations/11781327 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/11781327 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/11781327 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Citation |
| http://purl.uniprot.org/citations/11781327 | http://www.w3.org/2000/01/rdf-schema#comment | "The degradation of unsaturated fatty acids by beta-oxidation involves Delta(3),Delta(2)-enoyl-CoA isomerases (enoyl-CoA isomerases) that catalyze 3-cis --> 2-trans and 3-trans --> 2-trans isomerizations of enoyl-CoAs and the 2,5 --> 3,5 isomerization of dienoyl-CoAs. An analysis of rat liver enoyl-CoA isomerases revealed the presence of a monofunctional enoyl-CoA isomerase (ECI) in addition to mitochondrial enoyl-CoA isomerase (MECI) in mitochondria, whereas peroxisomes contain ECI and multifunctional enzyme 1 (MFE1). Thus ECI, which previously had been described as peroxisomal enoyl-CoA isomerase, was found to be present in both peroxisomes and mitochondria. This enzyme seems to be identical with mitochondrial long-chain enoyl-CoA isomerase (Kilponen, J.M., Palosaari, P.M., and Hiltunen, J.K. 1990. Biochem. J. 269, 223-226). All three hepatic enoyl-CoA isomerases have broad chain length specificities but are distinguishable by their preferences for one of the three isomerization reactions. MECI is most active in catalyzing the 3-cis --> 2-trans isomerization; ECI has a preference for the 3-trans --> 2-trans isomerization, and MFE1 is the optimal isomerase for the 2,5 --> 3,5 isomerization. A functional characterization based on substrate specificities and total enoyl-CoA isomerase activities in rat liver leads to the conclusion that the 3-cis --> 2-trans and 2,5 --> 3,5 isomerizations in mitochondria are catalyzed overwhelmingly by MECI, whereas ECI contributes significantly to the 3-trans --> 2-trans isomerization. In peroxisomes, ECI is predicted to be the dominant enzyme for the 3-cis --> 2-trans and 3-trans --> 2-trans isomerizations of long-chain intermediates, whereas MFE1 is the key enzyme in the 2,5 --> 3,5 isomerization."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.org/dc/terms/identifier | "doi:10.1074/jbc.m112228200"xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.org/dc/terms/identifier | "doi:10.1074/jbc.m112228200"xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Schulz H."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Schulz H."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Yu W."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Yu W."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Zhang D."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Zhang D."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Geisbrecht B.V."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Geisbrecht B.V."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Gould S.J."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Gould S.J."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Sprecher H."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/author | "Sprecher H."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/date | "2002"xsd:gYear |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/date | "2002"xsd:gYear |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/name | "J. Biol. Chem."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/name | "J. Biol. Chem."xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/pages | "9127-9132"xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/pages | "9127-9132"xsd:string |
| http://purl.uniprot.org/citations/11781327 | http://purl.uniprot.org/core/title | "Functional characterization of delta3,delta2-enoyl-CoA isomerases from rat liver."xsd:string |