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http://www.reactome.org/bio...rdf:typebiopax3:Evidencelld:biopax3
http://www.reactome.org/bio...biopax3:commentPeroxisomal HSD17B4 dimer catalyzes the reaction of 3-hydroxypristanoyl-CoA and NAD+ to form 3-ketoxypristanoyl-CoA and NADH + H+. The enzyme is bifunctional - an aminoterminal domain catalyzes the dehydrogenation of a variety of 3-hydroxyacyl-CoA's, the reaction annotated here, and a carboxyterminal domain catalyzes the hydration of a variety of trans-2,3-dehydroacyl-CoA's (Jiang et al. 1996, 1997). Defects in the enzyme are associated with a severe disorder of peroxisomal fatty acid metabolism in humans (Ferdinandusse et al. 2006).lld:biopax3
http://www.reactome.org/bio...biopax3:xrefhttp://identifiers.org/pubm...lld:biopax3
http://www.reactome.org/bio...biopax3:xrefhttp://identifiers.org/pubm...lld:biopax3
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http://www.reactome.org/bio...biopax3:evidenceCodehttp://www.reactome.org/bio...lld:biopax3
http://www.reactome.org/bio...biopax3:evidencehttp://www.reactome.org/bio...lld:biopax3