Phytol-induced pathology in 2-hydroxyacyl-CoA lyase (HACL1) deficient mice. Evidence for a second non-HACL1-related lyase

Author:

Mezzar Serena,De Schryver Evelyn,Asselberghs Stanny,Meyhi Els,Morvay Petruta L.,Baes Myriam,Van Veldhoven Paul P.

Funder

Fonds Wetenschappelijk Onderzoek

KU Leuven

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference85 articles.

1. Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolism;Van Veldhoven;J. Lipid Res.,2010

2. Alpha-oxidation of 3-Methylbranched Fatty Acids: Study of the Involved Enzymes Involved in the Reaction Sequence;Foulon,2001

3. Phytanic acid alpha-oxidation: decarboxylation of 2-hydroxyphytanoyl-CoA to pristanic acid in human liver;Verhoeven;J. Lipid Res.,1997

4. Purification, molecular cloning, and expression of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal thiamine pyrophosphate-dependent enzyme that catalyzes the carbon-carbon bond cleavage during alpha-oxidation of 3-methyl-branched fatty acids;Foulon;Proc. Natl. Acad. Sci. U. S. A.,1999

5. Comparison of the PTS1- and Rab8b-binding properties of Pex5p and Pex5Rp/TRIP8b;Fransen;Biochim. Biophys. Acta,2008

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