Molecular characterization of the human peroxisomal branchedchain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome

Peroxisomes in human liver contain two distinct acyl-CoA oxidases with different substrate specificities: (i) palmitoyl-CoA oxidase, oxidizing very long straight-chain fatty acids and eicosanoids, and (ii) a branched-chain acyl-CoA oxidase (hBRCACox), involved in the degradation of long branched fat...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Baumgart, Eveline, Vanhooren, Johannes C. T., Fransen, Mark, Marynen, Peter, Puype, Magda, Vandekerckhove, Joël, Leunissen, Jack A. M., Fahimi, H. Dariush, Mannaerts, Guy P., Van Veldhoven, Paul P.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1996
Assuntos:	Biological Sciences
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC19413/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8943006/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.93.24.13748
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