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  2. Carnitine palmitoyltransferase I - Wikipedia

    en.wikipedia.org/wiki/Carnitine_palmitoyl...

    Carnitine palmitoyltransferase I (CPT1) also known as carnitine acyltransferase I, CPTI, CAT1, CoA:carnitine acyl transferase (CCAT), or palmitoylCoA transferase I, is a mitochondrial enzyme responsible for the formation of acyl carnitines by catalyzing the transfer of the acyl group of a long-chain fatty acyl-CoA from coenzyme A to l-carnitine.

  3. Carnitine palmitoyltransferase I deficiency - Wikipedia

    en.wikipedia.org/wiki/Carnitine_palmitoyl...

    Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy. People with this disorder have a faulty enzyme, carnitine palmitoyltransferase I , that prevents these long-chain fatty acids from being transported into the mitochondria to be broken down.

  4. Fatty-acid metabolism disorder - Wikipedia

    en.wikipedia.org/wiki/Fatty-acid_metabolism_disorder

    Carnitor - an L-carnitine supplement that has shown to improve the body's metabolism in individuals with low L-carnitine levels. It is only useful for Specific fatty-acid metabolism disease. It is only useful for Specific fatty-acid metabolism disease.

  5. Carnitine - Wikipedia

    en.wikipedia.org/wiki/Carnitine

    Carnitine is a quaternary ammonium compound involved in metabolism in most mammals, plants, ... (also called carnitine palmitoyltransferase 1, CPT1). ...

  6. 2,4 Dienoyl-CoA reductase deficiency - Wikipedia

    en.wikipedia.org/wiki/2,4_Dienoyl-CoA_reductase...

    Laboratory investigations revealed elevated lysine, low levels of carnitine and an abnormal acylcarnitine profile in urine and blood. The abnormal acylcarnitine species was eventually identified as 2-trans,4-cis-decadienoylcarnitine, an intermediate of linoleic acid metabolism. [1]

  7. Carnitine palmitoyltransferase II - Wikipedia

    en.wikipedia.org/wiki/Carnitine_palmitoyl...

    12896 Ensembl ENSG00000157184 ENSMUSG00000028607 UniProt P23786 P52825 RefSeq (mRNA) NM_000098 NM_001330589 NM_009949 RefSeq (protein) NP_000089 NP_001317518 NP_034079 Location (UCSC) Chr 1: 53.2 – 53.21 Mb Chr 4: 107.76 – 107.78 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Carnitine O-palmitoyltransferase 2, mitochondrial is an enzyme that in humans is encoded by the CPT2 ...

  8. Carnitine palmitoyltransferase II deficiency - Wikipedia

    en.wikipedia.org/wiki/Carnitine_palmitoyl...

    Carnitine palmitoyltransferase II (CPT II) is a peripheral inner mitochondrial membrane protein ubiquitously found as a monomeric protein in all tissues that oxidize fatty acids. [12] It catalyzes the transesterification of palmitoylcarnitine back into palmitoyl-CoA which is now an activated substrate for β-oxidation inside the matrix.

  9. Carnitine-acylcarnitine translocase deficiency - Wikipedia

    en.wikipedia.org/wiki/Carnitine-acylcarnitine...

    Carnitine-acylcarnitine translocase deficiency has an autosomal recessive pattern of inheritance. Carnitine-acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long-chain fatty acids into energy, particularly during periods without food. [ 1 ]

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