-
oxidation have been identified. In case of
fatty acid
oxidation defects, acyl-
carnitines ac****ulate in
mitochondria and are
transferred into the cytosol, and then...
- working. Most cell
types appear to have
transporters to
import carnitine and
export acyl-
carnitines,
which seems to be a
mechanism to
dispose of longer-chain...
-
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. The
product is...
-
Carnitine palmitoyltransferase II deficiency,
sometimes shortened to CPT-II or CPT2, is an
autosomal recessively inherited genetic metabolic disorder...
-
stand for:
Carnitine palmitoyltransferase I (CPT1A, CPT1, CPT1-L, L-CPT1), a
mitochondrial enzyme responsible for the
formation of acyl
carnitines Carboxypeptidase...
-
Carnitine O-palmitoyltransferase 2,
mitochondrial is an
enzyme that in
humans is
encoded by the CPT2 gene.
Carnitine palmitoyltransferase II precursor...
- fatty-acid
metabolism disorders.
Carnitine Transport Defect Carnitine-acylcarnitine
translocase deficiency (CACT)
Carnitine Palmitoyl Transferase I & II (...
-
Carnitine biosynthesis is a
method for the
endogenous production of L-
carnitine, a
molecule that is
essential for
energy metabolism. In
humans and many...
-
Carnitine O-acetyltransferase also
called carnitine acetyltransferase (CRAT, or CAT) (EC 2.3.1.7) is an
enzyme that
encoded by the CRAT gene that catalyzes...
-
carnitine deficiency - SLC22A5 (
carnitine transporter)
Carnitine-acylcarnitine
translocase deficiency -
Carnitine-acylcarnitine
translocase Carnitine...
