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Carnitine palmitoyltransferase I (CPT1) also
known as
carnitine acyltransferase I, CPTI, CAT1, CoA:carnitine acyl
transferase (CCAT), or
palmitoylCoA transferase...
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Carnitine palmitoyltransferase II deficiency,
sometimes shortened to CPT-II or CPT2, is an
autosomal recessively inherited genetic metabolic disorder characterized...
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Carnitine palmitoyltransferase I
deficiency is a rare
metabolic disorder that
prevents the body from
converting certain fats
called long-chain
fatty acids(LCFA)...
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serine parti****te in a
condensation reaction catalyzed by
serine C-
palmitoyltransferase (SPT), in
which 3-ketosphinganine is formed.
These reactions occur...
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Carnitine O-
palmitoyltransferase 2,
mitochondrial is an
enzyme that in
humans is
encoded by the CPT2 gene.
Carnitine palmitoyltransferase II precursor...
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Carnitine O-
palmitoyltransferase (also
called carnitine palmitoyltransferase) is a
mitochondrial transferase enzyme (EC 2.3.1.21)
involved in the metabolism...
- In enzymology, a
serine C-
palmitoyltransferase (EC 2.3.1.50) is an
enzyme that
catalyzes the
chemical reaction: palmitoyl-CoA + L-serine ⇌ {\displaystyle...
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found in the
proteins predicted exosome complex RRP44 and
serine palmitoyltransferase, that are
exclusively shared by
species from
these two
subphyla but...
- co-A is then
exchanged with
carnitine (via the
enzyme carnitine palmitoyltransferase I) to
produce a
fatty acid-carnitine complex. This
complex is then...
-
synthesis begins with
formation of 3-keto-dihydrosphingosine by
serine palmitoyltransferase. The
preferred substrates for this
reaction are palmitoyl-CoA and...
