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1 arboxylase, or the frc gene, encoding formyl-CoA transferase.
2 nucleotide polymorphisms regulating an Acyl-CoA transferase.
3 lase or via butyryl-coenzyme A (CoA):acetate CoA-transferase.
4 which is similar to subunit B of glutaconate CoA-transferase.
5 that this mechanism is general among class I CoA-transferases.
6 A, a potent inhibitor of carnitine/palmitoyl-CoA transferase 1 (CPT1), releases CPT1 from inhibitory
7 that the brain-specific carnitine:palmitoyl-CoA transferase-1 (CPT1c) may be a regulated target of m
8 ne encoding butyryl-coenzyme A (CoA):acetate-CoA-transferase, a major enzyme in butyrate metabolism (
9 v2503c and Rv3272 possess itaconate:succinyl-CoA transferase activity, and Rv2499c and Rv3389c posses
11 essed high levels of succinyl-CoA:3-ketoacid-CoA transferase, an enzyme that forms acetoacetate in th
12 terizations of recombinant, wild type formyl-CoA transferase and a number of site-specific mutants, w
13 a pathway involving succinyl-CoA:3-ketoacid-CoA transferase and acetoacetyl-CoA synthetase to synthe
14 and LC/MS/MS analysis revealed that succinyl-CoA transferase and ATP synthase (F(1) complex, alpha-su
15 uinone Oxidoreductase 1, Carnitine Palmitoyl-CoA Transferase and mitochondrial respiratory complexes
16 he DeoR-family transcription factors, acetyl-CoA transferases and methenyltetrahydrofolate synthetase
17 carboxylase, YgfH is propionyl CoA:succinate CoA transferase, and Sbm is methylmalonyl CoA mutase.
19 irm that YfdW is a formyl coenzyme A (formyl-CoA) transferase, and YfdW appears to be more stringent
20 catalytic activity of succinyl-CoA:3-oxoacid CoA-transferase, and induces aggregation of mitochondria
21 886 (kstA) encodes beta-ketoadipate:succinyl-CoA transferase; and NRRL3_01526 (kctA) encodes beta-ket
22 ndrial acetate sources are acetate:succinate CoA-transferase (ASCT) and an unknown enzymatic activity
23 native TCA cycle, in which acetate:succinate CoA-transferase (ASCT) replaces the enzymatic step typic
24 that overexpress the acetoacetyl-CoA:acetyl-CoA transferase, AtoAD (EC 2.8.3.8), in media supplement
25 found for transcripts from genes in the acyl-coA transferase BAHD family, for which a role in AX feru
26 rial enzyme butyryl-coenzyme A (CoA):acetate CoA-transferase (BCoAT) in fecal nucleic acid extracts.
27 ly) and by upregulating the serine palmitoyl-CoA transferase catalytic subunit gene lace, the first g
29 a human eNOS promoter chloramphenicol acetyl-CoA transferase chimeric construct in a time-dependent f
30 g apo-citrate lyase phosphoribosyl-dephospho-CoA transferase citX, an Escherichia coli enzyme lacking
31 receptor-alpha (decreased by 51%), 3-oxoacid CoA transferase (decreased by 67%), and acetyl-CoA carbo
34 ent ATP synthesis and is the first Class III CoA-transferase for which a high resolution, three-dimen
35 oop in the active site of formyl-CoA:oxalate CoA transferase (FRC) play an important role in the cata
38 sal gene expression of SPT (serine palmitoyl-CoA transferase) (i.e., the rate-limiting enzyme in de n
39 ynthetase (3-8-fold) and carnitine palmitoyl-CoA transferase IA (2-4-fold) mRNAs that were dependent
43 class I CoA-transferase succinyl-CoA:acetate CoA-transferase is an acetic acid resistance factor (Aar
44 f ceramide biosynthesis via serine palmitoyl-CoA transferase (L-cycloserine, myriocin or ARN14494) we
45 ansporter, atoA, the beta subunit of acetate CoA-transferase likely to be involved in polyhydroxybuty
46 increase activity of succinyl-CoA:3-ketoacid-CoA transferase (SCOT) activity, the rate-limiting enzym
47 ated skeletal muscle succinyl CoA:3-ketoacid CoA transferase (SCOT) activity, the rate-limiting enzym
48 reased flux through succinyl-CoA-3-oxaloacid CoA transferase (SCOT), resulting in greater contractile
49 key ketolytic enzyme, succinyl-CoA:3-oxoacid CoA transferase (SCOT; encoded by Oxct1), as well as per
50 the ketolytic enzyme succinyl-CoA:3-oxo-acid CoA-transferase (SCOT), to demonstrate that ketone body
52 zyme CoA transferase (succinyl-CoA:3-oxoacid CoA transferase, SCOT, encoded by nuclear Oxct1) cannot
53 d myriocin to inhibit mouse serine palmitoyl-CoA transferase (SPT), the key enzyme for sphingolipid b
54 asmic reticulum (ER) enzyme serine palmitoyl-CoA transferase (SPT), the rate-limiting enzyme in sphin
56 ion in the extrahepatic mitochondrial enzyme CoA transferase (succinyl-CoA:3-oxoacid CoA transferase,
57 ivation by the enzyme succinyl-CoA:glutarate-CoA transferase (SUGCT) and become substrate for glutary
59 of the gene encoding succinyl-CoA:3-oxoacid-CoA transferase, the rate-limiting enzyme for myocardial
60 (acyl-CoA oxidase, liver carnitine palmitoyl-CoA transferase, very long chain acyl-CoA synthetase, ve
61 ated protein 78, transketolase, and succinyl-CoA transferase were primarily affected by presence or a
62 ilar to subunit A of glutaconate coenzyme A (CoA) transferase, which is involved in glutamate ferment
63 AarC is succinyl-coenzyme A (CoA):acetate CoA-transferase, which replaces succinyl-CoA synthetase
64 of methylmalonyl CoA mutases (Sbm) and acyl CoA transferases (YgfH) as well as a putative protein ki