ライフサイエンスコーパス: CoA transferase

1 arboxylase, or the frc gene, encoding formyl-CoA transferase.

2 lase or via butyryl-coenzyme A (CoA):acetate CoA-transferase.

3 which is similar to subunit B of glutaconate CoA-transferase.

4 that this mechanism is general among class I CoA-transferases.

5 A, a potent inhibitor of carnitine/palmitoyl-CoA transferase 1 (CPT1), releases CPT1 from inhibitory

6 that the brain-specific carnitine:palmitoyl-CoA transferase-1 (CPT1c) may be a regulated target of m

7 Butyryl-CoA:acetate CoA-transferase activity was detected in all 38 strains

8 essed high levels of succinyl-CoA:3-ketoacid-CoA transferase, an enzyme that forms acetoacetate in th

9 terizations of recombinant, wild type formyl-CoA transferase and a number of site-specific mutants, w

10 a pathway involving succinyl-CoA:3-ketoacid-CoA transferase and acetoacetyl-CoA synthetase to synthe

11 and LC/MS/MS analysis revealed that succinyl-CoA transferase and ATP synthase (F(1) complex, alpha-su

12 he DeoR-family transcription factors, acetyl-CoA transferases and methenyltetrahydrofolate synthetase

13 carboxylase, YgfH is propionyl CoA:succinate CoA transferase, and Sbm is methylmalonyl CoA mutase.

14 The enzymes YfdW, a formyl coenzyme A (CoA) transferase, and YfdU, an oxalyl-CoA decarboxylase,

15 irm that YfdW is a formyl coenzyme A (formyl-CoA) transferase, and YfdW appears to be more stringent

16 catalytic activity of succinyl-CoA:3-oxoacid CoA-transferase, and induces aggregation of mitochondria

17 ndrial acetate sources are acetate:succinate CoA-transferase (ASCT) and an unknown enzymatic activity

18 native TCA cycle, in which acetate:succinate CoA-transferase (ASCT) replaces the enzymatic step typic

19 that overexpress the acetoacetyl-CoA:acetyl-CoA transferase, AtoAD (EC 2.8.3.8), in media supplement

20 found for transcripts from genes in the acyl-coA transferase BAHD family, for which a role in AX feru

21 ly) and by upregulating the serine palmitoyl-CoA transferase catalytic subunit gene lace, the first g

22 Coenzyme A (CoA)-transferases catalyze transthioesterification react

23 a human eNOS promoter chloramphenicol acetyl-CoA transferase chimeric construct in a time-dependent f

24 receptor-alpha (decreased by 51%), 3-oxoacid CoA transferase (decreased by 67%), and acetyl-CoA carbo

25 ployed by all other members of the Class III CoA-transferase family.

26 ent ATP synthesis and is the first Class III CoA-transferase for which a high resolution, three-dimen

27 oop in the active site of formyl-CoA:oxalate CoA transferase (FRC) play an important role in the cata

28 Two hydroxycinnamoyl-CoA transferases (HCT/HQT) have been involved in CGA pro

29 ic acid, an inhibitor of carnitine-palmitoyl-CoA transferase I.

30 ynthetase (3-8-fold) and carnitine palmitoyl-CoA transferase IA (2-4-fold) mRNAs that were dependent

31 Formyl-CoA transferase is a critical enzyme in oxalate-dependen

32 zyme intermediate that is formed when formyl-CoA transferase is incubated with oxalyl-CoA.

33 The catalytic mechanism of formyl-CoA transferase is therefore established and is almost c

34 class I CoA-transferase succinyl-CoA:acetate CoA-transferase is an acetic acid resistance factor (Aar

35 ansporter, atoA, the beta subunit of acetate CoA-transferase likely to be involved in polyhydroxybuty

36 key ketolytic enzyme, succinyl-CoA:3-oxoacid CoA transferase (SCOT; encoded by Oxct1), as well as per

37 the ketolytic enzyme succinyl-CoA:3-oxo-acid CoA-transferase (SCOT), to demonstrate that ketone body

38 h partial sequence as succinyl-CoA:3-oxoacid CoA-transferase (SCOT; EC ).

39 zyme CoA transferase (succinyl-CoA:3-oxoacid CoA transferase, SCOT, encoded by nuclear Oxct1) cannot

40 d myriocin to inhibit mouse serine palmitoyl-CoA transferase (SPT), the key enzyme for sphingolipid b

41 asmic reticulum (ER) enzyme serine palmitoyl-CoA transferase (SPT), the rate-limiting enzyme in sphin

42 The class I CoA-transferase succinyl-CoA:acetate CoA-transferase is

43 ion in the extrahepatic mitochondrial enzyme CoA transferase (succinyl-CoA:3-oxoacid CoA transferase,

44 Mechanistic studies of class I CoA-transferases suggested that acyl-CoA binding energy

45 of the gene encoding succinyl-CoA:3-oxoacid-CoA transferase, the rate-limiting enzyme for myocardial

46 (acyl-CoA oxidase, liver carnitine palmitoyl-CoA transferase, very long chain acyl-CoA synthetase, ve

47 ated protein 78, transketolase, and succinyl-CoA transferase were primarily affected by presence or a

48 ilar to subunit A of glutaconate coenzyme A (CoA) transferase, which is involved in glutamate ferment

49 AarC is succinyl-coenzyme A (CoA):acetate CoA-transferase, which replaces succinyl-CoA synthetase

50 of methylmalonyl CoA mutases (Sbm) and acyl CoA transferases (YgfH) as well as a putative protein ki