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1 tudy expand the ASKHA superfamily to include acetyl-CoA synthetase.
2 M (S-adenosylmethionine) synthetases, and an acetyl-CoA synthetase.
3 istone deacetylase activity and up-regulated acetyl-coA synthetases.
4 of acetyl-CoA by the level of acetylation of acetyl-CoA synthetases.
7 values with the native acetylated substrate acetyl-CoA synthetase-1; measurement of Sirt1, Sirt2, an
10 genomics study revealed that the activity of acetyl-CoA synthetase 2 (ACSS2) contributes to cancer ce
12 AMP-activated protein kinase (AMPK)-mediated acetyl-CoA synthetase 2 (ACSS2) phosphorylation at S659,
13 ining acetyl lysine of its natural substrate acetyl-CoA synthetase 2, a reaction intermediate structu
17 resent here mutations to Salmonella enterica acetyl-CoA synthetase (Acs) and test the ability of the
18 enzyme A (acetyl-CoA) by means of the enzyme acetyl-CoA synthetase (Acs) and utilize it to generate e
19 obB is a bacterial sirtuin that deacetylates acetyl-CoA synthetase (Acs) at an active site lysine to
22 own to contain an unusual acetyl coenzyme A (acetyl-CoA) synthetase (ACS) which catalyzes the formati
25 ressing the expression of acetyl coenzyme A (acetyl-CoA) synthetase (Acss), leading to decreased acet
27 response to acetyl-CoA and the regulation of acetyl-CoA synthetase activity by the acetylation level.
33 th of a strain of S. enterica devoid of Acs (acetyl-CoA synthetase; AMP-forming) activity on 10 mm ac
34 tylates SlAacS more efficiently than it does acetyl-CoA synthetase, an enzyme known to be under acety
35 abidopsis seeds, we isolated cDNA clones for acetyl-CoA synthetase and for the ptE1alpha- and ptE1bet
36 rophosphate generated by reactions involving acetyl-CoA synthetase and luciferase can be readily dete
37 but two enzymes are thought to be involved: acetyl-CoA synthetase and plastidic pyruvate dehydrogena
38 s regulation of acetyl-CoA by acetylation of acetyl-CoA synthetase and raises the possibility that pr
42 ve determined the X-ray crystal structure of acetyl-CoA synthetase complexed with adenosine-5'-propyl
44 ighest level of accumulation of the mRNA for acetyl-CoA synthetase during silique development is with
45 inhibitors (lithium, allicin and sodium) of acetyl CoA synthetase (EC 6.2.1.1 acetate: CoA ligase),
47 and further develop a model to simulate the acetyl-CoA synthetase enzyme reaction network using the
49 cell eukaryotes relies on acetyl coenzyme A (acetyl-CoA) synthetase enzymes that use acetate to produ
50 diauxic shift, along with expression of both acetyl-CoA synthetase genes ACS1 and ACS2 We conclude th
51 ess elevated levels of ATP citrate lyase and acetyl-CoA synthetase genes, both of which are involved
54 nthesis of acetyl-coenzyme A (acetyl-CoA) by acetyl-CoA synthetase is used here as a case study for t
55 of acs, the gene encoding acetyl coenzyme A (acetyl-CoA) synthetase, leading to uptake of the excrete
56 c activity of key metabolic enzymes, such as acetyl-CoA synthetase, long-chain acyl-CoA dehydrogenase
59 yl-CoA was mainly produced from acetate (via acetyl-CoA synthetase) or citrate (via ATP citrate lyase
61 esulting structural features in AMP- and ADP-acetyl-CoA synthetase proteins in this study expand the
63 N- and C-terminal parts of the G. lamblia acetyl-CoA synthetase sequence were found to be homologo
64 CLY) from mitochondria-derived citrate or by acetyl-CoA synthetase short-chain family member 2 (ACSS2
67 embers of this enzyme family (exemplified by acetyl-CoA synthetase) use a large domain rotation to ca
68 coding these enzymes, as well as AMP-forming acetyl-CoA synthetase, were expressed at increased level
70 of ethanol and acetate on acetyl-coenzyme A (acetyl-coA) synthetases, which convert acetate to acetyl
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