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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.
5 -CoA by modulating the enzymatic activity of acetyl-CoA Synthetase 1 (AceCS1).
6                            The expression of acetyl-CoA synthetase 1, another cytosolic enzyme for pr
7  values with the native acetylated substrate acetyl-CoA synthetase-1; measurement of Sirt1, Sirt2, an
8 at these processes require acetate-dependent acetyl CoA synthetase 2 (ACSS2).
9                         We report that human acetyl-CoA synthetase 2 (AceCS2) is a mitochondrial matr
10 genomics study revealed that the activity of acetyl-CoA synthetase 2 (ACSS2) contributes to cancer ce
11       Here we show that the metabolic enzyme acetyl-CoA synthetase 2 (ACSS2) directly regulates histo
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
14                             Knockdown of the acetyl-coA synthetases abrogated the effect of ethanol o
15                We demonstrate that mammalian Acetyl-CoA synthetases (AceCSs) are regulated by reversi
16 yltransferase protein and is responsible for acetyl-CoA synthetase acetylation.
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
20 R2 function was required for activity of the acetyl-CoA synthetase (Acs) enzyme.
21                             The gene encodes acetyl-CoA synthetase (ACS), the cytosolic enzyme that a
22 own to contain an unusual acetyl coenzyme A (acetyl-CoA) synthetase (ACS) which catalyzes the formati
23                                  AMP-forming acetyl-CoA synthetase [ACS; acetate:CoA ligase (AMP-form
24                                        Yeast acetyl-CoA synthetases (Acs1p and 2p) are exceptional, a
25 ressing the expression of acetyl coenzyme A (acetyl-CoA) synthetase (Acss), leading to decreased acet
26                                              Acetyl-CoA synthetases (ACSS1, ACSS2) are involved in th
27 response to acetyl-CoA and the regulation of acetyl-CoA synthetase activity by the acetylation level.
28 acetylation of AceCS2 by SIRT3 activates the acetyl-CoA synthetase activity of AceCS2.
29 ular acetate levels resulting from decreased acetyl-CoA synthetase activity.
30                      The gene coding for the acetyl-CoA synthetase (ADP-forming) from the amitochondr
31                  The presence of homologs of acetyl-CoA synthetase (ADP-forming) in such human pathog
32       This gene codes for a 726 residue long acetyl-CoA synthetase (ADP-forming).
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
39 tion, control of p53 activity, regulation of acetyl-CoA synthetase, and aging.
40                                 Knockdown of acetyl-coA synthetases by short hairpin RNA (shRNA) was
41                            We also show that acetyl-CoA synthetase can be a significant contributor t
42 ve determined the X-ray crystal structure of acetyl-CoA synthetase complexed with adenosine-5'-propyl
43           In contrast, the level of mRNA for acetyl-CoA synthetase does not correlate in time and spa
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),
46 tients and was correlated with expression of acetyl-CoA synthetase enzyme 2, ACSS2.
47  and further develop a model to simulate the acetyl-CoA synthetase enzyme reaction network using the
48       Here, we show that the nucleocytosolic acetyl-CoA synthetase enzyme, ACSS2, supplies a key sour
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
52    Mxr1p is a key regulator of ACS1 encoding acetyl-CoA synthetase in cells cultured in YPA.
53                 The central metabolic enzyme acetyl-CoA synthetase is regulated in both bacteria and
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
57            They also suggest that the enzyme acetyl CoA synthetase mediates extracellular acetate upt
58        Here, genes encoding malic enzyme and acetyl-CoA synthetase (nucleoside diphosphate forming) w
59 yl-CoA was mainly produced from acetate (via acetyl-CoA synthetase) or citrate (via ATP citrate lyase
60                              The Arabidopsis acetyl-CoA synthetase preprotein has a calculated mass o
61 esulting structural features in AMP- and ADP-acetyl-CoA synthetase proteins in this study expand the
62 To our knowledge, this is the first reported acetyl-CoA synthetase sequence from a plant source.
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
65  more closely related to the Giardia lamblia acetyl-CoA synthetase than to those of archaea.
66                              The activity of acetyl-CoA synthetase, the first enzymatic step in aceta
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
69                           The E. histolytica acetyl-CoA synthetase, which converts acetyl-CoA to acet
70 of ethanol and acetate on acetyl-coenzyme A (acetyl-coA) synthetases, which convert acetate to acetyl

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