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1 M (S-adenosylmethionine) synthetases, and an acetyl-CoA synthetase.
2 tudy expand the ASKHA superfamily to include acetyl-CoA synthetase.
3 sphate needed for the synthesis of ATP by an acetyl-CoA synthetase.
4 istone deacetylase activity and up-regulated acetyl-coA synthetases.
5 of acetyl-CoA by the level of acetylation of acetyl-CoA synthetases.
6 -CoA by modulating the enzymatic activity of acetyl-CoA Synthetase 1 (AceCS1).
7                            The expression of acetyl-CoA synthetase 1, another cytosolic enzyme for pr
8  values with the native acetylated substrate acetyl-CoA synthetase-1; measurement of Sirt1, Sirt2, an
9                 Eukaryotic acetate-dependent acetyl CoA synthetase 2 (Acss2) is predominantly cytosol
10 at these processes require acetate-dependent acetyl CoA synthetase 2 (ACSS2).
11                         We report that human acetyl-CoA synthetase 2 (AceCS2) is a mitochondrial matr
12  production by regulating phosphorylation of acetyl-CoA synthetase 2 (ACSS2) by cyclin-dependent kina
13 genomics study revealed that the activity of acetyl-CoA synthetase 2 (ACSS2) contributes to cancer ce
14                                              Acetyl-CoA synthetase 2 (ACSS2) converts acetate to acet
15       Here we show that the metabolic enzyme acetyl-CoA synthetase 2 (ACSS2) directly regulates histo
16                               In particular, acetyl-CoA synthetase 2 (ACSS2) mediates histone acetyla
17 AMP-activated protein kinase (AMPK)-mediated acetyl-CoA synthetase 2 (ACSS2) phosphorylation at S659,
18 ate to citrate metabolism by down-regulating acetyl-CoA synthetase 2 (ACSS2) while maintaining ATP-ci
19  is produced from acetate by chromatin-bound acetyl-CoA synthetase 2 (ACSS2)(2).
20 dies have shown that cancer cells upregulate acetyl-CoA synthetase 2 (ACSS2), an enzyme that converts
21 ng acetyl-CoA synthesis from acetate through acetyl-CoA synthetase 2 (ACSS2).
22 part, from local acetate by metabolic enzyme acetyl-CoA synthetase 2 (ACSS2).
23 ction of cytosolic acetyl-CoA is mediated by acetyl-CoA synthetase 2 (ACSS2).
24 ining acetyl lysine of its natural substrate acetyl-CoA synthetase 2, a reaction intermediate structu
25                             Knockdown of the acetyl-coA synthetases abrogated the effect of ethanol o
26 pantothenamide MMV693183 as a first-in-class acetyl-CoA synthetase (AcAS) inhibitor to enter preclini
27                We demonstrate that mammalian Acetyl-CoA synthetases (AceCSs) are regulated by reversi
28 yltransferase protein and is responsible for acetyl-CoA synthetase acetylation.
29                            Acetate-dependent acetyl CoA synthetases (ACS) are de novo sources of acet
30 resent here mutations to Salmonella enterica acetyl-CoA synthetase (Acs) and test the ability of the
31 enzyme A (acetyl-CoA) by means of the enzyme acetyl-CoA synthetase (Acs) and utilize it to generate e
32 obB is a bacterial sirtuin that deacetylates acetyl-CoA synthetase (Acs) at an active site lysine to
33           In this study, we investigated the acetyl-CoA synthetase (ACS) enzyme from Leishmania infan
34 R2 function was required for activity of the acetyl-CoA synthetase (Acs) enzyme.
35                                              Acetyl-CoA synthetase (Acs) generates acetyl-coenzyme A
36 inctly localized acetate-activating enzymes, ACETYL-COA SYNTHETASE (ACS) in plastids and ACETATE NON-
37                             The gene encodes acetyl-CoA synthetase (ACS), the cytosolic enzyme that a
38                                              Acetyl-CoA synthetases (Acs) have emerged as drug target
39 own to contain an unusual acetyl coenzyme A (acetyl-CoA) synthetase (ACS) which catalyzes the formati
40                                  AMP-forming acetyl-CoA synthetase [ACS; acetate:CoA ligase (AMP-form
41                                        Yeast acetyl-CoA synthetases (Acs1p and 2p) are exceptional, a
42 ressing the expression of acetyl coenzyme A (acetyl-CoA) synthetase (Acss), leading to decreased acet
43                                              Acetyl-CoA synthetases (ACSS1, ACSS2) are involved in th
44 rial [ATP-citrate lyase (ACLY)]-, cytosolic [acetyl-CoA synthetase (ACSS2)]-, and peroxisomal [peroxi
45 response to acetyl-CoA and the regulation of acetyl-CoA synthetase activity by the acetylation level.
46 acetylation of AceCS2 by SIRT3 activates the acetyl-CoA synthetase activity of AceCS2.
47 ular acetate levels resulting from decreased acetyl-CoA synthetase activity.
48                      The gene coding for the acetyl-CoA synthetase (ADP-forming) from the amitochondr
49                  The presence of homologs of acetyl-CoA synthetase (ADP-forming) in such human pathog
50       This gene codes for a 726 residue long acetyl-CoA synthetase (ADP-forming).
51 th of a strain of S. enterica devoid of Acs (acetyl-CoA synthetase; AMP-forming) activity on 10 mm ac
52 tylates SlAacS more efficiently than it does acetyl-CoA synthetase, an enzyme known to be under acety
53 ional and/or posttranslational regulation of acetyl-CoA synthetase and ADP-Glc pyrophosphorylase, and
54 abidopsis seeds, we isolated cDNA clones for acetyl-CoA synthetase and for the ptE1alpha- and ptE1bet
55 rophosphate generated by reactions involving acetyl-CoA synthetase and luciferase can be readily dete
56  but two enzymes are thought to be involved: acetyl-CoA synthetase and plastidic pyruvate dehydrogena
57 s regulation of acetyl-CoA by acetylation of acetyl-CoA synthetase and raises the possibility that pr
58 tion, control of p53 activity, regulation of acetyl-CoA synthetase, and aging.
59                                 Knockdown of acetyl-coA synthetases by short hairpin RNA (shRNA) was
60                            We also show that acetyl-CoA synthetase can be a significant contributor t
61 ve determined the X-ray crystal structure of acetyl-CoA synthetase complexed with adenosine-5'-propyl
62           In contrast, the level of mRNA for acetyl-CoA synthetase does not correlate in time and spa
63 ighest level of accumulation of the mRNA for acetyl-CoA synthetase during silique development is with
64  inhibitors (lithium, allicin and sodium) of acetyl CoA synthetase (EC 6.2.1.1 acetate: CoA ligase),
65 tients and was correlated with expression of acetyl-CoA synthetase enzyme 2, ACSS2.
66  and further develop a model to simulate the acetyl-CoA synthetase enzyme reaction network using the
67       Here, we show that the nucleocytosolic acetyl-CoA synthetase enzyme, ACSS2, supplies a key sour
68 cell eukaryotes relies on acetyl coenzyme A (acetyl-CoA) synthetase enzymes that use acetate to produ
69 diauxic shift, along with expression of both acetyl-CoA synthetase genes ACS1 and ACS2 We conclude th
70 ess elevated levels of ATP citrate lyase and acetyl-CoA synthetase genes, both of which are involved
71 ology (CSH) module, flanked by four flexible acetyl-CoA synthetase homology (ASH) domains; CoA is bou
72    Mxr1p is a key regulator of ACS1 encoding acetyl-CoA synthetase in cells cultured in YPA.
73 ypnozoites was validated using MMV019721, an acetyl-CoA synthetase inhibitor that affects histone ace
74                 The central metabolic enzyme acetyl-CoA synthetase is regulated in both bacteria and
75 nthesis of acetyl-coenzyme A (acetyl-CoA) by acetyl-CoA synthetase is used here as a case study for t
76 of acs, the gene encoding acetyl coenzyme A (acetyl-CoA) synthetase, leading to uptake of the excrete
77 c activity of key metabolic enzymes, such as acetyl-CoA synthetase, long-chain acyl-CoA dehydrogenase
78            They also suggest that the enzyme acetyl CoA synthetase mediates extracellular acetate upt
79        Here, genes encoding malic enzyme and acetyl-CoA synthetase (nucleoside diphosphate forming) w
80 yl-CoA was mainly produced from acetate (via acetyl-CoA synthetase) or citrate (via ATP citrate lyase
81                              The Arabidopsis acetyl-CoA synthetase preprotein has a calculated mass o
82 esulting structural features in AMP- and ADP-acetyl-CoA synthetase proteins in this study expand the
83 To our knowledge, this is the first reported acetyl-CoA synthetase sequence from a plant source.
84    N- and C-terminal parts of the G. lamblia acetyl-CoA synthetase sequence were found to be homologo
85                                              Acetyl-CoA synthetase short-chain family member 1 (ACSS1
86 CLY) from mitochondria-derived citrate or by acetyl-CoA synthetase short-chain family member 2 (ACSS2
87                         Here, we report that acetyl-CoA synthetase short-chain family member 2 (ACSS2
88                         We further show that acetyl-CoA synthetase short-chain family member 2 (ACSS2
89  more closely related to the Giardia lamblia acetyl-CoA synthetase than to those of archaea.
90                              The activity of acetyl-CoA synthetase, the first enzymatic step in aceta
91 embers of this enzyme family (exemplified by acetyl-CoA synthetase) use a large domain rotation to ca
92 coding these enzymes, as well as AMP-forming acetyl-CoA synthetase, were expressed at increased level
93                           The E. histolytica acetyl-CoA synthetase, which converts acetyl-CoA to acet
94 of ethanol and acetate on acetyl-coenzyme A (acetyl-coA) synthetases, which convert acetate to acetyl
95 tion in bacteria involves the acetylation of acetyl-CoA synthetase, whose activity must be tightly re