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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.
8 values with the native acetylated substrate acetyl-CoA synthetase-1; measurement of Sirt1, Sirt2, an
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
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
20 dies have shown that cancer cells upregulate acetyl-CoA synthetase 2 (ACSS2), an enzyme that converts
24 ining acetyl lysine of its natural substrate acetyl-CoA synthetase 2, a reaction intermediate structu
26 pantothenamide MMV693183 as a first-in-class acetyl-CoA synthetase (AcAS) inhibitor to enter preclini
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
36 inctly localized acetate-activating enzymes, ACETYL-COA SYNTHETASE (ACS) in plastids and ACETATE NON-
39 own to contain an unusual acetyl coenzyme A (acetyl-CoA) synthetase (ACS) which catalyzes the formati
42 ressing the expression of acetyl coenzyme A (acetyl-CoA) synthetase (Acss), leading to decreased acet
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.
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
61 ve determined the X-ray crystal structure of acetyl-CoA synthetase complexed with adenosine-5'-propyl
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),
66 and further develop a model to simulate the acetyl-CoA synthetase enzyme reaction network using the
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
73 ypnozoites was validated using MMV019721, an acetyl-CoA synthetase inhibitor that affects histone ace
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
80 yl-CoA was mainly produced from acetate (via acetyl-CoA synthetase) or citrate (via ATP citrate lyase
82 esulting structural features in AMP- and ADP-acetyl-CoA synthetase proteins in this study expand the
84 N- and C-terminal parts of the G. lamblia acetyl-CoA synthetase sequence were found to be homologo
86 CLY) from mitochondria-derived citrate or by acetyl-CoA synthetase short-chain family member 2 (ACSS2
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
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