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1 ly unidentified acetyl-ADP-ribose product (1-O-acetyl-ADP ribose).
2  the ribose of NAD(+) or of the coproduct 2'-O-acetyl-ADP ribose.
3  requires Sir2, Sir3, Sir4, nucleosomes, and O-acetyl-ADP-ribose.
4 to deacetylated lysine, nicotinamide, and 2'-O-acetyl-ADP-ribose.
5 duction of deacetylated peptide and 1'-SH-2'-O-acetyl-ADP-ribose.
6 n and via formation of the novel compound 2'-O-acetyl-ADP-ribose.
7 ducing nicotinamide and the novel metabolite O-acetyl-ADP-ribose.
8 ellular enzymes that can efficiently utilize O-acetyl-ADP-ribose.
9 complex from telomeres was shown to generate O-acetyl-ADP-ribose.
10 enzymatic and structural characterization of O-acetyl-ADP-ribose.
11  of deacetylated lysine, nicotinamide, and 1-O-acetyl-ADP-ribose.
12 and beta-NAD(+) cleavage to the formation of O-acetyl-ADP-ribose, a newly described metabolite.
13  substrate are coupled with the formation of O-acetyl-ADP-ribose, a novel metabolite.
14 ed peptide and the 2' and 3' regioisomers of O-acetyl ADP ribose (AADPR), formed through an alpha-1'-
15 ydrolysis and the synthesis of a metabolite, O-acetyl-ADP-ribose (AAR), but the functional significan
16  techniques, and NMR structural analyses, 2'-O-acetyl-ADP-ribose and 3'-O-acetyl-ADP-ribose were foun
17 acetylation reaction generates two products: O-acetyl-ADP-ribose and nicotinamide, a precursor of nic
18 ansferred to the ADP-ribose of NAD, yielding O-acetyl-ADP-ribose and nicotinamide.
19 Possible mechanisms for the generation of 2'-O-acetyl-ADP-ribose are discussed.
20 der single-turnover conditions identified 2'-O-acetyl-ADP-ribose as the enzymatic product, whereas 3'
21 spreading in the absence of production of 2'-O-acetyl-ADP ribose by sir2p and Sir2p's enzymatic funct
22 y discovered metabolite, we demonstrate that O-acetyl-ADP-ribose causes a delay/block in oocyte matur
23  release into bulk solvent, where 2'- and 3'-O-acetyl-ADP-ribose exist in equilibrium (48:52).
24                                         This O-acetyl-ADP-ribose hydrolase belongs to a family of thr
25                                  The rate of O-acetyl-ADP-ribose hydrolysis by recombinant ARH3 was 2
26 he conclusion that the Sir2 reaction product O-acetyl-ADP-ribose is degraded by ARH3.
27        We demonstrate that the production of O-acetyl-ADP-ribose is evolutionarily conserved among Si
28 cule, a specific hydrolase would cleave the (O-acetyl)-(ADP-ribose) linkage.
29 /Dot1p competition, and the possible role of O-Acetyl ADP ribose (O-AADPR) in Sir3p/chromatin binding
30 rf130 catalyzes the efficient deacylation of O-acetyl-ADP-ribose, O-propionyl-ADP-ribose, and O-butyr
31 ize NAD(+) to deacetylate proteins, yielding O-acetyl-ADP-ribose (OAADPr) as a reaction product.
32 at these proteins produce a novel metabolite O-acetyl-ADP-ribose (OAADPr) during deacetylation.
33                                              O-Acetyl-ADP-ribose (OAADPR) is a metabolite produced fr
34 f acetyl-lysine residues to nicotinamide, 2'-O-acetyl-ADP-ribose (OAADPr), and deacetylated lysine.
35           A by-product of the Sir2 reaction, O-acetyl-ADP-ribose (OAADPr), is thought to aid spreadin
36                                              O-acetyl-ADP-ribose (OAADPr), produced by the Sir2-catal
37        Sirtuins form a unique metabolite, 2'-O-acetyl-ADP-ribose (OAADPr), shown to block oocyte matu
38 to nicotinamide, deacetylated lysine, and 2'-O-acetyl-ADP-ribose (OAADPr).
39 acetylated product, and the novel metabolite O-acetyl-ADP-ribose (OAADPR).
40 otinamide and a newly discovered metabolite, O-acetyl-ADP-ribose (OAADPr).
41 ae is a major regulator of cellular ADPr and O-acetyl-ADP-ribose (OAADPr).
42 c reaction between the deacetylation product O-acetyl-ADP-ribose (or its hydrolysis product ADP-ribos
43 ct, O-propionyl ADP-ribose, analogous to the O-acetyl ADP-ribose sirtuin product of deacetylation.
44 vent the release of deacetylated peptide and O-acetyl-ADP-ribose, the products of enzyme-catalyzed de
45 y(ADP-ribose) glycohydrolase ARH3 hydrolyzed O-acetyl-ADP-ribose to produce ADP-ribose in a time- and
46 n of poly(ADP-ribose) by ARH3, hydrolysis of O-acetyl-ADP-ribose was abolished by replacement of the
47 -ribose as the enzymatic product, whereas 3'-O-acetyl-ADP-ribose was formed by intramolecular transes
48 ARH3-catalyzed generation of ADP-ribose from O-acetyl-ADP-ribose was significantly faster than from p
49 previous conclusion, which suggested that 1'-O-acetyl-ADP-ribose was the solution product of the reac
50                     We hypothesized that, if O-acetyl-ADP-ribose were an important signaling molecule
51 ural analyses, 2'-O-acetyl-ADP-ribose and 3'-O-acetyl-ADP-ribose were found to be the solution produc

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