ライフサイエンスコーパス: acetyl group

1 , and the number of incorporated sulfate and acetyl groups).

2 to assign unambiguously the position of the acetyl group.

3 ant hydroxylamine was then protected with an acetyl group.

4 ine are secondary amines with at least one N-acetyl group.

5 degradation through their N(alpha)-terminal acetyl group.

6 ghtly higher than that for the removal of an acetyl group.

7 stent ~3.1 degrees C decrease in Tm per 2'-O-acetyl group.

8 ction other than the biologically relevant N-acetyl group.

9 ay result from Ile-313 packing against the N-acetyl group.

10 omers due to intramolecular migration of the acetyl group.

11 (dG-C8-AAF) adducts that differ by a single acetyl group.

12 nitro, trifluoromethyl, fluoro, chloro, and acetyl groups.

13 tion, alpha1 and alpha2 contained N-terminal acetyl groups.

14 e labeled methyl and carbonyl carbons of the acetyl groups.

15 ey were substituted with from zero to four O-acetyl groups.

16 chiometrically substituted with up to four O-acetyl groups.

17 2 promotes p53 degradation by removing these acetyl groups.

18 and each mutant produced alginate lacking O-acetyl groups.

19 A PS were specific for epitopes involving O-acetyl groups.

20 hat have the capacity to modify core histone acetyl groups.

21 serotyped, and had marked reduction in GXM O-acetyl groups.

22 ient protocol for on resin deprotection of O-acetyl groups.

23 thylation may lead to the decomposition of O-acetyl groups.

24 esterase (NanS) to confirm the presence of O-acetyl groups.

25 bunit is on average substituted with three O-acetyl groups.

26 starch more hydrophobic by the insertion of acetyl groups.

27 ncluding variations such as N-glycolyl and O-acetyl groups.

28 hydrolyze long-chain fatty acyl groups over acetyl groups.

29 V-1 integrase inhibitor containing aryl di-O-acetyl groups (Acetylated-Inhibitor).

30 Subsequent to the transfer of the acetyl group, acetylated aminoglycoside is released prio

31 r in the cytoplasm, (ii) the export of the O-acetyl group across the cytoplasmic membrane, and (iii)

32 assembles the thiazole functionality from an acetyl group and l-cysteine via condensation, cyclizatio

33 imetry titration, indicating that both the N-acetyl group and sugar type may be essential for donor s

34 intramolecular hydrogen bonds between the N-acetyl group and the protein backbone are an important i

35 Binding was enhanced by removal of 9-O-acetyl groups and attenuated by truncation of the glycer

36 (HDACs) are a family of enzymes that remove acetyl groups and control the acetylation status of hist

37 There were fewer O-acetyl groups and more phosphoethanolamine and sialic ac

38 ions between the degree of substitution with acetyl groups and properties of the modified preparation

39 d histone deacetylases (HDACs), which remove acetyl groups and silence transcription.

40 al and biological processes, the role of the acetyl groups and the complexity of their migration has

41 n isolated native oligomers with 13C labeled acetyl groups and the extraction of orientational constr

42 cally, the STM was used to cleave individual acetyl groups and to form Au-S bonds by manipulating sin

43 ygen to the Pd center, (4) hydrolysis of the acetyl group, and (5) reductive elimination of Pd(0), wh

44 ungal genes encoding enzymes that metabolise acetyl groups, and with genes for other hydrolyases such

45 orrelated with protection against disease, O-acetyl groups appear to be important in protection.

46 Although N-acetyl groups are common in nature, N-glycolyl groups ar

47 d their equatorial orientation but not the N-acetyl groups are critical for IRBC binding.

48 taining disaccharide thioglycoside with 6- O-acetyl group as donor building blocks for the alpha-dire

49 acyl esters, and tetra-acyl sucroses have an acetyl group as one of the acyl chains.

50 phosphates, (ii) the release of small excess acetyl groups as acetylcarnitine and ketone bodies, and

51 ation of the biaryl axis and the presence of acetyl groups as important structural elements for the b

52 it contains a carbonyl oxygen instead of an acetyl group at C17 on the steroid D ring.

53 The acetyl group at C17, but not that at C3, was essential f

54 troduction of small alkyl substituents or an acetyl group at C3 is also tolerated.

55 To accommodate the additional N-acetyl group at the C2 position of the sugar, the side c

56 The 2'-O-acetyl group at the ligation junction of the product RNA

57 Acetyl groups at C4 ensure alpha-selective galactosylati

58 O-acetylated ManNAc residues that contained acetyl groups at O-3, with some species acetylated at O-

59 indicate that GlcNAc residues on WTAs and O-acetyl groups at the 6-position of muramic acid residues

60 xylose has a hydroxyl group (instead of an N-acetyl group) at C2 and lacks the CH(2)OH group at C5; t

61 ed of a trisaccharide repeat unit with one O-acetyl group attached to each repeat unit.

62 has also been established that PDC flux and acetyl group availability limits aerobic ATP re-synthesi

63 pyruvate dehydrogenase complex activation or acetyl group availability occurred during the first 20 s

64 urately predicting which proteins receive an acetyl group based on their protein sequence is expected

65 -acylthio substituent, the benzoyl group and acetyl groups being removed 50 and 5 times as fast as th

66 and catalyzes the reversible transfer of an acetyl group between the alpha-amino groups of ornithine

67 tor-binding site on beta4Gal-T1, while the N-acetyl group-binding pocket in beta4Gal-T1 adjusts to ma

68 sugar-acceptor binding site, a hydrophobic N-acetyl group-binding pocket is found, formed by residues

69 ed-Control) that also contained an aryl di-O-acetyl group but did not inhibit HIV-1 integrase.

70 A that gets subsequently converted into a 3-acetyl group by 3-vinyl bacteriochlorophyllide a hydrata

71 deacetylase enzymes catalyze removal of the acetyl group by hydrolysis or by an NAD(+)-dependent rea

72 ides that results in the exchange of the 4-O-acetyl group by the glacial acetic acid that serves as e

73 OPV structures and can be converted to the S-acetyl group by treatment with sodium thiomethoxide and

74 lly active chromatin, whereas the removal of acetyl groups by histone deacetylases (HDACs) correlates

75 The presence of hydrophobic acetyl groups, carbonyl and carboxyl groups caused a par

76 thin 3.9 A of five aromatic residues and its acetyl group close to residues C187/188 of the principle

77 tural changes arise from rotations of the C3-acetyl group conformation and hydrogen bonding.

78 Ethynyl --> acetyl group conversion was also studied on ethynylated

79 ted, for the first time, the existence of an acetyl group deficit at the onset of contraction and has

80 d (P < 0.01), respectively, and overcame the acetyl group deficit at the onset of contraction.

81 ism by which dichloroacetate overcomes this "acetyl group deficit".

82 P re-synthesis at the onset of exercise (the acetyl group deficit).

83 ally decline (indicating the existence of an acetyl group deficit).

84 east in part attributable to a limitation in acetyl group delivery/availability at the onset of exerc

85 We examined the role of acetyl group-dependent and -independent epitopes on the

86 uents such as the fluoro, nitro, chloro, and acetyl groups do not.

87 losamine, utilizing acetyl-coenzyme A as the acetyl group donor.

88 the ER lumen where acetyl-CoA serves as the acetyl-group donor for Nepsilon-lysine acetylation.

89 these compounds are possible candidates for acetyl group-donors of 2AP, predominately in the form of

90 that develops on the carbonyl oxygen of the acetyl group during both the formation of the acyl-enzym

91 to encode acetyltransferases, which transfer acetyl groups either to internal lysine residues or to t

92 rgo two distinct steps, beginning with the N-acetyl group expelling water from the donor.

93 protease cathepsin L (CTSL) that remove the acetyl group first and then the unacetylated lysine grou

94 ethods, this synthetic approach introduces O-acetyl groups first, followed by N-acylation.

95 ha-azido may be inherently preferable to the acetyl group for N-terminal protection.

96 pecificity, we suggest that the bulky serine acetyl group forces a realignment of the omega end of th

97 Pure, acetyl group free oligonucleotides were isolated after d

98 the activated complex is the transfer of the acetyl group from acetyl CoA to the acceptor lysine resi

99 ic enzymes that catalyze the transfer of the acetyl group from acetyl coenzyme A (AcCoA) to the free

100 ric enzyme that catalyzes the transfer of an acetyl group from acetyl coenzyme A to polyamines such a

101 se gene product catalyzes the transfer of an acetyl group from acetyl coenzyme A to the C3 hydroxyl m

102 .3.1.8) catalyzes reversible transfer of the acetyl group from acetyl phosphate to coenzyme A (CoA),

103 .8) catalyzes the reversible transfer of the acetyl group from acetyl phosphate to coenzyme A (CoA),

104 .8) catalyzes the reversible transfer of the acetyl group from acetyl phosphate to coenzyme A (CoA):

105 re enzymes that catalyse the transfer of the acetyl group from acetyl-CoA to a primary amine.

106 that catalyze the reversible transfer of an acetyl group from acetyl-CoA to choline and L-carnitine,

107 se (EctA; EC 2.3.1.178), which transfers the acetyl group from acetyl-CoA to EctB-formed l-2,4-diamin

108 Acetyltransferase enzymes transfer the acetyl group from acetyl-CoA to lysine residues, while d

109 GCN5 catalyzes the transfer of an acetyl group from acetyl-CoA to the epsilon-amino of lys

110 ferase (EaDAcT) catalyzes the transfer of an acetyl group from acetyl-CoA to the sn-3 position of dia

111 yme was shown to catalyse the transfer of an acetyl group from acetyl-CoA to the terminal nitrogen of

112 ve been shown to catalyze the transfer of an acetyl group from acetyl-coenzyme A (Ac-CoA) to the amin

113 nal helix, such as removal of the N-terminal acetyl group from AcTM1aZip or striated muscle alpha-TM,

114 tylase 6 (HDAC6) catalyzes the removal of an acetyl group from lysine residues of several non-histone

115 le to catalyse the reversible transfer of an acetyl group from N-acetylornithine to glutamate, but no

116 show that LsrF catalyzes the transfer of an acetyl group from P-HPD to coenzyme A yielding dihydroxy

117 fied two enzyme activities that transfer the acetyl group from platelet-activating factor (PAF) in a

118 e deacetylases catalyze the hydrolysis of an acetyl group from post-translationally modified acetyl-l

119 ent enzymes catalyze a reaction in which the acetyl group from substrate is transferred to the ADP-ri

120 ccurs first, followed by the transfer of the acetyl group from the donor substrate to the ADP-ribose

121 ent protein/histone deacetylation, where the acetyl group from the lysine epsilon-amino group is tran

122 cetylase (HDAC) catalyzes the removal of the acetyl group from the lysine residues in the N-terminal

123 6 (HDAC6) primarily catalyzes the removal of acetyl group from the side chain of acetylated lysine re

124 ent in membranes of F. novicida, removes the acetyl group from undecaprenyl phosphate-N-acetylgalacto

125 llular function by catalyzing the removal of acetyl groups from -N-acetylated lysine residues of vari

126 erologously expressed PMR5 protein transfers acetyl groups from [(14) C]-acetyl-CoA to oligogalacturo

127 T) are two families responsible for removing acetyl groups from acetylated proteins.

128 transferase (SSAT) catalyzes the transfer of acetyl groups from acetylcoenzyme A to spermidine and sp

129 deacetylases (HDACs) catalyze hydrolysis of acetyl groups from acetyllysine side chains and are targ

130 (HDACs) are known to catalyze the removal of acetyl groups from both histones and non-histone protein

131 mily of enzymes that catalyze the removal of acetyl groups from core histones, resulting in a compact

132 gene expression by catalyzing the removal of acetyl groups from core histones.

133 r the enzyme is unknown, HerE hydrolyzes the acetyl groups from heroin to yield morphine and from phe

134 Histone deacetylases remove acetyl groups from histone proteins and play important r

135 press gene expression through the removal of acetyl groups from histone tails.

136 one deacetylases (HDACs) are known to remove acetyl groups from histone tails.

137 Hdac3 is a lysine deacetylase that removes acetyl groups from histones and additional proteins.

138 e of biological processes through removal of acetyl groups from histones as well as non-histone prote

139 By removal of acetyl groups from histones, HDACs create a non-permissi

140 press gene expression through the removal of acetyl groups from histones.

141 A second enzyme that removes acetyl groups from lysine residues in E. coli been disco

142 They regulate gene expression by removing acetyl groups from lysine residues in histone tails, res

143 Cs) are enzymes that catalyze the removal of acetyl groups from lysine residues of histone and nonhis

144 Histone deacetylases (HDACs) remove acetyl groups from lysine residues on histone tails, pro

145 atively regulate gene expression by removing acetyl groups from lysine residues present in histones a

146 nzymatic activity, preventing the removal of acetyl groups from lysine residues within histone tails.

147 as nonhistones by catalyzing the removal of acetyl groups from lysine residues.

148 eins (84% identity) that catalyze release of acetyl groups from modified N-terminal lysines of core h

149 ses that strip readily accessible methyl and acetyl groups from polymers like pectin and xylan, formi

150 Neisseria gonorrhoeae functions to release O-acetyl groups from the C-6 position of muramoyl residues

151 Gram-negative bacteria, the translocation of acetyl groups from the cytoplasm is performed by an inte

152 deacetylases (HDACs) catalyse the removal of acetyl groups from the N-terminal tails of histones.

153 harbors the activity that cleaves side chain acetyl groups from xylan-like substrates, and the bindin

154 malonyl and succinyl groups, rather than an acetyl group, from lysine residues.

155 tant strain that produced alginate lacking O-acetyl groups gave an amide II signal approximately five

156 tion of the GD3, de-N-acetylation of the 5-N-acetyl group (giving de-N-Ac-GD3).

157 The absence of the NodL-determined acetyl group greatly reduced the induction of calcium in

158 tide deformylase for the N-formyl over the N-acetyl group has been studied with N-alpha-fluoroacetyl

159 The modification of histones by acetyl groups has a key role in the regulation of chroma

160 MBPS-protein conjugate vaccines, in which N-acetyl groups have been replaced by propionyl groups (N-

161 hough the steady-state abundances of histone acetyl groups have been reported, the rate at which hist

162 The presence of the sn-3 acetyl group imparts acTAGs with different physical and

163 and 1,250 cm(-1) (C---O stretching of the O-acetyl group in alginate), as compared to biofilms of no

164 and O-acetyl groups in EPS-1 and a single O-acetyl group in EPS-2.

165 bel from water to the carbonyl oxygen of the acetyl group in OAADPr is consistent with water addition

166 duction by p53 inactivates p53 by removal of acetyl group in p53 molecule, thus functioning as an aut

167 ed acyl migration-resistant analogs using an acetyl group in place of the free hydroxyl group in orde

168 were traced to the absence of the N-terminal acetyl group in rWT that participates in an H-bond to th

169 t of native N-acetyl groups with 13C-labeled acetyl groups in a simple disaccharide derivative, (GlcN

170 substituent groups: 1-phosphoglycerol and O-acetyl groups in EPS-1 and a single O-acetyl group in EP

171 The method relies on the replacement of acetyl groups in isolated native oligomers with 13C labe

172 cetyl-coenzyme A transporting and delivering acetyl groups in many essential biochemical processes, w

173 e, for the first time, that the migration of acetyl groups in oligosaccharides and polysaccharides ma

174 ffect, indicating the critical role of the N-acetyl groups in the stimulation of proinflammatory cyto

175 The extent of the introduction of acetyl groups increased with increasing iodine levels as

176 emonstrated directly that the absence of the acetyl group increases the susceptibility of succinoglyc

177 immunogenicity associated with removal of O-acetyl groups indicates that O acetylation is essential

178 In the absence of the iMet, the N-acetyl group interacts with the central beta-sheet and s

179 ol resulted in the incorporation of labelled acetyl groups into gestating fetal brains.

180 The assignment of the two acetyl groups introduced is based on a novel combination

181 tional role of this modification and how the acetyl group is added to Lys-290 was unclear.

182 , but in all structures the binding of the N-acetyl group is conserved.

183 tiply acetylated residues, but in which each acetyl group is isotopically labeled, permit studies of

184 as expressed with a native level (>90%) of N-acetyl groups (MAbs F628 and F630).

185 An efficient intramolecular acetyl group migration from the C7 to C9-position of the

186 and quantum chemical modeling, we show that acetyl group migration is a much more complex phenomenon

187 Nod-factors made by the nodL mutant lack an acetyl group; mutation of nodF causes the nitrogen (N)-l

188 by positioning the carbonyl oxygen of the N-acetyl group near to the C1 atom.

189 ied enzyme catalyzed transacetylation of the acetyl group not only from PAF to lysoplasmalogen formin

190 rphyrin IX with strongly electron-polarizing acetyl groups not only leads to much lower meso-carbon r

191 proteins found in chromatin, by addition of acetyl groups occurs to a greater degree when the histon

192 s a ping-pong kinetic mechanism in which the acetyl group of acetyl-CoA is initially transferred to a

193 ct nucleophilic attack on the si-face of the acetyl group of acetyl-CoA.

194 uggested significant interaction between the acetyl group of acetylcholine and the alphaY93 residue.

195 In this study the N-acetyl group of BANA 113 was replaced with a 2-pyrrolidi

196 itates a keto-enol transition of the leaving acetyl group of EDTA.

197 gs suggests that Ser942 interacts with the 7-acetyl group of forskolin.

198 dditional hydrogen bond formed between the N-acetyl group of GalNAc moiety with the Tyr-289 side chai

199 s various N-acyl groups in addition to the N-acetyl group of GlcNAc.

200 de-N-acetylase capable of hydrolyzing the N-acetyl group of Lc(3)Cer was detected in bovine brain ex

201 CysM catalyzes the replacement of the acetyl group of O-acetylserine by CysO thiocarboxylate t

202 n 199 serves to hydrogen bond with the C2' N-acetyl group of sugar D, thus preventing the formation o

203 hevamine, the carbonyl oxygen atom of the N-acetyl group of the -1 sugar residue has rotated away fr

204 p of reactive Lys12 for direct attack of the acetyl group of the cofactor.

205 The acetyl group of the muscarinic agonist aceclidine 4 was

206 e regioisomer-selective interaction with the acetyl group of the stabilized regioisomers.

207 TL2)) forms no direct interaction with the N-acetyl group of the UDP-N-acetylhexosamine.

208 iosynthesis, catalyzing the removal of the N-acetyl group of UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylg

209 ng region displayed modes indicating that 3C-acetyl groups of BChl a are all involved in molecular in

210 To determine the role of the acetyl groups of low molecular mass hyaluronan in stimul

211 have an effect on the conformation of the C3-acetyl groups of the B820 molecules.

212 ble for accommodating both the hydroxy and N-acetyl groups of the substrate during sugar ring rotatio

213 Acetyl groups of unsaturated heparin disaccharides are w

214 n-391 in UGT3A1 is able to accommodate the N-acetyl group on C2 of UDP-GlcNAc so that the anomeric ca

215 of C1 and C3 configuration adjacent to the N-acetyl group on coupling behavior.

216 Mg(2+) on tRNA dynamics with and without an acetyl group on the A-site tRNA.

217 undertaken to determine the effect of the N-acetyl group on the chemistry of such compounds.

218 perties of the carbonyl moiety in the 17beta-acetyl group on the D-ring of the anesthetic steroids (3

219 ural occurrences of galactosamine lacking an acetyl group on the nitrogen, has been identified as a p

220 The presence of the acetyl group on the phenolic oxygen and the use of silve

221 inone ring was constructed in place of the N-acetyl group on the sialic acid.

222 we show that mitochondria provide 50% of the acetyl groups on H4-K16.

223 a feedforward circuit whereby HAT1 captures acetyl groups on nascent histones and drives H4 producti

224 uctural features including the location of O-acetyl groups on sialic acid (SA) moieties.

225 deacetylases (HDACs) catalyze the removal of acetyl groups on the amino-terminal lysine residues of c

226 one acetylation by catalyzing the removal of acetyl groups on the NH(2)-terminal lysine residues of t

227 to further investigate the effect of 2'/3'-O-acetyl groups on the stability of RNA duplex structure,

228 etyl-CoA), and catalyses the transfer of the acetyl group onto a specific lysine residue (K238).

229 d the dynamic incorporation of (13)C-labeled acetyl groups onto specific histone lysines with quantit

230 ture, being different only in their relative acetyl group orientations, cis (gamma' approximately 180

231 de additional specific interactions of the N-acetyl group oxygen and nitrogen with Lys-343 and Asp-32

232 The presence of O-acetyl groups plays an important role in the ability of

233 3)-enzymes that oppose Kac by buffering the acetyl group pool and catalyzing lysine deacetylation, r

234 , i.e. whether a limitation in mitochondrial acetyl group provision exists.

235 -methyl groups, whereas abstraction from the acetyl group represents a minor pathway, in line with th

236 The N-acetyl group slows down N-O bond cleavage by a factor of

237 rom oxidation of the methyl group and the N6-acetyl group stems from the methyl group and the adjacen

238 rationalized by the greater capacity of the acetyl group than the benzoyl group to conjugate with th

239 phobic interactions mimicking the N-terminal acetyl group that drives binding of UBE2M to DCN1.

240 urs in part through the direct deposition of acetyl groups that are derived from alcohol onto histone

241 contributing >50% of the fatty acid-derived acetyl groups that end up in malonyl-CoA.

242 A deacetylase can remove the acetyl group, thereby restoring activity.

243 Although G-AF and G-AAF differ by only an acetyl group, they exert different effects on DNA replic

244 uished only by the presence or absence of an acetyl group, they have profoundly different effects on

245 ch are metabolized into acetyl-coA, labeling acetyl groups through subsequent incorporation into prot

246 ic membrane, and (iii) the transfer of the O-acetyl group to a periplasmic protein or to alginate.

247 staglandin (PG) synthesis by transfer of its acetyl group to a serine residue in the cyclooxygenase (

248 CH(3) bond and the transfer of the resulting acetyl group to CoA.

249 from acetate and ATP and the transfer of the acetyl group to CoA.

250 idine acetyltransferase, which transfers the acetyl group to either the N-1 or N-8 position.

251 silon-amino group on AcCoA, transferring the acetyl group to H3 lysine residues.

252 the antibody (K(Ab)) on even addition of an acetyl group to P(1) of the peptide, the antibody fails

253 tif reveals that the tyrosine binds to the N-acetyl group to select for the "boat" conformation of N-

254 e carbonyl carbon of AcCoA, transferring the acetyl group to the acceptor peptide substrate (rate-lim

255 acyl carrier protein domain, transfer of the acetyl group to the acyl carrier protein domain is suppr

256 and undergo light-responsive addition of an acetyl group to the alpha-amino group of the amino-termi

257 Addition of an acetyl group to the amino terminus of peptide 145-159 al

258 rocess that can be blocked by addition of an acetyl group to the amino terminus of the peptide.

259 wn to transfer an 18O label from the peptide acetyl group to the ribose 1'-position of OAADPr, provid

260 I) triggers metal-mediated hydrolysis of the acetyl groups to afford a large, rapid, and zinc-induced

261 known to be essential for the addition of O-acetyl groups to alginate.

262 cetylase (HDAC) proteins that add and remove acetyl groups to and from target lysine residues within

263 strategy employs "light" and "heavy" labeled acetyl groups to block both N-termini and lysine residue

264 groups to DNA cytosine bases, of methyl and acetyl groups to proteins (histones) around which DNA is

265 YopJ catalyzes the transfer of acetyl groups to serine, threonine, and lysine residues

266 Covalent modification adding acetyl groups to the C terminus of the p53 protein has b

267 acetyltranferase involved in the transfer of acetyl groups to the glycopeptide core.

268 The importance of O-acetyl groups to the immunogenicity of Neisseria meningi

269 t the polymer level after the transport of O-acetyl groups to the periplasm.

270 mine N-acetyltransferases (NATs) catalyze an acetyl group transfer from AcCoA to primary arylamines,

271 mine N-acetyltransferases (NATs) catalyze an acetyl group transfer from acetyl coenzyme A (AcCoA) to

272 d with the lipoyl domains and intramolecular acetyl group transfer in the mechanism of active-site co

273 cotinamide-ribosyl cleavage is distinct from acetyl group transfer to the 2'-OH ribose.

274 des methyl group transfer, CO insertion, and acetyl group transfer, fitting to experimental traces re

275 chanism of nicotinamide-ribosyl cleavage and acetyl group transfer.

276 eactions, one of which involves catalysis of acetyl group transfer.

277 stone acetyltransferases (HATs) catalyze the acetyl-group transfer from acetyl-CoA to the epsilon-ami

278 A rhodium-catalyzed intramolecular acetyl-group transfer has been achieved through a "cut a

279 Decarboxylation precedes acetyl-group transfer, leading to acetyl-ACP(L) as the k

280 te in malonyl-CoA decarboxylation but not in acetyl-group transfer.

281 minal adapter domain was shown to facilitate acetyl-group transfer.

282 eavage of an amide bond, and transfer of the acetyl group ultimately to the 2'-ribose hydroxyl of ADP

283 Deprotection of the acetyl groups under basic conditions furnishes the free

284 TIPS-ethynyl group (via TIPS-acetylene), or acetyl group (via tributyl(1-ethoxyvinyl)tin, followed b

285 ersion of the trichloroacetyl group to the N-acetyl group was achieved under mild conditions, fully c

286 n acetate leaving group with or without an N-acetyl group, was cytotoxic and displayed significant in

287 The carboxyl, carbonyl, acetyl groups were determined in modified starches.

288 Antibodies to both backbone and O-acetyl groups were found to be opsonic against S. aureus

289 d possessing one specific internal 2'- or 3'-acetyl group, were used as synthetic standards in a rece

290 ith mice also showed an essential role for O-acetyl groups, where serum bactericidal titers following

291 s stems from steric hindrance effects of the acetyl group which significantly diminish the adduct-bas

292 reased hydrophobicity associated with adding acetyl groups, while the specific effects are a conseque

293 Replacement of the transmitter's ester acetyl group with a hydroxyl (ACh-->choline) results in

294 de, a modified mannosamine that replaced the acetyl group with a levulinate group (ManLev).

295 alyzed exchange of the methyl protons of the acetyl group with solvent; exchange is dependent on the

296 binds in the S1 site, predominantly via the acetyl group with the oxygen and acetamide nitrogen hydr

297 ecies undergoes reductive elimination of the acetyl group with the simultaneous release of two, low p

298 ts thereof, one obtained by substituting the acetyl group with the sulfonic amino acid taurine (Tau-L

299 n presented involves replacement of native N-acetyl groups with 13C-labeled acetyl groups in a simple

300 Replacement of the N-acetyl groups with bulky N-acyl or N-benzoyl substituent