ライフサイエンスコーパス: acetylate

1 ipids in Archaea but is dephosphorylated and acetylated.

2 howed that RhoGDIalpha is extensively lysine-acetylated.

3 sted that 1-pyrroline might be enzymatically acetylated.

4 6, K9, and K15) in Nt(17) were significantly acetylated.

5 Here, we report that the TUG C terminus is acetylated.

6 f the mature effector was found likely to be acetylated.

7 eta-MHC isoforms were found to be reversibly acetylated.

8 rged exopolysaccharide composed of partially acetylated 1-->4 glycosidic linkages of N-acetylgalactos

9 rotected 3-deoxy-3-fluorogalactopyranose and acetylated 4-deoxy-4-fluorogalactopyranose.

10 can act independently to posttranslationally acetylate a distinct set of substrates, notably actin.

11 acetylase) and therefore cannot N-terminally acetylate a majority of normally N-terminally acetylated

12 Thus, the Nt-acetylated Ac-MX-Rgs2 (X = Arg, Gln, Leu) proteins are s

13 The SMC3 subunit of cohesin is acetylated (ac) during S phase to establish cohesion bet

14 Here, we show that APE1 is acetylated (AcAPE1) after binding to the AP sites in chr

15 the physiological form of AS is N-terminally acetylated (AcAS).

16 This study was aimed at producing acetylated adipate of retrograded starch (ADA-R) with va

17 The study demonstrated that acetylated adipate of retrograded starch may be classifi

18 ves to the basal side and become extensively acetylated after the duplicated centrosomes reposition t

19 e treatment of control mitochondria with the acetylating agent acetic anhydride inhibits pyruvate upt

20 Because Naa10 is reported to acetylate all amino termini that are devoid of methionin

21 In addition, Naa50 acetylated all MXAA peptides except for MPAA.

22 mini that are devoid of methionine and Naa50 acetylates all other peptides that are followed by methi

23 which is composed of nonstoichiometrically O-acetylated alpha-1,4-linked N-acetylgalactosaminuronic a

24 N-acetylated alpha-linked acidic dipeptidase-like protein

25 so aimed to explore a potential mechanism of acetylated alpha-tubulin (alpha-Ac-Tub) regulation by Ac

26 hibition and the subsequent up-regulation of acetylated alpha-tubulin and FGF-21.

27 videnced by altered morphology and decreased acetylated alpha-tubulin and glu-tubulin.

28 fferentiation was demonstrated via increased acetylated alpha-tubulin and SOX9 proteins, the number o

29 Levels of acetylated alpha-tubulin were decreased in the ischemic

30 ion with different fibril structure than non-acetylated alphaS.

31 Using bacterially expressed acetylated-alphaS (NTAc-alphaS) and endogenous alphaS (E

32 om the slightly higher helical propensity of acetylated-alphaS in solution leading to a more homogeno

33 er effects of triacetylresveratrol (TRES, an acetylated analog of RES) which has higher bioavailabili

34 when a beta-amylase treatment was applied to acetylated and debranched potato starch.

35 f autophagy initiation and flux by affecting acetylated and dynamic microtubules in a reciprocal way.

36 The latter binds to acetylated and methylated lysine residues of histones.

37 s heparin and heparan sulfate occurring in N-acetylated and N-sulfated forms, and as the unmodified a

38 In Loxl3-/- mice, Stat3 is constitutively acetylated and naive CD4(+) T cells are potentiated in T

39 The degree of modification of acetylated and oxidized starches is dependent on the cat

40 Here, we show that mitochondrial GOT2 is acetylated and that deacetylation depends on mitochondri

41 Here, we report that both ERK1 and -2 are acetylated and that HDAC6 promotes ERK1 activity via dea

42 y examining the N-terminal sequences of many acetylated and unacetylated proteins and more recently b

43 We obtained curated N-terminally acetylated and unacetylated sequences from the UniProt d

44 owever, whether other regions of MSH2 can be acetylated and whether other histone deacetylases (HDACs

45 misfolded variants of cytosolic enzymes that acetylate arylamines and ubiquitinate proteins, respecti

46 The T-acetylated at aliphatic-OH and 3,5-diacetyl-R exhibited

47 effect only in serum oxidation, where the T-acetylated at aromatic-OH was the most active.

48 ctor alpha-induced protein 2 (TNFAIP2) to be acetylated at histone H4.

49 ctivity, lowered levels of total tau and tau acetylated at K174, rescued tau-induced memory deficits

50 s of histone H3 and of the BRD domain for H3 acetylated at Lys(14) (H3K14ac), the exact mode of H3 bi

51 -mediated association to histone H3 peptides acetylated at lysine 14 (H3K14Ac), validating the import

52 Here, we report that PGK1 is acetylated at lysine 220 (K220), which inhibits PGK1 act

53 cells to high glutamine concentration, GS is acetylated at lysines 11 and 14, yielding a degron that

54 due to a deletion in wciG Serotype 35C was O-acetylated at the 5- and 6-positions of 3-beta-galactofu

55 DNA damage the acetyltransferase Tip60 must acetylate ATM proteins prior to their full activation by

56 Two glycoclusters constituted by four fully acetylated beta-acetylmannosamine residues linked throug

57 Moreover, Ran was acetylated by CBP/p300 and Tip60 in vitro and on transfe

58 mutagenesis to identify major sites of ADA3 acetylated by GCN5 and p300.

59 s of a canonical nucleosome, is specifically acetylated by p300 in prenucleosomes relative to nucleos

60 oduce tri-acylsucroses, which can be further acetylated by Sl-ASAT4 (previously Sl-AT2).

61 tylation by TIP60, while this residue can be acetylated by TIP60 in vivo, blocking its ubiquitylation

62 Acetylated C/EBPalpha is enriched in human myeloid leuka

63 th regard to their suitability for detecting acetylated cellulosic key chromophores.

64 Naa10, suggesting that the substrates may be acetylated chemically rather than enzymatically.

65 Partially acetylated chito-oligosaccharides (paCOS) have diverse b

66 lled chromatin immunoprecipitation (ChIP) of acetylated chromatin (ChIPac).

67 ding of BRD2 to H4Ac protects the underlying acetylated chromatin from attack by histone deacetylases

68 tly targeting bromodomain proteins that bind acetylated chromatin marks.

69 A switch between methylated/acetylated chromatin underlies the tumor phenotypic evol

70 P) monitoring displacement of GFP-BAZ2A from acetylated chromatin.

71 el papers and historical papers in which the acetylated chromophores were detected successfully.

72 Eco1 acetylates cohesin's Smc3 subunit, which locks together

73 The essential MYST family Esa1 KAT acetylates core histones and many nonhistone substrates.

74 served primer-template looped structure, its acetylated counterpart uses a different mechanism, one c

75 -SOD1 (e.g., fibril Tm = 84.49 degrees C for acetylated D90A apo-SOD1 fibrils).

76 Binding of acetylated degron peptides to CRBN depends on an intact

77 ty of tyrosol (T), resveratrol (R) and their acetylated derivatives (AcD), as increased lipophilicity

78 Moreover, the acetylated derivatives were also detected but at lower f

79 ntained the greatest relative abundance of O-acetylated derivatives, Binocrit expressed the least Neu

80 low amylose rice starches, whether native or acetylated, did not form films with desirable characteri

81 fractory epilepsy persistently expressed the acetylated, disulfide HMGB1 isoforms.

82 nd required for transcription stimulation by acetylated double-variant chromatin.

83 ase1 and ATase2, two acetyltransferases that acetylate endoplasmic reticulum cargo proteins.

84 PAF-treatment had no effect on other acetylating enzymes (GCN5L2, PCAF) indicating it is not

85 rases CREB-binding protein and p300 both can acetylate ERK1/2.

86 Acetylated ERK1 exhibits reduced enzymatic activity towa

87 we observed elevated levels of CIDEC and its acetylated form in HDAC-deficient adipocytes as well as

88 omain readers, which preferentially bind the acetylated forms of their cognate ligands, the acidic do

89 We also found that acetylated FOXO3 preferentially bound JNK1, and a mutant

90 for HDAC8-catalyzed deacetylation of singly-acetylated, full-length protein substrates, revealing th

91 , an l-histidine methyl ester linker, and an acetylated galactose bonded to one of the aromatic nitro

92 The hydrolysis occurs at sites with fully acetylated GlcNAc moieties, with preference for uncross-

93 vity and led to increased GRP78 acetylation; acetylated GRP78 then bound to VPS34, a class III phosph

94 action was anthocyanin compounds, especially acetylated>diglucosylated forms than glucosylated ones.

95 In contrast, the expression of the acetylating gtrC gene is controlled by epigenetic phase

96 Here we show that chromatin containing acetylated H2AZ and H3.3 stimulates transcription in vit

97 Intriguingly, the accumulation of lysine 5-acetylated H2B was cell age-dependent and was associated

98 ccumulation of the epigenetic mark, lysine 5-acetylated H2B.

99 vealed a significantly higher association of acetylated H3 and H4 with the E-cadherin promoter in kid

100 Depletion of SMAD3 reduced PLOD2 acetylated H3 and H4, indicating that another as of yet

101 nscription, associated with an enrichment of acetylated H3 at several sites of Bdnf promoter I, more

102 termine that non-canonical histone signature acetylated H3 lysine 23 (H3K23ac)-binding protein tripar

103 decreased expression of Bcl-xL and increased acetylated H3, reversing the expression patterns observe

104 Histone acetylation, including acetylated H3K14 (H3K14ac), is generally linked to gene

105 articles (NCPs) containing site-specifically acetylated H3K14 or H3K56 and measured repair of uracil

106 ssociated with the ASS1 promoter to maintain acetylated H3K14ac and H3K27ac for ASS1 silencing.

107 find that the SAGA HAT module preferentially acetylates H3K4me3 nucleosomes in a mixture containing e

108 ansferase Rtt109 and promotes its ability to acetylate H3K56.

109 NuRD transcriptional repressor complex to de-acetylate H3K9 and repress RNA polymerase II recruitment

110 Direct association of BRD4 with acetylated H4 decreases in late spermatids as acetylated

111 of unacetylated, mono-, di-, tri-, and tetra-acetylated H4 histone tails using Replica Exchange Molec

112 Interestingly, the acetylated H4 lysine 16 (H4K16ac) is selectively augment

113 ncreased levels of acetylated pRb as well as acetylated H4K16 both globally and at telomeric regions.

114 e PU.1 promoter in progenitor cells, whereas acetylated HDAC1, which is inactive, is on the silenced

115 s, the secondary amides of peptides and of N-acetylated hexose sugars.

116 The films from acetylated high amylose starches had higher moisture con

117 They acetylate histone H3 and other nonhistone substrates and

118 rait loci, disease-associated polymorphisms, acetylated histone 3 lysine 27 (H3K27ac) and transcripti

119 -methylated histone 3 lysine 4 (H3K4me3) and acetylated histone 3 lysine 9 (H3K9ac) at the HER2 promo

120 additional repressive histone modifications, acetylated histone 3 on lysine 9 and 14 deacetylation, a

121 tone 3 on lysine 9 and 14 deacetylation, and acetylated histone 3 on lysine 9 methylation.

122 y by sodium butyrate enhances recruitment of acetylated histone 3 to the IL-10 promoter and increases

123 rified the increased enrichment of lysine-27 acetylated histone H3 at discrete loci, accompanied by e

124 HDAC8 selectively targeted acetylated histone H3 lysine 27 (H3K27Ac), which is know

125 In this study, we found that K27-acetylated histone H3 specifically recruited Super Elong

126 YEATS2 binds to acetylated histone H3 via its YEATS domain.

127 quencing analyses revealed that ENL binds to acetylated histone H3, and co-localizes with H3K27ac and

128 the conserved YEATS domain, which recognizes acetylated histone H3.

129 m molecular dynamics simulations of a doubly acetylated histone H4 peptide bound to the bromodomain o

130 fashion, selective disruption of bromodomain:acetylated histone interactions with chemical probes ser

131 T) proteins, which are epigenetic readers of acetylated histone lysine tail residues.

132 teins (BET) are chromatin adapters that bind acetylated histone marks via two tandem BDs, BD1 and BD2

133 ET proteins to chromatin by engaging cognate acetylated histone marks, and the extraterminal (ET) dom

134 eeper residue and binds relatively weakly to acetylated histone peptides.

135 Although both BD1 and BD2 bind acetylated histone residues, they may independently regu

136 BET proteins bind acetylated histone tails via their bromodomain, bringing

137 1 alters the direct association of BRD4 with acetylated histone-packaged promoters and reduces the tr

138 em in Drosophila, regulates gene activity by acetylating histone H4 preferentially at lysine 16.

139 gulator that localizes to DNA via binding to acetylated histones and controls the expression of thera

140 nal domain (BET) protein family, which binds acetylated histones and is a critical regulator of trans

141 of BRD4, a bromodomain protein that binds to acetylated histones and is a key transcriptional coactiv

142 eins are epigenetic "readers" that recognize acetylated histones and mark areas of the genome for tra

143 " proteins (BRD2, BRD3, BRD4, and BRDT) bind acetylated histones and serve as a scaffold for the recr

144 cetylated H4 decreases in late spermatids as acetylated histones are removed from the condensing nucl

145 n spermatids revealed enrichment of BRD4 and acetylated histones at the promoters of active genes.

146 ng factor chromatin assembly, which requires acetylated histones for efficient assembly.

147 l (BET) proteins are epigenetic "readers" of acetylated histones in chromatin and have been identifie

148 es the Adipoq gene by recruiting P-TEFb onto acetylated histones in the transcribed region of the gen

149 inhibit the association of BRD7 and BRD9 to acetylated histones in vitro and in cells.

150 dues in histone H3 enables deposition of pre-acetylated histones into cellular chromatin, via a pathw

151 t indicating that SEC recruitment to certain acetylated histones on a subset of genes stimulates the

152 the interaction between its YEATS domain and acetylated histones reduces the ATAC complex-dependent p

153 -forward loops of acetylation and binding of acetylated histones that drive transcription of underlyi

154 BRD7 simultaneously binds to acetylated histones to promote Smad-chromatin associatio

155 ecialized binding modules that interact with acetylated histones, linking chromatin recognition to ge

156 T) proteins, inhibiting them from binding to acetylated histones, which occurs preferentially at supe

157 RD3 isoforms display differential binding to acetylated histones.

158 bate and BETi blocked the binding of BRD4 to acetylated histones.

159 ins encoding acetyltransferases can directly acetylate host proteins to alter immunity.

160 Lower acetylated Hsp90, higher GR-Hsp90 association, and enhan

161 Acetylated htt also bound lipid membranes and disrupted

162 Several acetylated, hydroxylated, and/or sulfated metabolites we

163 oxylic acid cycle, has been identified to be acetylated in bacteria by proteomic studies, but no furt

164 erminal amino group, which is instead alphaN-acetylated in cells.

165 Lysines are acetylated in histone tails and the core domain/lateral

166 including the histone acetyltransferase p300 acetylated in its activation loop, which could explain s

167 n (alphaS) has been shown to be N terminally acetylated in its physiological state.

168 we discover that RhoGDIalpha is endogenously acetylated in mammalian cells, and we identify CBP, p300

169 We show here that one residue, Lys501, is acetylated in RNase II.

170 Here we show that SIRT3 is reversibly acetylated in the mitochondria and unexpectedly is a tar

171 considered that long-lived microtubules are acetylated inside their lumen and that microtubule acety

172 that the AXY9 protein may act to produce an acetylated intermediate that is part of the O-acetylatio

173 P300 acetylates IRS1/2 and inhibits its binding with the insu

174 ing in the induction of P300 which, in turn, acetylates IRS1/2, inhibits its association with the ins

175 nd muscle Arnt-like protein), CLOCK directly acetylates K165 and K176 of argininosuccinate synthase (

176 s modified forms of LDL, such as oxidized or acetylated LDL, and promotes ingestion by macrophages in

177 Chitosans, beta-1,4-linked partially N-acetylated linear polyglucosamines, are very versatile a

178 However, migratory SMCs did not uptake acetylated low-density lipoprotein or express the classi

179 Structural analysis reveals that acetylated Lys9 is sandwiched in an aromatic cage formed

180 ly, recent reports claim that Naa10 may also acetylate lysine residues of diverse targets, including

181 tivity as marked by histone 3 containing the acetylated lysine 27 (H3K27ac).

182 nalysis of DNA methylation, histone marking (acetylated lysine 9 in histone H3 and trimethylated lysi

183 ivity of the mammalian sirtuin SIRT7 targets acetylated lysine in the N-terminal tail of histone H3 (

184 omains, small protein modules that recognize acetylated lysine on histones, play a significant role i

185 Recent studies indicate that acetylated lysine residues mainly exhibit low acetylatio

186 ate transcription by selectively recognizing acetylated lysine residues on chromatin.

187 Bromodomains bind to acetylated lysine residues on histone tails and thereby

188 ility of Sirt1-3 to deacetylate two adjacent acetylated lysine residues.

189 es 18 enzymes that catalyze deacetylation of acetylated lysine residues; however, the specificity and

190 e interaction between BET proteins and their acetylated lysine substrates may provide a new therapeut

191 isrupt function by preventing recognition of acetylated lysine substrates.

192 Glutamine (or acetylated lysine) was neutral and thus caused the pocke

193 ac (histone H3, phosphorylated serine 10 and acetylated lysine-14), H3K4me3 (histone H3, trimethylate

194 ed lysine-to-glutamine (KQ) mutants to mimic acetylated lysines and screened 15 KQ mutants.

195 by mass spectrometry analysis, identifying 4 acetylated lysines in 3 distinct functional domains.

196 While acetylated lysines in histone tails are frequently recog

197 tandem bromodomains that mediate binding to acetylated lysines on target proteins to regulate gene e

198 JQ1, which blocks the functional readout of acetylated lysines, reduced heroin self-administration a

199 nteract with the RRS1 WRKY domain, and PopP2 acetylates lysines to block DNA binding.

200 hat all the tested GCN5-containing complexes acetylate mainly histone H3K14.

201 Herein we report that p300 and CBP acetylate Mastermind-like 1 (Maml1) on amino acid residu

202 ine acetyltransferase), Rv0998, specifically acetylates MbtA on lysine 546, in a cAMP-dependent manne

203 ed that acetyl-CoA or acetyl-phosphate could acetylate MDH chemically in vitro.

204 le the E. coli acetyltransferase YfiQ cannot acetylate MDH efficiently.

205 chia coli deacetylase CobB could deacetylate acetylated MDH, while the E. coli acetyltransferase YfiQ

206 However, acetylated microtubules are predominantly bundled, and b

207 human BRD4 protein, BRD4(BD1), identified an acetylated-mimic xanthine derivative inhibitor.

208 immunohistochemistry for SIRT3 activity via acetylated MnSOD(K68) Murine AEC SIRT3 and cleaved caspa

209 athogen KSHV, led to perinuclear wrapping by acetylated MT bundles and identified ORF52 as the viral

210 cally unlocks the nutritive potential of 9-O-acetylated mucus sialic acids for foraging by bacteria t

211 glycosylation using a metabolic label, tetra-acetylated N-azidoacetylgalactosamine (Ac4GalNAz).

212 We discover 20 sulfated and 4 acetylated N-glycans on IgGs.

213 he Golgi apparatus, and has a preference for acetylating N termini of the transmembrane proteins.

214 mutant virus encoding K229R, mimicking a non-acetylated NP lysine residue, is severely impaired compa

215 athway, which recognizes N(alpha)-terminally acetylated (Nt-acetylated) proteins.

216 complex to be recruited to chromatin and to acetylate nucleosomal histones.

217 in to aggregate, and lack of this ability in acetylated nucleosomal arrays.

218 2e are therefore critical for creating open, acetylated nucleosome structures and for controlling end

219 SMAD2 can bind pre-acetylated nucleosome-depleted sites.

220 ide produced by R7A is a monomer unit of the acetylated octasaccharide with the structure (2,3/3-OAc)

221 he transcriptionally active form of the p65 (acetylated on lysine 310) subunit of NF-kappaB exclusive

222 We found that alpha-synuclein is acetylated on lysines 6 and 10 and that these residues a

223 Expression of acetylated p53 and the conformationally active form of B

224 tuin-1 and Foxo3alpha with downregulation of acetylated p53 expression and prevented downregulation o

225 mulation of Foxo3alpha and downregulation of acetylated p53 expression.

226 sion resulting in constitutive activation of acetylated p65 (lysine 310).

227 The intensity and number of acetylated p65(+) cells was markedly elevated in LPLs of

228 y using a set of four enkephalin-related and acetylated peptides to generate 12 larger peptide sequen

229 the formation of robust and mature MurNAc O-acetylated peptidoglycan and infer its role in the divis

230 d in vitro using p-nitrophenyl acetate and O-acetylated PG as substrates.

231 SIRT6 levels correlate with elevated nuclear acetylated PKM2 levels in increasing grades of hepatocel

232 gae possesses acetyltransferase activity and acetylates plant proteins to facilitate infection.

233 has an allosteric polyamine-binding site and acetylating polyamines regulate their intracellular conc

234 tion of SIRT1 leading to increased levels of acetylated pRb as well as acetylated H4K16 both globally

235 Herein we report that the matrikine acetylated Pro-Gly-Pro (PGP) stimulates vascular inflamm

236 dipate and tryptophan, to their respective N-acetylated products in several plant species.

237 tudying protein acetylation is to get purely acetylated proteins at specific positions.

238 Some acetylated proteins such as Ras-related nuclear, p53, an

239 differentially expressed proteins and lysine acetylated proteins were involved in a number of differe

240 cetylate a majority of normally N-terminally acetylated proteins, including Hsp90 and most of its coc

241 d to effects on the in vivo half-lives of Nt-acetylated proteins.

242 ylation, leading to the identification of 24 acetylated proteins.

243 responsible for removing acetyl groups from acetylated proteins.

244 ecognizes N(alpha)-terminally acetylated (Nt-acetylated) proteins.

245 ates pyruvate dehydrogenase complex (PDC) by acetylating pyruvate dehydrogenase (PDH) and PDH phospha

246 , as does disruption of interactions between acetylated residues and 'reader' proteins.

247 alytic head we found that phosphorylated and acetylated residues are primarily on alpha/beta and beta

248 ng different interfaces the higher abundance acetylated residues are proximal to the regulatory sites

249 Mutation of the acetylated residues impaired insulin-responsive GLUT4 tr

250 Mutation of the acetylated residues in TUG abrogated these effects.

251 More importantly, Gcn5 directly acetylates Rph1 in vitro and in vivo, and Gcn5-containin

252 roup 2a CoVs, e.g., hCoV-OC43, for which 9-O-acetylated sialic acid (9-O-Ac-Sia) serves as a receptor

253 trate that hCoV-HKU1 uses certain types of O-acetylated sialic acid residues on glycoproteins to init

254 to slightly reduced retention times, while O-acetylated sialic acid-containing glycoforms are retaine

255 Most HEs (type I) target 9-O-acetylated sialic acids (9-O-Ac-Sias), but one group of

256 pends on a novel acetyltransferase domain to acetylate signalling proteins from plant and animal host

257 e natively folded, site-specific, and lysine-acetylated Sirt1-3 substrate proteins, namely Ras-relate

258 Acetylated Skp2 is exclusively localized to the cytosol,

259 totic factors FoxO1/3 are overly degraded by acetylated Skp2, resulting in polyploid cell division, g

260 tion of SpeG from V. cholerae showed that it acetylates spermidine and spermine.

261 hown that SpeG is the enzyme responsible for acetylating spermidine under stress conditions and for p

262 lied raw materials, production procedures of acetylated starch and correlations between the degree of

263 The insoluble complexes from the acetylated starch displayed the V-type pattern, whereas,

264 soluble and insoluble complexes for the low acetylated starch, but not for the high acetylated starc

265 The acetylated starch-based films had a lower decomposition

266 low acetylated starch, but not for the high acetylated starch.

267 Acetylated starches films exhibited more rapid degradati

268 The degree of substitution (DS) of the acetylated starches increased with the rise in catalyst

269 Biodegradable films from native or acetylated starches with different amylose levels were p

270 Acetylated STAT3 emerged upon HDAC inhibition was protec

271 ndings provide new insights into the role of acetylated STAT3-mediated activation of IGF2 transcripti

272 hanistically, p300-histone acetyltransferase acetylates STAT3, which, in turn, upregulates and activa

273 Both enzymes were active on acetylated substrates, although each showed a higher fer

274 aining monosaccharides, phosphorylated and N-acetylated sugars, polyols, carboxylic acids, nucleotide

275 ines and amides, primary amides, and novel N-acetylated sugars, which together account for nearly 50%

276 Acetylated TAF9 does not bind to the PU.1 gene promoter

277 We show that DPF2 interacts with the acetylated tails of both histones 3 and 4 via bipartite

278 in AD brains, Tracy et al. (2016) found that acetylated tau promotes synaptic dysfunction through dis

279 Importantly, acetylated TDP-43 lesions are found in ALS patient spina

280 uman Naa50 suggested the presence of CoA and acetylated tetrapeptide (AcMMXX) that have co-purified w

281 The human ESCO1 and ESCO2 paralogs acetylate the cohesin complex subunit SMC3 to regulate t

282 We demonstrate that KAT2A/2B acetylate the PLK4 kinase domain on residues K45 and K46

283 ctors including Ctf4 and Chl1, concomitantly acetylates the chromosomal cohesin complex to stabilize

284 NatA co-translationally acetylates the N termini of a wide variety of nascent po

285 gae T3SE HopZ1a is an acetyltransferase that acetylates the pseudokinase AtZED1 and triggers recognit

286 hed to prevent intramolecular arrangement by acetylating the N-terminal amino group prior to electroc

287 Histone acetyltransferase HBO1 might acetylate this residue.

288 oietic maturation system driven by GATA1, an acetylated transcription factor previously shown to inte

289 n TacT contributes to persister formation by acetylating tRNA, a novel mechanism of toxin action.

290 iary morphology accompanied by alteration of acetylated tubulin and IFT88 expression.

291 toma lanceolatum was reinvestigated by using acetylated tubulin immunohistochemistry, which specifica

292 While ATP depletion led to cell death, over-acetylated tubulin led to inhibition of motility and mit

293 We used antibodies against acetylated tubulin, human neuronal protein C/D, choline

294 tive stimulus, we demonstrate that p66Shc is acetylated under high glucose conditions and is deacetyl

295 of 10, 20, and 30g Cl/kg of starch, and then acetylated using acetic acid anhydride.

296 of the interactions between Ubc9 and its K65 acetylated variant (Ac-Ubc9K65) with three NDSMs derived

297 analysis has led to the identification of an acetylated variant of STX with unprecedented, low-nanomo

298 The presence of acetylated viosamine in vivo has also been confirmed on

299 r cells, we demonstrate that C/EBPepsilon is acetylated, which was confirmed by mass spectrometry ana

300 the dosage compensation complex (DCC), which acetylates X chromatin in males [11], becomes mis-locali