ライフサイエンスコーパス: acetyltransferase

1 nsferase activity of MOF, a H4K16ac-specific acetyltransferase.

2 which is generated at DSBs by the Tip60/KAT5 acetyltransferase.

3 pendently of Smc3p's regulation by the Eco1p acetyltransferase.

4 cant impact on the activities of arylamine N-acetyltransferase.

5 all domains of life that is carried out by N-acetyltransferases.

6 an important feedback mechanism to regulate acetyltransferases.

7 nit by members of the Eco1 family of cohesin acetyltransferases.

8 into the virulence activity of YopJ class of acetyltransferases.

9 We found that the enzyme arylalkylamine N-acetyltransferase 1 (AANAT1) is expressed by Drosophila

10 thelial growth factor, we identified histone acetyltransferase 1 (HAT1) as an induced gene that enhan

11 Histone acetyltransferase 1 (Hat1) catalyzes the acetylation of

12 Histone acetyltransferase 1 (HAT1) is responsible for the cytoso

13 Histone acetyltransferase 1 (HAT1), which catalyzes H4K5ac and H

14 Two different isoforms of this protein, N-acetyltransferase 1 (NAT1) and N-acetyltransferase 2 (NA

15 Arylamine N-acetyltransferase 1 (NAT1) is a drug-metabolizing enzyme

16 Arylamine N-acetyltransferase 1 (NAT1) is a phase II xenobiotic-meta

17 Human arylamine N-acetyltransferase 1 (NAT1), present in all tissues, is c

18 Spermidine/spermine N1-acetyltransferase 1 (SAT1), the rate-limiting enzyme in

19 f Arabidopsis (Arabidopsis thaliana) xylan O-acetyltransferase 1 (XOAT1), a member of the plant-speci

20 There is growing evidence that arylamine N-acetyltransferase 1 has an important cellular role in ad

21 the coactivator complexes SAGA (Spt-Ada-Gcn5-acetyltransferase)(1,2) and transcription factor IID (TF

22 Here, we show that ac4C and N-acetyltransferase 10 (NAT10), the enzyme that adds ac4C

23 N-alpha-acetyltransferase 10 protein (Naa10p) catalyzes N-alpha-

24 For isoniazid, mutations in the N-acetyltransferase 2 (NAT2) gene explain >88% of pharmaco

25 eotide polymorphism in the human arylamine N-acetyltransferase 2 (Nat2) gene has recently been identi

26 protein, N-acetyltransferase 1 (NAT1) and N-acetyltransferase 2 (NAT2), are expressed in human hepat

27 leus in human cell lines and binds to lysine acetyltransferase 2A (KAT2A, also known as GCN5) in the

28 cholangiocytes predominantly express Lysine Acetyltransferases 2A (KAT2A).

29 es and of overcoming the rare aminoglycoside acetyltransferase (3)-IV class of aminoglycoside-modifyi

30 The bacterial enzyme aminoglycoside acetyltransferase(6')-Ie/aminoglycoside phosphotransfera

31 Nalpha-Acetyltransferase 60 (Naa60 or NatF) was recently identi

32 K (lysine) acetyltransferase 8 (KAT8), an important component of th

33 K(lysine) acetyltransferase 8 (KAT8, also known as MOF) mediates t

34 encodes the neuronal NAA-synthetic enzyme N-acetyltransferase-8-like.

35 h is the catalytic subunit in the N-terminal acetyltransferase A (NatA) complex.

36 tylating enzyme in Gram-positive bacteria, O-acetyltransferase A (OatA), is a two-domain protein cons

37 eurons of melatonin-deficient aralkylamine N-acetyltransferase (AANAT) knockout mice.

38 After overexpression of arylalkylamine N-acetyltransferase (AANAT; the enzyme regulating melatoni

39 s insufficiently understood, Esco1 and Esco2 acetyltransferases acetylate the cohesin subunit Smc3, t

40 d identified five candidates that may encode acetyltransferases acting on HBsu.

41 mine (O-GlcNAc) hydrolase and cryptic lysine acetyltransferase activities.

42 Acetyltransferase activity assays of recombinant protein

43 4 fusions resulted in loss of histone lysine acetyltransferase activity in a dominant-negative fashio

44 sing a dominant negative p300 mutant lacking acetyltransferase activity in mouse muscle attenuated LL

45 study reveals an important role for tubulin acetyltransferase activity in presynaptic maintenance, w

46 We suggest that P300 acetyltransferase activity may be a promising therapeuti

47 or of LLC tumor-induced muscle wasting whose acetyltransferase activity may be targeted for therapeut

48 Importantly, the enzymatic acetyltransferase activity of ATAT-2 is required for syn

49 y in a set of genomic targets depends on the acetyltransferase activity of MOF, a H4K16ac-specific ac

50 emonstrate the essentiality of the polyamine acetyltransferase activity of SAT1 for its function as a

51 ion of RUVBL1 is critically required for the acetyltransferase activity of TIP60, promoting histone H

52 RSV infection activates BRD4 acetyltransferase activity on histone H3 Lys (K) 122, de

53 posttranslational modifications impact TIP60 acetyltransferase activity to influence the outcome of D

54 Targeted chemical inhibition of p300 acetyltransferase activity using a potent and selective

55 elucidated the regulatory mechanisms of p300 acetyltransferase activity, but it is not known whether

56 additional amino acid residues important for acetyltransferase activity, we isolated and characterize

57 nditions, PKM2 is a target of OGA-associated acetyltransferase activity, which facilitates O-GlcNAcyl

58 The Mtb Rv2170 protein shows lysine acetyltransferase activity, which is capable of post-tra

59 While in metazoa, NAA50 has N-acetyltransferase activity, yeast NAA50 is catalytically

60 romoters in eukaryotic cells via MOZ histone acetyltransferase activity.

61 ibrogenic genes through its atypical histone acetyltransferase activity.

62 lymerase II complex and inhibits its histone acetyltransferase activity.

63 polymerase II, and by its intrinsic histone acetyltransferase activity.

64 re transcriptional coactivators with histone acetyltransferase activity.

65 increased the protein level of HIPK2 via its acetyltransferase activity.

66 ssay that measures the inhibition of histone acetyltransferase activity.

67 Agmatine N-acetyltransferase (AgmNAT) catalyzes the formation of N-

68 We hypothesized that alpha-tubulin acetyltransferase (alphaTAT), which both stabilizes long

69 in this cluster that potentially encode an O-acetyltransferase, an N-acetylglucosamine transferase, a

70 to identify inhibitors targeting aspartate N-acetyltransferase (ANAT), a promising target for the tre

71 x structure with those of 14-3-3:serotonin N-acetyltransferase and 14-3-3:heat shock protein beta-6 c

72 SRP2BP, a coactivator for CRP2, is a histone acetyltransferase and a driver of smooth muscle gene exp

73 identified an essential role for the histone acetyltransferase and deubiquitinase SAGA complex in per

74 ive MORF complex as a histone H3K23-specific acetyltransferase and elucidate its mechanism of action.

75 rt that Poliota also interacts with the p300 acetyltransferase and is acetylated.

76 purified AtNAA50 displays N(alpha)-terminal acetyltransferase and lysine-epsilon-autoacetyltransfera

77 sis of garsubellin A, an enhancer of choline acetyltransferase and member of the large family of poly

78 Using histone acetyltransferase and methyltransferase inhibitors, we s

79 ce staining using antibodies against choline-acetyltransferase and neurofilament was performed to dif

80 w small molecule induced recruitment of P300 acetyltransferase and the acetylation of H3K27 at precis

81 ur work illustrates a causal role of histone acetyltransferases and acetylation in senescence and sug

82 Histone acetyltransferases and histone deacetylases (HDACs) are

83 controlled by the opposing action of histone acetyltransferases and histone deacetylases (HDACs).

84 bromodomains of the p300/KAT3B and CBP/KAT3A acetyltransferases and that this interaction is required

85 g protein (CBP) and p300 are closely related acetyltransferases and transcriptional coactivators.

86 se line with deficiencies in CrAT (carnitine acetyltransferase) and Sirt3 (sirtuin 3)-enzymes that op

87 pentanoate-originated acetyl-CoA for histone acetyltransferases, and by pentanoate-triggered enhancem

88 f microtubule stabilizers, including tubulin acetyltransferases; and (3) genetic epistasis suggests t

89 activating mutations of the CREBBP and EP300 acetyltransferases are among the most common genetic alt

90 es, and the biochemical functions of these O-acetyltransferases are evolutionarily conserved througho

91 rising that the targets of bacterial protein acetyltransferases are very diverse, making their bioche

92 d mass spectrometry, we identified the EP300 acetyltransferase as uniquely associated with BRD4 throu

93 F1 encodes a protein modifier of two histone acetyltransferases associated with ID: KAT6A (also known

94 in C.elegans, we show that the alpha-tubulin acetyltransferase ATAT-2 and the signaling hub RPM-1 are

95 Peptidoglycan O-acetyltransferase B (PatB) catalyzes the O-acetylation o

96 abidopsis and konjac is mediated by mannan O-acetyltransferases belonging to the Domain of Unknown Fu

97 ns belonging to the bacterial GCN5-related N-acetyltransferase (bGNAT) superfamily acetylate the epsi

98 eads to a specific activation of the histone acetyltransferase Brd2, which results in histone H3K27 a

99 on of TH with nitric oxide synthase, choline acetyltransferase, calbindin, calretinin, and serotonin,

100 own that pathogen effector proteins encoding acetyltransferases can directly acetylate host proteins

101 tically, DEX-bound GR recruits histone H3K27 acetyltransferase CBP to promote activation of C/EBPbeta

102 mutants is rescued by depleting the histone acetyltransferase CBP-1/p300 or the transcription factor

103 Inhibition of histone acetyltransferases CBP/p300 relieves the HMGN1-associate

104 ansferases MLL3/MLL4 (KMT2C/KMT2D) and H3K27 acetyltransferases CBP/p300 to recruit Brd4 to enhancers

105 Kat2a is a histone acetyltransferase central to promoter activity, that we

106 cortex contains neurons that express choline acetyltransferase (ChAT) and are a potential local sourc

107 immunohistochemical visualization of choline acetyltransferase (ChAT) and the low-affinity neurotroph

108 ridization to localize mRNA encoding choline acetyltransferase (ChAT) and vesicular acetylcholine tra

109 ally ubiquitinated proteins, reduced choline acetyltransferase (ChAT) enzyme expression, fragmented m

110 Choline acetyltransferase (ChAT) expressing retinal amacrine cel

111 iny neurons (MSNs) and D2-expressing choline acetyltransferase (ChAT) interneurons express Slc6a15, w

112 lutamic acid decarboxylase (GAD) and choline acetyltransferase (ChAT) revealed that all CG neurons ar

113 ported to potentiate the activity of choline acetyltransferase (ChAT), the enzyme that produces the n

114 Here, we show that the enzyme choline acetyltransferase (ChAT), which catalyzes the rate-limit

115 Neocortical choline acetyltransferase (ChAT)-expressing interneurons are a s

116 able to glaucomatous damage, whereas choline acetyltransferase (ChAT)-positive and glycinergic AC sub

117 developing CNS neurons that express choline acetyltransferase (ChAT).

118 ate decarboxylases (gad1, gad2), and choline acetyltransferase (chat).

119 veal how transcriptional regulators, histone acetyltransferases, chromatin remodelers, and transcript

120 e) cells lacking the N-terminal (Nt) protein acetyltransferase complex NatB exhibit an approximate 50

121 ead, functions as an ATP-independent histone acetyltransferase complex similar to the yeast NuA4, tar

122 ltransferase complex, ATAC (Ada2A containing acetyltransferase complex).

123 rsions of the SAGA complex and another large acetyltransferase complex, ATAC (Ada2A containing acetyl

124 acetyltransferase) complex and a smaller ADA acetyltransferase complex.

125 alleviated by mutations of the SAGA histone acetyltransferase complex.

126 hologous to subunits of a mammalian MOZ/MORF acetyltransferase complex.

127 Gcn5 is part of the large SAGA (Spt-Ada-Gcn5 acetyltransferase) complex and a smaller ADA acetyltrans

128 A) and Esa1-Yng2-Epl1 (Piccolo NuA4) histone acetyltransferase complexes have the capacity to crotony

129 Gcn5 acetyltransferase functions in multiple acetyltransferase complexes in yeast and metazoans.

130 nd humans, nucleosome remodeling and histone acetyltransferase complexes originate from gene duplicat

131 via the ectopic overexpression of eukaryotic acetyltransferase complexes.

132 The MOF acetyltransferase-containing Non-Specific Lethal (NSL) c

133 Furthermore, we identified the O-acetyltransferase Cps1D of App1 and used it to modify th

134 y creating mice lacking the enzyme carnitine acetyltransferase (CrAT) in the proximal tubules, thus l

135 We also noted that the acetyltransferases CREB-binding protein and p300 both ca

136 of epigenetic inhibitors, we found that the acetyltransferase CREBBP/EP300 is a major regulator of c

137 N-alpha-acetyltransferase D (NatD) mediates N-alpha-terminal ace

138 lphaH) and 10-deacetylbaccatin III-10-beta-O-acetyltransferase (DBAT) have been identified in this fu

139 Visualization of wild-type and acetyltransferase-deficient archaeal ribosomes by cryo-e

140 in response to increases in temperature, and acetyltransferase-deficient archaeal strains exhibit tem

141 Alteration of residues unique to the acetyltransferases did not alter the unique acyl donor s

142 was dependent on bacterial dihydrolipoamide acetyltransferase (DlaT), a major protein expressed on t

143 otransferase(2'')-Ia possesses an N-terminal acetyltransferase domain and a C-terminal phosphotransfe

144 rget with small-molecule inhibitors, but the acetyltransferase domain and the bromodomain in GCN5 mig

145 mass spectrometry, we identified the histone acetyltransferase domain of HBO1 as being essential in t

146 Fos eRNAs directly interact with the histone acetyltransferase domain of the enhancer-linked transcri

147 the role of missense mutations in the lysine acetyltransferase domain that are more frequently observ

148 ly of bacterial effectors depends on a novel acetyltransferase domain to acetylate signalling protein

149 The human N-terminal acetyltransferase E (NatE) contains NAA10 and NAA50 cata

150 ytes and uncovered that ETS1 and the histone acetyltransferase E1A-binding protein P300 (EP300 or p30

151 Euonymus alatus diacylglycerol acetyltransferase (EaDAcT) catalyzes the transfer of an

152 thesis is catalyzed by l-2,4-diaminobutyrate acetyltransferase (EctA; EC 2.3.1.178), which transfers

153 gh-throughput screens against an amino-sugar acetyltransferase enzyme, PglD, involved in biosynthesis

154 In turn, Hdac3 recruited histone acetyltransferase Ep300 to form an enhanceosome complex

155 nhancers together with SMAD3 and the histone acetyltransferase EP300, enabling transcription of TGF-b

156 gh induction of nuclear translocation of the acetyltransferase EP300, which increases histone H3K27 a

157 rongest differences for TP53 and the histone-acetyltransferase EP300.

158 arrangements of the ZNF384 gene with histone acetyltransferases EP300 and CREBBP ZNF384-rearranged AL

159 This provides the first evidence that acetyltransferase family TA systems, such as GmvAT, can

160 romatin-related genes, including the histone acetyltransferases for H3K27ac and H3K9ac.

161 Among them, the acetyltransferase from Euonymus fortunei possessed the h

162 rase activity, we isolated and characterized acetyltransferases from other acetyl-TAG-producing plant

163 The acetyltransferase function of the catalytic MORF subunit

164 The Gcn5 acetyltransferase functions in multiple acetyltransferas

165 that mice lacking enzymatic activity of the acetyltransferase GCN5 ((Gcn5(hat/hat) )), which were pr

166 Here we demonstrate a novel role of the acetyltransferase GCN5 in a previously undescribed mecha

167 The Arabidopsis thaliana histone acetyltransferase GCN5 regulates histone modifications a

168 We also find that the acetyltransferase Gcn5 synergizes with Spt3 to promote g

169 eletion of the previously implicated histone acetyltransferase Gcn5, but G1/S cell cycle regulated tr

170 onditional knockout mice for the key histone acetyltransferase Gcn5, which resulted in abnormal chrom

171 mr5) carries a mutation in a putative pectin acetyltransferase gene that confers enhanced resistance

172 hemophilic red alga with the chloramphenicol acetyltransferase gene, rendering this organism insensit

173 spartate (NAA) is synthesized by aspartate N-acetyltransferase (gene: Nat8l) from acetyl-coenzyme A a

174 tes of injury, paralleling increased histone acetyltransferase general transcription factor IIIC subu

175 was recently reported, but the presence of O-acetyltransferase genes in the serotype 35C cps locus su

176 ions in the regulation of BCL6, including in acetyltransferase genes, occur in clinically aggressive

177 coccal serotype 33A has two membrane-bound O-acetyltransferase genes, wciG and wcjE A 33A wcjE-defici

178 ical evidence that glucosamine 6-phosphate N-acetyltransferase (Gna1), a key enzyme in this pathway,

179 regulator with intrinsic kinase and histone acetyltransferase (HAT) activities that activates transc

180 n5 and sirtuins are highly conserved histone acetyltransferase (HAT) and histone deacetylase (HDAC) e

181 Using steady-state histone acetyltransferase (HAT) assays, we show that an RNA bind

182 Notch-binding region of MAML1 to the histone acetyltransferase (HAT) domain of p300 rescues expressio

183 The histone acetyltransferase (HAT) family of proteins performs hist

184 phthora sojae acts as a modulator of histone acetyltransferase (HAT) in plants.

185 Several histone acetyltransferase (HAT) inhibitors with these liabilitie

186 ng Tra1 module, the core module, the histone acetyltransferase (HAT) module and the histone deubiquit

187 Histone acetyltransferase (HAT) p300 and its paralog CBP acetyla

188 eport that PCAF is a fork-associated histone acetyltransferase (HAT) that regulates the stability of

189 and (2) auxin response factor (ARF)-histone acetyltransferase (HAT).

190 and (2) auxin response factor (ARF)-histone acetyltransferase (HAT).

191 modifications, largely regulated by histone acetyltransferases (HAT) and histone deacetylases, have

192 Histone acetyltransferases (HATs) and histone deacetylases (HDAC

193 ined by the antagonistic activity of histone acetyltransferases (HATs) and histone deacetylases (HDAC

194 The genes encoding the histone acetyltransferases (HATs) CREBB-binding protein (CREBBP)

195 We assess the ability of seven histone acetyltransferases (HATs) to catalyze acylations on hist

196 This process is controlled by histone acetyltransferases (HATs/KATs) found in multiprotein com

197 cetyltransferases (KATs, also termed histone acetyltransferases, HATs) catalyze the acetylation of su

198 Lysine acetyltransferases have been shown to regulate various s

199 MYST histone acetyltransferases have crucial functions in transcripti

200 s such as DNA methyltransferases and histone acetyltransferases have revealed a critical role for epi

201 We identify the MYST acetyltransferase HBO1 (also known as KAT7 or MYST2) and

202 , ten-eleven translocation proteins, histone acetyltransferases, histone deacetylases, BET bromodomai

203 ing that it is the second identified protein acetyltransferase in B. subtilis We propose that at leas

204 out to investigate whether the main histone acetyltransferases in budding yeast, Gcn5 and Esa1, poss

205 nts, and the evolutionary origin of mannan O-acetyltransferases in land plants has not yet been studi

206 tion, and presence of functional polyamine N-acetyltransferases in S. aureus and E. faecalis represen

207 ch encodes a plant-specific polysaccharide O-acetyltransferase involved in xylan acetylation.

208 We conclude that the CSRP2BP histone acetyltransferase is a coactivator for CRP2 that works s

209 ells lacking p300 suggested that the histone acetyltransferase is a negative regulator of Hippo pathw

210 ion, and a shortened isoform of Mst2 histone acetyltransferase is expressed.

211 , we explore an emerging concept that lysine acetyltransferase (KAT) enzymes drive cellular plasticit

212 The GCN5 lysine acetyltransferase (KAT) functions together with MYC both

213 th a second chaperone, Vps75, and the lysine acetyltransferase (KAT) Rtt109.

214 f the ubiquitin ligase HUWE1, or the histone acetyltransferase KAT5, top hits from our screens, robus

215 equired for the recruitment of the MYST-type acetyltransferase KAT7 to rDNA loci, resulting in enhanc

216 Lysine acetyltransferases (KATs, also termed histone acetyltran

217 Maternal depletion of MOF acetyltransferase leading to H4K16ac loss causes aberran

218 e compensatory induction of lecithin:retinol acetyltransferase (Lrat) or retinol dehydrogenase 11 (Rd

219 HIV-1 Tat-interacting protein 60 kDa (Tip60) acetyltransferase mediates acetylation at lysine residue

220 Here, we show that histone acetyltransferase MOF plays a critical role in this proc

221 chus, using in situ hybridization of choline acetyltransferase mRNA.

222 uvancy with a staphylococcal peptidoglycan O-acetyltransferase mutant reduces IL-10, increases IL-1be

223 vided a new molecular target, the N-terminal acetyltransferase Naa10p, for harnessing beige-fat bioge

224 be the role of an uncharacterized N-terminal acetyltransferase, NAA50, in the regulation of plant dev

225 ractor and regulator of the actin N-terminal acetyltransferase NAA80, and establish the modus operand

226 interaction partner of the actin N-terminal acetyltransferase NAA80, and further confirm this by ana

227 y identified as an unconventional N-terminal acetyltransferase (NAT) because it localizes to organell

228 NatB is one of three major N-terminal acetyltransferase (NAT) complexes (NatA-NatC), which co-

229 The dominant N-acetyltransferase (Nat) in Arabidopsis (Arabidopsis thal

230 Human N-acetyltransferases (NAT; EC 2.3.1.5) catalyze the N-acet

231 n humans, NTA is catalyzed by seven N(alpha)-acetyltransferases (NatA-F and NatH).

232 out by a family of enzymes called N-terminal acetyltransferases (NATs).

233 ino moiety of many proteins is modified by N-acetyltransferases (NATs).

234 HR), or channelrhodopsin-2 (ChR2) in Choline acetyltransferase neurons (ChAT(+)) or Arch in LIM-homeo

235 sion toxicity assays, we determined that the acetyltransferase NuA4 and deacetylase Rpd3 are primaril

236 n regulation in combination with the histone acetyltransferase NuA4 and histone H2A.Z exchanger SWR1.

237 n N-deacetylase PgdA and the peptidoglycan O-acetyltransferase OatA.

238 Histone modifications and acetyltransferase occupancy were confirmed using ChIP as

239 ype methyltransferases by 2-fold but also an acetyltransferase of another enzyme category when linked

240 ins important for the recruitment of histone acetyltransferases of the MYST family to chromatin.

241 ins important for the recruitment of histone acetyltransferases of the MYST family to chromatin.

242 T signaling, which in turn activates histone acetyltransferase p300 (p300 HAT), leading to changes in

243 ly to the transcriptional regulators histone acetyltransferase P300 (p300), NFkappaB, and CCAAT enhan

244 in protein activation, including the histone acetyltransferase p300 acetylated in its activation loop

245 the transcriptional coactivator and histone acetyltransferase p300 and activates gene expression in

246 We found PARN is primarily acetylated by the acetyltransferase p300 at Lys-566 and deacetylated by si

247 of reconstituting and locally activating the acetyltransferase p300 in mammalian cells.

248 horylation(17-19) stimulates activity of the acetyltransferase p300 in trans, suggesting that H3.3 ac

249 The histone acetyltransferase p300 is normally associated with the A

250 d multiple new players including the histone acetyltransferase p300 that was found to be a primary dr

251 tin association, and associates with histone acetyltransferase p300 to enhance Smad transcriptional a

252 mplex subunit)-1, and reduced recruitment of acetyltransferase p300.

253 ivity was necessary for c-Myc binding to the acetyltransferase p300.

254 nt evidence that FAAP20 is acetylated by the acetyltransferase p300/CBP on lysine 152, the key residu

255 l-CoA and isobutyryl-CoA interacted with the acetyltransferase P300/CBP-associated factor (PCAF) in l

256 ation was associated with elevated levels of acetyltransferase P300/CBP-associated factor (PCAF), whe

257 egradation system, we found that the histone acetyltransferases P300 and CBP maintained H3K27ac abund

258 creased by C646, an inhibitor of the protein acetyltransferases p300/CREB-binding protein (CBP).

259 by binding to the KIX domain of the histone acetyltransferase paralogues CREB-binding protein (CBP)

260 The histone acetyltransferase paralogues p300 and CREB-binding prote

261 laphos resistance (BAR) and phosphinothricin acetyltransferase (PAT) genes, which convey resistance t

262 Here, we report the histone acetyltransferase PCAF (p300/CBP-associated) as a fork-a

263 KAT5 encodes an essential lysine acetyltransferase, previously called TIP60, which is inv

264 ated in algae, their recruitment as mannan O-acetyltransferases probably occurred in bryophytes, and

265 (DHHC3)' was incorrectly referred to as an 'acetyltransferase' rather than an as an 'acyltransferase

266 acting at an early step to regulate histone acetyltransferase recruitment, histone acetylation, and

267 mitoyltransferase ZDHHC3 (DHHC3) as the main acetyltransferase required for the palmitoylation of PD-

268 Of the acetyltransferases responsible for H3K9ac, cholangiocyte

269 known to be N-terminally acetylated, and the acetyltransferases responsible for this modification bel

270 The Spt-Ada-Gcn5-acetyltransferase (SAGA) chromatin-modifying complex is

271 f the TBP-binding module of the Spt-Ada-Gcn5 Acetyltransferase (SAGA) complex, Spt8p and Spt3p.

272 ne modifications as part of the Spt-Ada-Gcn5 Acetyltransferase (SAGA) transcriptional coactivator com

273 r affinity for its natural inhibitor, serine acetyltransferase (SAT), as compared with its affinity f

274 Spermidine/spermine acetyltransferase (SAT1) is the rate-limiting enzyme in

275 ced flux is driven by spermidine/spermine N1-acetyltransferase (SSAT) activity, which acetylates poly

276 We show that spermidine/spermine N-acetyltransferase (SSAT) homologues encoded by S. aureus

277 permine oxidase and spermidine/spermine-N(1)-acetyltransferase (SSAT) when compared with 2,11-Me(2)Sp

278 campestris The P. syringae T3SE HopZ1a is an acetyltransferase that acetylates the pseudokinase AtZED

279 her, this study identifies the first histone acetyltransferase that activates ERalpha expression whic

280 a, suggesting MYST3 functioning as a histone acetyltransferase that activates ERalpha promoter.

281 2) that the Gcn5-related YiaC protein is the acetyltransferase that modifies CobB(L), and 3) that Yia

282 icant homology with some characterized sugar acetyltransferases that modify the C-4 amino group in th

283 We show that the lysine acetyltransferase Tip60 acetylates eEF1A1, whereas the h

284 ing phase of the circadian cycle, the lysine acetyltransferase TIP60 acetylates the transcriptional a

285 The histone acetyltransferase TIP60 was previously shown to suppress

286 uced MARCKS acetylation at lysine 165 by the acetyltransferase Tip60, which is a prerequisite for its

287 cluding histone demethylase LSD1 and histone acetyltransferase Tip60.

288 c leukemia zinc finger protein (MOZ) histone acetyltransferase to the viral promoter, which promoted

289 that AtaT2 is the first GNAT (Gcn5-related N-acetyltransferase) toxin that specifically targets charg

290 ion control, four were not acetylated by two acetyltransferases used in this work, and two were acety

291 Virginiamycin acetyltransferase (Vat) enzymes are resistance proteins

292 We demonstrated that the O-acetyltransferase WciG was functional in serotype 35C bu

293 s canonical role as a cytoplasmic histone H4 acetyltransferase, we isolated a HAT1-containing complex

294 ce, rice and poplar were mannan 2-O- and 3-O-acetyltransferases, whereas the two group I DUF231 membe

295 e kinase1 (SphK1) is an acetyl-CoA dependent acetyltransferase which acts on cyclooxygenase2 (COX2) i

296 e discovery of five cytochrome P450s and two acetyltransferases which catalyze a cascade of reactions

297 cohesion requires the activity of the ESCO2 acetyltransferase, which modifies the Smc3 subunit of co

298 his study enhances our understanding of PG O-acetyltransferases, which could guide the development of

299 s as a platform for recruiting Tip60 histone acetyltransferase with increased H4 acetylation and subs

300 stained association of NFAT and p300 histone acetyltransferase with the IP-10 gene required p38 and c