ライフサイエンスコーパス: transferase

1 alpha-4-amino-4-deoxy-l-arabinose arabinosyl transferase).

2 ched its function from oxidoreductase to FeS transferase.

3 indicated that AvrRpm1 may be an ADP-ribosyl transferase.

4 of cytochrome P450 1A but not glutathione S-transferase.

5 subunits of N-acetylglucosamine-1-phosphate transferase.

6 n and harbored arr-3, a rifampin ADP-ribosyl transferase.

7 -3, a rifampin adenosine diphosphate-ribosyl transferase.

8 mily, the polypeptide N-acetylgalactosaminyl transferases.

9 CGFS-type (class II) Grxs act as FeS cluster transferases.

10 noglycoside modifying enzymes or rRNA methyl transferases.

11 ence also occurs in MGAT4A and MGAT4B GlcNAc-transferases.

12 tose synthase and potentially other glycosyl-transferases.

13 uding MYB transcription factors and glycosyl transferases.

14 gh its interaction with arginyl-tRNA protein transferase 1 (Ate1), a component of the Arg/N-degron pa

15 through the key molecule carnitine palmitoyl transferase 1 (CPT1), it is possible to reverse or slowd

16 stal structure of WT human dimethyladenosine transferase 1 (DIMT1), an 18S rRNA N (6,6)-dimethyladeno

17 tein O-mannose beta1, 2-N-acetylglucosaminyl transferase 1 (POMGnT1), an enzyme involved in O-mannosy

18 nt ICA genes encoding two tRNA(His) guanylyl transferase 1 units evolved ~120 million years ago durin

19 ses in cyclophylin F and carnitine palmitoyl transferase 1A and reductions in mitofusin1, peroxiredox

20 increased expression of carnitine palmitoyl transferase 1a, the rate-limiting enzyme of FAO, in acti

21 calized polypeptide N-acetyl-d-galactosamine-transferase 2 isoenzyme.

22 res and degrees of terminal deoxynucleotidyl transferase 2'-deoxyuridine, 5'-triphosphate nick end la

23 Terminal deoxynucleotidyl transferase 2'-Deoxyuridine, 5'-Triphosphate nick end la

24 se, alkaline phosphatase, and gamma-glutamyl transferase: - 27.2, - 7.2, - 39.2, and - 16.3 IU/L, res

25 sociated with uridine diphosphate glucuronyl transferase 2B7 metabolism of morphine were identified.

26 %; P = 0.029 versus placebo), gamma-glutamyl transferase (-30%; P < 0.001), alanine aminotransferase

27 of 29 histone de-methylases, 5 of 20 acetyl-transferases, 5 of 19 de-acetylases, 1 of 4 DNA methyl-t

28 ted histone variants, 8 of 52 histone methyl-transferases, 5 of 29 histone de-methylases, 5 of 20 ace

29 ncoding butyryl-coenzyme A (CoA):acetate-CoA-transferase, a major enzyme in butyrate metabolism (OR =

30 y necessary alpha-helix in human glutathione transferase A1-1 (hGSTA1-1).

31 that it adopts the aryl-alkylamine-N-acetyl transferase (AANAT) fold, which is unprecedented in NRPS

32 However, carbene transferases accepting heterocyclic substrates are scarc

33 e hamster ovary cells with the core 2 GlcNAc transferase acting on a mucin-type O-glycoprotein displa

34 pe Grx with a CxxC/S-type loop abolished FeS transferase activity and activated the oxidative half re

35 nzyme activities but maintains glutathione S transferase activity and glutathione levels.

36 at.AG significantly increased histone acetyl-transferase activity and promoter histones H3 and H4 ace

37 these data indicate that AvrRpm1 ADP-ribosyl transferase activity contributes to virulence by promoti

38 Not only is this a report of carbene transferase activity in a completely de novo protein, bu

39 is not a substrate for the glutathione (GSH) transferase activity of GST P1-1.

40 -end of RNA template influences the terminal transferase activity of the RT.

41 Twelve transferase activity related genes had significant corre

42 te (UDP-GalNAc), nuclear polypeptide GalNAc -transferase activity, and a GalNAc transferase (polypept

43 active-site mutations on both stability and transferase activity, and identified new functional moti

44 In cells with chronically inhibited farnesyl transferase activity, in vitro farnesylation and electro

45 18 (K18), caspase cleaved K18, glutathione S-transferase alpha, alpha-fetoprotein, arginase-1, osteop

46 Here, we show that glutathione transferase alpha4 (GSTA4), a member of the Phase II det

47 of these species with a phosphopantetheinyl transferase and a ketoreductase domain are unaffected by

48 tes were functional, based on gamma glutamyl transferase and alkaline phosphatase activity and prolif

49 Levels of gamma glutamyl transferase and alkaline phosphatase were measured in ch

50 sis on large gene families for glutathione S-transferase and carboxylesterase detoxification enzymes.

51 rase, hemoglobin A1C (P<.05), gamma-glutamyl transferase and development of type 2 diabetes (P<.01).

52 ne Oxidoreductase 1, Carnitine Palmitoyl-CoA Transferase and mitochondrial respiratory complexes sugg

53 oaches, we identified WbmV as the UDP-GlcNAc transferase and noted that WbmW represents a UDP-Galf-de

54 the stress signaling and Gcn5 histone acetyl transferase and transcription factors, together altering

55 es, 5 of 19 de-acetylases, 1 of 4 DNA methyl-transferases and 0 of 3 DNA de-methylases were abundant

56 -terminal module similar to N(10)-formyl-THF transferases and a C-terminal module homologous to enoyl

57 ing scaffolds for the development of nitrene transferases and demonstrates the value of mechanism-dri

58 could be reduced by generating single-action transferases and immobilizing them on individual columns

59 ional modification synthetized by ADP-ribose transferases and removed by poly(ADP-ribose) glycohydrol

60 s of years, driven by CG-specific DNA methyl transferases and spontaneous methyl-cytosine deamination

61 O-acetyltransferase, an N-acetylglucosamine transferase, and a KDO transferase consistent with the s

62 m levels of aminotransferase, gamma-glutamyl transferase, and bilirubin.

63 osyltransferase, EptA, a phosphoethanolamine transferase, and the AlmEFG tripartite system, which is

64 -reactive absorbance capacity, glutathione-S-transferase, and total glutathione content.

65 omatin-modifiers such as PRC2 and DNA methyl-transferases, and proteins governing chromosome architec

66 spartate aminotransferase, or gamma-glutamyl transferase; and low numbers of platelets were associate

67 We used myriocin (a serine palmitoyl transferase antagonist) and two SK inhibitors (SKI-II an

68 The flavin transferase ApbE plays essential roles in bacterial phys

69 fs for S-acylation to occur, and many S-acyl transferases appear to have lax substrate specificity, w

70 novel hps loci, primarily encoding glycosyl transferases, are identified.

71 P450, GSH S-transferases, glucosyl and other transferases, aryl acylamidase, and others.

72 log of eptA, a predicted phosphoethanolamine transferase, as critical for antimicrobial defense.

73 dergoes efficient arginylation by an arginyl transferase (ATE1).

74 l link between the branched-chain amino acid transferase BCAT-1 and the neurodegenerative movement di

75 he nutrient-sensing protein modifier OGlcNAc transferase (betaOGTKO) causes beta-cell failure and dia

76 l PBP2x transpeptidase and its FtsW glycosyl transferase-binding partner relative to FtsZ treadmillin

77 Nmnat (nicotinamide mononucleotide adenylyl transferase), but requires the c-Jun N-terminal kinase (

78 , and increased expression of choline acetyl transferase by neurons (P < .001).

79 enaline-synthesizing enzyme, phenyl-N-methyl transferase, by adrenal chromaffin cells and changes in

80 as the SAM-dependent 3-amino-3-carboxypropyl transferase catalyzing this modification and thereby ext

81 KI-mediated activation of the histone-acetyl transferase CBP.

82 are limited by the lack of complete peptidyl transferase center (PTC) active site mutational analyses

83 on of the 5S RNP, maturation of the peptidyl transferase center (PTC) and the nascent polypeptide exi

84 al RNA segments that constitute the peptidyl transferase center (PTC) and those that connect PTC with

85 de rearrangements that suppress the peptidyl transferase center (PTC) catalytic activity stimulated b

86 e essential for the function of the peptidyl transferase center (PTC).

87 ance to antibiotics that target the peptidyl transferase center and exit tunnel of the ribosome.

88 ons at every rRNA nucleotide of the peptidyl transferase center and isolating gain-of-function varian

89 yo-EM analysis revealed a malformed peptidyl transferase center in the misassembled 50S subunits.

90 1 eviction from the pre-60S permits peptidyl transferase center maturation, and allows Yvh1 to mediat

91 ommodation corridor en route to the peptidyl transferase center of the large ribosomal subunit.

92 ction localized in proximity to the peptidyl transferase center of the large subunit of the ribosome.

93 graphy and reveals it to occupy the peptidyl transferase center P-site of the ribosome.

94 ed near the decoding center and the peptidyl transferase center, respectively.

95 perturbed by SrmB deletion, but the peptidyl transferase center, the uL7/12 stalk, and 30S contact si

96 d in the upper part close to the polypeptide transferase center, while in the lower part, it is subst

97 CCA end is improperly docked in the peptidyl transferase center.

98 end of deacyl-tRNA departs from the peptidyl transferase center.

99 he ribosome functional decoding and peptidyl transferase centers.

100 sions during accommodation into the peptidyl transferase centre.

101 imated by stereology) loss of choline acetyl-transferase (ChAT)-immunoreactive motoneurons which rema

102 and correlated with changes in alcohol acyl-transferase (CmAAT1) gene expression.

103 stroke included histo-blood group ABO system transferase, coagulation factor XI, scavenger receptor c

104 Nicotinamide adenylyl transferase condenses nicotinamide mononucleotide and (t

105 n N-acetylglucosamine transferase, and a KDO transferase consistent with the structure we report.

106 TE4 (which encodes a gamma-tocopherol methyl transferase converting gamma-tocopherol into alpha-tocop

107 evealed that all five known arabinofuranosyl transferases could process the exogenous lipid-linked su

108 active-site geometries, hemoprotein "carbene transferases" could provide an alternative to traditiona

109 factor CsMYB75 and phi (F) class glutathione transferase CsGSTF1 as being associated with anthocyanin

110 olangiocyte markers including gamma glutamyl transferase, cytokeratin 19, epithelial cellular adhesio

111 DNA methyl transferase (Dam MTase) and microRNA (miRNA).

112 th its cognate toxin Rv0059 (DNA ADP-ribosyl transferase, DarT(Mtb) ), to mediate reversible DNA ADP-

113 catalytic glutamate in the mono-ADP ribosyl transferase domain of the SdeA, thus blocking the ubiqui

114 Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and phospho-h

115 nick end labeling terminal deoxynucleotidyl transferase dutp nick end labeling [TUNEL] expression).

116 c acid-Schiff) and terminal deoxynucleotidyl transferase dUTP nick end labeling assay, Kim1 mRNA asse

117 emical techniques, terminal deoxynucleotidyl transferase dUTP nick end labeling staining, and immunoh

118 or A [VEGF-A], and terminal deoxynucleotidyl transferase dUTP nick end labeling terminal deoxynucleot

119 a lower density of terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL)-positive dyi

120 Terminal deoxynucleotidyl transferase dUTP nick end-labelling assay, SYTOX((R)) gr

121 evidenced by both terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) assay and imm

122 the commonly used terminal deoxynucleotidyl transferase dUTP nick-end labeling assay or methods base

123 ased the number of terminal deoxynucleotidyl transferase dUTP nick-end labeling positive cells in the

124 -CoA production by dihydrolipoamide succinyl-transferase (E2o).

125 n and zinc transporters were upregulated and transferase-encoding genes, for example UDP-glucoronosyl

126 CUTIN SYNTHASE1 (CUS1), an acyl transferase enzyme that links cutin monomers, contribute

127 ell as the activity of the ADP-ribose (ADPR) transferase enzymes (PARP family members) that catalyze

128 mentation assays, we probed recombinant flax transferase enzymes, previously shown to contribute to P

129 Through the addition of prenyl transferases, farnesyl diphosphates, (2E,6E)-FDP and (2Z

130 -O-Me globally by inhibiting the rRNA methyl-transferase fibrillarin in human cells.

131 l, the substrate for the ribitol-5-phosphate transferases FKRP and FKTN.

132 d MALDI-MS to verify eptA as an ethanolamine transferase for the lipid-A portion of V. fischeri lipop

133 As nucleotidyl transferases, formation of a covalent enzyme-adenylate i

134 onal modification of ribosomal peptides, and transferases from various biosynthesis pathways.

135 onfirmed the interaction using glutathione-S-transferase fusion pull-down.

136 Polypeptide N-acetylgalactosaminyl transferases (GalNAc-Ts) initiate mucin type O-glycosyla

137 al GlcNAc, followed by sialylation by sialyl transferases gave 12 differently fucosylated and sialyla

138 ote cytokinin biosynthesis by an ISOPENTENYL TRANSFERASE gene, PpIPT3.

139 henotypes, including elevated gamma-glutamyl transferase (GGT) and alanine aminotransferase (ALT), an

140 e aminotransferase (AST), and gamma-glutamyl transferase (GGT) at 52 weeks, for improvement in (1) li

141 gamma-glutamyl-transferase (GGT) is a key enzyme in GSH homeostasis, an

142 urinary biomarkers including gamma-glutamyl transferase (GGT), alanine aminopeptidase (AAP), and N-a

143 cumference, triglyceride, and gamma-glutamyl transferase (GGT).

144 prenoid chains via the enzyme geranylgeranyl transferase (GGTase) II.

145 resistances include cytochromes P450, GSH S-transferases, glucosyl and other transferases, aryl acyl

146 Fhb7 encodes a glutathione S-transferase (GST) and confers broad resistance to Fusari

147 Antioxidant enzymes from the glutathione S-transferase (GST) family may protect against these lung

148 r, potential interactions with glutathione S-transferase (GST) genes due to reduced antioxidant funct

149 e, we show that the Drosophila glutathione S-transferase (GST) Gfzf prevents mitochondrial hyperfusio

150 Here, we probed the role of glutathione transferase (GST) P1-1, an antiapoptotic protein often o

151 Glutathione S-transferase (GST) pull-down experiments found novel bind

152 g amino acids 313 to 549, by a glutathione S-transferase (GST) pulldown assay.

153 with or without an N-terminal glutathione S-transferase (GST) tag, resulting in monomeric or obligat

154 ously postulated function as a glutathione S-transferase (GST).

155 T) C(4) synthase (LTC(4)S) and glutathione S-transferases (GSTs) [microsomal GST (mGST)2, mGST3, and

156 ad bacteria use stereospecific glutathione S-transferases (GSTs) called beta-etherases to cleave the

157 Here, we report that glutathione S-transferases (GSTs), particularly GSTM1, promote proinfl

158 and co-IP demonstrated that the glutathione transferase GSTU4, which is coexpressed with Trp- and ca

159 s direct modification by one of three prenyl-transferases, has been an area of fairly settled science

160 The genes encoding the histone acetyl-transferases (HATs) CREB binding protein (CREBBP) and EP

161 es of MraY and its human paralog, GlcNAc-1-P-transferase, have provided insights into MraY inhibition

162 amoyl CoA:shikimate/quinate hydroxycinnamoyl transferase (HCT) or loss of function of cinnamoyl CoA r

163 amoyl-CoA:shikimate/quinate hydroxycinnamoyl transferase (HCT), and caffeoyl shikimate esterase (CSE)

164 proteins that classified as oxidoreductases, transferases, hydrolases, lyases, and ligases.

165 d receptor (PPAR)-alpha, carnitine palmitoyl transferase I (CPT1)a, peroxisomal membrane protein 70 (

166 ia targeted deletion of N-acetylglucosaminyl transferase I (Mgat1) markedly reduced cellularity in th

167 Acutely increased carnitine palmitoyl transferase I in normal rodent hearts has been shown to

168 th prenyl-transferase, namely geranylgeranyl-transferase-III (GGTase-III) (Kuchay et al, 2019; Shirak

169 sphingolipids by inhibiting serine palmitoyl transferase in response to elevated ceramide levels.

170 ith Pi*MZ had lower levels of gamma-glutamyl transferase in serum and lower LSMs than adults with the

171 (DeltaN)) functions as a phosphoethanolamine transferase in vitro with substrate preference for cellu

172 As glutathione transferases in other plants are known to act as transpo

173 upregulation of Trithorax group H3K4-methyl-transferases in StMSI1-OE Chromatin immunoprecipitation-

174 This effect was reversed by farnesyl transferase inhibitors and by the addition of geranylger

175 to block Rac1 prenylation as geranylgeranyl transferase inhibitors were effective in inhibiting HIV-

176 nt protein kinase A, a ubiquitous phosphoryl transferase involved in a myriad of cellular processes.

177 yl or geranylgeranyl), as well as the prenyl-transferases involved can be inferred by protein sequenc

178 port here that Gcn5, a paradigm lysyl-acetyl transferase (KAT) modifying both histone and non-histone

179 atients have mutations in the histone methyl-transferase KMT2D.

180 y hepatocyte proliferation and alanine amino transferase levels peaking at day 5 to 7 normalized agai

181 A short-chain cis-prenyl transferase (LfCPT1) first produces the rare diterpene p

182 atidylglycerol:prolipoprotein diacylglyceryl transferase (Lgt) recognizes a conserved lipobox motif w

183 cytochrome P450, shikimate hydroxycinnamoyl transferase, lysine decarboxylase, and acyltransferase g

184 eaved, and acylated by a membrane-bound acyl transferase (MBOAT).

185 determined by the terminal deoxynucleotidyl transferase mediated deoxyuridine triphosphate nick end

186 ssociation between a marker of glutathione S-transferase mediated metabolic resistance and Plasmodium

187 athway and OGT (O-linked N-acetylglucosamine transferase)-mediated protein O-GlcNAcylation.

188 is as shown by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling and DNA frag

189 NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay was pe

190 ath as assessed by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling staining and

191 munochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nickend labeling assay.

192 s confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling assay

193 Glutathione S-transferase metabolic resistance is potentially increasi

194 (extent of resection, methyl-guanine-methyl-transferase (MGMT) promoter methylation, age, Karnofsky

195 lpha, histone acetylation and histone acetyl-transferase modulate the increased replication of HIV-1-

196 3-Mercaptopyruvate sulfur transferase (MPST) catalyzes the desulfuration of 3-merc

197 GSTM1 encodes glutathione S-transferase mu-1 (GSTM1), which belongs to a superfamily

198 wisdom with the discovery of a fourth prenyl-transferase, namely geranylgeranyl-transferase-III (GGTa

199 telomerase was a specific telomere-terminal transferase necessary for the replication of chromosome

200 rt glucose to rhamnose and the five glycosyl transferases needed to build the repeating pentasacchari

201 f the nicotinic acid mononucleotide adenylyl-transferase Nma1 and can be bypassed by overexpressing t

202 lipidation across eukaryotes and N-myristoyl transferase (NMT) has been proposed as an attractive dru

203 habditis elegans and identified the O-GlcNAc transferase OGT-1 as an EEL-1 binding protein.

204 study, we probed the importance of O-GlcNAc transferase (OGT) activity for the survival of tamoxifen

205 er assays revealed that both O-GlcNAcylation transferase (OGT) and EZH2 are posttranscriptionally inh

206 e beta-d-GlcNAc sugar (O-GlcNAc) by O-GlcNAc-transferase (OGT) and O-GlcNAc removal by O-GlcNAcase (O

207 stablished by two opposing enzymes: O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA).

208 nce and accuracy of the assay using O-GlcNAc transferase (OGT) as a model system through detailed Mic

209 pathway (YAP) is O-GlcNAcylated by O-GlcNAc transferase (OGT) at serine 109.

210 O-Linked N-acetylglucosamine transferase (OGT) catalyzes O-GlcNAcylation of target pr

211 at countering age-related decreased O-GlcNAc transferase (OGT) expression and O-GlcNAcylation amelior

212 mine biosynthetic pathway (HBP) and O-GlcNAc transferase (OGT) for Drosophila homeodomain-interacting

213 ly, many transcriptional effects of O-GlcNAc transferase (OGT) inhibition were due to the activation

214 O-GlcNAc transferase (OGT) is an X-linked gene product that is es

215 O-GlcNAc transferase (OGT) is responsible for the addition of Glc

216 Suppressing O-GlcNAc signaling by O-GlcNAc transferase (OGT) knockout enhances macrophage proinflam

217 While in animals, O-GlcNAc transferase (OGT) modifies thousands of intracellular pr

218 lexed with O-linked beta-N-acetylglucosamine transferase (OGT) only in cells that had normal genomic

219 O-GlcNAc transferase (OGT) regulates a wide range of cellular pro

220 encode enzymes for its attachment (O-GlcNAc transferase (OGT)) and removal (O-GlcNAcase (OGA)).

221 Deletion of O-GlcNAc transferase (OGT), a key enzyme for protein O-GlcNAcylat

222 the enzyme that adds O-GlcNAc, the O-GlcNAc transferase (OGT), and the enzyme that removes O-GlcNAc,

223 me that catalyzes O-GlcNAcylation - O-GlcNAc-transferase (OGT), and the extent of protein O-GlcNAcyla

224 roteins with O-GlcNAc, catalyzed by O-GlcNAc transferase (OGT), is an abundant posttranslational even

225 A single essential enzyme, O-GlcNAc transferase (OGT), is responsible for all nucleocytoplas

226 ed that the nutrient-sensing enzyme O-GlcNAc transferase (Ogt), which catalyzes an O-GlcNAc-modificat

227 ilitates O-GlcNAcylation of PKM2 by O-GlcNAc transferase (OGT).

228 Glutathione S-transferase omega-1, an ECM-modifying enzyme, was signif

229 istones H3 and H4 by means of histone methyl transferases or histone demethylases.

230 the enzyme that installs O-GlcNAc (O-GlcNAc transferase, or OGT) and the enzyme that removes O-GlcNA

231 %) in the exopolysaccharide priming-glycosyl transferase (p-gtf).

232 be attenuated by silencing of glutathione S-transferase P1 (GSTP1), a mediator of metabolic alterati

233 ancer sites of genes regulated by the acetyl transferase p300 and by N1ICD or the N1ICD target MYC an

234 n and the recruitment of HBx, histone acetyl-transferase P300 and histone deacetylase 1 (HDAC1) to ci

235 ed that SvBAHD05 is a p-coumaroyl coenzyme A transferase (PAT) mainly involved in the addition of pCA

236 A family of Protein S-Acyl Transferases (PATs) is responsible for this reaction.

237 of RARalpha, RXRalpha and the lysine acetyl transferase PCAF in AGAP2 promoter.

238 xpression of phosphatidylethanolamine methyl transferase (PEMT).

239 athogenesis-related gene PR-1, glutathione-S-transferase, phospholipid hydroperoxide glutathione pero

240 ine on target proteins such as glutathione S-transferase pi (GSTP), serum albumin, or Keap1.

241 uinoneimine (NAPQI) with human glutathione S-transferase pi (hGSTP), human serum albumin (HSA), and b

242 re with two active subunits, the ADP ribosyl transferase PltA and the DNase CdtB, linked to a pentame

243 A gene cluster encoding a cryptic trans-acyl transferase polyketide synthase (PKS) was identified in

244 e GalNAc -transferase activity, and a GalNAc transferase (polypeptide GalNAc-T3).

245 and virulence depends on phosphopantetheinyl transferase (PptT), an enzyme that transfers 4'-phosphop

246 ication catalyzed by Protein aRginine Methyl Transferases (PRMTs).

247 TRANSPARENT TESTA19 (TT19), a glutathione S-transferase proposed to bind and stabilize anthocyanins,

248 ent enzymes from the luciferase-like hydride transferase protein superfamily in the biosynthesis of b

249 if IgG binding to the generic glutathione-S-transferase protein was observed, with 659 (2.0%) sample

250 The structures of these WTA transferases provide new insight into the binding of lip

251 sed site-directed mutagenesis, glutathione S-transferase pulldown experiments, immunofluorescence, mo

252 al approaches (colocalization, glutathione S-transferase pulldown, coimmunoprecipitation, yeast two-h

253 ON TRANSPORTER 4 (PvOCT4), and GLUTATHIONE S-TRANSFERASE (PvGSTF1) that are highly upregulated by ars

254 ccessive magnesium-dependent polynucleotidyl transferase reactions, 3' processing and strand transfer

255 ne 3-hydroxylase and different glutathione S-transferases related with their vacuolar transport were

256 e polyisoprenyl-phosphate hexose-1-phosphate transferase responsible for initiating repeat unit synth

257 e polyisoprenyl-phosphate hexose-1-phosphate transferase responsible for priming O-antigen synthesis.

258 resulting compounds by a recombinant fucosyl transferase resulted in only modification of the natural

259 ion of versatile trans-acting 2'-5' adenylyl transferase ribozymes for covalent and site-specific RNA

260 Ribonucleotidyl transferases (rNTases) add untemplated ribonucleotides t

261 ease activity of succinyl-CoA:3-ketoacid-CoA transferase (SCOT) activity, the rate-limiting enzyme of

262 yltransferase SPINDLY (SPY) and the O-GlcNAc transferase SECRET AGENT (SEC) are two prominent O-glyco

263 l. found that mutation of the histone methyl transferase SEDT2 affects alternative splicing fates of

264 +-dependent deacetylase and mono-ADP-ribosyl transferase SIRT6 stabilizes the genome by promoting DNA

265 Sugar nucleotidyl transferases (SNTs) catalyze nucleotidyltransfer reactio

266 W83) predicted to encode a serine palmitoyl transferase (SPT)-the enzyme that catalyzes the first co

267 mutation in N-acetylglucosamine-1-phosphate transferase subunits alpha and beta (GNPTAB) found in hu

268 lyomavirus(-) cells express serine palmitoyl transferase subunits and sphingosine kinase (SK) 1/2 mRN

269 -1 as a protein that binds recombinant GSH S-transferase-tagged PP2A-B55alpha.

270 e-resistant oligonucleotides and 3'-terminal transferase tailing.

271 uclease I (Exo I), terminal deoxynucleotidyl transferase (TdT) and methylene blue.

272 such as Pol mu and terminal deoxynucleotidyl transferase (TdT) are important components for the nonho

273 UV light activates Terminal deoxynucleotidyl Transferase (TdT) for spatially-selective synthesis on a

274 pendent polymerase terminal deoxynucleotidyl transferase (TdT) in kinetically controlled conditions.

275 trast to Poltheta, terminal deoxynucleotidyl transferase (TdT) is unable to use RNA as a substrate al

276 e features suggest terminal deoxynucleotidyl transferase (TdT) primes replication slippage through N-

277 e-stranded-DNA via terminal-deoxynucleotidyl-transferase (TdT) prior to initiation of BST-DSN reactio

278 Terminal deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end labeling

279 ssed low levels of terminal deoxynucleotidyl transferase (TdT).

280 leotides) added by terminal deoxynucleotidyl transferase (TdT).

281 sence of target by terminal deoxynucleotidyl transferase (TdT).

282 a leukemic marker (terminal deoxynucleotidyl transferase, TdT), and we successfully used spectral unm

283 s CCA to tRNAs in a eukaryote; a nucleotidyl transferase that adds nucleotides to RNA without apparen

284 MGAT1 is the GlcNAc-transferase that initiates complex and hybrid N-glycan s

285 existence of diversity for xanthophyll acyl transferases that could be exploited to increase lutein

286 l the presence of an assembly of interacting transferases that may facilitate the channeling of PUFA

287 r enzymes function as polymerising agents or transferases that modify lignins and facilitate interact

288 significantly higher levels of glutathione S-transferase theta 2 (GSTT2) mRNA in squamous mucosa from

289 , aspartate aminotransferase, gamma-glutamyl transferase, tissue inhibitor of metalloproteinase 1, C-

290 the expression of branched-chain amino acid transferase to terminate the reproductive cycle.

291 (TcdA), toxin B (TcdB) and the C. difficile transferase toxin (CDT)(2).

292 (TcdA), toxin B (TcdB), and the C. difficile transferase toxin (CDT).

293 abeling platform wherein a terminal uridylyl transferase (TUTase) was repurposed to generate clickabl

294 tochrome P450 (CYP), uridine glucuronic acid transferase (UGT), and sulfotransferase (SULT)) in their

295 had elevated liver weights and serum alanine transferase values.

296 Increasing level of gamma-glutamyl transferase was also associated with reduced odds of any

297 lucoronosyltransferase and Serine-glyoxylate transferase, were downregulated.

298 imarily mediated by the ZDHHC13 protein-acyl transferase, whether increasing MC1R palmitoylation repr

299 nce reveals the role of diverse acyl protein transferases (zDHHC) in controlling ion channel S-acylat

300 The protein acyl transferase ZDHHC5 was recently proposed to regulate tra