ライフサイエンスコーパス: glucosyltransferase

1 ts interaction with UDP-glucose:glycoprotein glucosyltransferase.

2 strate in vitro, demonstrating that Nss is a glucosyltransferase.

3 rotein and its characterization as the Ent C-glucosyltransferase.

4 ne promoter and the UDP-glucose:glycoprotein glucosyltransferase.

5 ha1-antitrypsin and UDP-glucose:glycoprotein glucosyltransferase.

6 is then glucosylated by a previously unknown glucosyltransferase.

7 types 6C/6D have wciNbeta encoding alpha-1,3-glucosyltransferase.

8 nd the glucose added by UDP-Glc:glycoprotein glucosyltransferase.

9 a CAP10 domain that functions as a protein O-glucosyltransferase.

10 aride alpha-galactosyltransferases and alpha-glucosyltransferases.

11 on the inhibition of alpha-glucosidases and glucosyltransferases.

12 This fraction contained other glucosyltransferases.

13 ilm-related factors such as antigen I/II and glucosyltransferases.

14 can binding epitopes of mutans streptococcal glucosyltransferases.

15 f similarity to previously characterized UDP-glucosyltransferases.

16 equence similarity to UDP-glucose: flavonoid glucosyltransferases.

17 poxide hydrolases, cytochrome P450s, and UDP-glucosyltransferases.

18 s mutans through the action of a family of 3 glucosyltransferases.

19 ino-acid sequences of several selected yeast glucosyltransferases.

20 ation of two UDP-glucose:monoterpenol beta-d-glucosyltransferases.

21 al ER-localized enzymes, including protein O-glucosyltransferase 1 (POGLUT1) and POFUT1.

22 -fucosyltransferase 1 (POFUT1), or protein O-glucosyltransferase 1 (POGLUT1).

23 exin cycle proteins UDP-glucose:glycoprotein glucosyltransferase 1 (UGGT1), which catalyzes monogluco

24 UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1) is a central quality contro

25 UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1) is a key quality control fa

26 UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1) serves as a folding sensor

27 between TAPBPR and UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1), a folding sensor in the ca

28 ncysting trophozoites, the giardial ceramide glucosyltransferase 1 gene (gglct-1) is transcribed only

29 ence for a role for UDP-glucose:glycoprotein glucosyltransferase 1 in MHC class I assembly.

30 nt and regulated by UDP-glucose:glycoprotein glucosyltransferase 1.

31 Thus we renamed Nss as glucosyltransferase 3 (Gtf3).

32 roteins targeted by UDP-glucose:glycoprotein glucosyltransferase, a chaperone implicated in quality c

33 The glucosyltransferase activities of both toxins are reduce

34 rain Challis derivatives was constructed and glucosyltransferase activities were determined.

35 cifically inhibit TcdB cysteine protease and glucosyltransferase activities, respectively.

36 as-yet-unidentified cytochrome P450 and UDP-glucosyltransferase activities.

37 ss in the presence of sucrose, but normal in glucosyltransferase activities.

38 ntly identified the gene responsible for the glucosyltransferase activity and constructed an isogenic

39 ghlighting the importance of targeting toxin glucosyltransferase activity for future therapy.

40 sinapoylmalate and sinapic acid:UDP-glucose glucosyltransferase activity in brt1 leaves suggest that

41 Additionally, screening for membrane glucosyltransferase activity in membranes from bacterial

42 of toxin A, suggesting that inhibiting toxin glucosyltransferase activity may be effective in combati

43 together, these data suggest that, while the glucosyltransferase activity of SS4 is important for gra

44 rogated the A1H3-mediated enhancement of the glucosyltransferase activity of TcdA in RAW 264.7 cells.

45 poptotic cell death that is dependent on the glucosyltransferase activity of the toxin.

46 Plasmid-borne rgg could increase glucosyltransferase activity only in strains which had a

47 h E. coli membranes revealed the presence of glucosyltransferase activity only in the species most cl

48 mulation of gtfBC recombinants whose reduced glucosyltransferase activity restores a less cariogenic

49 UDP-glucose:pABA glucosyltransferase activity was readily detected in fru

50 mes, we noted that, in addition to protein O-glucosyltransferase activity, both mammalian and Drosoph

51 A glucosyltransferase activity, capable of transferring on

52 The A1H3-dependent enhancement of glucosyltransferase activity, cytoskeleton disruption, a

53 ke fraction showed UDP-glucose: glycoprotein glucosyltransferase activity, the Golgi apparatus-like f

54 e rgg or gtfG promoter also showed decreased glucosyltransferase activity.

55 ing secondary structure, for Rgg to increase glucosyltransferase activity.

56 ted vector sequences had decreased levels of glucosyltransferase activity; plasmid-borne rgg could no

57 KCR1 and the yeast alpha-1,2-glucosyltransferase ALG10 exhibit sequence homology, and

58 wnstream action of the endoplasmic reticulum glucosyltransferases Alg6p, Alg8p and Alg10p, glucosidas

59 nking genes [NADH dehydrogenase (NDUFC2) and glucosyltransferase (ALG8)] appears to be conserved amon

60 fs associated with bacterial pathogenesis, a glucosyltransferase and a protease.

61 The N-terminal glucosyltransferase and autoprotease domains of the toxi

62 a orientalis) the benzoxazinoid-specific UDP-glucosyltransferase and beta-glucosidase that catalyze t

63 Subcellular fractionation indicated that the glucosyltransferase and esterase activities are predomin

64 ry domains, were analyzed for attenuation of glucosyltransferase and glucosylhydrolase activity.

65 lation of NAE 12:0 by a yet to be determined glucosyltransferase and its subsequent malonylation by P

66 vatives of zeatin have been characterized, O-glucosyltransferase and O-xylosyltransferase, occurring

67 ts indicated that lgt1 encodes an alpha(1-2) glucosyltransferase and the lgt2 encodes a beta(1-4) gal

68 vity against mouse-derived ceramide-specific glucosyltransferase and was about half as potent as NB-D

69 uced amino-acid sequences of glucansucrases (glucosyltransferases and dextransucrases) from oral stre

70 ucreyi heptosyltransferase III, the putative glucosyltransferase, and both glycosyltransferases were

71 active against rat-derived ceramide-specific glucosyltransferase, and four of the other eight-membere

72 chemical studies reveal that the domain is a glucosyltransferase, and it catalyses the transfer of gl

73 s including glucan-binding protein B (GbpB), glucosyltransferases, and fructosyltransferase.

74 chaperone; cyclophilin B; ERp72; GRP170; UDP-glucosyltransferase; and SDF2-L1.

75 d to be involved in the translocation of the glucosyltransferase, appears as a large solvent-exposed

76 8 (N-butyldeoxynojirimycin), an inhibitor of glucosyltransferase, as a novel oral treatment for non-n

77 ubsequently, we found that S. mutans-derived glucosyltransferase B (GtfB) itself can promote C. albic

78 g those encoding fructosyltransferase (Ftf), glucosyltransferase B (GtfB), and GtfC, by reverse trans

79 mediated by the S. mutans-derived exoenzyme glucosyltransferase B (GtfB); GtfB readily binds to C. a

80 tion with glucans synthesized using purified glucosyltransferase B, the adherence was significantly e

81 lot analysis revealed that the expression of glucosyltransferases B and D was lower in the RopA-defic

82 sults from recessive mutations affecting the glucosyltransferase B3GLCT, leading to congenital cornea

83 We focus on three enzymes, beta-1,3-glucosyltransferase (B3GLCT), beta-galactoside alpha-2,3

84 FUT2) and is elongated with glucose by beta3-glucosyltransferase (B3GLCT).

85 This protocol involves beta-glucosyltransferase (beta-GT)-mediated protection of 5-h

86 beta-Glucosyltransferase (BGT) is a DNA-modifying enzyme enco

87 r the cysteine-rich UDP-glucose:glycoprotein glucosyltransferase-binding domain.

88 Thus, glucosyltransferase but not cysteine protease activity i

89 d glycosylation 10 homolog (yeast, alpha-1,2-glucosyltransferase); butyrylcholinesterase; dipeptidyl-

90 lly with a crude antigen preparation rich in glucosyltransferase (C-GTF) from Streptococcus mutans, a

91 free or liposomal Streptococcus mutans crude glucosyltransferase (C-GTF) with or without MPL-AF added

92 ependent QC of folding (UDP-Glc:glycoprotein glucosyltransferase, calreticulin, and/or calnexin) was

93 e pathogenesis are TcdA and TcdB, homologous glucosyltransferases capable of inactivating small GTPas

94 Our studies show that Rumi is a protein O-glucosyltransferase, capable of adding glucose to serine

95 of conserved residues typically involved in glucosyltransferase catalysis impairs DNA glucosylation

96 Cell-associated glucosyltransferases catalyze the sucrose-dependent synt

97 e responsible for GlcCer synthesis, ceramide glucosyltransferase (CerGlc transferase), during keratin

98 Ceramide glucosyltransferase (CGT) activity was similar between t

99 o investigate how Gb3 is augmented, ceramide glucosyltransferase (CGT), lactosylceramide synthase (Ga

100 e was also observed in the mRNA for ceramide:glucosyltransferase (CGT), the first of three glycosyltr

101 eported that IroB is an enterobactin (Ent) C-glucosyltransferase, converting the siderophore into mon

102 In-frame mutations of C. rodentium lifA glucosyltransferase (CrGlM21) and protease (CrPrM5) were

103 The gene encoding chlorobactene glucosyltransferase (CT1987) has been named cruC, and th

104 moiety by autoproteolytic processing, and a glucosyltransferase-dependent inactivation of Rho family

105 bimodal mechanism; it induces apoptosis in a glucosyltransferase-dependent manner at lower concentrat

106 Our in vitro data also revealed that glucosyltransferase-derived EPS is a key mediator of cos

107 , which is also an in vitro substrate of the glucosyltransferase, did not influence the toxic effects

108 ed endocytosis, translocation of a catalytic glucosyltransferase domain across the membrane, release

109 single, highly conserved epitope on the TcdB glucosyltransferase domain and blocks productive translo

110 at least two enzymatic domains: an effector glucosyltransferase domain for inactivating host Rho GTP

111 We present crystal structures of the TcdA glucosyltransferase domain in the presence and absence o

112 ), the autoprotease cleaves and releases the glucosyltransferase domain into the cytosol, where GTP-b

113 oteolysis event that releases the N-terminal glucosyltransferase domain into the cytosol.

114 avage of the toxins, releasing an N-terminal glucosyltransferase domain into the host cell cytosol.

115 It was shown that the glucosyltransferase domain of TpeL modifies Ras in vitro

116 restored with autoproteolytic activation and glucosyltransferase domain release.

117 translocation and delivery of an N-terminal glucosyltransferase domain that inactivates host GTPases

118 idomain proteins, each harboring a cytotoxic glucosyltransferase domain that is delivered into the cy

119 ional proteins disrupt cell function using a glucosyltransferase domain that is translocated into the

120 nd autoprocessing activities but vary in the glucosyltransferase domain, consistent with the differen

121 ysteine protease domain, located next to the glucosyltransferase domain.

122 in two beta-sandwiches tightly clasping the glucosyltransferase domain.

123 rocessing occurs after cysteine protease and glucosyltransferase domains translocate into the cytosol

124 ficant structural change in the delivery and glucosyltransferase domains, and thus provides a framewo

125 t, corresponding to the receptor-binding and glucosyltransferase domains, respectively.

126 The C-terminal region contains the catalytic glucosyltransferase domains, which are widely conserved

127 The enzyme UDPglucose:zeatin O-glucosyltransferase (EC 2.4.1.203) was previously isolat

128 nverts benzoic acid to SA, and UDPglucose:SA glucosyltransferase (EC 2.4.1.35), which catalyzes conve

129 solubilizing and purifying UDP-Glc:ceramide glucosyltransferase (EC 2.4.1.80; glucosylceramide synth

130 Distinct from 1,4-alpha-glucan 6-alpha-glucosyltransferases (EC 2.4.1.24) and 4-alpha-glucanotr

131 O-Glucosylation is stereo-specific: the O-glucosyltransferase encoded by the Phaseolus lunatus ZOG

132 H pylori expression of cholesterol-alpha-glucosyltransferase (encoded by cgt) is required for gas

133 ly activates UFGT (UDP-glucose:flavonoid-3-O-glucosyltransferase), encoding the first enzyme of the a

134 The Streptococcus gordonii (Challis) glucosyltransferase-encoding determinant gtfG is regulat

135 d twice, within a seven-day interval, with a glucosyltransferase-enriched preparation (E-GTF) adminis

136 -encoded water-insoluble glucan-synthesizing glucosyltransferase enzyme (GTF-I) from Streptococcus mu

137 model and demonstrates that JGT is the only glucosyltransferase enzyme required for the second step

138 ng (GLU) regions of the mutans streptococcal glucosyltransferase enzymes (GTF) can provide immunity t

139 ngle Glc residue to fully trimmed glycans by glucosyltransferase enzymes (reglucosylation).

140 Glucans synthesized by glucosyltransferase enzymes of oral streptococci facilit

141 g is a positive transcriptional regulator of glucosyltransferase expression.

142 was refined using the T4 bacteriophage beta-glucosyltransferase fold.

143 brane surface charge and the presence of the glucosyltransferase for metabolic channeling.

144 Streptococcus mutans glucosyltransferases form extracellular glucans from suc

145 w type of bacterial 1,4-alpha-glucan 4-alpha-glucosyltransferase from GH31.

146 e of the gene ZOG1 encoding a trans-zeatin O-glucosyltransferase from Phaseolus (EC ), a cis-zeatin-s

147 heless, our data indicate that the alpha-1,2-glucosyltransferase function is a key component of the m

148 on of the NH2-terminal remainder of HUGT1 to glucosyltransferase function is presently unknown.

149 (Kr) drug sensitivity, protects HERG through glucosyltransferase function.

150 precipitates not only AbpA and AbpB but also glucosyltransferase G (Gtf-G) from S. gordonii supernata

151 ielded loss-of-function mutations in the UDP-glucosyltransferase gene UGT74F2.

152 In this paper, the cloning of a glucosyltransferase gene using polymerase-chain-reaction

153 The Streptococcus gordonii glucosyltransferase gene, gtfG, is positively regulated

154 es carrying insertions in the UDP-Glc:sterol glucosyltransferase genes, UGT80A2 and UGT80B1.

155 ransferase (GT), and galactosylhydroxylysine-glucosyltransferase (GGT) activities.

156 about 130 genes in the large gallate 1-beta-glucosyltransferase (GGT) superfamily were detected.

157 lc) from UDP-Glc to GlcNAc, constituting the glucosyltransferase (Glc-T) activity, albeit at an effic

158 port a role for SloR in S. mutans control of glucosyltransferases, glucan binding proteins, and genes

159 A UDP-Glc:glycoprotein glucosyltransferase glucosylates N-glycans of misfolded

160 R proteins, the kinase/nuclease Ire1 and the glucosyltransferase Gpt1, act together to mount an ER st

161 lding sensor enzyme UDP-glucose:glycoprotein glucosyltransferase (GT) as a unique and sensitive indic

162 A glucosyltransferase (GT) of Arabidopsis, UGT71B6, recogn

163 15 co-purifies with UDP-glucose:glycoprotein glucosyltransferase (GT), an essential regulator of qual

164 determine physical and kinetic properties of glucosyltransferase (GTF) adsorbed onto hydroxyapatite (

165 Glucosyltransferase (GTF) enzymes of mutans streptococci

166 ic (CAT) and glucan-binding (GLU) domains of glucosyltransferase (GTF) of mutans streptococci has res

167 Glucans produced by the glucosyltransferase (GTF) of Streptococcus gordonii conf

168 nse factor in human saliva that inhibits the glucosyltransferase (GTF) of Streptococcus mutans, a vir

169 The enzyme glucosyltransferase (GTF) produced by mutans streptococc

170 Streptococcus sobrinus glucosyltransferase (GTF), an enzyme involved in dental

171 nese Nutgall, exhibited strong inhibition of glucosyltransferase (GTF), in vitro adherence and glucan

172 y in the salivary gland vicinity with GBP59, glucosyltransferase (GTF), or phosphate-buffered saline

173 he glucan-binding domain (GLU) of the enzyme glucosyltransferase (GTF), which is an important virulen

174 alytic barrel domain of Streptococcus mutans glucosyltransferase (GTF).

175 pen-reading-frame putatively identified as a glucosyltransferase (gtf-1).

176 combining epitopes from mutans streptococcal glucosyltransferases (GTF) and glucan binding protein B

177 Mutans streptococcal glucosyltransferases (GTF) have been demonstrated to be

178 m functional domains of Streptococcus mutans glucosyltransferases (GTF) have been shown to induce pro

179 Mutation of a glucosyltransferase (Gtf1) gene led to accumulation of a

180 A glucosyltransferase (Gtf3) catalyzes the second step of

181 -binding proteins (AbpA/AbpB), and S. mutans glucosyltransferase (GtfB), affect their respective oral

182 mutans employs a key virulence factor, three glucosyltransferase (GtfBCD) enzymes to establish cariog

183 S. gordonii glucosyltransferase (GtfG) and amylase-binding proteins

184 omparison of the amino acid sequences of the glucosyltransferases (GTFs) of mutans streptococci with

185 been implicated in the enzymatic activity of glucosyltransferases (GTFs) of the mutans group streptoc

186 mostly glucans synthesized by streptococcal glucosyltransferases (Gtfs), provide binding sites that

187 ilarity in its carboxyl-terminal domain with glucosyltransferases (GTFs), the enzymes responsible for

188 lar pattern of key enzymes that produce EPS, glucosyltransferases (Gtfs), while Cheng et al. reported

189 lgt3 was introduced into a defined beta(1-4) glucosyltransferase Haemophilus ducreyi 35000glu- mutant

190 DNAs encoding human UDP-glucose:glycoprotein glucosyltransferase homologues.

191 Mutants of glucosyltransferase I were constructed in which this glu

192 this enzyme is an N-methylanthranilic acid O-glucosyltransferase implicated in the synthesis of avena

193 n, calreticulin and UDP-glucose:glycoprotein glucosyltransferase in the folding and quality control o

194 tein folding sensor UDP-glucose:glycoprotein glucosyltransferase in the Golgi complex.

195 onse in Arabidopsis and interacts with a UDP-glucosyltransferase in the nucleus.

196 clones) and demonstrated the LH3 function as glucosyltransferase in type I collagen.

197 characterize nine ripening-related UGTs (UDP-glucosyltransferases) in Fragaria that function in the g

198 cose (UDP-Glc) is a common substrate used by glucosyltransferases, including certain bacterial toxins

199 dependent manner at lower concentrations and glucosyltransferase-independent necrotic death at higher

200 eling of UGT2B7 with related plant flavonoid glucosyltransferases indicates human UGTs share a common

201 regulation of uda-1 favors hydrolysis of the glucosyltransferase inhibitory product UDP to UMP, and t

202 We demonstrate that a CesA glucosyltransferase initiates glucan polymerization by u

203 These data suggest that lgt3 encodes a glucosyltransferase involved in the addition of a beta(1

204 (ER) protein GT1 (UDP-glucose: glycoprotein glucosyltransferase) is the central enzyme that modifies

205 UGT707B1 is a new glucosyltransferase isolated from saffron (Crocus sativu

206 hibitory product of the UDP-Glc:glycoprotein glucosyltransferase, it is likely to promote reglucosyla

207 possible candidate for the base J-associated glucosyltransferase (JGT) in trypanosomatid genomes.

208 ne effector of Legionella pneumophila is the glucosyltransferase Lgt1, which modifies serine 53 in ma

209 oethanolamine (PEA) transferase, and LgtG, a glucosyltransferase, mediate the substitution of PEA or

210 ytosis, pore formation, autoproteolysis, and glucosyltransferase-mediated modification of host substr

211 Taken together, we conclude that this new glucosyltransferase mediates the second step of Fap1 gly

212 The N-glucosyltransferase (N-GT) responsible for this activity

213 characterized by a mutation in the protein O-glucosyltransferase, Notch signaling is impaired in a te

214 The glucosyltransferase of M. luteus, which participates in

215 A second ORF had homology to the LgtF (glucosyltransferase) of Neisseria meningitidis.

216 is catalyzed either by UDP-glucose:ceramide glucosyltransferase or by UDP-galactose:ceramide galacto

217 analog is turned over by the toxin in either glucosyltransferase or glucosylhydrolase reactions.

218 In this study, the UDP-glucose:pABA acyl-glucosyltransferase (pAGT) activity in Arabidopsis extra

219 The Drosophila protein O-glucosyltransferase (Poglut) Rumi regulates Notch signal

220 A UDP-glucose:protein O-glucosyltransferase (Poglut/Rumi) transfers O-glucose to

221 wed that BRT1 (At3g21560) encodes UGT84A2, a glucosyltransferase previously shown to be capable of us

222 1 activation controlled UDP-glucose ceramide glucosyltransferase production, thereby tipping the bala

223 r aspartate 162 in the chemical step for the glucosyltransferase reaction and a role for aspartate 15

224 consequent loss of activity in the membrane glucosyltransferase reaction of membrane-derived oligosa

225 eins as active or inhibitory in the membrane glucosyltransferase reaction.

226 ions of the protein for participation in the glucosyltransferase reaction.

227 Implications for glucosyltransferase regulation and applicability to othe

228 4-HPAA reductase and tyrosol:UDP-glucose 8-O-glucosyltransferase, respectively, to complete salidrosi

229 These contained the glucosyltransferase responsible for reglucosylation of m

230 ensitive to the gene dosage of the protein O-glucosyltransferase Rumi.

231 analysis confirmed the absence of a 155-kDa glucosyltransferase S (Gtf-S) from GMS315 protein profil

232 The tobacco UDP-glucose:salicylic acid glucosyltransferase (SA GTase) capable of forming both S

233 A cDNA encoding solanidine glucosyltransferase (SGT) was isolated from potato.

234 aize (Zea mays) gene (cisZOG1) encoding an O-glucosyltransferase specific to cis-zeatin lends further

235 Because UDP-glucose:glycoprotein glucosyltransferase sustains calnexin binding, its alter

236 Rumi is a protein O-glucosyltransferase that adds glucose to EGF repeats wit

237 This gene encodes an O-glucosyltransferase that attaches glucose sugars to seri

238 2), which is made by a UDP-Glc: glycoprotein glucosyltransferase that is part of a conserved N-glycan

239 lgtF gene of C. jejuni encodes a two-domain glucosyltransferase that is responsible for the transfer

240 l antiserum against UDP-glucose:glycoprotein glucosyltransferase that likely functions in glycoprotei

241 lity control is the UDP-glucose:glycoprotein glucosyltransferase that targets unfolded glycoproteins

242 d B of Clostridium difficile are UDP-glucose glucosyltransferases that exert their cellular toxicity

243 C. difficile toxins TcdA and TcdB are UDP-glucosyltransferases that monoglucosylate and thereby in

244 ively), homologous (47% amino acid identity) glucosyltransferases that target small GTPases within th

245 ively), homologous (47% amino acid identity) glucosyltransferases that target small GTPases within th

246 Structures of the N-terminal glucosyltransferase, the cysteine protease, and the C-te

247 ace proteins for maximum host cell invasion: glucosyltransferase, the sialic acid-binding protein Hsa

248 These include glucosyltransferases, their glucan products, and protein

249 We use the T4 bacteriophage beta-glucosyltransferase to transfer an engineered glucose mo

250 ial toxins, including all of the clostridial glucosyltransferase toxins and various MARTX toxins.

251 on porcine tissue, encoded for by the enzyme glucosyltransferase UDP galactose:beta-D-galactosyl-1, 4

252 The enzyme UDP-glucose ceramide glucosyltransferase (Ugcg) catalyzes the initial step of

253 GSL biosynthetic enzyme UDP-glucose ceramide glucosyltransferase (UGCG).

254 1) and GSLs by deleting UDP-glucose ceramide glucosyltransferase (UGCG).

255 to glucosylceramide via UDP-glucose ceramide glucosyltransferase (UGCG).

256 UDP-glucose:glycoprotein glucosyltransferase (UGGT) is a presumed folding sensor

257 eyed by the 170-kDa UDP-glucose:glycoprotein glucosyltransferase (UGGT).

258 UDP-glucose:glycoprotein glucosyltransferase (UGGT1) acts as a central component

259 lity control factor UDP-glucose:glycoprotein glucosyltransferase (UGGT1) in a novel, BiP- and CNX-ind

260 functional characterization of a phenol UDP-glucosyltransferase (UGT) from the silkworm, Bombyx mori

261 UDP-glucose:glycoprotein glucosyltransferase (UGT) is a soluble protein of the en

262 chinery, the enzyme UDP glucose glycoprotein glucosyltransferase (UGT1).

263 Sterol glucosyltransferase, Ugt51/Atg26, is essential for both

264 The Arabidopsis type 1 UDP-glucose-dependent glucosyltransferase UGT72B1 is highly active in conjugat

265 A UDP-glucosyltransferase, UGT72E1 (At3g50740), was identified

266 ize a putative UDP-glucose:thiohydroximate S-glucosyltransferase, UGT74B1, to determine its role in t

267 In particular, the glucosyltransferase UGT78G1, previously identified as sh

268 In previous work we identified the glucosyltransferase UgtP as a division inhibitor respons

269 n was identified as UDP-glucose:glycoprotein glucosyltransferase (UGTR), the endoplasmic reticulum (E

270 analysis of the multigene family of Group 1 glucosyltransferases (UGTs) of Arabidopsis thaliana reve

271 O-glucose (D3G), by secondary metabolism UDP-glucosyltransferases (UGTs).

272 This epitope is synthesized by the enzyme glucosyltransferase uridine 5'-diphosphate galactose:bet

273 ication of a UDP-glucose:monoterpenol beta-d-glucosyltransferase (VvGT7).

274 of its mobility on native gradient gel, the glucosyltransferase was estimated to have a molecular ma

275 rom Phaseolus (EC ), a cis-zeatin-specific O-glucosyltransferase was isolated from maize.

276 For one cis-eQTL (at B3GALTL, beta-1,3-glucosyltransferase), we conducted follow-up single nucl

277 Two uridine diphosphate glucosyltransferases were functionally characterized; UG

278 ese cytokinins to serve as substrates to the glucosyltransferases were in a large part correlated wit

279 ipid synthases (DGD1, DGD2, and Chloroflexus glucosyltransferase) were introduced into the dgd1-1 mut

280 at lgtF encodes the UDP-glucose:LOS-beta-1,4-glucosyltransferase which attaches the first glucose res

281 cription of fatty acid elongase and ceramide glucosyltransferase, which are critical for the synthesi