ライフサイエンスコーパス: glucosyltransferase

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

2 ts interaction with UDP-glucose:glycoprotein glucosyltransferase.

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

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

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

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

7 is then glucosylated by a previously unknown glucosyltransferase.

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

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

10 lyzed by uridine diphosphate (UDP)-dependent glucosyltransferases.

11 aride alpha-galactosyltransferases and alpha-glucosyltransferases.

12 on the inhibition of alpha-glucosidases and glucosyltransferases.

13 This fraction contained other 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 ilm-related factors such as antigen I/II and glucosyltransferases.

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

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

20 ino-acid sequences of several selected yeast glucosyltransferases.

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

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

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

24 associated proteins UDP-glucose:glycoprotein glucosyltransferase 1 (UGGT1) and glucosidase II (GlucII

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

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

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

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

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

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

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

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

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

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

35 The glucosyltransferase activities of both toxins are reduce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 monstrate that PI3P binding activates LtpM's glucosyltransferase activity toward protein substrates.

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

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

54 A glucosyltransferase activity, capable of transferring on

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 8 (N-butyldeoxynojirimycin), an inhibitor of glucosyltransferase, as a novel oral treatment for non-n

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

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

82 es revealed that S. mutans-derived exoenzyme glucosyltransferase B (GtfB), which binds to the fungal

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

84 ALG10B (alpha-1,2-glucosyltransferase B protein) is a known interacting pr

85 ) was identified in ALG10B-encoded alpha-1,2-glucosyltransferase B protein.

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

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

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

89 dactyly, is caused by mutations in the beta3-glucosyltransferase (B3GLCT) gene.

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

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

92 a1-3-fucose (GlcFuc) disaccharide by beta1,3-glucosyltransferase (B3GLCT).

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

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

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

96 Thus, glucosyltransferase but not cysteine protease activity i

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

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

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

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

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

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

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

104 Cell-associated glucosyltransferases catalyze the sucrose-dependent synt

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

106 Ceramide glucosyltransferase (CGT) activity was similar between t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

124 restored with autoproteolytic activation and glucosyltransferase domain release.

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

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

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

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

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

130 body that binds to an epitope on the toxin B glucosyltransferase domain.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

149 Glucans synthesized by glucosyltransferase enzymes of oral streptococci facilit

150 g is a positive transcriptional regulator of glucosyltransferase expression.

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

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

153 Streptococcus mutans glucosyltransferases form extracellular glucans from suc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 15 co-purifies with UDP-glucose:glycoprotein glucosyltransferase (GT), an essential regulator of qual

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

174 Glucosyltransferase (GTF) enzymes of mutans streptococci

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

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

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

178 The enzyme glucosyltransferase (GTF) produced by mutans streptococc

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

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

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

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

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

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

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

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

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

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

189 A glucosyltransferase (Gtf3) catalyzes the second step of

190 oreover, S. parasanguinis inhibits S. mutans glucosyltransferase (GtfB) activity, which is important

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

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

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

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

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

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

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

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

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

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

201 Mutants of glucosyltransferase I were constructed in which this glu

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

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

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

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

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

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

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

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

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

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

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

213 ) and in POGLUT1, an endoplasmic reticulum O-glucosyltransferase involved in Notch signaling.

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

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

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

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

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

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

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

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

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

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

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

225 The glucosyltransferase of M. luteus, which participates in

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

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

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

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

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

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

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

233 1 activation controlled UDP-glucose ceramide glucosyltransferase production, thereby tipping the bala

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

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

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

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

238 Implications for glucosyltransferase regulation and applicability to othe

239 4-HPAA reductase and tyrosol:UDP-glucose 8-O-glucosyltransferase, respectively, to complete salidrosi

240 These contained the glucosyltransferase responsible for reglucosylation of m

241 Regulator gene of glucosyltransferase (Rgg) family proteins, such as Rgg2

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

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

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

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

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

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

248 The glucosyltransferase TcdB from Clostridium difficile, a w

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

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

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

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

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

254 NULE BOUND STARCH SYNTHASE (GBSS), the major glucosyltransferase that synthesises amylose, and the di

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

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

257 o toxins, toxin A (TcdA) and toxin B (TcdB), glucosyltransferases that modulate monomeric G-protein f

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

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

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

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

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

263 These include glucosyltransferases, their glucan products, and protein

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

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

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

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

268 y enzyme encoded by the UDP-glucose ceramide glucosyltransferase (UGCG) gene.

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

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

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

272 UDP-glucose:glycoprotein glucosyltransferase (UGGT) 1 and 2 are central hubs in t

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

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

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

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

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

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

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

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

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

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

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

284 Here, we report the 3D structure of the UDP-glucosyltransferase UGT76G1, including a complex of the

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

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

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

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

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

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

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

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

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

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

295 Two uridine diphosphate glucosyltransferases were functionally characterized; UG

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

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

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

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

300 UGGT1 was the dominant glucosyltransferase with a preference toward large plasm