ライフサイエンスコーパス: glycosyltransferase

1 l diacylglycerol synthesized by a processive glycosyltransferase.

2 by cellulose synthase, a processive family-2 glycosyltransferase.

3 ucleotide-activated form, acting as a Leloir glycosyltransferase.

4 nes encodes a protein that is likely to be a glycosyltransferase.

5 perty not previously described for any other glycosyltransferase.

6 a systemic supply of FKRP protein acting as glycosyltransferase.

7 ransferase domain and a predicted C-terminal glycosyltransferase.

8 d serine-rich repeat adhesins by a series of glycosyltransferases.

9 process regulated by the availability of key glycosyltransferases.

10 ntrasted with common properties of canonical glycosyltransferases.

11 to the cell membrane and is hence exposed to glycosyltransferases.

12 endogenous nucleotide sugar transporters and glycosyltransferases.

13 nto LacNAc and then elaborated by a panel of glycosyltransferases.

14 s, whose interactions can be tuned by Fringe glycosyltransferases.

15 cy of IgA1 via coordinated modulation of key glycosyltransferases.

16 new mechanistic insight into this family of glycosyltransferases.

17 ns of functionally distinct glycosidases and glycosyltransferases.

18 anisms responsible for Golgi localization of glycosyltransferases.

19 novel feature not observed before for lipid glycosyltransferases.

20 mmalian expression vectors encoding specific glycosyltransferases.

21 tion of sequentially acting glycosidases and glycosyltransferases.

22 T/JBP, pyrimidine hydroxymethylases, Mom and glycosyltransferases.

23 cture even in the presence of the other five glycosyltransferases.

24 sting that they are synthesized by retaining glycosyltransferases.

25 diverse range of substrates required for the glycosyltransferases.

26 the nucleotide-sugar substrates required by glycosyltransferases.

27 separately from related Golgi-resident GT32 glycosyltransferases.

28 hat CgT represents a new member of GT-A-type glycosyltransferases.

29 s then extended to up to 11 HMOs by 4 robust glycosyltransferases.

30 by virtue of the inherent specificity of the glycosyltransferases.

31 amine (UDP-GlcNAc), a substrate for cellular glycosyltransferases.

32 inds the sugar nucleotide UDP-glucose, as do glycosyltransferases.

33 ouse model was generated to excise exostosin glycosyltransferase 1 (Ext1) in keratin 14-positive cell

34 dentified a unique hybrid protein dGT1 (dual glycosyltransferase 1) that contains two distinct domain

35 We show that the glycosyltransferases 1 and 2 (GT1 and GT2) are responsib

36 yzed by the integral membrane lipid-to-lipid glycosyltransferase 4-amino-4-deoxy-L-arabinose transfer

37 18 from SW1990 cells increased levels of UDP-glycosyltransferase 8 and miR-218 was found to bind to i

38 H3 looks like a glycosyltransferase, a family of enzymes that transfer c

39 ped FKRP might circulate as an extracellular glycosyltransferase, able to exert a "glycan remodelling

40 at such that the cleavage region lies in the glycosyltransferase active site above uridine diphosphat

41 ure of a previously disordered region in the glycosyltransferase active site and discuss its implicat

42 action of a polymerase (WbdA) containing two glycosyltransferase active sites.

43 d have widespread and significant impacts on glycosyltransferase activities and would be responsible

44 oreover, so far unknown chitin hydrolase and glycosyltransferase activities were detected using GlcNA

45 d TarS with respective alpha- and beta-(1-4) glycosyltransferase activities.

46 ase and five sequentially acting cytoplasmic glycosyltransferase activities.

47 Cargos of sugar donor substrates for glycosyltransferase activity have also been reported in

48 NleB glycosyltransferase activity inhibited GAPDH-TRAF3 bindi

49 Heparin binding and glycosyltransferase activity may be involved in the func

50 tein-protein interaction and crucial for the glycosyltransferase activity of CgT in vitro and in vivo

51 l number of enzyme activities comprising the glycosyltransferase activity of class A PBP1b and the D,

52 rate Srr2-GlcNAc, concurrently abolished the glycosyltransferase activity of GtfC, and also altered g

53 Inhibition was dependent on the glycosyltransferase activity of NleB.

54 The glycosyltransferase activity of PBP1A, which aids in the

55 bpX is responsible for most of the essential glycosyltransferase activity.

56 Homologous glycosyltransferases alpha-(1-->3)-N-acetylgalactosaminy

57 nstrated that the enzyme is active as both a glycosyltransferase and an HCF-1 protease.

58 njugates that takes advantage of recombinant glycosyltransferases and a corresponding sugar nucleotid

59 ile lineages by mutagenesis of five putative glycosyltransferases and biosynthetic genes.

60 ivity of a repertoire of proteins, including glycosyltransferases and glycosidases.

61 ately related to the spatial distribution of glycosyltransferases and glycosyl hydrolases within the

62 nzymatic labeling (or SEEL) uses recombinant glycosyltransferases and nucleotide-sugar analogues to a

63 neer glycans using different permutations of glycosyltransferases and to investigate biosynthetic pat

64 such as the kinetoplastid J-base generating glycosyltransferase (and its homolog GREB1), the catalyt

65 PG synthase with glycan chain polymerizing (glycosyltransferase) and peptide cross-linking (transpep

66 iver is the most noted among the circulatory glycosyltransferases, and decorates marrow hematopoietic

67 ent signaling pathways regulated by O-GlcNAc glycosyltransferase are thus fundamental for T cell biol

68 Cells containing PbpX as their sole glycosyltransferase are viable, and the loss of pbpX lea

69 g target for control of the pathogen, as the glycosyltransferases are absent from mammalian hosts.

70 Multiple glycosyltransferases are essential for the proper modifi

71 Sizable pools of freely circulating glycosyltransferases are in blood, but understanding the

72 y ligation assay, we found that all examined glycosyltransferases are in the vicinity of these UDP-su

73 y conserved, the specific roles of different glycosyltransferases are poorly understood.

74 genetic analyses, we found that Caulobacter glycosyltransferases are primarily redundant but that Pb

75 Two closely related glycosyltransferases are responsible for the final step

76 O-linked-beta-N-acetylglucosamine (O-GlcNAc) glycosyltransferase as compared with naive cells.

77 neer glycans using different permutations of glycosyltransferases as well as to investigate biosynthe

78 Homologous glycosyltransferases assemble a similar core trisacchari

79 nvolving BcsE and the PilZ domain containing glycosyltransferase BcsA.

80 pparatus by a series of glycan synthases and glycosyltransferases before export to the wall.

81 a protein-specific transfer of GalNAc by the glycosyltransferases beta4GalNAc-T3/T4.

82 in the center of the plant secondary product glycosyltransferase box (A389V) reduced the enzymatic ac

83 gle amino acid changes in cps genes encoding glycosyltransferases can alter substrate specificities,

84 ts a convenient strategy to rapidly optimize glycosyltransferase catalysts for the synthesis of compl

85 A series of glycosyltransferases catalyze sequential glycosylation o

86 integration of the general reversibility of glycosyltransferase-catalyzed reactions, artificial glyc

87 Mutations in several known or putative glycosyltransferases cause glycosylation defects in alph

88 that they both belong to the branch-forming glycosyltransferase cluster, but are distantly related a

89 we examined the functions of three capsular glycosyltransferases (Cps2F, Cps2G, and Cps2I) involved

90 ike-acetylglucosaminyltransferase (LARGE)--a glycosyltransferase critical for DG function.

91 ly required for induction of Fut7 and Gcnt1, glycosyltransferases critical for selectin ligand biosyn

92 mal and pathological conditions, but several glycosyltransferase-deficient mice exhibit no or only mi

93 cdB-L543A, delayed toxicity in mice, whereas glycosyltransferase-deficient TcdB demonstrated no toxic

94 Here we show that microinjection of the glycosyltransferase domain Afp18(G) into zebrafish embry

95 llographic model for inhibition of the PBP1b glycosyltransferase domain by the potent substrate analo

96 The peptidoglycan glycosyltransferase domain of PBP1b is also considered a

97 cated between the coiled-coil region and the glycosyltransferase domain of SS4.

98 proteolytic fragment containing the putative glycosyltransferase domain was tested in isolation for a

99 mer in which each blade contains a GT-B-type glycosyltransferase domain with a typical Rossmann fold.

100 The csaA gene product contains a predicted glycosyltransferase domain with structural homology to G

101 mes (ORFs) were found to contain a conserved glycosyltransferase domain.

102 a helices in addition to a typical GT-A-type glycosyltransferase domain.

103 we propose the linkage specificities of the glycosyltransferase domains are conserved in KpsC homolo

104 KpsC contains two retaining beta-Kdo glycosyltransferase domains belonging to family GT99 tha

105 rases (ppGalNAc-Ts) on catalytic activity of glycosyltransferases during O-GalNAc glycan biosynthesis

106 n vivo glycoengineering technologies and the glycosyltransferase-enabled in vitro engineering method,

107 pids are synthesized by a single promiscuous glycosyltransferase encoded by the ORF atu2297, with UDP

108 of Xoc flagellin was altered by deletion of glycosyltransferase-encoding rbfC, but this had little e

109 or is regulated in part by the repertoire of glycosyltransferase enzymes (which make the glycan ligan

110 beta-Kdo counterparts were not identified as glycosyltransferase enzymes by bioinformatics tools and

111 The precise glycosyltransferase enzymes that mediate selectin-ligand

112 Analyses of glycosyltransferase expression identified fucosyltransfe

113 ypoxia, suggesting that hypoxia up-regulates glycosyltransferase expression required for F77 antigen

114 f the STELLO proteins indicate that they are glycosyltransferases facing the Golgi lumen.

115 epresented among the 98 currently recognized glycosyltransferase families in the Carbohydrate-Active

116 Mammalian members of glycosyltransferase family 6 (GT6) of the CAZy database

117 gene, At3g57630, in clade E of the inverting Glycosyltransferase family GT47 as a candidate for the t

118 e of the adaptation by trypanosomes of beta3-glycosyltransferase family members to catalyze beta1-2 g

119 ests that the parasite has adapted the beta3-glycosyltransferase family to catalyze beta1-2 linkages.

120 hat TbGT15, another member of the same beta3-glycosyltransferase family, encodes an equally divergent

121 ted C-terminal GT-B domain and defines a new glycosyltransferase family, GT97, in CAZy (Carbohydrate-

122 ses with similarity to the mammalian beta1-3-glycosyltransferase family.

123 Distinct features of a novel glycosyltransferase fold from a domain of unknown functi

124 erases; therefore, we designate it as a GT-D glycosyltransferase fold.

125 IBP was first catalyzed by P450, and then by glycosyltransferase, followed by further storage or meta

126 rimetric screen to enable the engineering of glycosyltransferases for combinatorial sugar nucleotide

127 ngs to a large family of membrane-associated glycosyltransferases for which the understanding of the

128 how that due to the asymmetric effect of the glycosyltransferase Fringe, different outcomes are gener

129 found that Toxoplasma utilizes a cytoplasmic glycosyltransferase from an ancient clade of CAZy family

130 tidine monophosphate-Kdo-dependent alpha-Kdo glycosyltransferase from LPS assembly is well characteri

131 f new mechanisms to regulate the activity of glycosyltransferases from the Golgi apparatus.

132 An isogenic mutant of the glycosyltransferase gacI, which is defective for GlcNAc

133 -undecaprenol (GlcNAc-P-Und) produced by the glycosyltransferase GacI.

134 Our results also suggested that a GT-C glycosyltransferase, GacL, transfers GlcNAc from GlcNAc-

135 ene, a lipB (kpsS)-like gene, and a putative glycosyltransferase gene designated csaA (capsule synthe

136 ant (DeltaepsE) lacking the putative priming glycosyltransferase gene located within a predicted eps

137 Furthermore, inactivation of each glycosyltransferase gene resulted in differentially impa

138 agellin glycosylation, including a predicted glycosyltransferase gene that is linked to the flagellin

139 The glycosyltransferase gene, Ext1, is essential for heparan

140 P716Y1 with oxidosqualene cyclase, P450, and glycosyltransferase genes available from other plant spe

141 I (TbGnTI) among a set of putative T. brucei glycosyltransferase genes belonging to the beta3-glycosy

142 Analysis of the expression of key glycosyltransferase genes revealed that p38alpha signali

143 an biosynthesis in mycobacteria involves two glycosyltransferases, GlfT1 and GlfT2, which have been t

144 ormation of this polymer is catalyzed by the glycosyltransferase GlfT2, a processive carbohydrate pol

145 tribution of processing machineries, such as glycosyltransferases, glycosidases, and nucleotide sugar

146 s created by the collaborative activities of glycosyltransferases, glycosidases, nucleotide-sugar tra

147 Although the glycosyltransferases (glycoTs) constructing selectin-lig

148 discovered that the gene Mgat3 encoding the glycosyltransferase GnT-III is elevated in epithelial ov

149 ified by five sugars via the action of three glycosyltransferases, Gnt1, PgtA, and AgtA, which are re

150 The movement of a putative glycosyltransferase, GntB, requires the Sar1 and ARF1 GT

151 re members of the carbohydrate-active enzyme glycosyltransferase (GT) 31 family (CAZy GT31) involved

152 in validates the overall fold of the modeled glycosyltransferase (GT) domain.

153 Bioinformatics analyses identified two glycosyltransferase (GT) domains in CslB.

154 rstood, largely because of the resistance of glycosyltransferase (GT) enzymes to structural character

155 es, however, have only revealed two distinct glycosyltransferase (GT) folds, GT-A and GT-B.

156 WbbB contains three glycosyltransferase (GT) modules.

157 We have extracted putative glycosyltransferase (GT) sequences from the grape genome

158 mannosyltransferase A (PimA) is an essential glycosyltransferase (GT) that initiates the biosynthetic

159 e EpsHIJK proteins suggest EpsH and EpsJ are glycosyltransferases (GT) with a GT-A fold; EpsI is a GT

160 SuS belongs to family 4 of the glycosyltransferases (GT4) and contains an E-X7-E motif

161 lyzed the mechanism by which the cytosolic O-glycosyltransferase GtfA/B of Streptococcus gordonii mod

162 own previously that gtfA and gtfB encode two glycosyltransferases, GtfA and GtfB, that catalyze the t

163 O-antigen can be modified by the activity of glycosyltransferase (gtr) operons acquired by horizontal

164 The glycosyltransferases (GTs) are an important and function

165 Three glycosyltransferases (GTs) are involved (WbdN, WbdO and

166 zymes such as glycoside hydrolases (GHs) and glycosyltransferases (GTs) are of growing importance as

167 al MUCILAGE-RELATED (MUCI) genes that encode glycosyltransferases (GTs) involved in the production of

168 c analysis identified six main proteins: two glycosyltransferases (GTs) TaGT43-4 and TaGT47-13; two p

169 core subset of 152 genes encoding cell wall glycosyltransferases (GTs).

170 Like glycosyltransferases, H3 binds UDP-glucose, as shown by

171 the first time that a Michaelis complex of a glycosyltransferase has been described, and it clearly s

172 More than 33,000 glycosyltransferases have been identified.

173 their organizational interplay and show that glycosyltransferase homomers are assembled in the endopl

174 is predicted to possess a typical GT-A-type glycosyltransferase, however, the activity remains unkno

175 ion of a dual specificity cis-AB blood group glycosyltransferase in complex with a synthetic UDP-GalN

176 previously unrecognized role for a specific glycosyltransferase in driving a CSC state.

177 nd instead promotes the phosphorylation of a glycosyltransferase in the biosynthetic pathway, thereby

178 e regulated by a protein that helps retain a glycosyltransferase in the Golgi.

179 understanding of the function of glycan and glycosyltransferase in the tumorigenesis, progression an

180 d as essential for the Golgi localization of glycosyltransferase in yeast.

181 Predictions for the function of two UDP-glycosyltransferases in flavonoid metabolism were confir

182 However, the function of other glycosyltransferases in glycosylation of Srr2 is unknown

183 l processes mediated by 2 distinct groups of glycosyltransferases in oral streptococci that are impor

184 Consistently, new evidences reported glycosyltransferases in the blood, freely circulating or

185 sugars, which serve as donor substrates for glycosyltransferases in the lumen of Golgi vesicles and

186 rcially available and recombinantly produced glycosyltransferases including key N-acetylglucosaminylt

187 creased abundance of transcripts for several glycosyltransferases indicated the enzymes that may be i

188 kely be exploited for the development of new glycosyltransferase inhibitors and probes.

189 RG-II in cell elongation and the utility of glycosyltransferase inhibitors as new tools for studying

190 udy, we show that using moenomycin and other glycosyltransferase inhibitors as templates, we were abl

191 The approach can generate highly specific glycosyltransferase inhibitors.

192 ations affecting exostosin-like 3 (EXTL3), a glycosyltransferase involved in heparan sulfate (HS) bio

193 e genes identified was lpsB, which encodes a glycosyltransferase involved in lipopolysaccharide (LPS)

194 nt with the predicted functions of the WbkD (glycosyltransferase involved in the biosynthesis of the

195 R XYLEM9-LIKE [IRX9L]) encodes a family GT43 glycosyltransferase involved in xylan backbone biosynthe

196 d most known dystroglycanopathy genes encode glycosyltransferases involved in glycan synthesis.

197 fold of ppGalNAc-Ts in enzymatic activity of glycosyltransferases involved in the O-glycan biosynthes

198 role in the process; thus understanding the glycosyltransferases involved is key to identifying new

199 role in the process, thus understanding the glycosyltransferases involved is key to identifying new

200 These data indicate that the glycosyltransferase is surprisingly promiscuous in its s

201 This glycosyltransferase is thus a prime target for the devel

202 and dependent on the expression of both like-glycosyltransferase (LARGE) and partially functional FKR

203 HepII) are controlled by phase-variable LOS glycosyltransferase (lgt) genes; we sought to define how

204 We show that this process requires the glycosyltransferase lh3 and that post-injury expression

205 this binding requires Mg(2+) Mutation of the glycosyltransferase-like metal ion binding motif in H3 g

206 synthesis, while UPEX1 encodes a family GT31 glycosyltransferase likely involved in galactosylation o

207 dentified colonization genes, epaX encodes a glycosyltransferase located in a variable region of the

208 Thus, bryophytes and algae likely lack the glycosyltransferase machinery required to synthesize api

209 In harmony with their natural tasks, glycosyltransferases may in vitro complete the imperfect

210 y studies have suggested the significance of glycosyltransferase-mediated macromolecule glycosylation

211 ontaining multiple cellulose synthase (CESA) glycosyltransferases mediates cellulose microfibril form

212 ing transcription factors, cytochrome P450s, glycosyltransferases, methyltransferases and transporter

213 on between nucleotide sugar transporters and glycosyltransferases might be a more common phenomenon t

214 These results explain how the glycosyltransferase modifies a progressively changing su

215 We study the functional role of glycosyltransferases modifying type B flagellin in the 0

216 Substitution of the predicted DXD glycosyltransferase motif with alanine residues abolishe

217 nt fibroblasts, while microarray analysis of glycosyltransferase mRNAs detected modestly increased ex

218 nd LAM molecules produced by three different glycosyltransferase mutants of Mycobacterium smegmatis w

219 s only partially disrupted in several of the glycosyltransferase mutants.

220 the cytoplasm and is mediated by a soluble N-glycosyltransferase (NGT) that uses nucleotide-activated

221 glycosylation system mediated by a soluble N-glycosyltransferase (NGT).

222 One such effector is the arginine glycosyltransferase NleB1 (NleB(CR) in C. rodentium) tha

223 We identified the bacterial glycosyltransferase NodC as an appropriate model system

224 uences is cleaved by the nutrient-responsive glycosyltransferase, O-linked N-acetylglucosamine (O-Glc

225 ransferase referred to here as PgfS (protein glycosyltransferase of streptococci).

226 This is based on the observation that glycosyltransferases often tolerate chemical modificatio

227 ar mechanism of the toxin component Afp18 as glycosyltransferase opens new perspectives in studies of

228 Phloretin-2'-O-glycosyltransferase (P2'GT) catalyzes the last glycosyla

229 example, Caulobacter crescentus encodes six glycosyltransferase paralogs of largely unknown function

230 T-IV, and GnT-V in cells revealed that these glycosyltransferases, particularly GnT-IV, play importan

231 previously shown that loss of a conserved O-glycosyltransferase (PGANT4) in Drosophila results in ab

232 These synthetic enzymes each possess a PG glycosyltransferase (PGT) domain and a transpeptidase (T

233 ers to the pathway in which Protein N- and O-glycosyltransferases (PGTases) sequentially add monosacc

234 mpounds that bind to bacterial peptidoglycan glycosyltransferases (PGTs) and inhibit cell wall biosyn

235 that perform these reactions, polyisoprenyl-glycosyltransferases (PI-GTs) include dolichol phosphate

236 Bacterial glycosyltransferases play important roles in bacterial f

237 t, mice double heterozygous for Jag1 and the glycosyltransferase, Poglut1 (Rumi), start showing a sig

238 l interaction between GOLPH3 and a mammalian glycosyltransferase, POMGnT1, which is involved in the O

239 n display unexpected promiscuity, with human glycosyltransferase pp-alpha-GanT2 able to utilize both

240 saminyltransferase (LARGE) is a bifunctional glycosyltransferase previously shown to hyperglycosylate

241 Such a dual glycosyltransferase-protease activity, which occurs in t

242 Thus, from a dual glycosyltransferase-protease, essentially single-activit

243 Levels of UDP-glycosyltransferase protein and messenger RNA were assoc

244 The H3 crystal structure shows that it has a glycosyltransferase protein fold.

245 Reconstitution of the glycosyltransferase reactions in extracts with radioacti

246 Mammalian glycosyltransferases recognize only the terminal LacNAc

247 anscribed with SMU.2067, encoding a putative glycosyltransferase referred to here as PgfS (protein gl

248 h the physiological function of blood stream glycosyltransferases remains unclear, they are likely re

249 cell surface glycans where remotely produced glycosyltransferases remodel surfaces of target cells an

250 transferase 1 gene (Pofut1), which encodes a glycosyltransferase required for NotchR-mediated cell-ce

251 Typically, glycosyltransferases reside within the intracellular sec

252 fferent SD proteins that are modified by two glycosyltransferases, SdgA and SdgB.

253 The glycosyltransferase ST6Gal-I, which adds alpha2-6-linked

254 The S-glycosyltransferase SunS is a recently discovered enzyme

255 osyltransferase genes belonging to the beta3-glycosyltransferase superfamily.

256 Among these is the glycosyltransferase TarM, a component of the WTA de novo

257 reatly increased in CSCs; (ii) among various glycosyltransferases tested, mRNA levels for ST3GAL5, B4

258 O-GlcNAc transferase (OGT) is the glycosyltransferase that acts to install O-GlcNAc onto p

259 Thus, UGT708A6 is a bifunctional glycosyltransferase that can produce both C- and O-glyco

260 deletion of bshA (sa1291), which encodes the glycosyltransferase that catalyzes the first step of BSH

261 thin a GBS-specific gene encoding a putative glycosyltransferase that confers resistance to HMOs, sug

262 Lunatic Fringe (Lfng), a glycosyltransferase that enhances Notch activation by Dl

263 FKRP gene encodes for a glycosyltransferase that in vivo transfers a ribitol pho

264 mannosyltransferase A (PimA) is an essential glycosyltransferase that initiates the biosynthetic path

265 cNAc transferase (OGT) is a serine/threonine glycosyltransferase that is essential for development an

266 demonstrated that lymphostatin is a putative glycosyltransferase that is important in intestinal colo

267 NleB is a glycosyltransferase that modifies host proteins with N-a

268 Glycosyltransferases that act on polyprenol pyrophosphat

269 l, deeply conserved family of plant-specific glycosyltransferases that add arabinose sugars to divers

270 hway nor the roles of many known or putative glycosyltransferases that are essential for this process

271 mediators in vivo by engineering solubilized glycosyltransferases that attach galactose or sialic aci

272 ted organizational interplay between Golgi N-glycosyltransferases that involves dynamic and organelle

273 ically relevant substrates of small-molecule glycosyltransferases that often show broad sugar accepto

274 esized by membrane-integrated and processive glycosyltransferases that polymerize UDP-activated gluco

275 It is synthesized by membrane-embedded glycosyltransferases that processively polymerize UDP-ac

276 Quantitative PCR gene expression studies of glycosyltransferases that regulate display of sLe(X) rev

277 model, we highlight new features of several glycosyltransferases that sequentially modify the serine

278 motile DeltahpsE-G strain, which lacks three glycosyltransferases that synthesize hormogonium polysac

279 n to chaperones or other known regulators of glycosyltransferases, the ENPP3-mediated hydrolysis of n

280 This step is vital because glycosyltransferases, the enzymes mediating the glycosyl

281 Thus, DUF1792 represents a new family of glycosyltransferases; therefore, we designate it as a GT

282 is study reports the discovery of a second S-glycosyltransferase, ThuS, and shows that ThuS catalyzes

283 d compounds could be selectively extended by glycosyltransferases to give libraries of asymmetrical m

284 ic strategy, using a limited number of human glycosyltransferases, to access a collection of 60 asymm

285 e detected; however, activities of the other glycosyltransferases together with bioinformatic analyse

286 N-terminal DUF1792 is a novel GT-D-type glycosyltransferase, transferring Glc residues to Glc-Gl

287 s study, we determine that CgT is a distinct glycosyltransferase, transferring GlcNAc residues to Glc

288 cluding a phage protein and a phase-variable glycosyltransferase ubiquitous among the diverse set of

289 UDP-glycosyltransferase (UGT) plays a major role in the dive

290 The human UDP glycosyltransferase (UGT) superfamily comprises four fam

291 ed to involve a family 1 UDP-sugar dependent glycosyltransferase (UGT) to facilitate acetophenone acc

292 th similarity to terpene URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASES (UGTs) from Arabidopsis (Arabidopsi

293 The glycosyltransferase WaaG is involved in the synthesis of

294 uding cytochrome P450 monooxygenases and UDP-glycosyltransferases, was shared between both treatments

295 As expected for a glycosyltransferase, we found that RDN1 and RDN2 protein

296 candidate gene in this region encodes a GT61 glycosyltransferase, which has been implicated in arabin

297 ntibiotic moenomycin that inhibits bacterial glycosyltransferases, which are essential for peptidogly

298 I pilins are O-glycosylated through the TfpO glycosyltransferase with a single subunit of O-antigen (

299 arge clostridial toxins, which are retaining glycosyltransferases with a DXD motif involved in bindin

300 ted a family of putative UDP-sugar-dependent glycosyltransferases with similarity to the mammalian be

301 Glycosyltransferases WreG, WreE, WreS, and WreT would ea