ライフサイエンスコーパス: glycosyl

1 has been developed to obtain enantiopure 2-C-glycosyl-3-nitrochromenes.

2 -elimination, yielded chiral enantiopure 2-C-glycosyl-3-nitrochromenes.

3 vel boronic acid-amine copromoter system for glycosyl acceptor activation.

4 ond tethering between the glycosyl donor and glycosyl acceptor counterparts while providing a practic

5 he beneficial effects may include moving the glycosyl acceptor further out into solution and providin

6 antly regenerated upon its consumption until glycosyl acceptor has reacted.

7 zide analogue of 1, which may be useful as a glycosyl acceptor in the synthesis of alpha-galactosylce

8 nsfer of the anomeric sulfide group from the glycosyl acceptor to the C(2)-benzylidene donor and can

9 nsfer of the anomeric sulfide group from the glycosyl acceptor to the glycosyl donor.

10 may diminish with the increased bulk of the glycosyl acceptor, and may be an important factor for th

11 to differentiate OH groups in an unprotected glycosyl acceptor, followed by substrate-controlled reac

12 that these derivatives are suitable for both glycosyl acceptor-bound and glycosyl donor-bound strateg

13 he oxocarbenium ion that was attacked by the glycosyl acceptor.

14 lycosylation reaction around the immobilized glycosyl acceptor.

15 ete facial selectivity for the attack of the glycosyl acceptor.

16 on between 2,6-dideoxy-sugar hemiacetals and glycosyl acceptors in good yield and high alpha-selectiv

17 ity when glycosylated with a wide variety of glycosyl acceptors including properly protected amino ac

18 ized by coupling thiophenyl 4-DP donors with glycosyl acceptors using BSP/Tf2O activation, whereas be

19 It is possible that surface-immobilized glycosyl acceptors with a longer spacer (C8-O-C8)-lipoic

20 To facilitate access to glycosyl acceptors, we assembled phosphonophosphate anal

21 in glycosylation reactions on more demanding glycosyl acceptors.

22 in case of unreactive glycosyl donors and/or glycosyl acceptors.

23 resence of the anomeric sulfide group on the glycosyl acceptors.

24 otolyl donors as well as differently crowded glycosyl acceptors; subtle differences in the stereochem

25 ution-phase synthesis of thioglycosides from glycosyl acetates and thiols in the presence of In(III)

26 of sepsis, a major cause of ALI, 3-O-beta-d-glycosyl aesculin significantly enhanced the survival of

27 Unlike aesculin, 3-O-beta-d-glycosyl aesculin significantly suppressed neutrophilic

28 Mechanistically, 3-O-beta-d-glycosyl aesculin suppressed ubiquitination of Nrf2, ret

29 w that the glycosylated aesculin, 3-O-beta-d-glycosyl aesculin, robustly activated Nrf2, inducing the

30 The key step in the synthesis of C-glycosyl aldehydes is the aryl driven reductive dehydrat

31 ydrate modification, (b) oligosaccharide and glycosyl amino acid synthesis, (c) assembly of glycoclus

32 otrityl resin as the solid-phase support and glycosyl amino acids as building blocks.

33 talysis to allow the convergent synthesis of glycosyl amino acids bearing M6P residues.

34 the sequential installation of four O-linked glycosyl-amino acid cassettes into closely spaced O-glyc

35 divergent approach to C(2)-C(3) unsaturated glycosyl and alpha-D-mannopyranosyl sulfones has been de

36 set of N-substituted peptides (with methyl, glycosyl and amino acids as N-substituents), cyclic N-me

37 r of 2-deoxy-2-C-alkyl glycosides, with both glycosyl and nonglycosyl moieties at the reducing end, a

38 rough combinatorial enumeration of aglycone, glycosyl, and acyl subunits.

39 ying in the number and position of hydroxyl, glycosyl, and methyl groups about their aromatic core st

40 chanisms of LTA modifications with D-alanyl, glycosyl, and phosphocholine residues will be discussed

41 ed biflavonone, morelloflavone-4'''-O-beta-d-glycosyl, and the known compounds 1,3,6,7-tetrahydroxyxa

42 o- and stereospecific construction of the C5 glycosyl angucycline framework of mayamycin.

43 eptide substrate; moreover, once formed, the glycosyl aspartate reacts further to form a succinimide

44 The reducing end is activated as a glycosyl azide and masked as a 1,6-anhydro sugar, while

45 By employing 1,4-naphthoquinone and glycosyl azides undergoing a [3 + 2] cycloaddition, we h

46 one-pot protocol for the synthesis of novel glycosyl-beta-azido ester 3 from glycosyl olefinic ester

47 -catalyzed diazotransfer reaction to furnish glycosyl-beta-azido ester.

48 dPer adopts the anti conformation about the glycosyl bond and forms a less stable wobble pairing int

49 londG adopts the anti conformation about the glycosyl bond and that the etheno moiety is accommodated

50 After the hydrolysis of the N-glycosyl bond between a damaged base and C1' of a deoxyr

51 When N-glycosyl bond cleavage is prevented, unhooking occurs vi

52 n-bonding to the water molecule required for glycosyl bond hydrolysis may explain this sequence requi

53 droxyl groups in mediating both this aqueous glycosyl bond-forming reaction and the site-selectivity

54 ex and adopts the syn conformation about the glycosyl bond.

55 lity over tetrahydrouridine (THU) 5 at its N-glycosyl bond.

56 dG maintains the anti-conformation about the glycosyl bond.

57 d, the ICL is unhooked when one of the two N-glycosyl bonds forming the cross-link is cleaved by the

58 ydrolyze O-glycosidic bonds in addition to N-glycosyl bonds.

59 mation by enzymes catalyzing the cleavage of glycosyl bonds.

60 the in situ synthesis from the corresponding glycosyl bromides and activation of the OFox imidates co

61 nophosphate (Dol-P) functions as an obligate glycosyl carrier lipid in protein glycosylation reaction

62 ir enzyme that has been shown to stabilize a glycosyl cation reaction intermediate and a related tigh

63 Cl4 activation or intermediate generation of glycosyl chloride as the real donor could be excluded.

64 ospecific invertive substitution pathways of glycosyl chlorides.

65 structure of CPS34 and, in conjunction with glycosyl composition analyses, revealed the following re

66 lar as determined by gel electrophoresis and glycosyl composition analysis using gas chromatography/m

67 polysaccharide, HF-PS, was characterized by glycosyl composition and linkage analyses, mass spectrom

68 Any attempt to fit the best glycosyl composition match by mass only is problematic p

69 transfer of anomeric configuration make the glycosyl cross-coupling reaction a practical tool for th

70 The versatility of the glycosyl cross-coupling reaction was probed in the total

71 We demonstrated that the glycosyl cross-coupling resulted in consistently high an

72 rm the presence of motifs with evenly spaced glycosyl decorations on the xylan backbone, together wit

73 ycosphingolipids, as well as microbial alpha-glycosyl diacylglycerolipids.

74 Binding of the two (13)C-labelled glycosyl diastereomers to NKA were studied by solid-stat

75 d oxidative aromatization with the preformed glycosyl diene and dienophiles.

76 The glycosyl dienes were obtained from simple sugars by tand

77 A series of protected and unprotected glycosyl dipeptides, glycopeptide I, which contained the

78 In this article, we evaluate glycosyl dithiocarbamates (DTCs) with unprotected C2 hyd

79 intermolecular H-bond tethering between the glycosyl donor and glycosyl acceptor counterparts while

80 date activation revealed low affinity to the glycosyl donor but high affinity to the hydroxy group of

81 osyl-(1-->6)](7) -D-mannopyranoside, and the glycosyl donor C(50) -polyprenol-phosphate-[(14) C]-mann

82 The glycosyl donor employed in this study is stable and easi

83 ween acceptor and catalyst and then with the glycosyl donor enables self-organization of an ordered t

84 eospecific glycosylation with an enantiopure glycosyl donor followed by separation of the derived dia

85 promising as it enables us to regenerate the glycosyl donor for further utilization.

86 , thereby providing supplies of this complex glycosyl donor for future studies of lipopolysaccharide

87 kyne reductive coupling reactions and as the glycosyl donor for subsequent intramolecular glycosylati

88 roups, which decreased the reactivity of the glycosyl donor relative to the parent benzyl ether (Bn)

89 xy-2-C-alkyl glycal derivative is a suitable glycosyl donor to prepare 2-deoxy-2-C-alkyl glycosides,

90 along a reaction path involving an activated glycosyl donor with a covalent bond between the glycosyl

91 uitable for both glycosyl acceptor-bound and glycosyl donor-bound strategies, commonly employed in re

92 novel benchtop stable and readily available glycosyl donor.

93 poor reactivity is employed as an efficient glycosyl donor.

94 nucleofuge that has been reconverted to the glycosyl donor.

95 behave as an efficient, partially protected glycosyl donor.

96 fide group from the glycosyl acceptor to the glycosyl donor.

97 ve to the parent benzyl ether (Bn) protected glycosyl donor.

98 f the axial azide and hence formation of the glycosyl donor.

99 stereochemical information intrinsic to the glycosyl donor.

100 pwise extensions using excess monosaccharide glycosyl donors (trichloroacetimidates and thioglycoside

101 g blocks, which can easily be converted into glycosyl donors and acceptors.

102 nthesis of 3,3-difluoro-3H-indol-2-yl (OFox) glycosyl donors and activation thereof can be conducted

103 articularly pronounced in case of unreactive glycosyl donors and/or glycosyl acceptors.

104 These glycosyl donors are capable of coupling to a wide variet

105 Substitution of the participating group of glycosyl donors by a halogen atom is shown to specifical

106 ng blocks that can readily be converted into glycosyl donors for glycosylations that give reliably hi

107 l (TBDMS) protected fucose thioglycosides as glycosyl donors for oligosaccharide synthesis is describ

108 With a view to the eventual synthesis of glycosyl donors for the stereocontrolled synthesis of ps

109 Anomeric sulfonium ions are attractive glycosyl donors for the stereoselective installation of

110 ohexopyranosyl-1-thioglycosides were used as glycosyl donors for the stereoselective synthesis of 2-d

111 a continuum of reactivity exists where some glycosyl donors form oxacarbenium ions in glycosylation

112 old(III) activation of unprotected propargyl glycosyl donors has been shown to be effective for the s

113 e reactivity and selectivity of 3,6-tethered glycosyl donors have been studied using acceptors with d

114 ages with complete anomeric control by using glycosyl donors having a participating (S)-(phenylthiome

115 st glycosylation reactions require activated glycosyl donors in the form of nucleotide sugars to driv

116 functionality at the C(2)-amino position of glycosyl donors is crucial for the high alpha-selectivit

117 on of the C(1)-trichloroacetimidate group on glycosyl donors is necessary for the coupling process to

118 r protecting groups affect the reactivity of glycosyl donors of the thioglycoside type with the N-iod

119 A complementary concept for superarming glycosyl donors through the use of common protecting gro

120 Thioglycosides were employed as glycosyl donors to construct two key pseudotrisaccharide

121 Eight (four anomeric pairs) 3,6-bridged-glycosyl donors were synthesized in high yields from the

122 ltransferase-catalyzed reactions, artificial glycosyl donors, and a high throughput colorimetric scre

123 7, 25, or 26, using trichloroacetimidates as glycosyl donors, led to the corresponding branched dithi

124 ptosyl derivatives served as alpha-selective glycosyl donors.

125 iously discovered with S-benzoxazolyl (SBox) glycosyl donors.

126 to encompass a wide array of common, stable glycosyl donors.

127 spoke N-glycans using N-glycan oxazolines as glycosyl donors.

128 Glycosyl DTC couplings are highly beta-selective despite

129 Glycosyl DTCs are readily activated with Cu(I) or Cu(II)

130 ild, one-pot conversion of glycals into beta-glycosyl DTCs via DMDO oxidation with subsequent ring op

131 ement mechanism with formation of a covalent glycosyl-enzyme intermediate (CGE), new experimental and

132 irst crystallographic structure of a natural glycosyl-enzyme intermediate (GEI) of Saccharomyces cere

133 (1)C(4) (chair) conformation and a covalent glycosyl-enzyme intermediate in (3)S(1) (skew-boat).

134 s no effect on the rates of formation of the glycosyl-enzyme intermediate, but it accelerates turnove

135 double displacement mechanism via a covalent glycosyl-enzyme intermediate, CGE) by using density func

136 h resolution structure of a trapped covalent glycosyl-enzyme intermediate, indicating that the 1,3-xy

137 omplex with a full cellononaose ligand and a glycosyl-enzyme intermediate, that reveal details of the

138 of a simpler mechanism involving a covalent glycosyl-enzyme intermediate, the most plausible mechani

139 -displacement mechanism involving a covalent glycosyl-enzyme intermediate, which was directly detecte

140 ophilic attack on the anomeric carbon of the glycosyl-enzyme intermediate.

141 -step mechanism that includes formation of a glycosyl-enzyme intermediate.

142 -dexoynojirimycin and two different covalent glycosyl-enzyme intermediates obtained with fluorinated

143 o the upregulation of CsAOG, involved in ABA glycosyl ester (ABAGE) synthesis, and to a moderate indu

144 n intramolecular rearrangement of a covalent glycosyl ester adduct of the HCF-1 polypeptide was propo

145 The MceIJ-catalyzed formation of the glycosyl ester linkage between MccE492 and the sideropho

146 l enzyme system for which the formation of a glycosyl ester within the enzyme active site has been sh

147 Maysin is a C-glycosyl flavone that, when present in silks, confers na

148 Of these, two C-glycosyl flavones (lucenin-2 and vicenin-2) and an O-tri

149 irst time we reported the presence of five C-glycosyl flavones (lucenin-2, vicenin-2, stellarin-2, lu

150 dentified for the first time, namely, four C-glycosyl flavones (lucenin-2, vicenin-2, stellarin-2, lu

151 ituents in the polyphenolic extracts were C- glycosyl flavones, including schaftoside, isoschaftoside

152 irst step in the formation of insecticidal C-glycosyl flavones.

153 cation and characterisation of nine C- and O-glycosyl flavonoids in Moro (Citrus sinensis (L.) Osbeck

154 er, the influence of the identified C- and O-glycosyl flavonoids on the antioxidant and acetylcholine

155 of the identified polymethoxylated, C- and O-glycosyl flavonoids on the total antioxidant activity ha

156 er, the influence of the identified C- and O-glycosyl flavonoids on the total antioxidant activity of

157 n, characterised by the presence of C- and O-glycosyl flavonoids.

158 and scoparin), a 3-hydroxy-3-methylglutaryl glycosyl flavonol (3-hydroxy-3-methylglutaryl glycosyl q

159 tion reaction between sucrosyl acceptors and glycosyl fluoride donors to yield the derived trisacchar

160 (fukugetin) and morelloflavone-7''-O-beta-d-glycosyl (fukugeside) were isolated from the epicarp of

161 revealed the molecular basis for nitrile and glycosyl functionalization.

162 action between a substituted naphthyne and a glycosyl furan and a subsequent O-->C-glycoside rearrang

163 ically bound aroma precursors, determined as glycosyl glucose content by HPLC-IR, in Monastrell grape

164 The N-glycosyl group is then processed, and the protein is tra

165 Glycosyl groups are an essential mediator of molecular i

166 Herein, O- and N-glycosyl groups are characterized in their sugar monomer

167 hemical groups such as phosphate, acetyl and glycosyl groups from one protein to another protein.

168 from genome-sequenced microbes by targeting glycosyl groups in microbial metabolomes.

169 d after the enzymatic hydrolysis of specific glycosyl groups.

170 nesulfonate donors are prepared in situ from glycosyl hemiacetals, and are coupled under mild, operat

171 is covered by two templates corresponding to glycosyl hydrolase 15 family members and the A subunit o

172 malian chitinase (AMCase) is a member of the glycosyl hydrolase 18 family (EC 3.2.1.14) that has been

173 ss diverse environments, generating the only glycosyl hydrolase 25 muramidases in plants and archaea.

174 e activity of alpha-l-arabinofuranosidase, a glycosyl hydrolase acting on the side chains of pectin i

175 REEZING 2 (SFR2) is classified as a family I glycosyl hydrolase but has recently been shown to have g

176 Glycosyl hydrolase family 28 (GH28) is a set of structur

177 Xylanases of glycosyl hydrolase family 30 (GH30) have been shown to c

178 The protein is a member of glycosyl hydrolase family 31.

179 enes encoding putative cellulases, including glycosyl hydrolase family 7 (GH7) cellobiohydrolases.

180 gnated jiaoyao1 (jia1), in the second of the glycosyl hydrolase family 9 active site signature motifs

181 The 18 glycosyl hydrolase family of chitinases is an ancient ge

182 The concept of expressing non-plant glycosyl hydrolase genes in plant tissue is nearly two d

183 unctata reveals a transcriptome dominated by glycosyl hydrolase genes.

184 ns a domain showing sequence homology to the glycosyl hydrolase motif in the heparanase (HPSE) gene,

185 esponse pathway in the tunable regulation of glycosyl hydrolase production in response to changes in

186 ase, annotated as a member of the TIM barrel glycosyl hydrolase superfamily, was characterized.

187 H9A1/KORRIGAN1 is a membrane-bound, family 9 glycosyl hydrolase that is important for cellulose synth

188 es of the BT_1012 protein identifies it as a glycosyl hydrolase, expanding an already impressive cata

189 notation revealed unknown functions (37.2%), glycosyl hydrolases (26.5%) and redox enzymes (11.5%) as

190 Salmonella contains 47 glycosyl hydrolases (GHs) that may degrade the glycan.

191 Natural occurrences of apparent glycosyl hydrolases acting as transferases are interesti

192 oides thetaiotaomicron genome identified 172 glycosyl hydrolases and a large number of uncharacterize

193 Three regions disparate from glycosyl hydrolases are identified as required for trans

194 Genes encoding glycosyl hydrolases are significantly more abundant than

195 cteristics to the heterologous production of glycosyl hydrolases in a high yielding bioenergy crop, h

196 ridium species organize cellulases and other glycosyl hydrolases into large complexes known as cellul

197 Chitosanases (EC 3.2.1.132) are glycosyl hydrolases that catalyse the endohydrolysis of

198 encodes a mannanase, representing a class of glycosyl hydrolases that has not previously been reporte

199 Cellobiohydrolases are exo-active glycosyl hydrolases that processively convert cellulose

200 ial distribution of glycosyltransferases and glycosyl hydrolases within the Golgi apparatus.

201 pically found in C-terminal domains of other glycosyl hydrolases, however these domains are typically

202 d cell wall-associated transglycosidases and glycosyl hydrolases, which are responsible for remodelin

203 Intercellular glycosyl hydrolases-mediated decomposition of the dextri

204 te is highly conserved with that of family 1 glycosyl hydrolases.

205 nd increased polysaccharide accessibility to glycosyl hydrolases.

206 2, each of which shares sequence homology to glycosyl hydrolases.

207 of pectin is aided by digestion assays with glycosyl hydrolases.

208 BcsZ belongs to family eight of glycosyl-hydrolases, and its activity is required for op

209 Study of the highly glycosylated glycosyl inositol phosphorylceramide (GIPC) sphingolipid

210 Glycosyl inositol phosphorylceramide (GIPC) sphingolipid

211 cus on highly polar sphingolipids, so-called glycosyl inositol phosphorylceramides (GIPCs).

212 achieved using one-pot per-O-trimethylsilyl glycosyl iodide glycosidation.

213 ective silyl exchange technology (ReSET) and glycosyl iodide glycosylation have now been integrated t

214 -beta-pinene as acid scavenger and work with glycosyl iodides under mild conditions.

215 To meet this demand, glycosyl iodides were enlisted in the synthesis of these

216 overcome this obstacle, per-O-trimethylsilyl glycosyl iodides were investigated and shown to undergo

217 Glycosyl isoquinoline-1-carboxylate was developed as a n

218 tis MSMEG2785 resulted in altered growth and glycosyl linkage analysis revealed the absence of AG alp

219 rmined by enzyme degradation, permethylation glycosyl linkage analysis, electron microscopy, and muta

220 m each of the rgt mutants were elucidated by glycosyl linkage analysis.

221 ate component of the cell wall with multiple glycosyl linkages and no repeating units.

222 e presence of a diarylborinic acid catalyst, glycosyl methanesulfonates engage in regio- and stereose

223 atic chains with chlorine substituents and C-glycosyl moieties, is reported.

224 ntually solvent-separated ion pairs with the glycosyl moiety and the leaving group being separated by

225 cosyl donor with a covalent bond between the glycosyl moiety and the leaving group, followed by forma

226 minations highlighted that the presence of a glycosyl moiety bound to the chalcone structure dramatic

227 es to promote apparent transfer of the donor glycosyl moiety from nucleobase to hydroxyl.

228 c Sm1 is produced as a glycoprotein, but the glycosyl moiety is missing from its dimeric form, and Ep

229 d by formation of contact ion pairs with the glycosyl moiety loosely bound to the leaving group, and

230 is of novel glycosyl-beta-azido ester 3 from glycosyl olefinic ester 1 under mild conditions has been

231 lation/disproportionation reactions in which glycosyl or dextrinyl units are transferred among linear

232 dified dATP and South-MC-dATP each adopt syn glycosyl orientations to form Hoogsteen base pairs with

233 tricyclic systems, invoking an intermediate glycosyl oxocarbenium ion reacting through a boat confor

234 ement of a conformationally mobile transient glycosyl oxocarbenium ion.

235 nucleophilic attack of putative intermediate glycosyl oxocarbenium ions suggests that the observed se

236 thylphosphono(difluoromethyl) iminosugars as glycosyl phosphate and sugar nucleotide mimics.

237 ducts to the endoplasmic reticulum (ER), the glycosyl phosphatidylinositol (GPI)-anchor likely functi

238 Expression of CD24, a glycosyl phosphatidylinositol (GPI)-linked sialoglycopro

239 Here, we report that the glycosyl phosphatidylinositol-anchored cell surface glyc

240 The association of glycosyl phosphatidylinositol-anchored MT4-MMP with ADAM

241 Overexpression of CD24, a glycosyl phosphatidylinositol-linked sialoglycoprotein,

242 The glycosyl-phosphatidylinositol (GPI) membrane anchor is a

243 investigated whether reverse signaling via a glycosyl-phosphatidylinositol (GPI)-linked ephrin contro

244 CD14 antigen is a glycosyl-phosphatidylinositol (GPI)-linked glycoprotein

245 zed by the partial or complete deficiency of glycosyl-phosphatidylinositol (GPI)-linked membrane prot

246 n that is tethered to the cell membrane by a glycosyl-phosphatidylinositol anchor.

247 ional transmembrane domain, and a C-terminal glycosyl-phosphatidylinositol anchor.

248 The glycosyl-phosphatidylinositol anchored folate receptor (

249 In this approach, the key glycosyl phosphodiester bond-forming reaction proceeds w

250 -PLC) capable of hydrolyzing PI and cleaving glycosyl-PI (GPI)-linked proteins from cell surfaces.

251 The processive reaction mechanisms of beta-glycosyl-polymerases are poorly understood.

252 lycosyl flavonol (3-hydroxy-3-methylglutaryl glycosyl quercetin) and a flavone O-glycosides (chrysoer

253 uits, enzymatically hydrolysed to remove the glycosyl residues from the phenolic ingredients was able

254 The O-acetylation occurs on the four glycosyl residues in a non-stoichiometric ratio, and eac

255 ment of expressed msp2(p44) paralogs and the glycosyl residues modifying Msp2(P44) varied considerabl

256 y analysis of derivatized neutral and acidic glycosyl residues).

257 The OPS is composed of several unusual glycosyl residues, including 6-deoxy-3-O-methyl-d-talose

258 Microbial GNPs consist of aglycone and glycosyl structure groups in which the sugar unit(s) are

259 lecular dynamic simulations suggest that the glycosyl substitutions in xylan are not only sterically

260 ate pyrimidine metabolic flux to provide the glycosyl subunits required for protein glycosylation and

261 condition for the exclusive preparation beta-glycosyl thiol derivatives has been developed successful

262 Further reaction of glycosyl thiol derivatives with Michael acceptors and al

263 14, where both pseudosugar conformation and glycosyl torsion angle are opposite with respect to the

264 zed in the anti orientation about the pseudo-glycosyl torsion angle, which mimics precisely the mutag

265 al is quantitatively converted into an alpha-glycosyl tosylate, which is presumably the reactive spec

266 Enzymatic prenyl and glycosyl transfer are seemingly unrelated reactions that

267 echanistic insights into the function of the glycosyl transfer polymerase that is related to the viru

268 our understanding of the structural basis of glycosyl transfer.

269 oth a transcriptional regulator (ExpG) and a glycosyl transferase (ExpC).

270 Genes within two glycosyl transferase (GT) families, GT43 (IRREGULAR XYLE

271 domain, followed by its transmission to the glycosyl transferase active site.

272 rom the Carbohydrate-Active Enzymes database glycosyl transferase families GT61, GT47, and GT43, prev

273 In Arabidopsis thaliana, a glycosyl transferase family 37 (GT37) fucosyltransferase

274 imary wall CesAs, several Csl genes, and GT8 glycosyl transferase genes, and are correlated with the

275 Escherichia coli LpxB, an inverting glycosyl transferase of the GT-B superfamily and a membe

276 ely, as they do not carry out glycosidase or glycosyl transferase reactions, and they are of nonimmun

277 the order Rhizobiales, where bgsA encodes a glycosyl transferase with domain resemblance and phyloge

278 Cytochrome P450 monooxygenase, glycosyl transferase, and glutathione S-transferase are

279 on patterns of their genes, (5) other HRGPs, glycosyl transferase, prolyl 4-hydroxylase, and peroxida

280 ndicated that LpsB is a core oligosaccharide glycosyl transferase.

281 rmed four contigs (two cytochromes P450, one glycosyl-transferase and one glutathione-S-transferase)

282 ty acid omega-hydroxylase CYP704B1, putative glycosyl transferases At1g27600 and At1g33430, 4-coumara

283 rhamnose, suggesting that one or more of the glycosyl transferases encoded by the epaBCD operon are n

284 o-enzymatic methods, which employ a range of glycosyl transferases to modify a synthetic oligosacchar

285 s of endoplasmic reticulum and Golgi-located glycosyl transferases whose activities are difficult to

286 hesis of HS involves an array of specialized glycosyl transferases, epimerase, and sulfotransferases,

287 level through activation of their associated glycosyl transferases.

288 eral flavonol glycosides and some associated glycosyl transferases.

289 his residue to become exposed to appropriate glycosyl transferases.

290 tuned process that involves the activity of glycosyl-transferases and hydrolases.

291 secretory cargo and exogenous Golgi resident glycosyl-transferases are exchanged between separated Go

292 beta-selectivity at the anomeric carbon of N-glycosyl trichloroacetamides depends on the nature of th

293 The resulting alpha- and beta-N-glycosyl trichloroacetamides were further coupled with a

294 Gold(III) chloride as catalyst for O-glycosyl trichloroacetimidate activation revealed low af

295 ol % of Pd(CH(3)CN)(4)(BF(4))(2) to activate glycosyl trichloroacetimidate donors at room temperature

296 ethod for stereoselective glycosylation with glycosyl trichloroacetimidate donors employing cationic

297 d to the protein through a complex series of glycosyl trimming and addition steps.

298 amino acids to afford O-tert-butyl-protected glycosyl tripeptides, glycopeptide II.

299 The research on the area of glycosyl urea derivatives, in which the O- and N-glycosi

300 en nucleophiles to provide the corresponding glycosyl ureas in moderate to good yields and with no lo