ライフサイエンスコーパス: glycosidic

1 Millingtonine is a glycosidic alkaloid that exists as a pair of pseudo-enan

2 The well-defined conformation of glycosidic and aglyconic bonds in alpha-, beta-, and gam

3 Using fluoranthene or xenon, both glycosidic and cross-ring cleavages are observed, as wel

4 Both glycosidic and cross-ring cleavages are promoted by hydr

5 r five model glycans, ISD produced extensive glycosidic and cross-ring cleavages in the positive ion

6 oss, and that produced complete sets of both glycosidic and cross-ring fragment ions.

7 s that fragments to produce information-rich glycosidic and cross-ring product ions which can be used

8 acterization and found to produce a range of glycosidic and proteolytic enzymes.

9 C-glycosidic antagonists may serve such a purpose.

10 wine odorant aglycones from odourless grape glycosidic aroma precursors previously isolated from whi

11 extract in order to determine the effect on glycosidic aroma precursors.

12 Thus, this study proved a change in the glycosidic aroma profile in grapes after the oak applica

13 ed carbohydrate amino acid core, followed by glycosidic attachment of thymine at C-1, and peptidic li

14 CID and HCD generated mainly glycosidic B/Y and C/Z cleavages of the oligosaccharides

15 docked state, which requires an unusual syn glycosidic base conformation at A38 for active site asse

16 asic sites from the formal hydrolysis of the glycosidic bond (AP) and several oxidized abasic lesions

17 re due to the metabolic instability of the O-glycosidic bond (O-mannosides).

18 omodeoxyuridine, dT) or have a more stable N-glycosidic bond (such as dT).

19 from the double-stranded DNA, cleaves the N-glycosidic bond and leaves the C1' hydrolyzed abasic sug

20 formation from 1 involves rotation about the glycosidic bond and that the rate constant for this proc

21 in a high number of distance restraints per glycosidic bond and, consequently, a well-defined struct

22 bose moiety of the substrate and cleaves the glycosidic bond at the very last stage.

23 acetolysis susceptible, indicative of a 1,6 glycosidic bond between CPS and the GlcNAc C-6.

24 rns in terms of preferential cleavage of the glycosidic bond between O- and fructose C2 in both inuli

25 es early stage assembly of the acidic labile glycosidic bond between sugar and 2-methylchromone aglyc

26 ol+base)-H]-, resulting from cleavage of the glycosidic bond between the 2'-deoxyribose and base, cor

27 in three-stranded DNA via hydrolysis of the glycosidic bond between the crosslinked base and deoxyri

28 Endoglycosidases F2 and H, which cleave the glycosidic bond between the two primary GlcNAc residues,

29 s (GH) are enzymes that mainly hydrolyze the glycosidic bond between two carbohydrates or a carbohydr

30 city of the alpha-face on replacement of the glycosidic bond by the hydroxylamine linkage.

31 e kinetics and thermodynamics of gas-phase N-glycosidic bond cleavage induced by nucleophilic attack

32 by its insertion into the active site where glycosidic bond cleavage is catalyzed.

33 N-Glycosidic bond cleavage is much slower, taking place on

34 NDTs catalyze N-glycosidic bond cleavage of 2'-deoxynucleosides via a co

35 n maintaining genome integrity by catalyzing glycosidic bond cleavage of 8-oxoguanine (oxoG) lesions

36 ase, protects genome integrity by catalyzing glycosidic bond cleavage of 8-oxoguanine (oxoG) lesions,

37 genic 8-oxoguanine (oxoG) lesion, catalyzing glycosidic bond cleavage of oxoG to initiate base excisi

38 RCL is an enzyme that catalyzes the N-glycosidic bond cleavage of purine 2'-deoxyribonucleosid

39 RCL is an enzyme that catalyzes the N-glycosidic bond cleavage of purine 2'-deoxyribonucleosid

40 -ethenoadenine (A) lesion, and the rate of N-glycosidic bond cleavage was identical to that of the wi

41 reported accounts that IRMPD results only in glycosidic bond cleavage, the fragmentation of singly pr

42 ergy barrier and largest exothermicity for N-glycosidic bond cleavage.

43 lease of the abasic product is faster than N-glycosidic bond cleavage.

44 lyzed protonation of the nucleobase promotes glycosidic bond cleavage.

45 sion deoxyribose participate in catalysis of glycosidic bond cleavage.

46 ylation of crystalline cellulose, leading to glycosidic bond cleavage.

47 The glycan-specific ions mainly arose from glycosidic bond cleavages (B, Y, C, and Z ions) in addit

48 vatized glycans predominately generates C1-O glycosidic bond cleavages retaining the charge on the re

49 acts to yield abundant cross-ring cleavages, glycosidic bond cleavages, and combinations of these typ

50 all possible heparin/HS sequences solely by glycosidic bond cleavages, without the need to generate

51 accharide and disaccharide ions derived from glycosidic bond cleavages.

52 es (G4 and G6 in (rGACGAGUGUCA)(2)) in a syn glycosidic bond conformation and forming a sheared GG pa

53 of the templating base to maintain the anti glycosidic bond conformation in the binary complex in a

54 udouridine synthase, strongly prefer the syn glycosidic bond conformation, while that of the nonreact

55 In both cases, the modified C adopts an anti glycosidic bond conformation; the equilenin distal ring

56 sociated with the nucleophilic cleavage of N-glycosidic bond constitutes a major factor contributing

57 ines by reversible homolytic scission of the glycosidic bond following the dictates of the Fischer-In

58 s a control element in enzymic processes for glycosidic bond formation and hydrolysis are discussed.

59 Formidable challenges include glycosidic bond formation between ribose and the canonic

60 They catalyze a glycosidic bond formation between sugar donors and sugar

61 a modification not directly involved in the glycosidic bond formation, 6F-N-acetyl-d-galactosamine (

62 g protecting groups on the donor favor alpha-glycosidic bond formation.

63 containing the characteristic ribose-ribose glycosidic bond formed during poly(ADP-ribosyl)ation.

64 onfiguration is retained following gas-phase glycosidic bond fragmentation during tandem mass spectro

65 ism in which the key amino acids driving the glycosidic bond hydrolysis act as catalytic acid/base an

66 Previous studies show that N-glycosidic bond hydrolysis follows a stepwise (S(N)1) me

67 the active site by exclusively impairing the glycosidic bond hydrolysis step.

68 icient despite the relatively slow rate of N-glycosidic bond hydrolysis.

69 be facilitated by binding the bases with the glycosidic bond in the anti and syn conformation, respec

70 s the polyoxygenated saccharide and a labile glycosidic bond in the nucleosides, these reactions can

71 and two hydrogen bond acceptors because the glycosidic bond is C-C rather than C-N as in uridine.

72 te transition state in which cleavage of the glycosidic bond is coupled to the transfer of a proton f

73 displacement mechanism: the cleavage of the glycosidic bond is facilitated by the nucleophilic parti

74 lity of the deficient variants to cleave the glycosidic bond of beta-NAD(+) into nicotinamide and ADP

75 nd 26, hydrolyze glucomannan by cleaving the glycosidic bond of mannosides at the -1 subsite.

76 at LytB cleaves the GlcNAc-beta-(1,4)-MurNAc glycosidic bond of peptidoglycan building units.

77 ine DNA glycosylase (Tdg), which cleaves the glycosidic bond of the bases to give potentially harmful

78 Nucleosides fragmented at the N-glycosidic bond provide nucleobase and/or ribose or 2'-d

79 ein, we disclose that compounds having the O-glycosidic bond replaced with carbon linkages had improv

80 on on the mannoside phenyl ring ortho to the glycosidic bond results in large potency enhancements se

81 The presence of the glycosidic bond results in the stereoselective induction

82 ces induce differences in the sugar puckers, glycosidic bond rotation, and backbone conformations.

83 iring, base stacking, backbone conformation, glycosidic bond rotation, and sugar puckering in the stu

84 N-glycosidic bond scission is then facilitated by a backbo

85 ase cleavage is dependent on the intrinsic N-glycosidic bond stability.

86 g mispair formation, but it also renders the glycosidic bond susceptible to base cleavage by DNA repa

87 Cleavage of the N-glycosidic bond that connects the nucleobase to the back

88 In contrast, the beta-D-GlcNAc-(1-->3)-D-Gal glycosidic bond that connects the two Le(x) trisaccharid

89 esions and catalyzes the hydrolysis of the N-glycosidic bond to initiate the base excision repair pat

90 osine, and catalyzes the hydrolysis of the N-glycosidic bond to release the lesion base and initiate

91 n bonds, permitting dA* to rotate around the glycosidic bond to syn and incorporate dT via a Hoogstee

92 e on the nucleophilic aspartate (264) as the glycosidic bond to the aspartate is broken during the br

93 ss units to its molecular mass and makes the glycosidic bond unusually labile during mass spectral an

94 demonstration of the anomeric memory of the glycosidic bond upon fragmentation.

95 ing flipping and the conformation of the 1,4-glycosidic bond was observed.

96 xist in anti or syn conformations around the glycosidic bond when paired opposite to U or G in the co

97 which selectively cleaves the nicotinamide's glycosidic bond yielding (tz)ADP-ribose.

98 tivities: N-glycosylase (hydrolysis of the N-glycosidic bond) and AP lyase (elimination of the 3'-pho

99 eonine residues of a protein via an O-linked glycosidic bond) are largely unknown.

100 h a 3-OH group and a 4-OH group (or alpha1-4-glycosidic bond) at the acceptor subsite +1 for the cata

101 Due to the lability of the glycosidic bond, 8-nitrodG cannot be incorporated into o

102 n by the C2-alkoxide, an essentially cleaved glycosidic bond, and a slight shortening of the endocycl

103 ering by the value of the Psi angle for this glycosidic bond, are populated in solution.

104 f uracil-DNA glycosylase hydrolysis of the N-glycosidic bond, converting 2'-deoxyuridine in DNA to an

105 The wild-type enzyme cleaves the N-glycosidic bond, leaving the ribose ring in the flipped

106 ed in cellular DNA due to instability of the glycosidic bond, particularly at purines and various oxi

107 tion through a spontaneous hydrolysis of the glycosidic bond, the ability of Rev1 to stabilize an aba

108 Following cleavage of the glycosidic bond, the liberated hemiacetal spontaneously

109 )-meG adopts an anti conformation around its glycosidic bond, with the methyl group in the proximal o

110 the hyaluronic acid polymer at the beta-1,4 glycosidic bond.

111 talysis to achieve selective cleavage of the glycosidic bond.

112 uite indirect because of the lability of the glycosidic bond.

113 of the l-histidine through a hydrolyzable N-glycosidic bond.

114 sidue and thereby facilitate cleavage of the glycosidic bond.

115 lting in a Schiff base intermediate at the N-glycosidic bond.

116 ell characterized in cells due to its labile glycosidic bond.

117 thesis of the so-called difficult classes of glycosidic bond: the 2-deoxy-beta-glycopyranosides, the

118 uanosine adopts a syn conformation about the glycosidic bond; thermal melting studies and molecular m

119 ing cycle, which likely includes energy from glycosidic bonds and other sources.

120 degrees of conformational change around the glycosidic bonds and subsequently alter its function as

121 catalyze the highly specific biosynthesis of glycosidic bonds and, as such, are important both as dru

122 n of SEC and FTIR data showed that alpha-1,6-glycosidic bonds are more frequently split in pressurize

123 osyl urea derivatives, in which the O- and N-glycosidic bonds are replaced with the urea-glycosidic l

124 pore cortex PG and catalyzes the cleavage of glycosidic bonds between N-acetylmuramic acid (NAM) and

125 One of these LPMOs cleaves glycosidic bonds by oxidation of the C1 carbon, whereas

126 nsition states are late with largely cleaved glycosidic bonds coupled to pyranosyl ring flattening ((

127 on is reversed by hydrolases that cleave the glycosidic bonds either between ADP-ribose units or betw

128 G and AlkA are therefore able to hydrolyze O-glycosidic bonds in addition to N-glycosyl bonds.

129 Cellulase enzymes cleave glycosidic bonds in cellulose to produce cellobiose via

130 dicating the ability of MGIIa_P to hydrolyse glycosidic bonds in complex sugars in PRE.

131 nsertion and subsequent elimination to break glycosidic bonds in crystalline cellulose.

132 To achieve cleavage of the glycosidic bonds in host glycans, S. pneumoniae deploys

133 opening polymerization to generate multiple glycosidic bonds in one simple chemical step, allowing u

134 structurally related enzymes that hydrolyze glycosidic bonds in pectin, and are important extracellu

135 s (LPMOs) catalyze the oxidative cleavage of glycosidic bonds in recalcitrant polysaccharides, such a

136 e of electrons to oxidize the C1 position of glycosidic bonds in starch substrates, but not in cellul

137 -xylanases (xylanases) hydrolyse the beta1,4 glycosidic bonds in the backbone of xylan.

138 ases (LPMO10s) use redox chemistry to cleave glycosidic bonds in the two foremost recalcitrant polysa

139 ncorrelated rotations are observed about the glycosidic bonds of a partially de-methyl-esterified dec

140 talline cellulose and hydrolyze the beta-1,4-glycosidic bonds of cellulose to produce fermentable sug

141 s suggested that phenolic hydroxyls, but not glycosidic bonds of melanoidin-bound phenolics are cleav

142 yses reveal that correlated rotations around glycosidic bonds of monosaccharide subunits at and immed

143 that catalyse the endohydrolysis of beta-1,4-glycosidic bonds of partially acetylated chitosan to rel

144 soamylase is essential to debranch alpha-1,6-glycosidic bonds of starch, yielding linear amylodextrin

145 he fungus Trichoderma reesei that hydrolyzes glycosidic bonds on cellulose randomly.

146 Glucosidases are enzymes that hydrolyze beta-glycosidic bonds to release non-reducing terminal glucos

147 ermore, lysozyme catalyzed the hydrolysis of glycosidic bonds to the end of the linear substrate but

148 enzymes that catalyze oxidative cleavage of glycosidic bonds using molecular oxygen and an external

149 ttention owing to their abilities to disrupt glycosidic bonds via oxidation instead of hydrolysis and

150 saccharides linked through 1,3- and 1,4-beta glycosidic bonds with subtle differences in structure th

151 fragment ions predominantly from cleavage of glycosidic bonds without breaking the peptide bond.

152 The two most stable structures had trans glycosidic bonds, but distinct pairing geometries, i.e.

153 atalytic itineraries" during the cleavage of glycosidic bonds, illustrating the relationship between

154 nitial substrate; with increasing numbers of glycosidic bonds, less glucose is formed.

155 ectivity in the formation of 1,2-cis-2-amino glycosidic bonds, the glycosylation reaction is hampered

156 ither cross-ring cleavages or rupture of the glycosidic bonds, thereby allowing an unambiguous assign

157 de thioglycosides containing 1,2-cis-2-amino glycosidic bonds, via cationic nickel-catalyzed glycosyl

158 ion 1175-1157cm(-1), linked with breakage of glycosidic bonds, were the most useful for diagnostic mo

159 nd sialic acid receptors linked via alpha2-3 glycosidic bonds, while human-adapted hemagglutinins bin

160 , that are linked by amide, ether, ester, or glycosidic bonds.

161 the LPMO mechanism for oxidative cleavage of glycosidic bonds.

162 es may utilize in catalyzing the cleavage of glycosidic bonds.

163 , for example, that Cel7A cleaves about four glycosidic bonds/s during processive hydrolysis.

164 linked GalNAc polymers that lack significant glycosidic branching and may be connected by glycine pep

165 l chain C-O, C-N, and C-C bond cleavages and glycosidic C-O and cross ring cleavages, thus providing

166 By contrast, glycosidic cleavages dominate in IRMPD although cross-ri

167 bonds were still preferably cleaved over the glycosidic cleavages under ETD fragmentation.

168 e oligo-porphyrans, with many cross-ring and glycosidic cleavages.

169 nteraction was observed by the change in the glycosidic CO, and the CH stretch vibrations of the treh

170 erties, permeabilities, zeta potentials, and glycosidic compositions of capsules from young and old c

171 Characteristic glycosidic conformational patterns along the G-strands,

172 ymorphisms of G-quadruplexes relate to these glycosidic conformational patterns and the lengths of th

173 of anthocyanin pigments comprising multiple glycosidic conjugates of cyanidin.

174 on among species were assigned as kaempferol glycosidic conjugates, with kaempferol-3-O-[glucopyranos

175 cones show higher bioavailability than their glycosidic counterparts and thus may have greater potenc

176 ations, and the release of aromas from their glycosidic counterparts in model cherry juices.

177 ose B, as well as a viable sequencing of the glycosidic couplings.

178 strong sensitizer, so this compound and its glycosidic derivative can contribute to the allergic pot

179 ans accommodated mostly in their cyclic beta-glycosidic form.

180 e oak extract were assimilated and stored as glycosidic forms in both cultivars.

181 They exist in various glycosidic forms.

182 vonols are accumulating in a large number of glycosidic forms.

183 Positive ion ESI-MS generates B/Y-type glycosidic fragment ions under collisional-induced disso

184 e charge results in the generation of C-type glycosidic fragments, highly informative A-type cross-ri

185 ed oligopeptide tree structure appended with glycosidic groups at its multiple N-termini were investi

186 e production of beta-glucosidase and convert glycosidic isoflavones in aglycones.

187 a nonreducing end GlcNAc that has a beta1-6-glycosidic link and that are analogous to either N-glyca

188 For the alpha-O-GalNAc-Ser derivative, the glycosidic linkage adopts a high-energy conformation, ba

189 tions from AF4, carbohydrate composition and glycosidic linkage analysis for the dominating populatio

190 iomers possessing the natural sugar in alpha-glycosidic linkage are the most potent inhibitors of the

191 GlycoSeq employs rules of glycosidic linkage as defined by glycan synthetic pathwa

192 flight mass spectrometry confirmed a direct glycosidic linkage between CPS and PG and showed that a

193 s involved were the synthesis of the 1,2-cis-glycosidic linkage between galactose and the linker (spa

194 They cleave the glycosidic linkage between N-acetylmuramoyl and N-acetyl

195 re symmetrically joined, by a "head-to-head" glycosidic linkage between their carbonyl groups (Chart

196 trehalose oxygen atoms most distant from the glycosidic linkage fluctuated around 7.5 x 10(-14) m(2)/

197 ) that sulfur-for-oxygen substitution in the glycosidic linkage fundamentally alters the energeticall

198 ds a disaccharide that closely resembles the glycosidic linkage in the polylegionaminic acid from the

199 The construction of the 1,2-trans-glycosidic linkage in the terminal anthrose moiety was a

200 n-bond acceptor at the position ortho to the glycosidic linkage may not be required.

201 ygromycin B identified an orientation of one glycosidic linkage of hygromycin B consistent with metal

202 The glycosidic linkage positions are often determined by per

203 e chemoselective introduction of a 1,2-trans glycosidic linkage prior to other linkages.

204 dihedral angles has been determined for each glycosidic linkage relevant for the conformational prefe

205 A direct glycosidic linkage to PG was also demonstrated for serot

206 terized and revealed that in the complex the glycosidic linkage torsion angles between the two reduci

207 free energy landscapes obtained for the same glycosidic linkage within different oligosaccharides.

208 ural substrates harboring the Fucalpha1-2Gal glycosidic linkage, a xyloglucan-derived nonasaccharide,

209 instance, the sugar is aminoglucose in beta-glycosidic linkage, and in the other, two enantiomers ha

210 n the sugar itself, the presence and form of glycosidic linkage, and the environment in the crystal,

211 uctural information, including sugar pucker, glycosidic linkage, hydrogen bonding patterns and stacki

212 t high concentration was key to making the C-glycosidic linkage.

213 to be assigned to the nonreducing side of a glycosidic linkage.

214 he natural sugar N-methylfucosamine in alpha-glycosidic linkage.

215 n, regiochemistry and stereochemistry of the glycosidic linkage.

216 was connected to the sequence by a beta(1-6) glycosidic linkage.

217 y known enzymes to be able to hydrolyze this glycosidic linkage.

218 the inversion of the configuration of the N-glycosidic linkage.

219 te preference for alpha(1-6) over alpha(1-4) glycosidic linkages and produces glucose from isomaltose

220 nt structural conformation i.e. variation in glycosidic linkages and sulphate group orientation.

221 e mutant glycosidases, that can readily form glycosidic linkages are addressing a lack of a wide rang

222 enzyl, and p-bromobenzyl ethers, esters, and glycosidic linkages are stable to these reaction conditi

223 glycoconjugates bearing the 1,2-cis-2-amino glycosidic linkages because the saccharide thioglycoside

224 ymers of different lengths containing labile glycosidic linkages between monomer units necessitating

225 monosaccharide composition, the position of glycosidic linkages between monosaccharides, and the pos

226 an be characterized by the torsion angles of glycosidic linkages between relatively rigid carbohydrat

227 matic detection and annotation of sugars and glycosidic linkages between sugar units and to proteins,

228 h sugar residues are all connected by native glycosidic linkages found in natural N-glycans.

229 es (GT) to catalyse formation of the various glycosidic linkages found in the polymer.

230 a reduction of alpha(1-->6) and alpha(1-->2) glycosidic linkages illustrating a reduced degree of bra

231 complementary specificities to hydrolyze the glycosidic linkages in agarose, a linear polymer compris

232 Glycoside hydrolases (GHs) cleave glycosidic linkages in carbohydrates, typically via inve

233 Cellulases hydrolyze beta-1,4 glycosidic linkages in cellulose, which are among the mo

234 rize anomeric configurations of newly formed glycosidic linkages in complex oligosaccharide synthesis

235 Cellobiohydrolases processively hydrolyze glycosidic linkages in individual polymer chains of cell

236 is a paradigm for the study of other unusual glycosidic linkages in model and parasitic organisms.

237 n and a reducing agent to oxidatively cleave glycosidic linkages in polysaccharides.

238 Challenging glycosidic linkages including alpha-gluco, beta-manno, a

239 de thioglycosides containing 1,2-cis-2-amino glycosidic linkages is challenging.

240 An immense variety of sugars and glycosidic linkages leads to an almost unlimited diversi

241 enzyme known to catalyse hydrolysis of the O-glycosidic linkages of ADP-ribose polymers, thereby reve

242 aride composed of partially acetylated 1-->4 glycosidic linkages of N-acetylgalactosamine and N-acety

243 s ability to catalyze the hydrolysis of beta-glycosidic linkages once endocytosed, whereas equal conc

244 C-H protons is indicative of the position of glycosidic linkages or other substituents and can be rea

245 fficient and stereoselective construction of glycosidic linkages remains one of the most formidable c

246 A review of its repertoire of glycosidic linkages suggests a minimum of 38 glycosyltra

247 ately 10(7) y),(5) of the 1-4 "head-to-tail" glycosidic linkages that join the common glucose polymer

248 te alternating beta-(1-->5) and beta-(1-->6) glycosidic linkages using a single active site.

249 xtend this study to the synthesis of various glycosidic linkages using different sugar series.

250 trols stereoselective formation of 1,2-trans-glycosidic linkages via the arming participation effect.

251 ferases was performed, and the nature of the glycosidic linkages was determined by NMR.

252 ortant glucoside containing multiple 1,2-cis-glycosidic linkages with complete anomeric control by us

253 ransferase in the GT41 family that creates N-glycosidic linkages with glucose and galactose at aspara

254 rocycles, melamine and barbituric acid, form glycosidic linkages with ribose and ribose-5-phosphate i

255 can show that the torsions of the different glycosidic linkages within the GPI tetrasaccharide can b

256 types, sugar types, chemical modifications, glycosidic linkages, and anomeric states.

257 ha-glucan with (alpha1-->3) and (alpha1-->6) glycosidic linkages, and was similar in structure to a p

258 sis of their monosaccharide building blocks, glycosidic linkages, chain length, as well as additional

259 Of the two possible glycosidic linkages, chemically, 1,2-trans linkage is re

260 -glycosidic bonds are replaced with the urea-glycosidic linkages, has recently emerged with applicati

261 ain of xylose residues connected by beta-1,4 glycosidic linkages, has remained elusive.

262 To prevent hydrolysis of acid-labile glycosidic linkages, optimal reaction conditions that ma

263 Moreover, glycans with unique glycosidic linkages, particularly from prokaryotes, whic

264 families acting on both axial and equatorial glycosidic linkages, respectively.

265 an-II, cleaving all but 1 of its 21 distinct glycosidic linkages.

266 ight on gas-phase dissociation mechanisms of glycosidic linkages.

267 ansferase family members to catalyze beta1-2 glycosidic linkages.

268 g is an exo-alpha-neuraminidase that cleaves glycosidic-linked sialic acids.

269 Thermal treatment of the glycosidic mixture at native pH of fruit gave furanoid c

270 By HPLC-ESI-MS analyses of glycosidic mixtures and GC-MS analyses of volatiles rele

271 ains a polycyclic ring system (rings A-D), a glycosidic moiety at C4, and a pendant ring (E-ring) at

272 d of a polycyclic ring system (rings A-D), a glycosidic moiety at the C4 position, and a pendent ring

273 ising from the C-ring, the D-ring, or the C4 glycosidic moiety were observed with either enzyme, sugg

274 residue was found to be too distant from the glycosidic oxygen (>4.3 A) to serve directly as a genera

275 thuss proton shuttle between Glu-796 and the glycosidic oxygen, permitting this residue to serve as t

276 riables, such as coordination numbers of the glycosidic oxygen, yielded a variety of chemical reactio

277 oned between the catalytic acid/base and the glycosidic oxygen.

278 nsted acidic OH-defect sites and constrained glycosidic oxygens (i.e., those juxtaposed adjacent to t

279 However, an explanation for these featured glycosidic patterns has not emerged.

280 eral acid/base Glu-288 nearest the predicted glycosidic position, whereas the open conformation possi

281 PMO1s and PMO2s hydroxylate glycosidic positions C1 and C4, respectively.

282 The aim of this work was to identify the glycosidic precursors of the key volatile compounds resp

283 ships among odour-active volatiles and their glycosidic precursors were also proposed.

284 Glycosidic precursors were isolated from juice by adsorp

285 ntargeted approach with 3 custom-synthesized glycosidic precursors.

286 ne bearing redox-active osmium complexes and glycosidic residues (lactose) is used to create a self-a

287 peating ADP-ribose units linked via a unique glycosidic ribose-ribose bond, and is synthesized from N

288 f long chains of ADP-ribose units, linked by glycosidic ribose-ribose bonds, and is critical for a wi

289 SoArsAB also activated DMB to its alpha-N-glycosidic ribotide.

290 aMN) to phenol or p-cresol, yielding alpha-O-glycosidic ribotides.

291 This work aimed to define the glycosidic simple phenolic profile of a large selection

292 piperidine ring of the iminosugar and the C-glycosidic structure of alpha-D-GlcNAc.

293 Presence of alpha and beta-glycosidic structures such as glucans and glucan-protein

294 After a glycan search is complete, each glycosidic torsion angle distribution is displayed in te

295 wever, for K14M with adenyl nucleotides, the glycosidic torsion angle was 30 +/- 5 degrees with MgATP

296 omplexes, GKy.MgADP.[u-(13)C]GMP, the guanyl glycosidic torsion angle, chi, is 51 +/- 5 degrees for R

297 For R41M with adenyl nucleotides, the glycosidic torsion angle, chi, was 55 +/- 5 degrees with

298 ww.glycanstructure.org, is a database of the glycosidic torsion angles derived from the glycan struct

299 The analysis of the glycosidic torsional angles and the pair interaction ene

300 The changes in glycosidic torsional linkage and the receptor conformati