ライフサイエンスコーパス: glucuronic acid

1 sulfate to the iduronic acid but not to the glucuronic acid.

2 fated heparosan, a polysaccharide containing glucuronic acid.

3 DP-N-acetylglucosamine (UDP-GlcNAc), and UDP-glucuronic acid.

4 ansformed cells on minimal medium containing glucuronic acid.

5 h as hormones by reversible conjugation with glucuronic acid.

6 daily diet and environment by conjugation to glucuronic acid.

7 s two oxidations of UDP-glucose to yield UDP-glucuronic acid.

8 position 6 with glucuronic acid or rhamnosyl glucuronic acid.

9 d environmental chemicals via conjugation to glucuronic acid.

10 mediate that is synthesized by ArnA from UDP-glucuronic acid.

11 neurotoxic bilirubin by conjugating it with glucuronic acid.

12 a pathway for l-Ara4N biosynthesis from UDP-glucuronic acid.

13 e polysaccharide contained galactosamine and glucuronic acid.

14 the related IAG sequence, where G is alpha-D-glucuronic acid.

15 inked mannan substituted with D-xylose and D-glucuronic acid.

16 e HA or any other molecules known to contain glucuronic acid.

17 e hydroxyl groups in glycosidic linkage with glucuronic acid.

18 ha-D-glucose, beta-D-glucose, rhamnose and D-glucuronic acid.

19 lycyrrhizin (GL) by hydrolysing one terminal glucuronic acid.

20 polymer from UDP-N-acetylglucosamine and UDP-glucuronic acid.

21 cid, rhamnose, mannose, xylose and traces of glucuronic acid.

22 UDP-glycosyltransferase UGT co-substrate UDP-glucuronic acid.

23 applied to develop a synthesis of protected glucuronic acid 1, a key intermediate in the synthesis o

24 ed a rare sequence consisting of consecutive glucuronic acid 2-O-sulfate residues as selectively targ

25 boring nodes of Ranvier stained for unmasked glucuronic acid 3-SO4 and chondroitin 6-SO4.

26 ies against carbohydrate epitopes, including glucuronic acid 3-SO4 and chondroitins 6-SO4 and 4-SO4.

27 tive cleavage of myo-inositol (MI) to give d-glucuronic acid, a committed step in MI catabolism.

28 gh content of the nonsulfated disaccharide D-glucuronic acid-acetylated glucosamine (GlcA-GlcNAc).

29 metabolites (methylated and conjugated with glucuronic acid) across hCMEC/D3 cells (a blood-brain ba

30 inant UAS homologs all form UDP-Api from UDP-glucuronic acid albeit in different amounts.

31 Mutations in a previously identified UDP-glucuronic acid allosteric binding site decreased the bi

32 nd glycolipid, termed Gl-X (mannose-alpha1-4-glucuronic acid-alpha1-diacylglycerol), which function a

33 s for the sugar donors UDP-galactose and UDP-glucuronic acid, although UDP-glucose was always preferr

34 des UDP-glucose dehydrogenase which produces glucuronic acid, an essential component for the synthesi

35 ssive oxidations of UDP-glucose to yield UDP-glucuronic acid, an essential precursor for matrix polys

36 DP-glucose dehydrogenase (Ugd) generates UDP-glucuronic acid, an important precursor for the producti

37 shown to hydrolyze terminal alpha-1,2-linked glucuronic acid and 4-O-methylated glucuronic acid from

38 backbone of xylosyl residues substituted by glucuronic acid and 4-O-methylglucuronic acid (collectiv

39 that although wild-type xylans contain both glucuronic acid and 4-O-methylglucuronic acid residues,

40 ranosiduronic acids (glucuronides) using UDP-glucuronic acid and acceptor substrates such as drugs, s

41 lation, we identified O-acetylation of alpha-glucuronic acid and alpha-glucose in 9A PS.

42 es with low ratios of xylose to 4-O-methyl-D-glucuronic acid and appears to require two 4-O-methyl-D-

43 in itself, and this binding was inhibited by glucuronic acid and chondroitin sulfate.

44 hesized in the assay was composed of Glc and glucuronic acid and could be degraded to a low molecular

45 dependent oxidation of the 4''-OH of the UDP-glucuronic acid and decarboxylation of the UDP-4-keto-gl

46 f acidic O-linked glycoconjugates containing glucuronic acid and galactose as well as a reduction of

47 microfibrils had a higher content of (methyl)glucuronic acid and galactose in tension wood than in no

48 dation of not only alginate, but poly-beta-D-glucuronic acid and hyaluronic acid as well.

49 o its ability to sequester intracellular UDP-glucuronic acid and inhibition of hyaluronan synthase tr

50 tabolites; quercetin-3'-sulfate, quercetin-3-glucuronic acid and isorhamnetin-3-glucuronic acid were

51 ed that the resulting mutant lacked both UDP-glucuronic acid and its downstream product, UDP-xylose,

52 ible for the oxidation of UDP-glucose to UDP-glucuronic acid and its subsequent decarboxylation to UD

53 accommodation of alpha1,2-linked 4-methyl-D-glucuronic acid and L-arabinofuranose side chains.

54 ase responsible for the interconversion of d-glucuronic acid and l-iduronic acid residues encodes a t

55 DG42 encoded on a plasmid incorporated [14C]glucuronic acid and N-[3H]acetylglucosamine from exogeno

56 ide composed of repeating disaccharides of D-glucuronic acid and N-acetyl-D-glucosamine (GlcNAc).

57 nctional chondroitin synthase K4CP catalyzes glucuronic acid and N-acetylgalactosamine transfer activ

58 block, and the two monosaccharide components glucuronic acid and N-acetylglucosamine and identify mar

59 ted HA synthase capable of transferring both glucuronic acid and N-acetylglucosamine groups.

60 long linear polymer composed of alternating glucuronic acid and N-acetylglucosamine residues, is an

61 inear polysaccharide composed of alternating glucuronic acid and N-acetylglucosamine residues, is an

62 onsisting of repeating disaccharide units of glucuronic acid and N-acetylglucosamine.

63 reaction of appropriately substituted azido-glucuronic acid and propargyluted N-acetyl glucosamine a

64 and two quercetin metabolites (quercetin-3-O-glucuronic acid and quercetin-3-O-sulfate) significantly

65 e propose a binding model for NAD(+) and UDP-glucuronic acid and the involvement of residues T(432),

66 catalyzes the conjugation of bilirubin with glucuronic acid and thus enhances bilirubin elimination;

67 eds in three chemical steps via UDP-4-keto-D-glucuronic acid and UDP-4-keto-pentose intermediates.

68 UXNAcS is specific and cannot utilize UDP-glucuronic acid and UDP-galacturonic acid as substrates.

69 at synthesize the building blocks of HA, UDP-Glucuronic acid and UDP-N-Acetyl-Glucosamine, as well as

70 ynthases (HAS1-3), which use cytoplasmic UDP-glucuronic acid and UDP-N-acetylglucosamine as substrate

71 Chondroitin sulfate type C (CSC) contains glucuronic acid, and 90% of the GalNAc residues are sulf

72 Chondroitin sulfate type A (CSA) contains glucuronic acid, and 90% of the GalNAc residues are sulf

73 xylosyl residues is decorated by occasional glucuronic acid, and approximately one-half of the xylos

74 dic, alpha-fucosidic, alpha-mannosidic, beta-glucuronic acid, and beta-glucosamine linkages upon acti

75 ow that hemicellulose branches of arabinose, glucuronic acid, and especially glucuronate strengthen t

76 al other monosaccharides, including glucose, glucuronic acid, and N-acetylmannosamine, do not express

77 gy, we used purified S. equisimilis HAS, UDP-glucuronic acid, and UDP[beta-32P]-Glc-NAc to radiolabel

78 The UGT1 and UGT2 enzymes use UDP-glucuronic acid, and UGT3 enzymes use UDP-N-acetylglucos

79 s beta-glucuronidase enzymes that remove the glucuronic acid as a carbon source, effectively reversin

80 by the ORF atu2297, with UDP-glucose or UDP-glucuronic acid as sugar donors.

81 A Cer analogue with a D-glucuronic acid attached at the primary hydroxyl of N-pa

82 a variety of monodisperse hyaluronan (beta 4-glucuronic acid-beta 3-N-acetylglucosamine (HA)) oligosa

83 magnetic resonance studies confirmed that a glucuronic acid beta1,4-xylose disaccharide synthesized

84 duced repeating units of [-3-xylose-alpha1,3-glucuronic acid-beta1-].

85 uctions in the amount of [-3-xylose-alpha1,3-glucuronic acid-beta1-]n (hereafter referred to as LARGE

86 accharide repeating unit [-3-xylose-alpha1,3-glucuronic acid-beta1-]n by like-acetylglucosaminyltrans

87 ctive UDP-sugars to the non-reducing end of [glucuronic acid]beta1-3[galactose]beta1-O-naphthalenemet

88 with UDP and the acceptor substrate analog [glucuronic acid]beta1-3[galactose]beta1-O-naphthalenemet

89 resolution apo crystal structure of the UDP-glucuronic acid binding domain of human UGT isoform 2B7

90 ncoded protein is closely related to the UDP-glucuronic acid binding site consensus sequence, and the

91 A calcium-dependent glucuronic acid binding site shows distinctive structura

92 n to grow with N-acetylglucosamine but not d-glucuronic acid (both components of HA) as a sole carbon

93 The deletion of either sequence abolishes glucuronic acid but not N-acetylgalactosamine transfer a

94 ectins, is produced from the precursor UDP-D-glucuronic acid by the action of glucuronate 4-epimerase

95 Biosynthesis of UDP-glucuronic acid by UDP-glucose 6-dehydrogenase (UGDH) oc

96 M) enhanced the potency of UDPG (but not UDP-glucuronic acid) by 7-fold.

97 scovered that the published sequence for the glucuronic acid C5-epimerase responsible for the interco

98 t has an overall 37% homology to the human D-glucuronic acid C5-epimerase.

99 residues predicted to interact with the UDP-glucuronic acid cofactor exhibited significantly impaire

100 Compound 5e was converted to beta-glucuronic acid conjugate 6e by the action of pig liver

101 or each analyte; a mixture of 1-pyOH and its glucuronic acid conjugate can be analyzed in 30 min.

102 nantly excreted (>87%) in human urine as the glucuronic acid conjugate, whereas the relative abundanc

103 Minor compounds were glucuronic acid conjugates of 9,10-dihydroxy-octadecanoi

104 iver, intestine and kidney, and catalyze the glucuronic acid conjugation of both endogenous compounds

105 recombinant human UGT isoforms, we show that glucuronic acid conjugation of the model substrate, (-)-

106 Only glucuronic acid-containing ligands produced complexes, a

107 e content of UDP-N-acetylhexosamines and UDP-glucuronic acid, correlating with the expression level o

108 Addition of the terminal residue (glucuronic acid) could not be detected; however, activit

109 (UDP-GlcA) is irreversibly catalyzed by UDP-glucuronic acid decarboxylase (UXS).

110 iosynthesis of UDP-xylose is mediated by UDP-glucuronic acid decarboxylase, which converts UDP-glucur

111 ransmembrane protein that functions as a UDP-glucuronic acid decarboxylase.

112 coccal sequence as putatively encoding a UDP-glucuronic acid decarboxylase.

113 Acetate or glucuronic acid decorations are exclusively found on eve

114 uronic acid degradation at pH 5, poly-beta-D-glucuronic acid degradation at pH 7, and alginate degrad

115 enosine diphosphate-activated platelets, UDP-glucuronic acid-dependent bilirubin conjugation was dete

116 ndogenous and exogenous chemicals by linking glucuronic acid donated by UDP-glucuronic acid to a lipo

117 o glycoside (25) with a trichloroacetimidate glucuronic acid donor (13), using a catalytic amount of

118 The Glc-GlcA disaccharide, featuring the glucuronic acid donor moiety, proved to be the most prod

119 We demonstrated that lpsL encoded a UDP-glucuronic acid epimerase activity that was reduced in t

120 a gene previously predicted to encode a UDP-glucuronic acid epimerase.

121 espect to chain length, sulfate content, and glucuronic acid epimerization content, resulting in a di

122 Although glucuronic acid esters are often considered to be of ver

123 eactions revealed that the reactivity of the glucuronic acid esters studied is sufficient to provide

124 The relative reactivity of glucuronic acid esters was established in a series of co

125 4" oxidation and C-6" decarboxylation of UDP-glucuronic acid, followed by the C-4" transamination of

126 and C-6" decarboxylation of [alpha-(32)P]UDP-glucuronic acid, followed by transamination to generate

127 ,2-linked glucuronic acid and 4-O-methylated glucuronic acid from the plant cell wall polysaccharide

128 ol g(-1)), whereas binding of the competitor glucuronic acid (GA) and other monosaccharides was consi

129 xtracts of the mutants completely lacked UDP-glucuronic acid:Galbeta1,3Gal-R glucuronosyltransferase

130 formation occurs by the copolymerization of glucuronic acid (GlcA) and N-acetylglucosamine (GlcNAc)

131 lcNAc) or N-sulfated glucosamine (GlcNS) and glucuronic acid (GlcA) as the primary sites and the link

132 uishing the epimers iduronic acid (IdoA) and glucuronic acid (GlcA) has been a long-standing challeng

133 corporation of radioactive glucose (Glc) and glucuronic acid (GlcA) into lipid-linked disaccharides i

134 ore-shell particles specifically recognizing glucuronic acid (GlcA) or N-acetylneuraminic acid (NANA)

135 glycan decorations that include a conserved glucuronic acid (GlcA) residue and various additional su

136 ries a pentose linked 1-2 to the alpha-1,2-d-glucuronic acid (GlcA) side chains on the beta-1,4-Xyl b

137 ta-glucuronidase (GUS) enzymes that liberate glucuronic acid (GlcA) sugars from small-molecule conjug

138 the 2-OH position of iduronic acid (IdoA) or glucuronic acid (GlcA) within HS.

139 MIPs were prepared with the templates D-glucuronic acid (GlcA), a substructure of hyaluronan, an

140 The distribution of 13C in the Man, Xyl, glucuronic acid (GlcA), and O-acetyl constituents of nat

141 merase (Hsepi) catalyzes C5-epimerization of glucuronic acid (GlcA), converting it to iduronic acid (

142 residues substituted with alpha(1,2)-linked glucuronic acid (GlcA).

143 Glucuronic acid (GlcAp) and/or methylglucuronic acid (Me

144 6OSO3), but contained a higher proportion of glucuronic acid GlcUA-GlcNSO3(6OSO3) and IdUA-GlcNSO3(6O

145 is a membrane-bound enzyme that utilizes UDP-glucuronic acid (GlcUA) and UDP-GlcNAc to synthesize HA.

146 at transfer N-acetylglucosamine (GlcNAc) and glucuronic acid (GlcUA) in alternative positions in the

147 sed of alternating beta-1,3-Glc and beta-1,4-glucuronic acid (GlcUA) linkages.

148 atalyzes sugar transfer from UDP-Glc and UDP-glucuronic acid (GlcUA) to a polymer with the repeating

149 yltransferase that catalyzes the transfer of glucuronic acid (GlcUA) to the common growing linker reg

150 s comprising 3-sulfated rhamnose linked to d-glucuronic acid (GlcUA), l-iduronic acid (IdoUA), or d-x

151 PmHAS possesses both GlcNAc-transferase and glucuronic acid (GlcUA)-transferase activities.

152 Reaction of beta-glucuronic acid glycoside of 4-hydroxy-3-nitrobenzyl alc

153 al preparations resulted in no metabolite or glucuronic acid-HPPH conjugate production.

154 ogether with the aglycon and alpha- and beta-glucuronic acid hydrolysis products.

155 may be close to the 3-hydroxyl group of beta-glucuronic acid in a HNK-1 acceptor.

156 esonance that revealed a crucial role of the glucuronic acid in antibody binding.

157 w that the carboxyl group on nonreducing end glucuronic acid in dodecasaccharide motif is important f

158 o distinguish the epimers iduronic acid from glucuronic acid in heparan sulfate tetrasaccharides and

159 a1-4 linkage between N-acetylglucosamine and glucuronic acid in hyaluronan polymers via a substrate-a

160 s undergo detoxification by conjugation with glucuronic acid in the liver via the action of UDP-glucu

161 Nrf2 promoted conjugation of ABP with glucuronic acid in the liver, increasing urinary excreti

162 n, ideal for decarboxylation of UDP-4-keto-D-glucuronic acid in the second chemical step.

163 E, quercetin-3-O-glucoside and quercetin-3-O-glucuronic acid inhibited significantly (p<0.05) ACE act

164 c acid and decarboxylation of the UDP-4-keto-glucuronic acid intermediate.

165 The oxidative decarboxylation of UDP-glucuronic acid is catalyzed by the 345-residue C-termin

166 d-Glucuronic acid is further metabolized to xylitol via th

167 ctivity of B3GAT1, we were able to show that glucuronic acid is present on antennae of plasma glycopr

168 In humans, conjugation with glucuronic acid is the most important phase II metabolic

169 In mammalian organisms, UDP-glucuronic acid is typically used in the transfer reacti

170 at is specific for the l-rhamnose-alpha1,4-d-glucuronic acid linkage that caps the side chains of com

171 Glucuronic acid linked prodrugs of O(6)-benzylguanine an

172 ated Az29, possesses two PEtn moieties and a glucuronic acid linked to a Gal-extended Nz28.

173 ranched surface structure containing glucose-glucuronic acid linked to a glucose-rhamnose-rhamnose-rh

174 vered that heparanase cleaves the linkage of glucuronic acid linked to glucosamine carrying 6-O-sulfo

175 n those measured on a mixture of pyruvic and glucuronic acids (logK = 2.2), which are the two constit

176 Glucuronic acid modification was observed in E. coli B,

177 f sugar residues and epimerizations of their glucuronic acid moieties.

178 etraazacyclododecane) bearing a pendant beta-glucuronic acid moiety connected by a self-immolative li

179 GlcAT-I transfers a glucuronic acid moiety from the uridine diphosphate-gluc

180 cid hydrolysis, resulting in a Xyl:arabinose:glucuronic acid molar ratio of approximately 105:34:1.

181 fucose, d-mannose, d-galactose, d-glucose, d-glucuronic acid, N-acetyl-d-galactosamine, and N-acetyl-

182 -ribofuranose and 3-O-[(R)-1-carboxyethyl]-D-glucuronic acid (nosturonic acid) pendant groups.

183 ccus neoformans comprises manose, xylose and glucuronic acid, of which mannose is the major constitue

184 scribed, which arises due to the addition of glucuronic acid on the third heptose with a concomitant

185 transferase GUX1, and so the even pattern of glucuronic acid on the xylan is lost.

186 residues in the capsule are derived from UDP-glucuronic acid or its metabolites.

187 di- or trisaccharide and at position 6 with glucuronic acid or rhamnosyl glucuronic acid.

188 highly sulfated polysaccharide consisting of glucuronic acid (or iduronic acid) linked to glucosamine

189 of acidic sugars N-acetylneuraminic acid and glucuronic acid out of lysosomes.

190 ctivity against hyaluronan (HA), poly-beta-d-glucuronic acid (poly-GlcUA), and poly-beta-d-mannuronic

191 lation of the bacterial N-acetylglucosaminyl-glucuronic acid polymer K5 under conditions where the ho

192 effects in rodents, and are conjugated with glucuronic acid prior to excretion in human urine.

193 We propose that the regulation of UDP-glucuronic acid production in a specific subset of vulva

194 indicating that an alternate pathway for UDP-glucuronic acid production was not used.

195 d from partial desulfation demonstrated that glucuronic acid rather than iduronic acid residues are i

196 lysaccharide composed of N-acetylglucosamine-glucuronic acid repeats, is found in the extracellular m

197 acid and appears to require two 4-O-methyl-D-glucuronic acid residues for substrate recognition and/o

198 on, BtGH115A, hydrolyzes terminal 4-O-methyl-glucuronic acid residues from decorated arabinogalactan

199 dase was used to remove nonreducing-terminal glucuronic acid residues from oligosaccharides.

200 ily 2 glycosylhydrolases that cleaves beta-D-glucuronic acid residues from the nonreducing termini of

201 ly incorporated xylose (Xyl), arabinose, and glucuronic acid residues from their corresponding uridin

202 Odd-numbered oligosaccharides with terminal glucuronic acid residues isolated from hyaluronidase dig

203 ults in a specific defect in the addition of glucuronic acid residues onto xylans.

204 iency, both contain a trisaccharide with two glucuronic acid residues that enabled the identification

205 ride of alternating N-acetyl-glucosamine and glucuronic acid residues, is ubiquitously expressed in v

206 ride units of N-acetyl-D-galactosamine and d-glucuronic acid residues, modified with sulfated residue

207 idues but lacks any 2-O-sulfated iduronic or glucuronic acid residues.

208 rface than thought previously, such that a D-glucuronic acid ring makes stacking and ionic interactio

209 ynthesis mutants, such as the replacement of glucuronic acid side chains with methylglucuronic acid s

210 (GXMT) that catalyzes 4-O-methylation of the glucuronic acid substituents of this polysaccharide.

211 xylan, generating products with a 4-O-methyl-glucuronic acid-substituted xylose residue one position

212 GUX1 (glucuronic acid substitution of xylan 1) and GUX2, recen

213 noglycan composed of N-acetylglucosamine and glucuronic acid subunits.

214 ernating beta1,3-N-acetylglucosamine-beta1,4-glucuronic acid sugar chain by the sequential addition o

215 nd xenobiotic compounds by linking them to a glucuronic acid sugar for GI excretion.

216 UGTs catalyze the covalent addition of glucuronic acid sugar moieties to a host of therapeutics

217 ects observed for amino acids closest to the glucuronic acid sugar transferred to the acceptor molecu

218 ansport rate for N-acetylneuraminic acid and glucuronic acid, suggesting that it may be directly invo

219 (Ssp) show homology to genes involved in UDP-glucuronic acid synthesis.

220 specificity and allows phosphorylation of d-glucuronic acid, the 4-epimer of GalA.

221 charides containing terminal 4,5-unsaturated glucuronic acid, the nonreducing end disaccharide moiety

222 found in natural polysaccharides containing glucuronic acid, the oxidation of the primary alcohol at

223 nts may be linked to the availability of UDP-glucuronic acid; therefore UGDH is an intriguing therape

224 ls by linking glucuronic acid donated by UDP-glucuronic acid to a lipophilic acceptor substrate.

225 "reversible" catalytic mode by converting a glucuronic acid to an iduronic acid residue, and vice ve

226 lso serve as a one-way catalyst to convert a glucuronic acid to an iduronic acid residue, displaying

227 coded by PsUGT1 catalyzes conjugation of UDP-glucuronic acid to an unknown compound.

228 Chst10 adds sulfate to glucuronic acid to form a carbohydrate antigen, HNK-1, i

229 precedented oxidative decarboxylation of UDP-glucuronic acid to form uridine 5'-(beta-l-threo-pentapy

230 )-dependent oxidative decarboxylation of UDP-glucuronic acid to generate a UDP-4'-keto-pentose sugar

231 ehydrogenase, which is capable of converting glucuronic acid to glucaric acid.

232 ylgalactosamine may precede epimerization of glucuronic acid to iduronic acid during dermatan sulfate

233 san with C(5)-epimerase converts some of the glucuronic acid to iduronic acid, thus becoming a substr

234 The HS C(5)-epimerase converts glucuronic acid to iduronic acid.

235 fication reactions is the epimerization of D-glucuronic acid to its C5-epimer L-iduronic acid, which

236 UGT1As add glucuronic acid to many drugs, modifying their activity

237 UGT1As add glucuronic acid to many drugs.

238 3)-glucuronyltransferases, one of which adds glucuronic acid to protein-linked galactose-beta(1, 4)-N

239 the NAD(+)-dependent decarboxylation of UDP-glucuronic acid to UDP-4-keto-arabinose and (ii) the N-1

240 One activity is to decarboxylate UDP-glucuronic acid to UDP-beta-l-threo-pentopyranosyl-4''-u

241 hase (AXS) catalyzes the conversion of UDP-D-glucuronic acid to UDP-D-apiose and UDP-D-xylose.

242 neoformans gene catalyzed conversion of UDP-glucuronic acid to UDP-xylose, as confirmed by NMR analy

243 ronic acid decarboxylase, which converts UDP-glucuronic acid to UDP-xylose.

244 ase (UXS) catalyzes decarboxylation of UDP-D-glucuronic acid to UDP-xylose.

245 +-dependent oxidative decarboxylation of UDP-glucuronic acid to yield the UDP-4''-ketopentose, uridin

246 olase-like catalytic mechanism to facilitate glucuronic acid transfer.

247 into two single-action glycosyltransferases (glucuronic acid transferase and N-acetylglucosamine tran

248 ) to the key metabolic precursor UDP-alpha-d-glucuronic acid (UDP-GlcA) and display specificity for U

249 e authentic sugar nucleotide precursors, UDP-glucuronic acid (UDP-GlcA) and UDP-N-acetylglucosamine (

250 together with UDP-xylose is formed from UDP-glucuronic acid (UDP-GlcA) by UDP-Api synthase (UAS).

251 The biosynthesis of UDP-Xyl from UDP-glucuronic acid (UDP-GlcA) is irreversibly catalyzed by

252 UDP-glucuronic acid (UDP-GlcA) is the precursor of many plan

253 ing (1) the oxidative decarboxylation of UDP-glucuronic acid (UDP-GlcA) to the UDP-4' '-ketopentose [

254 ) catalyzes the epimerization of UDP-alpha-D-glucuronic acid (UDP-GlcA) to UDP-alpha-D-galacturonic a

255 is synthesized by the decarboxylation of UDP-glucuronic acid (UDP-GlcA).

256 nverts UDP-2-acetamido-3-amino-2,3-dideoxy-d-glucuronic acid (UDP-GlcNAc3NA) to UDP-2,3-diacetamido-2

257 NAc3NA) to UDP-2,3-diacetamido-2,3-dideoxy-d-glucuronic acid (UDP-GlcNAc3NAcA).

258 ed nucleotide sugars UDP-2-acetamido-2-deoxy-glucuronic acid (UDP-GlcNAcA) and UDP-2-acetamido-2-deox

259 te (Glc-6-P) --> Glc-1-P --> UDP-Glc --> UDP-glucuronic acid (UDP-GlcUA) --> (GlcUA-Glc)(n).

260 accharide units from the donor molecules UDP-glucuronic acid (UDP-GlcUA) and UDP-N-acetylglucosamine

261 oniae requires UDP-glucose (UDP-Glc) and UDP-glucuronic acid (UDP-GlcUA) for production of the [3)-be

262 resence of protein-mediated transport of UDP-glucuronic acid (UDP-GlcUA) in rat liver endoplasmic ret

263 lcUA-(1-] from UDP-glucose (UDP-Glc) and UDP-glucuronic acid (UDP-GlcUA) is catalysed by the type 3 s

264 nic acid moiety from the uridine diphosphate-glucuronic acid (UDP-GlcUA) to the common linkage region

265 trate for all glucuronidation reactions, UDP-glucuronic acid (UDP-GlcUA), was determined using a rapi

266 cerevisiae expressing SQV-7 transported UDP-glucuronic acid, UDP-N-acetylgalactosamine, and UDP-gala

267 The abundance of the 4-O-methyl-alpha-d-glucuronic acid was not previously reported.

268 use steroid hormones are often conjugated to glucuronic acid, we hypothesized that Chst10 sulfates gl

269 ercetin-3-glucuronic acid and isorhamnetin-3-glucuronic acid were effective at physiological concentr

270 synthase for UDP-N-acetylglucosamine and UDP-glucuronic acid were estimated to be approximately 75 an

271 talyzes the conversion of UDP-glucose to UDP-glucuronic acid, which is essential for the biosynthesis