ライフサイエンスコーパス: UDP glucose

1 milar to the native substrate of the toxins (UDP-glucose).

2 eristics similar to their natural substrate, UDP-glucose.

3 embranes and the nucleotide-sugar substrate, UDP-glucose.

4 50 values (323, 132, and 72 nM) observed for UDP-glucose.

5 d is also the first nonplant transporter for UDP-glucose.

6 max, but a 165-fold decrease in affinity for UDP-glucose.

7 substrate rather than the more commonly used UDP-glucose.

8 etabolism, interconverting UDP-galactose and UDP-glucose.

9 se-1P, elevated UDP-galactose, and deficient UDP-glucose.

10 in contains the binding sites for NAD(+) and UDP-glucose.

11 1G1 from Medicago truncatula bound to UDP or UDP-glucose.

12 ease in extracellular levels of both ATP and UDP-glucose.

13 th galactose metabolism and the synthesis of UDP-glucose.

14 e synthesis by degrading Suc to fructose and UDP-glucose.

15 and in a ternary complex with bound NADH and UDP-glucose.

16 otif in H3 greatly diminished its binding to UDP-glucose.

17 strate specificity of cellulose synthase for UDP-glucose.

18 s mediterranei which derives kanosamine from UDP-glucose.

19 the presence and absence of the co-substrate UDP-glucose.

20 he sugar donor preference from UDP-GlcNAc to UDP-glucose.

21 8-A resolution structure of the complex with UDP/glucose.

22 ot hair defective1 (rhd1) lacks a functional UDP-glucose 4-epimerase gene, UGE4, which is involved in

23 ligosaccharide biosynthesis, three annotated UDP-glucose 4-epimerase genes of B. anthracis were clone

24 Uge5 is the dominant UDP-glucose 4-epimerase in A. fumigatus and is essential

25 enome contains three genes encoding putative UDP-glucose 4-epimerases, uge3, uge4, and uge5.

26 The first gene encodes a UDP-glucose-4,6-dehydratase that converts UDP-glucose to

27 oof of principle work were cyclophilin A and UDP-glucose-4-epimerase, both of which are known to inte

28 In Arabidopsis, mutation of RHD1, a UDP-glucose-4-epimerase, causes root-specific phenotypes

29 transport operon and galE, which encodes the UDP-glucose-4-epimerase.

30 Biosynthesis of UDP-glucuronic acid by UDP-glucose 6-dehydrogenase (UGDH) occurs through the fo

31 Similarly, knockdown of UDP-glucose 6-dehydrogenase (UGDH) using lentiviral shRN

32 rated that recombinant HasB2 is a functional UDP-glucose 6-dehydrogenase enzyme.

33 ding hyaluronan synthase, and hasB, encoding UDP-glucose 6-dehydrogenase, are essential for capsule p

34 Classical UDP-glucose 6-dehydrogenases (UGDHs; EC 1.1.1.22) cataly

35 The identification of redundant UDP-glucose 6-dehydrogenases underscores the importance

36 the subsequent 4-HPAA reductase and tyrosol:UDP-glucose 8-O-glucosyltransferase, respectively, to co

37 Pase; EC 2.7.7.9) is an enzyme that produces UDP-glucose, a key precursor for sucrose metabolism and

38 d Ca(2+)-regulated apical release of ATP and UDP-glucose, a substrate of glycosylation reactions with

39 UDP and UDP-glucose activate the P2Y14 receptor (P2Y14R) to modu

40 llular UDP-glucose levels, expression of the UDP-glucose-activated P2Y(14) receptor in COS-7 cells re

41 ologically relevant tissues and suggest that UDP-glucose acts as an autocrine activator of the P2Y(14

42 n UGDH involves Lys(220) as general base for UDP-glucose alcohol oxidation and for oxyanion stabiliza

43 UDP and UDP-glucose also stimulated extracellular signal-regulat

44 UDP-glucose also was observed at levels that equaled or

45 a high-affinity manner influenced in part by UDP glucose, an intracellular proxy for nutrient availab

46 zes the interconversion of UDP-galactose and UDP-glucose, an important step in galactose catabolism.

47 hexose 6-phosphates, but predominantly from UDP-glucose; an alternative to the textbook pentose-phos

48 ose (Suc) synthase (SUS) cleaves Suc to form UDP glucose and fructose, and exists in soluble and memb

49 Approximate K(m) values of 150 microm for UDP-glucose and 10 microm for sulfite were established f

50 crystallizing E161Q in the presence of 5 mm UDP-glucose and 2 mm NAD(+), we succeeded in trapping a

51 The involvement of SUS in the synthesis of UDP-glucose and ADP-glucose linked to Arabidopsis cellul

52 tSus1) has been determined as a complex with UDP-glucose and as a complex with UDP and fructose, at 2

53 Similar rates of basal release of UDP-glucose and ATP (72 and 81 fmol/min/10(6) cells) com

54 gonists as the human receptor, responding to UDP-glucose and closely related molecules with similar a

55 -galactosyltransferase from UDP-galactose to UDP-glucose and decreased the cost for the synthesis of

56 Mr of 43 kDa which had dual specificity for UDP-glucose and ethanol.

57 Furthermore, co-administration of UDP-glucose and G-CSF led to greater HSPC mobilization t

58 halose-6-phosphate (T6P) is synthesized from UDP-glucose and glucose-6-phosphate (catalyzed by T6P sy

59 c synthesis of Galalpha1,3Galbeta1,4Glc from UDP-glucose and lactose, the genetically fused enzymes f

60 Both UDP-glucose and LTD(4) increased GPR17 internalization,

61 as a G protein-coupled receptor activated by UDP-glucose and other nucleotide sugars.

62 rst, the assembly of UDP-sulfoquinovose from UDP-glucose and sulfite, and second, the transfer of the

63 sponsible for the recognition and binding of UDP-glucose and the catalytic manganese ion and implicat

64 4-epimerase catalyzes the interconversion of UDP-glucose and UDP-galactose during normal galactose me

65 he common UDP moiety in substrate/inhibitor, UDP-glucose and UDP-hexanol amine caused competitive inh

66 ant uridine-containing cell wall precursors, UDP-Glucose and UDP-N-acetylglucosamine are efficiently

67 effects due to each mutation using both the UDP-glucose and UDP-N-acetylglucosamine bound structures

68 r, and the isoform from C24 can utilize both UDP-glucose and UDP-xylose but with a higher affinity to

69 prenyl transfers (IPP), glucosyl transfers (UDP-glucose), and electron and ADP-ribosyl transfers (NA

70 or hexose-, pentose-, and triose-phosphates, UDP-glucose, and adenosine monophosphate (AMP).

71 eotides, including GDP-mannose, ADP-mannose, UDP-glucose, and ADP-glucose.

72 structure of Gal10p in complex with NAD(+), UDP-glucose, and beta-D-galactose determined to 1.85-A r

73 , S-adenosylmethionine, carbamoyl phosphate, UDP-glucose, and Delta(2)-isopentenyl-PP play similar ro

74 nd UGT3 enzymes use UDP-N-acetylglucosamine, UDP-glucose, and UDP-xylose to conjugate xenobiotics, in

75 hydroximic acid (approximately 6 microm) and UDP-glucose (approximately 50 microm) strongly suggest t

76 eptors, and utilizes either UDP-galactose or UDP-glucose as donor substrates.

77 sfers glucose to diacylglycerol (DAG), using UDP-glucose as its substrate.

78 ugation reaction, with free anthranilate and UDP-glucose as substrates, that yielded the same fluores

79 All tested UGTs preferred UDP-glucose as sugar donor.

80 The Km for UDP-glucose as the glucosyl donor was approximately 18 m

81 ently glucosylates vancomycin aglycone using UDP-glucose as the glycosyl donor to form desvancosaminy

82 monstrate that H3 binds the sugar nucleotide UDP-glucose, as do glycosyltransferases.

83 Like glycosyltransferases, H3 binds UDP-glucose, as shown by saturation transfer difference

84 GALE), which interconverts UDP-galactose and UDP-glucose, as well as UDP-N-acetylgalactosamine and UD

85 aided by development of a novel bioassay for UDP-glucose based on signaling through heterologously ex

86 P-glucose, with ADP-glucose, GDP-glucose and UDP-glucose being the preferred substrates.

87 ified residues that are required for UDP- or UDP-glucose binding and for oligomerization of Gtf3 and

88 This region contains the UDP-glucose binding domain and the glycosyltransferase d

89 Stimulation of GBS and depletion of UDP-glucose both correlated with an early and rapid rise

90 zyme recognizes as substrates cis-zeatin and UDP-glucose but not cis-ribosylzeatin, trans-zeatin, or

91 ly was the human P2Y14 receptor activated by UDP-glucose, but it also was activated by UDP.

92 was greatly stimulated in its utilization of UDP-glucose by polyanions such as heparin, the recombina

93 for the interconversion of UDP-galactose and UDP-glucose by reversibly mediating their dehydrogenatio

94 s through the four-electron oxidation of the UDP-glucose C6 primary alcohol in two NAD(+)-dependent s

95 ctivity accumulate WT levels of ADP-glucose, UDP-glucose, cellulose and starch.

96 The enzyme UDP-glucose ceramide glucosyltransferase (Ugcg) catalyze

97 NAc-transferase (MGAT1) and GSLs by deleting UDP-glucose ceramide glucosyltransferase (UGCG).

98 fication of ceramide to glucosylceramide via UDP-glucose ceramide glucosyltransferase (UGCG).

99 epression of the key GSL biosynthetic enzyme UDP-glucose ceramide glucosyltransferase (UGCG).

100 Subsequent C5aR1 activation controlled UDP-glucose ceramide glucosyltransferase production, the

101 , the action of which is catalyzed either by UDP-glucose:ceramide glucosyltransferase or by UDP-galac

102 to model conformational heterogeneity in the UDP-glucose complex followed by the use of multiconforme

103 The N-terminal domain of the UDP-glucose complex was found to be 13.3 degrees more cl

104 unt for the observed electron density of the UDP-glucose complex.

105 sophila Sugarless, a uridine 5'-diphosphate (UDP)-glucose dehydrogenase required for heparan sulfate,

106 UDP-glucose dehydrogenase (Ugd) generates UDP-glucuronic

107 UDP-glucose dehydrogenase (UGDH) catalyzes the formation

108 UDP-glucose dehydrogenase (UGDH) catalyzes two oxidation

109 on in zebrafish revealed a critical role for UDP-glucose dehydrogenase (UGDH) in valve development, s

110 Human UDP-glucose dehydrogenase (UGDH) is a homohexameric enzy

111 UDP-glucose dehydrogenase (UGDH) oxidizes UDP-glucose to

112 UDP-glucose dehydrogenase (UGDH) provides precursors for

113 hich disrupts the single mouse gene encoding UDP-glucose dehydrogenase (Ugdh), an enzyme required for

114 we have generated a mesenchymal ablation of UDP-glucose dehydrogenase (Ugdh), an essential biosynthe

115 ced the IPUT1 gene together with genes for a UDP-glucose dehydrogenase from Arabidopsis and a human U

116 ns of cps2K, cps2J, or cps2H, which encode a UDP-glucose dehydrogenase necessary for side chain synth

117 uronate arose predominantly by the action of UDP-glucose dehydrogenase rather than through the postul

118 Comparison of the GMD structure with that of UDP-glucose dehydrogenase reveals the structural basis o

119 tion induces transcription of the Salmonella UDP-glucose dehydrogenase ugd gene in an RcsA- and RcsB-

120 e sugars in C. neoformans, the gene encoding UDP-glucose dehydrogenase was disrupted.

121 -d-carboxylethyl)-l-norvaline dehydrogenase, UDP-glucose dehydrogenase, and 6-phosphogluconate dehydr

122 A second UDP-glucose dehydrogenase, corresponding to the monospec

123 ound that sqv-4 encodes a protein similar to UDP-glucose dehydrogenases and showed that the SQV-4 pro

124 cloned with high similarity to the family of UDP-glucose dehydrogenases.

125 The Arabidopsis type 1 UDP-glucose-dependent glucosyltransferase UGT72B1 is hig

126 ined, both in its 'Michaelis' complex with a UDP-glucose-derived donor and the acceptor kaempferol an

127 S, and a reduction in steady-state levels of UDP-glucose due to increased precursor utilization.

128 zes the interconversion of UDP-galactose and UDP-glucose during normal galactose metabolism.

129 The positioning of the bound UDP-glucose far from Tyr194 in the glycogenin structure

130 he reduction of the anthocyanin-related gene UDP glucose:flavonoid 3-O-glucosyl transferase (UFGT), w

131 The red grape enzyme UDP-glucose:flavonoid 3-O-glycosyltransferase (VvGT1) is

132 nin pathway and specifically activates UFGT (UDP-glucose:flavonoid-3-O-glucosyltransferase), encoding

133 uconeogenesis, and uridine-diphosphoglucose (UDP)-glucose flux were measured using [3-(3)H]glucose, d

134 On the other hand, total UDP-glucose flux (13.2 +/- 1.7 and 12.5 +/- 1.0 vs. 8.1

135 .5 +/- 1.3 micro mol x kg(-1) x min(-1)) and UDP-glucose flux (5.0 +/- 0.4 vs. 5.0 +/- 0.3 vs. 4.0 +/

136 ion of the direct (extracellular) pathway to UDP-glucose flux was minimal and constant during all ins

137 UDP-glucose flux, a measure of glycogen synthesis, was a

138 lycogenolysis occurred without a decrease in UDP-glucose flux, this implies that insulin inhibits EGP

139 ution of the extracellular direct pathway to UDP-glucose flux.

140 The concentration-effect curve of UDP-glucose for promoting inhibition of adenylyl cyclase

141 inetically characterized in the direction of UDP-glucose formation, and the enzyme activity was affec

142 ese results indicate constitutive release of UDP-glucose from physiologically relevant tissues and su

143 ene encoding sucrose synthase that generates UDP-glucose from sucrose for cell wall biosynthesis.

144 We propose that UGT1 may transfer UDP-glucose from sucrose synthase to the callose synthas

145 s partially reversed by enzymatic removal of UDP-glucose from the medium.

146 gher UTP values might be related to elevated UDP-glucose/galactose, which was found to be at higher c

147 Both proteins were able to convert UDP-glucose (Glc) to UDP-Gal, but only the BAS5304-encod

148 Xyl also feedback inhibits upstream enzymes (UDP-glucose [Glc] dehydrogenase, UDP-Glc pyrophosphoryla

149 al levels of sinapoylmalate and sinapic acid:UDP-glucose glucosyltransferase activity in brt1 leaves

150 of the quality control machinery, the enzyme UDP glucose glycoprotein glucosyltransferase (UGT1).

151 e endoplasmic reticulum-like fraction showed UDP-glucose: glycoprotein glucosyltransferase activity,

152 The endoplasmic reticulum (ER) protein GT1 (UDP-glucose: glycoprotein glucosyltransferase) is the ce

153 ep15 remains elusive, Sep15 co-purifies with UDP-glucose:glycoprotein glucosyltransferase (GT), an es

154 UDP-glucose:glycoprotein glucosyltransferase (UGGT) is a

155 ere their folding is surveyed by the 170-kDa UDP-glucose:glycoprotein glucosyltransferase (UGGT).

156 UDP-glucose:glycoprotein glucosyltransferase (UGGT1) act

157 e p97 and the luminal quality control factor UDP-glucose:glycoprotein glucosyltransferase (UGGT1) in

158 The latter protein was identified as UDP-glucose:glycoprotein glucosyltransferase (UGTR), the

159 ORC1v2 interact with calnexin cycle proteins UDP-glucose:glycoprotein glucosyltransferase 1 (UGGT1),

160 UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1) is

161 UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1) is

162 UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1) se

163 e identify an interaction between TAPBPR and UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1), a

164 also provide direct evidence for a role for UDP-glucose:glycoprotein glucosyltransferase 1 in MHC cl

165 er that is glycan-dependent and regulated by UDP-glucose:glycoprotein glucosyltransferase 1.

166 estration of the glycoprotein folding sensor UDP-glucose:glycoprotein glucosyltransferase in the Golg

167 Because UDP-glucose:glycoprotein glucosyltransferase sustains ca

168 R) lumenal sensor for quality control is the UDP-glucose:glycoprotein glucosyltransferase that target

169 ation of N-glycosylated proteins targeted by UDP-glucose:glycoprotein glucosyltransferase, a chaperon

170 the Sep15 gene coding for the cysteine-rich UDP-glucose:glycoprotein glucosyltransferase-binding dom

171 protein folding through its interaction with UDP-glucose:glycoprotein glucosyltransferase.

172 ontrol of the BiP chaperone promoter and the UDP-glucose:glycoprotein glucosyltransferase.

173 tivity by at least 260-fold but only reduced UDP-glucose hydrolytic activity by 4-14-fold.

174 ated self-glucosylation activity and reduced UDP-glucose hydrolytic activity by at least 190-fold.

175 ctosylated oligosaccharides from inexpensive UDP-glucose in a multigram scale.

176 evidence demonstrating a potential role for UDP-glucose in HSPC mobilization and may provide an attr

177 erase (GALE) interconverts UDP-galactose and UDP-glucose in the final step of the Leloir pathway.

178 ctively condenses undecaprenyl phosphate and UDP-glucose in vitro to form undecaprenyl phosphate-gluc

179 antioxidant agent NAC significantly reduced UDP-glucose-induced mobilization, coinciding with a redu

180 The bioconversion of UDP-glucose into kanosamine along with the bioconversion

181 l aligned near the entrance of the substrate UDP-glucose into the active site.

182 o-opt the host transporter SLC35D2 to import UDP-glucose into the vacuole, where it serves as substra

183 n UDP-rhamnose synthase (RHS1) that converts UDP-glucose into UDP-l-rhamnose.

184 Extracellular UDP-glucose is a natural purinergic receptor agonist, bu

185 It has recently been shown that UDP-glucose is a potent agonist of the orphan G-protein-

186 Because cellular UDP-glucose is concentrated in the lumen of the endoplas

187 t of cellulose synthase, where the substrate UDP-glucose is consumed at the cytosolic side of the Gol

188 uridine diphosphate (UDP) into fructose and UDP-glucose, is a key enzyme in sucrose metabolism in hi

189 GPR105, a G protein-coupled receptor for UDP-glucose, is highly expressed in several human tissue

190 stead alters the terminal destination of the UDP-glucose it generates.

191 argets Ugp1 to the cell periphery, where the UDP-glucose it produces is in proximity to the site of g

192 of a G protein-coupled receptor activated by UDP-glucose led us to develop a sensitive and specific a

193 ned to resting extracellular levels of 3 nM, UDP-glucose levels attained a steady state that exceeded

194 g level; consequently, resting extracellular UDP-glucose levels exceeded those of ATP by 5- to 10-fol

195 lysis account for the elevated extracellular UDP-glucose levels on resting cells.

196 oubled by 10 min (t(1/2) of <5 min), whereas UDP-glucose levels were concomitantly decreased during t

197 the observation of significant extracellular UDP-glucose levels, expression of the UDP-glucose-activa

198 5 min) was accompanied by the restoration of UDP-glucose levels.

199 alactose 1-phosphate <--> UDP-galactose <--> UDP-glucose <--> glucose 1-phosphate <--> glucose 6-phos

200 o develop a sensitive and specific assay for UDP-glucose mass and to test whether this sugar nucleoti

201 mol/min/10(6) cells) combined with a rate of UDP-glucose metabolism approximately three times lower t

202 ructure and a complex between glycogenin and UDP-glucose/Mn2+ were solved by molecular replacement to

203 UDP-glucose-mobilized cells possessed the capacity to ac

204 Compared with G-CSF-mobilized cells, UDP-glucose-mobilized cells preferentially supported lon

205 m in which the Mn2+ that associates with the UDP-glucose molecule functions as a Lewis acid to stabil

206 sphate uridylyltransferase which synthesizes UDP-glucose monomers.

207 ndidate genes led to the identification of a UDP-glucose:monoterpenol beta-d-glucosyltransferase (VvG

208 is approach led to the identification of two UDP-glucose:monoterpenol beta-d-glucosyltransferases.

209 l produced via UDP-glucuronate) stemmed from UDP-glucose, not glucose 6-phosphate; therefore, UDP-glu

210 asmic reticulum-like vesicles with K(m)s for UDP-glucose of approximately 2-4 microm.

211 change also resulted in rapid appearance of UDP-glucose on the luminal surface of highly differentia

212 ion of configuration occurs about C-4 of the UDP-glucose or UDP-galactose substrates, in the reaction

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

214 gnificantly influence which donor substrate (UDP-glucose or UDP-Xyl) is used.

215 c acid, GDP-fucose, UDP-N-acetylglucosamine, UDP-glucose, or GDP-mannose.

216 In this study, the UDP-glucose:pABA acyl-glucosyltransferase (pAGT) activit

217 UDP-glucose:pABA glucosyltransferase activity was readil

218 In contrast, both flux through the UDP-glucose pool (P < 0.05) and the contribution of the

219 l; the C5-to-C3 ratio was measured in the in UDP-glucose pool using nuclear magnetic resonance and th

220 UDP-glucose-promoted chemotaxis of differentiated HL-60

221 UDP-glucose-promoted chemotaxis of freshly isolated huma

222 A UDP-glucose:protein O-glucosyltransferase (Poglut/Rumi)

223 nucleoside triphosphates, two new enzymes, a UDP-glucose pyrophosphatase and a CoA pyrophosphatase, w

224 UDP-glucose pyrophosphorylase (UGP) alternatively makes

225 east PAS kinases Psk1 and Psk2 phosphorylate UDP-glucose pyrophosphorylase (Ugp1), the primary produc

226 UDP-glucose pyrophosphorylase (UGPase; EC 2.7.7.9) is an

227 A cis-QTL for UDP-glucose pyrophosphorylase activity in the UGP1 promo

228 PAS kinase was also found to phosphorylate UDP-glucose pyrophosphorylase and glycogen synthase, the

229 uperoxide dismutase, quinone oxidoreductase, UDP-glucose pyrophosphorylase and phosphoglycerate kinas

230 The structure of the UDP-glucose pyrophosphorylase encoded by Arabidopsis tha

231 genes, and a silent site polymorphism in the UDP-glucose pyrophosphorylase gene (UGPase).

232 accumulation) through the disruption of the UDP-glucose pyrophosphorylase gene exemplifies the power

233 he expression of Sucrose phosphate synthase, UDP-glucose pyrophosphorylase, and ADP-glucose pyrophosp

234 SVEN_3027 is a UDP-glucose pyrophosphorylase, SVEN_3972 is an unusual I

235 drates through phosphorylation of the enzyme UDP-glucose pyrophosphorylase.

236 upported by decreased rates of ATP, AMP, and UDP-glucose release in response to the secretory inhibit

237 An increased rate of UDP-glucose release in ymd8Delta was reduced by deletion

238 the endoplasmic reticulum, we speculate that UDP-glucose release may occur as a result of vesicle tra

239 Using this assay, an elevated rate of UDP-glucose release was demonstrated in mutants lacking

240 The genetic basis of UDP-glucose release was explored through analysis of del

241 However, unlike ATP release, UDP-glucose release was not dependent on glucose stimula

242 deed, total adenine nucleotide release, like UDP-glucose release, did not vary with glucose concentra

243 ession of YEA4 or HUT1 increased the rate of UDP-glucose release.

244 i cell-free lysate of glutamine and NAD with UDP-glucose resulted in the formation of kanosamine.

245 t shares twin Rossmann-like domains with the UDP-glucose-specific OtsA from Escherichia coli However,

246 genes UGDH in complex with NAD+ cofactor and UDP-glucose substrate to generate a model of the enzyme

247 hosphorylase (Ugp1), the primary producer of UDP-glucose, the glucose donor for glucan biosynthesis.

248 ment in a coupled exchange with the entry of UDP-glucose, thereby further relieving ER stress by favo

249 Here, we characterize a putative UDP-glucose:thiohydroximate S-glucosyltransferase, UGT74

250 d forms, with the latter proposed to channel UDP glucose to the cellulose-synthase complex on the pla

251 or KDELC2, catalyze transfer of glucose from UDP-glucose to an EGF repeat from human factor VII.

252 in E. coli catalyses glucosyl transfer from UDP-glucose to cholesterol.

253 nusual property of transferring glucose from UDP-glucose to form an oligosaccharide covalently attach

254 ALT), which converts galactose-1-phosphate + UDP-glucose to glucose-1-phosphate + UDP-galactose.

255 presence of the substrates/products UTP and UDP-glucose to nominal resolutions of 1.64 Angstroms and

256 he coupling of 2-thioglucose 6-phosphate and UDP-glucose to produce 2-thiotrehalose 6-phosphate, whic

257 74F1 and UGT74F2) that transfer glucose from UDP-glucose to SA.

258 t as a subunit of callose synthase that uses UDP-glucose to synthesize callose, a 1,3-beta-glucan.

259 a UDP-glucose-4,6-dehydratase that converts UDP-glucose to UDP-4-keto-6-deoxyglucose.

260 UDP-glucose dehydrogenase (UGDH) oxidizes UDP-glucose to UDP-glucuronate, an essential precursor f

261 the enzymes responsible for the oxidation of UDP-glucose to UDP-glucuronic acid and its subsequent de

262 ein specifically catalyzes the conversion of UDP-glucose to UDP-glucuronic acid, which is essential f

263 The pathway from UDP-glucose to UDP-xylose has been characterised in diff

264 that catalyzes two successive oxidations of UDP-glucose to yield UDP-glucuronic acid, an essential p

265 drogenase (UGDH) catalyzes two oxidations of UDP-glucose to yield UDP-glucuronic acid.

266 solated an Arabidopsis cDNA encoding a novel UDP-glucose transferase (UGT1).

267 ociated proteins, phragmoplastin and a novel UDP-glucose transferase that copurifies with the CalS co

268 gest that plant CalS may form a complex with UDP-glucose transferase to facilitate the transfer of su

269 UDP-glucose transferase, Rop1 and, possibly, annexin.

270 ing they are in the lumen; (e) characterized UDP-glucose transport activities in Golgi apparatus and

271 Further evidence for UDP-glucose transport was obtained by expression of ZK 8

272 as well as a candidate endoplasmic reticulum UDP-glucose transporter (HUT1L) and several pseudogenes.

273 hoid-biased differentiation, suggesting that UDP-glucose triggers the mobilization of functionally di

274 rs were released from keratinocytes and that UDP-glucose (UDP-Glc) added into keratinocyte cultures i

275 UDP-glucose (UDP-Glc) and glycogen levels in skeletal mu

276 [-4)-beta-d-Glc-(1-3)-beta-d-GlcUA-(1-] from UDP-glucose (UDP-Glc) and UDP-glucuronic acid (UDP-GlcUA

277 charide of Streptococcus pneumoniae requires UDP-glucose (UDP-Glc) and UDP-glucuronic acid (UDP-GlcUA

278 lla pneumoniae bound to the substrate analog UDP-glucose (UDP-Glc) was solved by X-ray crystallograph

279 an P2Y(14) receptor is potently activated by UDP-glucose (UDP-Glc), UDP-galactose (UDP-Gal), UDP-N-ac

280 ate-N-acetylglucosamine (UDP-GlcNAc) but not UDP-glucose (UDP-Glc).

281 xpression did not respond to P2Y14 R agonist UDP-glucose (UDP-Glu) while hCPCs with higher P2Y14 R ex

282 .9 encodes a Golgi apparatus transporter for UDP-glucose, UDP-galactose, UDP- N-acetylglucosamine, an

283 uted human epimerase complexed with NADH and UDP-glucose, UDP-galactose, UDP-GlcNAc, or UDP-GalNAc.

284 d, we identified and quantified the pools of UDP-glucose, UDP-galactose, UDP-N-acetylglucosamine, GDP

285 tle or no activity is seen with ADP-glucose, UDP-glucose, UDP-GlcNAc, or UDP-galactose.

286 c location of pAGT activity and on cytosolic UDP-glucose/UDP ratios, this K(eq) value allowed estimat

287 UDP-glucose (UDPG) and derivatives are naturally occurri

288 ratio of the infusate was 1.07, the ratio in UDP-glucose was <1.0 in all subjects both before (0.75 +

289 -galactose and UDP-glucuronic acid, although UDP-glucose was always preferred.

290 ture of the human enzyme with bound NADH and UDP-glucose was determined.

291 m as well as forms bound to the peptides and UDP-Glucose was performed.

292 Similar to ATP, UDP-glucose was released by S. cerevisiae at a rate that

293 r this substrate was approximately 7 mm when UDP-glucose was the glucosyl donor and approximately 4 m

294 The model proposed that UDP-glucose was then channeled to cellulose synthase in

295 vels of ATP, ADP, ADP-glucose, UTP, UDP, and UDP-glucose were altered in a light-dependent manner.

296 The apparent efficacies of UDP and UDP-glucose were similar, and the EC50 values (74, 33, a

297 dy, we demonstrated that a nucleotide sugar, UDP-glucose, which is released into extracellular fluids

298 ants, these transfer reactions generally use UDP-glucose with acceptors that include hormones such as

299 e, CDP-glucose, GDP-glucose, TDP-glucose and UDP-glucose, with ADP-glucose, GDP-glucose and UDP-gluco

300 has been shown to epimerize UDP-galactose to UDP-glucose without the addition of NAD+.