ライフサイエンスコーパス: galactosyltransferase

1 LT gene encoding Gb3/CD77 synthase (alpha1,4-galactosyltransferase).

2 the lgt2 gene of D4, which encodes beta(1-4)-galactosyltransferase.

3 the product of one of these genes encodes a galactosyltransferase.

4 transferase and the lgt2 encodes a beta(1-4) galactosyltransferase.

5 It is the first pH-sensitive method for galactosyltransferase.

6 port here a new pH-indicator-based assay for galactosyltransferase.

7 tively, using domains from mannosidase-1 and galactosyltransferase.

8 ly distinguished from the trans-Golgi marker galactosyltransferase.

9 ans bre-5, which encodes a putative beta-1,3-galactosyltransferase.

10 m for the substrate binding of the alpha1, 3-galactosyltransferase.

11 em containing equal amounts of epimerase and galactosyltransferase.

12 nd a UDP-galactose dependent (1-->6)-alpha-D-galactosyltransferase.

13 antigen is not synthesized in the absence of galactosyltransferase.

14 ar to be regulated by the specificity of the galactosyltransferase.

15 f UDP-galactose:glucosylceramide beta(1-->4)-galactosyltransferase.

16 B gene encoding the terminal oligosaccharide galactosyltransferase.

17 ity of another Mn-dependent enzyme, beta-1,4-galactosyltransferase.

18 matically galactosylated by bovine beta(1,4)-galactosyltransferase.

19 ctive toward T-synthase but not another beta-galactosyltransferase.

20 conversion of UDP-Gal to UDP, using 1-4-beta-galactosyltransferase.

21 ntaining conserved domains of core-1 beta1,3-galactosyltransferases.

22 ced expression of the enzyme core 1, beta1,3-galactosyltransferase 1 (C1GALT1) may contribute.

23 this phenotype using Mutant [core 1 beta1,3-galactosyltransferase 1 (C1galt1)(FF):zona pellucida gly

24 beta-1,4-Galactosyltransferase 1 (Gal-T1) transfers galactose (Ga

25 evated levels of the long isoform of beta1,4-galactosyltransferase 1 (GalT), a proportion of which is

26 rystallographic structures of bovine beta1,4-galactosyltransferase 1 and human glucuronyltransferase

27 The enzymes alpha(1,3)galactosyltransferase (1,3GT) and isoglobotriaosylcerami

28 es are due largely to the vertebrate beta1,4-galactosyltransferase-1 (beta4Gal-T1), which is found as

29 During the catalytic cycle of beta1,4-galactosyltransferase-1 (Gal-T1), upon the binding of Mn

30 osaminyltansferase-7 (beta3GnT7) and beta1,4-galactosyltransferase-4 (beta4GalT4), in the production

31 n by knockdown of the gene encoding beta-1,3-galactosyltransferase 5 (beta3GalT5) in the globo-series

32 sylceramide (LacCer) synthesized by beta-1,4-galactosyltransferase 6 (B4GALT6) is upregulated in the

33 The beta-1,4-galactosyltransferase 7 (beta4GalT7) enzyme is involved

34 GAG) biosynthetic enzymes, the human beta1,4-galactosyltransferase 7 (hbeta4GalT7) is characterized b

35 The beta1,4-galactosyltransferase-7 (beta4Gal-T7) enzyme, one of sev

36 ese-dependent enzymes, most notably beta-1,4-galactosyltransferase, a Golgi enzyme essential for bios

37 because of mutation of the gene for ceramide galactosyltransferase, a key enzyme for galactosphingoli

38 omologue of cj1136, which encodes a putative galactosyltransferase according to the annotation of the

39 nephropathy indicated a decrease in beta1,3-galactosyltransferase activity and an increase in N-acet

40 ity by nearly 1000-fold, while enhancing its galactosyltransferase activity by 80-fold.

41 ydrolase but has recently been shown to have galactosyltransferase activity in Arabidopsis thaliana.

42 jection of zebrafish beta4GalT1 mRNA returns galactosyltransferase activity to control levels and res

43 -terminal region of FT85 abolishes Skp1 beta-galactosyltransferase activity with minimal effects on t

44 lumen with a K(m) of 2.7 microm;(c) detected galactosyltransferase activity(ies) in the lumen of the

45 me that has in vitro galactomannan alpha-1,6-galactosyltransferase activity.

46 kp1, suggesting that FT85 may also have beta-galactosyltransferase activity.

47 serving the secretion of galactomannan alpha-galactosyltransferase activity.

48 pendent ancestral genes encoding sialyl- and galactosyltransferase activity.

49 zymatic treatment with recombinant alpha 1,3 galactosyltransferase (alpha 1,3GT).

50 cells expressing the suicide gene alpha(1,3)Galactosyltransferase (alpha GT).

51 why family GT6 members, like bovine alpha1,3-galactosyltransferase (alpha1,3-GalT), have a nucleophil

52 The alpha1,3-galactosyltransferase (alpha1,3GT or GGTA1) gene display

53 The enzyme alpha1,3-galactosyltransferase (alpha1,3GT or GGTA1) synthesizes

54 Disruption of the gene encoding pig alpha1,3-galactosyltransferase (alpha1,3GT) by homologous recombi

55 because of the inactivation of the alpha1,3-galactosyltransferase (alpha1,3GT) gene in these species

56 the UDP-galactose:beta-galactoside-alpha1-3-galactosyltransferase (alpha1,3GT) gene, which ablated t

57 Alpha1,3-galactosyltransferase (alpha1,3GT) is an enzyme that pro

58 hich requires the enzyme product of alpha1,3-galactosyltransferase (alpha1,3GT), are sugar chains on

59 I, and an increase in the expression of the galactosyltransferase, alpha1-3GalT.

60 the function of PgtA, a dual function beta3-galactosyltransferase/alpha2-fucosyltransferase that con

61 UDP-galactose:beta-galactosyl-alpha1,3-galactosyltransferase (alpha3GT) catalyzes the synthesis

62 alpha-1,3-Galactosyltransferase (alpha3GT) catalyzes the transfer

63 Alpha-1,3 galactosyltransferase (alpha3GT) catalyzes the transfer

64 The retaining glycosyltransferase, alpha-1,3-galactosyltransferase (alpha3GT), is mutationally inacti

65 In contrast, galactosyltransferase, an enzyme that does not interact

66 Notably, two domains harbored by beta-1,3 galactosyltransferase, an essential enzyme in forming pl

67 demonstrated an increase in overall beta(1,3)galactosyltransferase and alpha(2,3)sialyltransferase ac

68 ian beta1,4-galactosyltransferase or beta1,4-galactosyltransferase and alpha2,6-sialyltransferase gen

69 ectors designed to express mammalian beta1,4-galactosyltransferase and alpha2,6-sialyltransferase gen

70 the porcine submaxillary gland core 1 beta 3-galactosyltransferase and alpha2-fucosyltransferase exhi

71 tracts with [3H]galactose in the presence of galactosyltransferase and subsequent analyses of sacchar

72 ntiviral vector expressing porcine alpha 1,3 galactosyltransferase and transplanted into lethally irr

73 eins that are lipooligo/polysaccharide alpha-galactosyltransferases and alpha-glucosyltransferases.

74 The T-synthase (core 1 beta3-galactosyltransferase) and its molecular chaperone Cosmc

75 from the pIgR, asialoglycoprotein receptor, galactosyltransferase, and CD89 is constitutively expres

76 cleus, the medial/trans-Golgi by fusion with galactosyltransferase, and the mitochondrial matrix by u

77 The principles of using pH indicator in galactosyltransferase assay should be applicable to othe

78 ids predominant in photosynthetic membranes, galactosyltransferases associated with these membranes t

79 n-dependent kinases related to the mammalian galactosyltransferase-associated protein kinase p58, and

80 transgenic animals with a heterozygous alpha-galactosyltransferase background (Tg Gal-/+), and from n

81 and/or resialylated TNFR-IgG using beta-1,4-galactosyltransferase (beta1,4GT) and/or alpha-2,3-sialy

82 on enzyme (iGnT) and a member of the beta1,4-galactosyltransferase (beta4Gal-T) gene family.

83 Beta-1,4-galactosyltransferase (beta4Gal-T1) in the presence of m

84 then demonstrate that among various beta1, 4-galactosyltransferases (beta4Gal-Ts), beta4Gal-TI is mos

85 Six beta4-galactosyltransferase (beta4GalT) genes have been cloned

86 method to assay UDP-Gal:beta-d-GlcNAcbeta1,4-galactosyltransferase (beta4GalT-I) enzymatic activity.

87 beta1,4-Galactosyltransferase (beta4GalT-I) participates in both

88 hepatoma cDNA library with a bovine beta1,4-galactosyltransferase (beta4GT) cDNA clone.

89 er genes encoding the LPG side chain beta1,3-galactosyltransferases (betaGalTs).

90 form of the N-terminal region exhibits beta-galactosyltransferase but not fucosyltransferase activit

91 strongly inhibited modification by the PgtA galactosyltransferase but not the fucosyltransferase.

92 We have also confirmed the identity of the galactosyltransferase by inserting the cDNA in frame int

93 ion catalyzed by lipopolysaccharyl-alpha-1,4-galactosyltransferase C (LgtC) from Neisseria meningitid

94 Human core 1 beta3-galactosyltransferase (C1beta3Gal-T) generates the core

95 ate directly via decreased expression of the galactosyltransferase C1GalT1 and, indirectly, via incre

96 e Golgi-targeting mechanisms of core 1 beta3 galactosyltransferase (C1GalT1) and core 2 beta1,6-N-ace

97 The core 1 beta1,3-galactosyltransferase (C1GALT1) controls the formation o

98 that there are three different sets of lipid galactosyltransferases capable of galactoglycerolipid bi

99 ponse to proton release that accompanies the galactosyltransferase-catalyzed galactose transfer.

100 The putative galactosyltransferase cDNA encodes a 51282 Da protein, w

101 osyltransferase or by UDP-galactose:ceramide galactosyltransferase (CGalT).

102 zyme to generate GCs, UDP-galactose:ceramide galactosyltransferase (CGT(-/-)), exhibit severe postnat

103 he axonal protein NCP1 or the glial ceramide galactosyltransferase (CGT) display disruptions in AGJs

104 at encodes the enzyme UDP-galactose:ceramide galactosyltransferase (Cgt), which is responsible for ca

105 om UDP-Gal to GalNAcalpha1-R by core 1 beta3-galactosyltransferase (core 1 beta3-Gal-T).

106 er/Thr is UDP-Gal:GalNAc-alpha-Ser/Thr beta3-galactosyltransferase (core1 beta3-Gal-T).

107 g galactose alpha 1,3 galactose in alpha 1,3 galactosyltransferase deficient (gal knockout) mice usin

108 were used as heart graft donors to alpha1,3-galactosyltransferase deficient (GalT KO; B6, H-2) recip

109 ow cells (BMC) were transplanted to alpha1,3-galactosyltransferase deficient (GalT-/-) mice condition

110 UDP-galactose ceramide galactosyltransferase-deficient (Cgt(-/-)) mice exhibit

111 s for an anti-Gal IgM antibody into an alpha-galactosyltransferase-deficient (Gal-/-) background.

112 We have used alpha1,3-galactosyltransferase-deficient (GalT(-/-)) mice, which,

113 alpha1,3-Galactosyltransferase-deficient (GalT-/-) mice were trea

114 a similar splenic subpopulation of alpha1, 3-galactosyltransferase-deficient and wild-type mice.

115 from animals with the transgene in an alpha-galactosyltransferase-deficient background (Tg Gal-/-),

116 s study, we take advantage of the ability of galactosyltransferase-deficient knockout (GT-Ko) mice to

117 nd (Tg Gal-/+), and from nontransgenic alpha-galactosyltransferase-deficient littermates (Gal-/-) dem

118 -) 493(-) cells) in the spleens of alpha1, 3-galactosyltransferase-deficient mice.

119 dgd1 mutant, which is defective in the lipid galactosyltransferase, DGD1.

120 Domestic and alpha1,3-galactosyltransferase double knockout porcine KC culture

121 DP-galactose 4-epimerase, EC ) and alpha1, 3-galactosyltransferase (EC ) with an N-terminal His(6) ta

122 osyl-1, 4-N-acetyl-D-glucosaminide alpha(1-3)galactosyltransferase (EC 2.4.1.151) or simply alphaGT.

123 This study confirms that a putative galactosyltransferase encoded by cj1136 is involved in L

124 Golgi preparations were analyzed for galactosyltransferase enrichment (>40-fold above cell ho

125 ing effect on Drosophila melanogaster core 1 galactosyltransferase enzyme activity and a predominant

126 uorescent or biotin tags using an engineered galactosyltransferase enzyme and [3 + 2] azide-alkyne cy

127 zymatic approach that exploits an engineered galactosyltransferase enzyme to selectively label O-GlcN

128 The T-synthase is the key beta 3-galactosyltransferase essential for biosynthesis of core

129 In addition, the galactosyltransferase exhibited an atypical concentratio

130 a2 treatment increased cell surface beta-1,4-galactosyltransferase expression.

131 Flavonol 3-O-galactosyltransferase (F3GalTase) is a pollen-specific e

132 We identified a flavonol 3-O-galactosyltransferase (F3GalTase) that is expressed excl

133 The newly identified beta4-galactosyltransferase family member had unusually broad

134 formatics, but its identification as a beta4-galactosyltransferase family member was experimentally c

135 p is predicted to be a member of the beta1,3-galactosyltransferase family, and Pvg3p-green fluorescen

136 ains exists among other members of the beta3-galactosyltransferase family, recombinant enzyme did not

137 is only distantly related to the known beta3-galactosyltransferase family.

138 gene family that includes: murine alpha1, 3-galactosyltransferase, Forssman (Gb(5)) synthase, and th

139 in both organisms, and a bifunctional alpha-galactosyltransferase from CAZy family GT77 mediates the

140 the initial characterization of recombinant galactosyltransferase from crude cell extract.

141 e changed the donor requirement of alpha1, 3-galactosyltransferase from UDP-galactose to UDP-glucose

142 amine (GlcNAc), which constitutes its normal galactosyltransferase (Gal-T) activity.

143 UDP-Gal:betaGlcNAc beta1,3-galactosyltransferase (Gal-T-II) is responsible for synt

144 re of the catalytic domain of bovine beta1,4-galactosyltransferase (Gal-T1) co-crystallized with UDP-

145 AGP galactosyltransferase (GalT) activities in tobacco (Nico

146 SV-G (VSV), and the trans/TGN enzyme beta1,4-galactosyltransferase (GalT) fused to GFP.

147 mammals, humans lack a functional alpha-1,3-galactosyltransferase (GalT) gene and produce abundant a

148 s-mediated gene transfer of porcine alpha1,3 galactosyltransferase (GalT) is able to induce tolerance

149 the characterization of a zebrafish beta1,4-galactosyltransferase (GalT), which has substantial homo

150 CLS) and beta-N-acetylglucosaminyl-beta-1,4 galactosyltransferase (GalT).

151 Galactosyltransferases (GalT) are important molecular ta

152 ucosylceramide synthase and LacCer synthase (galactosyltransferase, GalT-2) inhibitor, inhibited LPS/

153 Bioinformatics indicated that AGP galactosyltransferases (GALTs) are members of the carboh

154 otype were linked to variation of a putative galactosyltransferase gene (beta-(1,3)galT); mutagenesis

155 Due to inactivation of the alpha1,3-galactosyltransferase gene (GGTA1, or the alpha1,3GT gen

156 as a result of up-regulation of the alpha1,3-galactosyltransferase gene and concomitant reduction in

157 homozygous for the knockout of the alpha1-3 galactosyltransferase gene appear to express low but det

158 alpha1,3-Galactosyltransferase gene knockout (GTKO) pigs reduced

159 -accelerating factor transgenic or alpha-1,3-galactosyltransferase gene knockout miniature swine.

160 urvival of cardiac xenografts from alpha 1-3 galactosyltransferase gene knockout pigs, which express

161 Decreased survivals of alpha1,3-galactosyltransferase gene knockout renal xenografts in

162 rtent introduction of pCMV into our alpha1,3-galactosyltransferase gene knockout swine herd.

163 availability of pigs homozygous for alpha1,3-galactosyltransferase gene knockout, and improved immuno

164 mammals, duplication of the ancestral beta4-galactosyltransferase gene occurred over 250 million yea

165 Southern blot analysis of the alpha1-3 galactosyltransferase gene showed that we had produced (

166 nerated by homologous disruption of alpha1,3-galactosyltransferase gene, is capable of producing natu

167 erminus (f2) of a truncated bovine alpha1, 3-galactosyltransferase gene, respectively.

168 l antibodies (Abs) in baboons after alpha1,3-galactosyltransferase gene-knockout (GalT-KO) pig heart

169 The recent generation of alpha1,3-galactosyltransferase gene-knockout (GalT-KO) pigs has a

170 ic cardiac xenotransplantation from alpha1,3-galactosyltransferase gene-knockout (GalT-KO) swine to b

171 radiated human or wild type (WT) or alpha1,3-galactosyltransferase gene-knockout (GT-KO) pig PBMC in

172 rombotic microangiopathy (TM) after alpha1,3-galactosyltransferase gene-knockout (GTKO) pig organ tra

173 in response to wild-type (WT) and alpha-1,3-galactosyltransferase gene-knockout (GTKO) porcine aorti

174 in baboons after Tx of livers from alpha1,3-galactosyltransferase gene-knockout (GTKO, n=1) or GTKO

175 s from genetically engineered pigs (alpha1,3-galactosyltransferase gene-knockout [GTKO] pigs and pigs

176 etic cells from pigs homozygous for alpha1,3-galactosyltransferase gene-knockout is reported.

177 peracute rejection did not occur in alpha1,3-galactosyltransferase gene-knockout kidney xenografts.

178 After alpha1,3-galactosyltransferase gene-knockout pig artery patch xen

179 Antibody binding to alpha1,3-galactosyltransferase gene-knockout pig cells was less t

180 We examined pathologic changes in alpha1,3-galactosyltransferase gene-knockout pig kidneys transpla

181 ononuclear cells from wild-type and alpha1,3-galactosyltransferase gene-knockout pigs) and anti-Gal I

182 s that do not express Gal epitopes (alpha1,3-galactosyltransferase gene-knockout pigs) might remove t

183 heterozygous knockout (+/-) of the alpha1-3 galactosyltransferase gene.

184 ely eliminated by disruption of the alpha1,3 galactosyltransferase gene.

185 by using comparative genomics with known XyG galactosyltransferase genes from Arabidopsis.

186 from SLA identical wild type (WT), alpha1, 3-galactosyltransferase (GGTA1) KO, GGTA1/ cytidine monoph

187 RISPR/Cas9 system to inactivate the collagen galactosyltransferase GLT25D1 and GLT25D2 genes in osteo

188 ases, mannan synthase (MS) and galactomannan galactosyltransferase (GMGT).

189 odifying enzyme possessing LH, hydroxylysine galactosyltransferase (GT), and galactosylhydroxylysine-

190 eins to express high levels of human beta1,4-galactosyltransferase (GT, E.C. 2.4.1.38) and/or alpha2,

191 tosaminyltransferase (GTA) and alpha-(1-->3)-galactosyltransferase (GTB) catalyze the final step in A

192 he donor binding site of human blood group B galactosyltransferase (GTB).

193 The solubilised galactosyltransferase has an absolute requirement for ad

194 A family of five beta1,3-galactosyltransferases has been characterized that catal

195 ain SS1 or SS1::0826kan, in which a beta-1,4-galactosyltransferase (HP0826), an LPS biosynthetic enzy

196 se 2, Drosophila melanogaster core 1 beta1,3-galactosyltransferase, human alpha2,3-sialyltransferase,

197 Beta-1,4-galactosyltransferase I (beta4Gal-T1) normally transfers

198 beta1,4-Galactosyltransferase I (Gal-T1) normally transfers Gal

199 ona pellucida glycoprotein, ZP3, via beta1,4-galactosyltransferase I (GalT I), a lectin-like receptor

200 of sperm lacking the long isoform of beta1,4-galactosyltransferase I (GalT I), a sperm surface protei

201 surface-associated, long isoform of beta1,4-galactosyltransferase I (GalT I).

202 d forms of five of the biosynthetic enzymes: galactosyltransferase I and glucuronosyltransferase I, r

203 Relocating either galactosyltransferase I or glucuronosyltransferase I had

204 zymes of the pathway (xylosyltransferase and galactosyltransferase I) show that the assembly of the p

205 5B2, which encode glucuronosyltransferase I, galactosyltransferase I, and the 3'-phosphoadenosine 5'-

206 the zebrafish ortholog of mammalian beta1,4-galactosyltransferase I, beta4GalT1, and its requirement

207 er with the lbgA gene, which encodes for the galactosyltransferase I.

208 Beta1,4-galactosyltransferase-I (beta4Gal-T1) catalyzes the tran

209 The beta1-4-galactosyltransferase-I (beta4Gal-T1) enzyme is responsi

210 beta-1,4-Galactosyltransferase-I (beta4Gal-T1) transfers galactos

211 beta1,4-Galactosyltransferase-I (beta4Gal-T1) undergoes critical

212 g in late pachytene spermatocytes, the beta4-galactosyltransferase-I (beta4GalT-I) gene is transcribe

213 evidence suggests that ZP3 binds to beta-1,4-galactosyltransferase-I (GalTase) on the sperm surface.

214 Using four enzymes, beta1,4-galactosyltransferase-I, beta1,3-N-acetylglucosaminyltra

215 d-galactosyl-1,4-glucosylceramide alpha-1, 3-galactosyltransferase (iGb(3) synthase) from a rat place

216 In contrast to the murine alpha1, 3-galactosyltransferase, iGb(3) synthase preferentially mo

217 A recombinant SQV-2 fusion protein had galactosyltransferase II activity with substrate specifi

218 indicating that beta3GalT6 is the so-called galactosyltransferase II involved in glycosaminoglycan b

219 sqv-2 encodes a protein similar to human galactosyltransferase II.

220 bstrate specificity similar to that of human galactosyltransferase II.

221 upon O-glycosylation mediated by C1GALT1, a galactosyltransferase implicated in other cancers.

222 ave cloned Gb(3) synthase, the key alpha1, 4-galactosyltransferase in globo-series glycosphingolipid

223 ent or by knocking down the relevant enzyme, galactosyltransferase in Sb(R)LD (KD Sb(R)LD), compromis

224 indicate a gatekeeper function for the beta3-galactosyltransferase in the PgtA dual reaction, and ide

225 The assay was used to compare three galactosyltransferases in our collection.

226 , suggesting that the disrupted genes encode galactosyltransferases in plant cell wall synthesis.

227 ulted in the inactivation of a gene (beta1,3-galactosyltransferase) in the woolly monkey.

228 conclude that the R2866 lgtC gene encodes a galactosyltransferase involved in synthesis of the 4C4 e

229 Plant lipid galactosyltransferases involved in both pathways are ass

230 beta1,4-Galactosyltransferase is one such enzyme.

231 DP-galactose:glycoprotein-alpha-GalNAc beta3-galactosyltransferase) is most sensitive to the presence

232 s specific client T-synthase (Core 1 beta1-3-galactosyltransferase) is required for folding of the en

233 The development of alpha-1,3-galactosyltransferase knock-out (GalT-KO) swine that pro

234 the absence of alphaGAL epitopes, humans and galactosyltransferase knock-out (GALT/ KO) mice express

235 ineered porcine cartilage s.c. into alpha1,3-galactosyltransferase knockout (Gal KO) mice.

236 e report our initial results using alpha-1,3-galactosyltransferase knockout (GalT-KO) donors and a to

237 The recent availability of alpha1,3-galactosyltransferase knockout (GalT-KO) miniature swine

238 demonstrated that skin grafts from alpha-1,3 galactosyltransferase knockout (GalT-KO) miniature swine

239 previously reported life-supporting alpha1,3-galactosyltransferase knockout (GalTKO) thymokidney xeno

240 ncompatible carbohydrate antigen in alpha1,3-galactosyltransferase knockout (KO) mice.

241 this treatment was demonstrated in alpha1,3-galactosyltransferase knockout mice producing anti-Gal a

242 This hypothesis was tested in alpha-1,3-galactosyltransferase knockout mice, which produce anti-

243 melanoma (B16Null) tumors in the alpha(1,3)-galactosyltransferase knockout mouse model.

244 Hearts from alpha1,3-galactosyltransferase knockout pigs (GalT-KO, n = 8) wer

245 ages were highly specific for NPIs (alpha1,3-galactosyltransferase knockout) compared with AIs.

246 llagen type IV alpha-1 (COL4A1) and Beta-1,3-galactosyltransferase-like (B3GALTL) have been reported

247 Isolation of the gene DGD1, encoding a galactosyltransferase-like protein, now provides insight

248 re swine with a null allele of the alpha-1,3-galactosyltransferase locus (GGTA1) by nuclear transfer

249 ve pigs in which one allele of the alpha-1,3-galactosyltransferase locus has been knocked out.

250 nsertions in the genes encoding the putative galactosyltransferase (lpcA) and the distal Kdo-transfer

251 We find that galactosyltransferase mRNA expression begins at the late

252 binds to the acceptor site of human beta1-4-galactosyltransferase much like the acceptor trisacchari

253 with the previously characterized xyloglucan galactosyltransferase, MUR3, but is required for galacto

254 d its serum-sensitive phenotype and that the galactosyltransferase mutant retained its serum-resistan

255 ty of strain A77 cannot be attributed to the galactosyltransferase mutation in strain A77.

256 nsertionally inactivated the gene encoding a galactosyltransferase necessary for serotype O1 O-antige

257 t are closely related to the MUR3 xyloglucan galactosyltransferase of Arabidopsis.

258 family Pasteurellaceae and the LgtB and LgtE galactosyltransferases of Neisseria meningitidis and N.

259 the addition of either galactose by beta1,3-galactosyltransferase or a terminal sialic acid by a N-a

260 tosyl-1,4-N-acetyl-D-glucosaminide alpha(1-3)galactosyltransferase or alphaGT.

261 nsect cell lines that have mammalian beta1,4-galactosyltransferase or beta1,4-galactosyltransferase a

262 tter, no obvious homologues of known beta1-4-galactosyltransferase or beta1-2- or beta1-6-N-acetylglu

263 bohydrate-active enzyme database family GT4 (galactosyltransferases) or to family GT64 (C-terminal do

264 ongly influenced UDP-Gal:betaGlcNAc beta-1,4-galactosyltransferase, polypeptide 5 (B4GALT5) expressio

265 was termed XLT2 for Xyloglucan L-side chain galactosylTransferase position 2.

266 the asialoglycoprotein receptor or beta-1, 4-galactosyltransferase, previously described on HT-29 cel

267 Platelet-associated galactosyltransferase produces efficient galactosylation

268 identification on gels of a putative 51 kDa galactosyltransferase protein, and the isolation, clonin

269 ccharides have relied on the use of beta-1,3-galactosyltransferases recently cloned and characterized

270 o knockdown c1galt1 (T-synthase), a critical galactosyltransferase required for the synthesis of core

271 iously yielded iGb(3) synthase, the alpha1,3-galactosyltransferase required in isoglobo-series GSL.

272 f culmination, cells lacking AgtA, an alpha3-galactosyltransferase required to extend the trisacchari

273 was demonstrated unambiguously as a beta-1,3 galactosyltransferase responsible for converting GM2-lik

274 nt of a group of putative bacterial beta-1,3-galactosyltransferases revealed the presence of two cons

275 P-P-LU-galactan, catalyzed by a bifunctional galactosyltransferase (Rv3808c) capable of adding altern

276 he X-linked gene that encodes core 1 beta1,3-galactosyltransferase-specific chaperone 1 (C1GALT1C1, a

277 equences found in previously described beta3-galactosyltransferases, suggesting this enzyme is only d

278 rior studies suggested that the core 1 beta3-galactosyltransferase (T-synthase) is a specific client

279 The core 1 beta1-3-galactosyltransferase (T-synthase) transfers Gal from UD

280 lNAc-transferases (GALNT), the core 1 beta-3-galactosyltransferase (T-synthase), three alpha2-6-sialy

281 the primary follicle stage of core 1 beta1,3-galactosyltransferase (T-synthase; generates core 1-deri

282 ions 310-322) which is also found in beta1,4-galactosyltransferases (termed the Gal/GalNAc-T motif).

283 ositionally and shown to encode a xyloglucan galactosyltransferase that acts specifically on the thir

284 smic reticulum for T-synthase, a Golgi beta3-galactosyltransferase that generates the core 1 O-glycan

285 cated that Rv3789 interacts in vivo with the galactosyltransferase that initiates the elongation of t

286 GalT5 is a previously unidentified zebrafish galactosyltransferase that is essential for proper patte

287 e inactivation of the gene encoding alpha1-3 galactosyltransferase, the enzyme that synthesizes the g

288 ing protein, or subsequently modified with a galactosyltransferase to build more complex carbohydrate

289 f beta-galactosides using a bacterial beta-4-galactosyltransferase/-UDP-4'-gal-epimerase fusion prote

290 Although these galactosyltransferases use UDP-Gal as the galactose dono

291 Secondarily, a processive galactosyltransferase was activated, leading to the accu

292 eviously uncharacterized putative xyloglucan galactosyltransferase was identified.

293 Also, expression of beta1,3-galactosyltransferase was significantly lower, and that

294 d lysosomal trafficking of the Golgi protein galactosyltransferase was sortilin independent and occur

295 hemically characterized a bacterial beta-1,3-galactosyltransferase (WbiP) from Escherichia coli O127,

296 ecretory pathway compartments (p63, p53, and galactosyltransferase) were not stained by antibodies in

297 pes 6A/6B have wciNalpha, encoding alpha-1,3-galactosyltransferase, whereas serotypes 6C/6D have wciN

298 sferases that includes vertebrate beta(1, 4)-galactosyltransferases, which create galactose-beta(1, 4

299 rized grafts in the combination of alpha 1,3-galactosyltransferase wild-type (GalT(+/+)) and deficien

300 he detergent solubilisation of the fenugreek galactosyltransferase with retention of activity, the id