ライフサイエンスコーパス: acetylglucosamine

1 ucosamine (neosamine) series prepared from N-acetylglucosamine.

2 well as UDP-N-acetylgalactosamine and UDP-N-acetylglucosamine.

3 idic linkages of N-acetylgalactosamine and N-acetylglucosamine.

4 ic reactions involving uridine diphosphate N-acetylglucosamine.

5 ose, alpha-glucose, beta-glucose, and beta-N-acetylglucosamine.

6 inked sialic acid, galactose, and bisected N-acetylglucosamine.

7 sion of UDP-N-acetylgalactosamine with UDP-N-acetylglucosamine.

8 (OGT) modifies intracellular proteins with N-acetylglucosamine.

9 lipoprotein YceK, toxin HicA, or MurA (UDP-N-acetylglucosamine 1-carboxyvinyltransferase) suppressed

10 tic identified two signaling muropeptides (N-acetylglucosamine-1,6-anhydro-N-acetylmuramyl pentapepti

11 DP-GlcNAc biosynthesis, converting UTP and N-acetylglucosamine-1-phosphate (GlcNAc-1P) to UDP-GlcNAc.

12 Eight N-acetylglucosamine-1-phosphate and N-acetylgalactosamine-

13 Engineering a mutation in N-acetylglucosamine-1-phosphate transferase subunits alpha

14 ich encodes the alpha and beta subunits of N-acetylglucosamine-1-phosphate transferase.

15 al and chemoenzymatic syntheses relying on N-acetylglucosamine-1-phosphate uridylyltransferase (GlmU)

16 n the mammalian transmembrane glycoprotein N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosa

17 he Golgi enzyme UDP-GlcNAc:lysosomal enzymeN-acetylglucosamine-1-phosphotransferase (GlcNAc-1-phospho

18 UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (GlcNAc-1-phospho

19 ta subunits of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase (phosphotransfera

20 The Golgi-resident N-acetylglucosamine-1-phosphotransferase (PT) complex is c

21 ineered to carry a mutation in the Gnptab (N-acetylglucosamine-1-phosphotransferase subunits alpha/be

22 sosomal storage disorder caused by loss of N-acetylglucosamine-1-phosphotransferase, which tags lysos

23 protein with key enzymatic activities, UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine ki

24 Using UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

25 he key enzyme of sialic acid biosynthesis, N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

26 paucimannosylation (mannose(1-3)fucose(0-1)N-acetylglucosamine(2)Asn).

27 sis of sialic acid is the bifunctional UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase

28 etylmannosamine kinase (MNK) domain of UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase

29 e (UDP)-sugar donors, UDP-4-deoxy-4-fluoro-N-acetylglucosamine (4FGlcNAc) and UDP-4-deoxy-4-fluoro-N-

30 Sulf1 codes for an N-acetylglucosamine 6-O-endosulfatase, an enzyme that spec

31 Mice deficient in N-acetylglucosamine-6-O-sulfotransferase-1 (GlcNAc6ST-1) f

32 clear cells and identified 2 autoantigens, N-acetylglucosamine-6-sulfatase (GNS) and filamin A (FLNA)

33 Uridine diphospho-N-acetylglucosamine, a product of the hexosamine synthetic

34 ,4-linked glucosamine (deacetylated/D) and N-acetylglucosamine (acetylated/A) units.

35 UDP-N-acetylglucosamine acyltransferase (LpxA) and UDP-3-O-(ac

36 UDP-N-acetylglucosamine acyltransferase (LpxA) and UDP-3-O-(R-

37 ase of the structures containing bisecting N-acetylglucosamine along with bi- and trisialylated trian

38 rted by epimerization to the corresponding N-acetylglucosamine analog by the epimerase N-acetylgalact

39 t resulting in IgG molecules with only one N-acetylglucosamine and a fucose residue was fully able to

40 the C6 and C1 hydroxyl groups of mannose, N-acetylglucosamine and glucose respectively.

41 e based NPs that incorporate both sulfated N-acetylglucosamine and hydrophobic monomers were optimize

42 in a ligand-free form, in complex with the N-acetylglucosamine and N-acetylgalactosamine products of

43 These structures showed N-acetylglucosamine and N-acetylgalactosamine to be recogn

44 to catalyze the in vitro incorporation of N-acetylglucosamine and N-acetylgalactosamine to oligosacc

45 tion-dependent manner and was inhibited by N-acetylglucosamine and N-acetylgalactosamine.

46 ypical M. xanthus lipids, fucose, mannose, N-acetylglucosamine and N-acetylgalactoseamine carbohydrat

47 repeating beta-1,4-linked disaccharide of N-acetylglucosamine and N-acetylmuramic acid appended with

48 n esculentum lectin, which recognizes poly-N-acetylglucosamine and poly-N-acetyllactosamine.

49 ll producing an identical polymer from UDP-N-acetylglucosamine and UDP-glucuronic acid.

50 2 able to utilize both uridine diphosphate N-acetylglucosamine and uridine diphosphate N-acetylgalact

51 n three different carbon sources (glucose, N-acetylglucosamine, and glycerol).

52 cell wall precursors, UDP-Glucose and UDP-N-acetylglucosamine are efficiently used to initiate trans

53 ne O-GlcNAcylation (O-GlcNAc=O-linked beta-N-acetylglucosamine) are largely unexplored.

54 successive coupled enzyme assays using UDP-n-acetylglucosamine as the initial sugar substrate.

55 inin (HA) of influenza virus with a single N-acetylglucosamine at each of the N-glycosylation sites [

56 Similar to alginate and poly-beta-1,6 N-acetylglucosamine, bacterial cellulose is implicated in

57 fer of GalNAc to the simple sugar acceptor N-acetylglucosamine-beta-p-nitrophenol (GlcNAcbeta-pNP) is

58 trisaccharide [N-acetylgalactosamine-beta3-N-acetylglucosamine-beta4-(phosphate-6-)mannose] is requir

59 ctivity, resulting in higher levels of UDP-N-acetylglucosamine biosynthesis and protein O-GlcNAcylati

60 utation using both the UDP-glucose and UDP-N-acetylglucosamine bound structures of the wild-type prot

61 tor endocytosis and signaling by promoting N-acetylglucosamine branching of Asn (N)-linked glycans.

62 of uridyldiphospho-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine by the enzyme LpxC.

63 Inhibition of hexokinase by N-acetylglucosamine causes its dissociation from mitochond

64 et al. (2016) report that detection of the N-acetylglucosamine component of peptidoglycan by the glyc

65 ns confer recognitional specificity toward N-acetylglucosamine-containing signaling molecules, such a

66 nhibitor of UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase (LpxC) in Gram-negative ba

67 mined and found to be a member of the PIG-LN-acetylglucosamine deacetylase family; GalB is structural

68 made of repeating N-acetylmuramic acid and N-acetylglucosamine disaccharides cross-linked by pentapep

69 synthetic pathway (HBSP) that produces UDP-N-acetylglucosamine for O-linked N-acetylglucosamine modif

70 e pools of UDP-glucose, UDP-galactose, UDP-N-acetylglucosamine, GDP-mannose, and GDP-fucose in Plasmo

71 hase 1-3 (HAS1-3) isoenzymes that transfer N-acetylglucosamine (GlcNAc) and glucuronic acid (GlcUA) i

72 sugar-aromatic interactions, with glucose, N-acetylglucosamine (GlcNAc) and mannose in between.

73 on of nucleocytoplasmic proteins with beta-N-acetylglucosamine (GlcNAc) and regulates numerous biolog

74 particular with higher levels of beta-1,6-N-acetylglucosamine (GlcNAc) branched N-glycans.

75 production of the high value nutraceutical N-acetylglucosamine (GlcNAc) could be balanced and optimiz

76 on is altered by deleting two Bdellovibrio N-acetylglucosamine (GlcNAc) deacetylases, one of which we

77 N-acetylglucosamine (GlcNAc) exists ubiquitously as a comp

78 ate addition and removal, respectively, of N-acetylglucosamine (GlcNAc) from intracellular protein su

79 -GlcNAc transferase (OGT), which transfers N-acetylglucosamine (GlcNAc) from the nucleotide sugar don

80 outstanding affinities for derivatives of N-acetylglucosamine (GlcNAc) in aqueous solution.

81 (OGT) mediates post-translational O-linked N-acetylglucosamine (GlcNAc) modification.

82 usly that varphi11 requires alpha- or beta-N-acetylglucosamine (GlcNAc) moieties on cell wall teichoi

83 ase that mediates the O-linked addition of N-acetylglucosamine (GlcNAc) moieties to Ser and Thr resid

84 proteins via O-linked addition of a single N-acetylglucosamine (GlcNAc) moiety.

85 scribed here, is attached to the remaining N-acetylglucosamine (GlcNAc) of IgG, using a mutant endogl

86 To study the effect of short N-acetylglucosamine (GlcNAc) oligosaccharides on the physi

87 Dynamic cycling of N-Acetylglucosamine (GlcNAc) on serine and threonine resid

88 ide variety of substrates which contain an N-acetylglucosamine (GlcNAc) residue to act as an 'accepto

89 ranslationally modified by adding O-linked N-acetylglucosamine (GlcNAc) residue to serine or threonin

90 dules recognize polysaccharides containing N-acetylglucosamine (GlcNAc) residues including peptidogly

91 reducing end glucose of CPS and the beta-D-N-acetylglucosamine (GlcNAc) residues of peptidoglycan (PG

92 Chitin, a homopolymer of beta1,4-linked N-acetylglucosamine (GlcNAc) residues, is a key component

93 lyrhamnose backbone with an immunodominant N-acetylglucosamine (GlcNAc) side chain, which is the basi

94 d consists of a polyrhamnose polymer, with N-acetylglucosamine (GlcNAc) side chains, which is an esse

95 MX regulates formation of N-acetylglucosamine (GlcNAc) terminated N-glycans that par

96 core-2 O-glycan branch through addition of N-acetylglucosamine (GlcNAc) to a core-1 O-glycan structur

97 The transfer of N-acetylglucosamine (GlcNAc) to Ser or Thr in cytoplasmic

98 odifies protein function by attaching beta-N-acetylglucosamine (GlcNAc) to serine and threonine resid

99 ions of PgaB show a binding preference for N-acetylglucosamine (GlcNAc) to the N-terminal domain and

100 O-linked N-acetylglucosamine (GlcNAc) transferase (OGT) is the only

101 Here, we show that O-linked N-acetylglucosamine (GlcNAc) transferase (OGT), an enzyme

102 nctional homologue of the Candida albicans N-acetylglucosamine (GlcNAc) transporter NGT1, and represe

103 e for glycolysis and chitobiose to produce N-acetylglucosamine (GlcNAc), a key component of the bacte

104 ved by the treatment of P. aeruginosa with N-acetylglucosamine (GlcNAc), a widespread chemical presen

105 Various stimuli, including N-acetylglucosamine (GlcNAc), induce the fungal pathogen C

106 hesis of a tetra-antennary glycan that has N-acetylglucosamine (GlcNAc), N-acetyllactosamine (LacNAc)

107 entation of culture media with uridine and N-acetylglucosamine (GlcNAc), precursors for the hexosamin

108 nslational modification with O-linked beta-N-acetylglucosamine (GlcNAc), promoted apoptosis through a

109 to form hyphae in response to the inducer N-acetylglucosamine (GlcNAc), suggesting that a basal leve

110 death domain-containing host proteins with N-acetylglucosamine (GlcNAc), thereby blocking extrinsic a

111 ry glycan [A3(2,4,2) type] terminated with N-acetylglucosamine (GlcNAc), which is generated by N-acet

112 We previously demonstrated that certain N-acetylglucosamine (GlcNAc)-containing polysaccharides ca

113 rom the cheaper and commercially available N-acetylglucosamine (GlcNAc).

114 ne residues modified by the monosaccharide N-acetylglucosamine (GlcNAc).

115 are mainly composed of virally synthesized N-acetylglucosamine (GlcNAc).

116 results of many cysteine residues bound to N-acetylglucosamine (GlcNAc).

117 n, demonstrating that the 6-O-sulfation of N-acetylglucosamine (GlcNAc-6-O-sulfation) is highly conse

118 n lysine residues (+128.1 Da), and loss of N-acetylglucosamine (GlcNAc; -203.1 Da).

119 amine transferase (OGT), and O-linked beta-N-acetylglucosamine hydrolase in control and IPAH cells an

120 ial cells as demonstrated by inhibition of N-acetylglucosamine incorporation into polymeric cell wall

121 N-Acetylglucosamine is a key component of bacterial and fu

122 In H. jecorina-produced HjCel3A, a single N-acetylglucosamine is present at both sites, whereas in P

123 toring the relative abundance of bisecting N-acetylglucosamine is relevant to physiological processes

124 Also, N-acetylglucosamine is selectively oxidized at C3.

125 Chitin, a biopolymer of N-acetylglucosamine, is abundant in invertebrates and fung

126 on of chitin, a beta-1,4 linked polymer of N-acetylglucosamine, is of major interest in areas varying

127 Specificity studies with human N-acetylglucosamine kinase and hexokinase IV indicated a h

128 es residues that are already modified with N-acetylglucosamine, likely by converting into a relaxed c

129 O-linked N-acetylglucosamine linkage (O-GlcNAcylation) to serine or

130 osphate-N-acetylmuramic acid(pentapeptide)-N-acetylglucosamine (lipid II), which is readily accessibl

131 for a unique phosphotransferase system and N-acetylglucosamine metabolism suggests an important ecolo

132 duces UDP-N-acetylglucosamine for O-linked N-acetylglucosamine modification (O-GlcNAcylation) of prot

133 ed by cAMP (EPAC), involving also O-linked N-acetylglucosamine modification downstream of the hexosam

134 s resulted in reduced global O-linked beta-N-acetylglucosamine modification levels and abrogated PASM

135 We measured the levels of O-linked beta-N-acetylglucosamine modification, O-linked beta-N-acetylgl

136 iosynthetic pathway, which allows O-linked N-acetylglucosamine modifications of proteins.

137 he addition of the phosphothreonine to the N-acetylglucosamine moiety and CD0243 transfers the methyl

138 ongest interactions are established by the N-acetylglucosamine moiety in the central region of the en

139 omposed of N-acetylmuramic acid-(beta-1,4)-N-acetylglucosamine (MurNAc-GlcNAc) disaccharides associat

140 g amino sugars [i.e., N-acetylmuramic acid-N-acetylglucosamine (MurNAc-GlcNAc)] from attached peptido

141 enzymes phosphomannomutase (PMM), phospho-N-acetylglucosamine mutase (PAGM) and phosphoglucomutase (

142 o the monosaccharides l-fucose, d-mannose, N-acetylglucosamine, N-acetylgalactosamine, and galactose)

143 uniform responses (d-lactose, d-galactose, N-acetylglucosamine, N-acetylneuraminic acid), 'all-or-non

144 vitro in the presence of acetyl-CoA, UDP- N-acetylglucosamine, NADPH, and ATP, we have developed a s

145 g azides and alkynes were installed on tri-N-acetylglucosamine (NAG)3, a PG mimic, as well as PG isol

146 onal addition and removal of O-linked beta-N-acetylglucosamine (O-GlcNAc) also occurs on serine resid

147 ion controlled by the enzyme O-linked-beta-N-acetylglucosamine (O-GlcNAc) glycosyltransferase as comp

148 sis and impaired addition of O-linked beta-N-acetylglucosamine (O-GlcNAc) groups to proteins importan

149 ar and cytosolic proteins by O-linked beta-N-acetylglucosamine (O-GlcNAc) has been shown to play an i

150 c post-translational modification O-linked N-Acetylglucosamine (O-GlcNAc) has emerged as an attractiv

151 (OGA) is an enzyme harboring O-linked beta-N-acetylglucosamine (O-GlcNAc) hydrolase and cryptic lysin

152 O-Linked beta-N-acetylglucosamine (O-GlcNAc) is a carbohydrate post-tran

153 O-Linked beta-N-acetylglucosamine (O-GlcNAc) is a post-translational mod

154 O-linked N-acetylglucosamine (O-GlcNAc) is a post-translational mod

155 ational protein modification O-linked beta-N-acetylglucosamine (O-GlcNAc) is a proposed nutrient sens

156 O-linked N-acetylglucosamine (O-GlcNAc) is a reversible posttransla

157 Glycosylation with O-linked beta-N-acetylglucosamine (O-GlcNAc) is one of the protein glyco

158 Cellular O-linked N-acetylglucosamine (O-GlcNAc) levels are modulated by two

159 O-Linked beta-N-acetylglucosamine (O-GlcNAc) modification found on the s

160 We studied O-linked beta-N-acetylglucosamine (O-GlcNAc) modification of contractile

161 O-linked beta-N-acetylglucosamine (O-GlcNAc) modification of cytoplasmic

162 efute the hypothesis of extensive O-linked N-acetylglucosamine (O-GlcNAc) modification of endogenous

163 Although the O-linked N-acetylglucosamine (O-GlcNAc) modification of the RNA pol

164 O-linked N-acetylglucosamine (O-GlcNAc) modifications regulate the

165 how that Oct1 is modified by O-linked beta-N-acetylglucosamine (O-GlcNAc) moieties.

166 ranslational modification by O-linked beta-N-acetylglucosamine (O-GlcNAc) moieties.

167 ttranslational modification by beta-linked N-acetylglucosamine (O-GlcNAc) on HDAC4 were investigated

168 osttranslational addition of O-linked beta-N-acetylglucosamine (O-GlcNAc) on intracellular proteins.

169 Dynamic cycling of O-linked beta-N-acetylglucosamine (O-GlcNAc) on nucleocytoplasmic protei

170 tification and precise mapping of O-linked N-acetylglucosamine (O-GlcNAc) post-translational modifica

171 Evidence suggests that the O-linked N-acetylglucosamine (O-GlcNAc) posttranslational modificat

172 is study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNA

173 t-translational modification O-linked beta-N-acetylglucosamine (O-GlcNAc) regulates thousands of nucl

174 ss of interest is the addition of O-linked N-acetylglucosamine (O-GlcNAc) residues onto nuclear and c

175 inflammatory function of the O-linked beta-N-acetylglucosamine (O-GlcNAc) signaling associated with t

176 ted role of nutrient-sensing O-linked beta-N-acetylglucosamine (O-GlcNAc) signaling in suppressing ma

177 posttranslational modification by O-linked N-Acetylglucosamine (O-GlcNAc) stabilizes FOXP3 and activa

178 the covalent addition of an O-linked beta-N-acetylglucosamine (O-GlcNAc) sugar moiety to hydroxyl gr

179 ed, in part, by the attachment of O-linked N-acetylglucosamine (O-GlcNAc) to proteins (O-GlcNAcylatio

180 plasmic and nuclear protein by transfer of N-acetylglucosamine (O-GlcNAc) to serine and threonine hyd

181 ational addition of a single O-linked beta-N-acetylglucosamine (O-GlcNAc) to serine or threonine resi

182 O-linked N-acetylglucosamine (O-GlcNAc) transferase (OGT) is an ess

183 Here we demonstrate that O-linked beta-N-acetylglucosamine (O-GlcNAc) transferase (OGT) is requir

184 The nutrient sensor O-linked-beta-N-acetylglucosamine (O-GlcNAc) transferase (OGT) modifies

185 N-Acetylglucosamine (O-GlcNAc) transferase (OGT) regulates

186 w that DELLAs are modified by the O-linked N-acetylglucosamine (O-GlcNAc) transferase (OGT) SECRET AG

187 ine biosynthesis pathway and O-linked beta-N-acetylglucosamine (O-GlcNAc) transferase (OGT) to potent

188 TET2 and TET3 associate with O-linked beta-N-acetylglucosamine (O-GlcNAc) transferase (OGT), an enzym

189 We identifed O-linked-N-acetylglucosamine (O-GlcNAc) transferase (OGT), an X-lin

190 AMPK directly phosphorylates O-linked beta-N-acetylglucosamine (O-GlcNAc) transferase (OGT).

191 t-responsive glycosyltransferase, O-linked N-acetylglucosamine (O-GlcNAc) transferase (OGT).

192 We demonstrate that O-linked N-acetylglucosamine (O-GlcNAc), a post-translational modif

193 ttranslational modification, O-linked beta-N-acetylglucosamine (O-GlcNAc), in NSCs promotes a glial f

194 One such signal, O-linked beta-N-acetylglucosamine (O-GlcNAc), is an essential post-trans

195 h a modification in the amount of O-linked N-acetylglucosamine (O-GlcNAc)-modified proteins and in th

196 n of serine/threonine residues by O-linked N-acetylglucosamine (O-GlcNAc).

197 ovalent modification of CaMKII by O-linked N-acetylglucosamine (O-GlcNAc).

198 olic and nuclear proteins by O-linked beta-N-acetylglucosamine (O-GlcNAc).

199 Glycosylation with O-linked beta-N-acetylglucosamine (O-GlcNAcylation) is a reversible post

200 modification of proteins with beta-linked N-acetylglucosamine (O-GlcNAcylation) via overexpression o

201 eased modification of proteins by O-linked N-acetylglucosamine (O-GlcNAcylation).

202 de beta-N-acetylmuramic acid, (1-->4)-beta-N-acetylglucosamine of staphylococcal peptidoglycan.

203 ation, sialylation, and level of bisecting N-acetylglucosamine of the IgG glycans.

204 fy the pattern of O-glycosylation (21 mono-N-acetylglucosamines) of its AST domain.

205 mmatory and stress responses, and O-linked N-acetylglucosamine (OGN) transferase (OGT), an enzyme tha

206 he reaction of free MurA and substrate UDP-N-acetylglucosamine or isomer UDP-N-acetylgalactosamine.

207 hydrolyze the beta-linkages joining either N-acetylglucosamine or N-acetylgalactosamine to a wide var

208 O-Linked beta-N-acetylglucosamine, or O-GlcNAc, is a dynamic post-transl

209 ubstrates (a mix of substrates, glutamine, N-acetylglucosamine, or pyruvate) revealed contrasting cap

210 lly predicted putative miR-185 targets UDP-N-acetylglucosamine-peptide N-acetylglucosaminyltransferas

211 ct O antigen, a capsule mutant, and a poly-N-acetylglucosamine (PGA) mutant.

212 ysaccharide intercellular adhesin, or poly N-acetylglucosamine (PIA/PNAG).

213 Poly-N-acetylglucosamine (PNAG) is a major component of the Sta

214 The exopolysaccharide poly-beta-(1->6)-N-acetylglucosamine (PNAG) is a major structural determina

215 rved microbial surface polysaccharide poly-N-acetylglucosamine (PNAG) that is expressed on numerous p

216 conserved cell surface polysaccharide poly-N-acetylglucosamine (PNAG) were effective at mediating red

217 encoding the biosynthesis of poly-beta-1,6-N-acetylglucosamine (PNAG), a major biofilm matrix compone

218 isolate and found to be negative for poly-N-acetylglucosamine (PNAG)-like material by immunoblot ass

219 adly expressed microbial carbohydrate poly-N-acetylglucosamine (PNAG).

220 Chitin is a natural N-acetylglucosamine polymer and a major structural compone

221 Two intracellular enzymes, UDP-N-acetylglucosamine-polypeptide beta-N-acetylglucosaminyl

222 UDP-N-acetylglucosamine pyrophosphorylase (UAP) is the final e

223 mmy codes for the single UDP-N-acetylglucosamine pyrophosphorylase in Drosophila, and i

224 FGFR1c2 can tolerate an HS chain having an N-acetylglucosamine residue at its non-reducing end.

225 d to the proximal (reducing-terminal) core N-acetylglucosamine residue of N-glycans by beta1,4-linked

226 tode glycan cores, specifically the distal N-acetylglucosamine residue; this result is in accordance

227 glycan structure of seven mannosyl and two N-acetylglucosamine residues (Man7GlcNAc2) on misfolded gl

228 linear tetrasaccharide that contained two N-acetylglucosamine residues and a free OH group gave two

229 ties of N-acetylneuraminic acid as well as N-acetylglucosamine residues and nucleophilic sites of an

230 Cnm and strongly suggested the presence of N-acetylglucosamine residues attached to Cnm.

231 nds between N-acetylmuramic acid (NAM) and N-acetylglucosamine residues with concomitant formation of

232 alpha2-6-linked sialic acid, and bisected N-acetylglucosamine, respectively.

233 bon substrates, For example, for growth on N-acetylglucosamine, S. marcescens exhibits high pentose p

234 lus niger in deglycosylated and Asn-linked N-acetylglucosamine-stub forms reveal a 10(2/3)-turn paral

235 magnetic resonance and shown to contain an N-acetylglucosamine substituted with a phosphorylated N-me

236 on of intracellular proteins with a single N-acetylglucosamine sugar (O-GlcNAcylation) regulates sign

237 e for the selective phosphorylation of the N-acetylglucosamine sugar in a teicoplanin A2-2 derivative

238 dynamically modified with an O-linked beta-N-acetylglucosamine sugar in response to hypoxia.

239 The enzymatic addition of a single beta-D-N-acetylglucosamine sugar molecule on serine and/or threon

240 ion consisting of the addition of a single N-acetylglucosamine sugar to serine and threonine residues

241 ated post-translational addition of beta-D-N-acetylglucosamine sugars to nuclear and cytoplasmic prot

242 vidently, hexosamine pathway activation or N-acetylglucosamine supplementation induces distinct prote

243 c forms of either N-acetylgalactosamine or N-acetylglucosamine target hepatic antigen-presenting cell

244 The dynamic cycling of N-acetylglucosamine (termed O-GlcNAcylation) on serine or

245 idue is in closer proximity (7.6 A) to the N-acetylglucosamine than the two other sugar rings present

246 Chitin is a polymer of N-acetylglucosamine that is abundant and widely found in t

247 mmasome activation is caused by release of N-acetylglucosamine that is detected in the cytosol by the

248 tic itineraries for other sugars; for beta-N-acetylglucosamine, the key N-acetyl arm confounds the pu

249 These results demonstrate that glucose and N-acetylglucosamine, the most readily available chiral bui

250 K3, which is essential for the transfer of N-acetylglucosamine to arginine residues (arginine-GlcNAcy

251 etylmannosamine kinase that transforms UDP-N-acetylglucosamine to N-acetylmannosamine (ManNAc) follow

252 l modification involving O-linkage of beta-N-acetylglucosamine to Ser/Thr residues on target proteins

253 such modification is addition of O-linked N-acetylglucosamine to serine or threonine residues, known

254 dification involving the O-linkage of beta-N-acetylglucosamine to serine/threonine residues of membra

255 Addition of the N-glycan precursor N-acetylglucosamine to the growth medium slows aging in wi

256 nctions as a ligase that adds the terminal N-acetylglucosamine to the lipooligosaccharide core of Y.

257 They catalyze the addition of the N-acetylglucosamine to the N-acetyl-lactosamine repeat as

258 involved in cell metabolism: O-linked beta-N-acetylglucosamine transferase (OGT) and isocitrate dehyd

259 O-Linked N-acetylglucosamine transferase (OGT) catalyzes O-GlcNAcyl

260 O-Linked beta-N-acetylglucosamine transferase (OGT) is an essential huma

261 O-linked N-acetylglucosamine transferase (OGT) is found in all meta

262 umors from colon tumor cells with O-linked N-acetylglucosamine transferase (OGT) knockdown grew signi

263 at TRIM28 was complexed with O-linked beta-N-acetylglucosamine transferase (OGT) only in cells that h

264 tylglucosamine modification, O-linked beta-N-acetylglucosamine transferase (OGT), and O-linked beta-N

265 es in proteins by the enzyme O-linked beta-N-acetylglucosamine transferase (OGT), whereas the enzyme

266 s an essential substrate for O-linked beta-N-acetylglucosamine transferase (OGT), which glycosylates

267 s a putative serine and threonine O-linked N-acetylglucosamine transferase (OGT).

268 ine biosynthetic pathway and OGT (O-linked N-acetylglucosamine transferase)-mediated protein O-GlcNAc

269 entially encode an O-acetyltransferase, an N-acetylglucosamine transferase, and a KDO transferase con

270 also interacts with the O-GlcNAc (O-linked N-acetylglucosamine) transferase SPINDLY required for prop

271 LPH3 supports incorporation of both core 2 N-acetylglucosamine-transferase 1 and alpha-2,6-sialyltran

272 o control the Golgi localization of core 2 N-acetylglucosamine-transferase 1.

273 hat EXTL2 exhibited much stronger in vitro N-acetylglucosamine-transferase activity related to elonga

274 SLC35A3 is considered the main UDP-N-acetylglucosamine transporter (NGT) in mammals.

275 lactose transporter (UGT; SLC35A2) and UDP-N-acetylglucosamine transporter (NGT; SLC35A3) form hetero

276 UDP-N-acetylglucosamine (UDP-GlcNAc) acyltransferase (LpxA) ca

277 000) as an ER-localized facilitator of UDP-N-acetylglucosamine (UDP-GlcNAc) and UDP-N-acetylgalactosa

278 osamine biosynthetic pathway, increase UDP-N-acetylglucosamine (UDP-GlcNAc) availability, and lead to

279 thatlymphostatin binds uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc) but not UDP-glucose (UDP-

280 athway (HBP) generates uridine diphosphate N-acetylglucosamine (UDP-GlcNAc) for glycan synthesis and

281 The sugar nucleotide UDP-N-acetylglucosamine (UDP-GlcNAc) is an essential metabolit

282 Uridine 5'-diphosphate-N-acetylglucosamine (UDP-GlcNAc) is the donor sugar substr

283 The HBP end product UDP-N-acetylglucosamine (UDP-GlcNAc) is used in enzymatic post

284 kingly, addition of the HBP metabolite UDP-N-acetylglucosamine (UDP-GlcNAc) to CRPC-like cells signif

285 mine are precursors of uridine diphosphate N-acetylglucosamine (UDP-GlcNAc), a substrate for cellular

286 iosynthesis precursor, uridine diphosphate N-acetylglucosamine (UDP-GlcNAc), was monitored by recordi

287 In complex with the cosubstrate UDP-N-acetylglucosamine (UDP-GlcNAc),O-linked-GlcNAc transfera

288 eventually synthesize uridine diphosphate N-acetylglucosamine (UDP-GlcNAc).

289 es UDP-glucuronic acid (UDP-GlcUA) and UDP-N-acetylglucosamine (UDP-GlcNAc).

290 way (HBP), to increase uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc).

291 -glucuronic acid, and UGT3 enzymes use UDP-N-acetylglucosamine, UDP-glucose, and UDP-xylose to conjug

292 , ChiA variants with weaker binding of the N-acetylglucosamine unit either in substrate-binding site

293 de the cell (to produce the monosaccharide N-acetylglucosamine), using this beta-glucan to obtain car

294 five-member consortium of sialic acid and N-acetylglucosamine utilizers that impedes C. difficile's

295 tion of ethoximated and trimethylsilylated N-acetylglucosamines was developed.

296 ties for uncharged substrates (glucose and N-acetylglucosamine) were also enhanced, despite competiti

297 ans with different modifications including N-acetylglucosamine, which bisects the mannose core.

298 ep in the synthesis of uridine diphosphate N-acetylglucosamine, which is required for the biosynthesi

299 rsion of UDP-N-acetylgalactosamine and UDP-N-acetylglucosamine while the bacterial enzyme cannot.

300 beta4 addition of N-acetylgalactosamine to N-acetylglucosamine with formation of the N,N-diacetyllact