ライフサイエンスコーパス: glucosylate

1 irst, the cyanogenic glycoside linamarin was glucosylated 1-4 times in succession in a reaction catal

2 DB-JBP1 to oligonucleotides containing J or glucosylated 5-hydroxymethylcytosine (glu-5-hmC) using a

3 hat using the natural T4 DNA, which contains glucosylated, 5-hydoxymethylated cytosine residues, affe

4 containing 5-hydroxymethylctosine (5hmC) and glucosylated 5hmC (g5hmC), but not DNA containing unmodi

5 idopsis thaliana) GTs whose encoded proteins glucosylate a diversity of terpenes.

6 howed a rather broad substrate tolerance and glucosylated a range of aroma compounds in vitro, wherea

7 nthesis, we show that C. elegans selectively glucosylates a series of modified purines but not the ca

8 eumoniae) to produce a unique set of defined glucosylated adhesin proteins.

9 odel mixed micelles consisting of a nonionic glucosylated alkane surfactant from the maltoside and th

10 in barrier (BBB) in guinea pigs, whereas its glucosylated analogue is unable to do so.

11 TcdB contain domains that use UDP-glucose to glucosylate and inactivate host Rho GTPases, resulting i

12 are hydroxylated by the enzyme CrtC and then glucosylated and acylated to produce chlorobactene gluco

13 seedlings treated with NAE 12:0 accumulated glucosylated and malonylated forms of this NAE species,

14 The glucosylated and non-glucosylated samples adopt a random

15 ng proteins of the Rho/Ras family are mono-O-glucosylated and, thereby, inactivated.

16 he parasitic plant Phtheirospermum japonicum glucosylates and inactivates its haustorium-inducing fac

17 ,366-amino-acid, multidomain bacterial toxin glucosylates and inactivates small GTPases in the cytoso

18 ajor Clostridium difficile virulence factor, glucosylates and inactivates the small GTP-binding prote

19 le, toxin A (TcdA) and toxin B (TcdB) act by glucosylating and inactivating Rho and Ras family small

20 rget sites of the human JAG1 are efficiently glucosylated, and loss of Rumi in VSMCs results in incre

21 etries, the site at EGF 27 is only partially glucosylated, and the occupancy of the site at EGF 4 var

22 onoplast and is involved in the transport of glucosylated anthocyanidins.

23 branched-chain rhamnosylation of flavonoids glucosylated at positions 3 or 7.

24 methylation analysis; stevioside was mainly glucosylated at the steviol C-19 glucosyl moiety.

25 One of these (UGT74H6) is able to glucosylate both N-methylanthranilic acid and benzoic ac

26 In contrast, GtfE is much more efficient at glucosylating both its natural substrate, vancomycin agl

27 bolished the ability of glycogenin-2 to self-glucosylate but not to interact with glycogenin-1.

28 hmU is then glucosylated by a previously unknown glucosyltransferase

29 genous eEF1A but harbored a mutant eEF1A not glucosylated by Lgt1, were resistant toward the bacteria

30 ed by showing that salicyl salicylate can be glucosylated by recombinant UGT71L1, providing a potenti

31 omers are (R) and (S) diastereomers at their glucosylated C21 positions.

32 Among the phenylamides, several glucosylated caffeoyl and/or dihydrocaffeoyl derivatives

33 In contrast, glucosylated ceramides have profound effects in adipocyt

34 nce, and sphingolipids such as ceramides and glucosylated-ceramides (e.g., GM3) are putative nutritio

35 ATP-dependent accumulation of glucosylated chlorsulfuron by vacuolar membrane vesicles

36 Other glucosylated compounds of the phenylpropanoid pathway we

37 age anthocyanins, predominantly acylated and glucosylated cyanidin derivatives.

38 The major virulence factors are two large glucosylating cytotoxins.

39 late-type siderophores, enterobactin and its glucosylated derivative salmochelin.

40 y either with the aglycones (GtfB, E) or the glucosylated derivatives (GtfC, D) of vancomycin and tei

41 We demonstrate that C-glucosylated derivatives of Ent produced by iroA-encoded

42 der substrate specificity in vitro and could glucosylate diverse steroid and flavonoid substrates.

43 ice show that the initial binding of JBP1 to glucosylated DNA is very fast with a second order rate c

44 olates (enterobactin, degraded enterobactin, glucosylated enterobactin, dihydroxybenzoate, dihydroxyb

45 show that the terminally pyruvylated versus glucosylated EPS require specific repeating unit translo

46 ated by construction of heterodimers able to glucosylate exclusively by intrasubunit or intersubunit

47 The analysis of the glucosylated flavonoids present in Crocus tepals reveals

48 cultivars transformed deoxynivalenol to its glucosylated form at conversion rates between 6 and 22%.

49 The glucosylated form of the O-antigen mediated enhanced sur

50 lated to the ability to conjugate DON into a glucosylated form, deoxynivalenol-3-O-glucose (D3G), by

51 5 degrees C accumulated SA, particularly in glucosylated form.

52 e major function of LH3 in osteoblasts is to glucosylate galactosylhydroxylysine residues in type I c

53 Whereas VvGT14a glucosylated geraniol, R,S-citronellol, and nerol with s

54 estriction nuclease that targets and digests glucosylated (glc)-hydroxymethylcytosine (HMC) DNAs.

55 cosylation extent (MSAE) produced by the non-glucosylated glycogenin monomer is 13.3 +/- 1.9 glucose

56 The MSAE of non-glucosylated glycogenin produced by dimer intrasubunit g

57 However, partially glucosylated glycogenin was able to almost complete its

58 lar determinants by which GS recognizes self-glucosylated GN, the first step in glycogenesis, are unk

59 ctive in self-glucosylation assays, and self-glucosylated GN-2 can be elongated by skeletal muscle gl

60 ure sequence rendered the expression of this glucosylating gtr operon uniform in the population.

61 for multiple sapogenins and was confirmed to glucosylate hederagenin at the C28 position.

62 yltransferases, UGT73F18 and UGT73F19, which glucosylate hemolytic sapogenins at the C-3 position, we

63 lucosylated hmC (5betaghmC) but also 5-alpha-glucosylated hmC (5alphaghmC).

64 enzymes not only have specificity for 5-beta-glucosylated hmC (5betaghmC) but also 5-alpha-glucosylat

65 glycosylase defenses that target phages with glucosylated hydroxymethyl cytosines, and 5ara-ara-hC pr

66 overy in the 1960s of modifying enzymes that glucosylate hydroxymethylcytosine in T-even phages and o

67 d a gene, UGT84B1, whose recombinant product glucosylated indole-3-acetic acid (IAA) in vitro.

68 Copolypeptides of L-glutamate and glucosylated L-/DL-allyl- or DL-propargylglycine were sy

69 Second, both linamarin and the glucosylated linamarin derivatives were phosphorylated.

70 zed as the fructose homopolymer levan, and a glucosylated lipoteichoic acid (LTA) was identified in a

71 identically but at different efficiencies to glucosylate low-molecular-weight Rho GTPases, underlie t

72 18-30-fold reduction in its ability to trans-glucosylate maltose.

73 ontrol lectin-like chaperone, interacts with glucosylated mannose glycans presented by empty major hi

74 dase capable of catalyzing the hydrolysis of glucosylated methymycin/neomethymycin produced by S. ven

75 of the desR gene led to the accumulation of glucosylated methymycin/neomethymycin products, all of w

76 ons including the calreticulin-engulfed mono-glucosylated MHC I glycan, which only becomes accessible

77 UGTR functions by glucosylating misfolded proteins, retaining them in the

78 A UDP-Glc:glycoprotein glucosyltransferase glucosylates N-glycans of misfolded proteins, which are

79 Here, we show that UGT76B1 also glucosylates N-hydroxypipecolic acid (NHP), which is syn

80 sylated adhesin is the first example of an N-glucosylated native antigen that can be considered a rel

81 siological substrates revealed that UGGT can glucosylate nonnative glycoproteins by recognizing subtl

82 These data indicate that by O-glucosylating Notch in the ER, Rumi regulates its foldin

83 Glucosylated oligomannose N-linked oligosaccharides (Glc

84 riants, and these clients are preferentially glucosylated on their most C-terminal glycan.

85 ecially acetylated>diglucosylated forms than glucosylated ones.

86 ex natural products and synthetic drugs were glucosylated or xylosylated by Sv0189.

87 ty of the galactosyltransferase, 18 unique O-glucosylated peptides were identified on the EGF domain

88 responding host activities that restrict non-glucosylated phage DNA: rglA and rglB (restricts glucose

89 plications of the terminally pyruvylated and glucosylated polymers and their potential contribution t

90 Glycogenin is the autocatalytic, self-glucosylating primer for glycogen synthesis, providing t

91 hrough the isolation and characterization of glucosylated products.

92 te that POGLUT2 and 3 function together to O-glucosylate protein substrates and that these modificati

93 Glycogenin, a self-glucosylating protein involved in the initiation of glyc

94 Glycogenin is a self-glucosylating protein involved in the initiation of glyc

95 Glycogenin is a self-glucosylating protein involved in the initiation phase o

96 Glycogenin-2 is a recently described self-glucosylating protein potentially involved in the initia

97 Glycogenin-2 is one of two self-glucosylating proteins involved in the initiation phase

98 The self-glucosylating proteins, Glg1p and Glg2p, are required fo

99 csL) is a large clostridial toxin (LCT) that glucosylates Ras, Rac, and Ral.

100 LFnTcdB(1-556) was enzymatically active and glucosylated recombinant RhoA, Rac, Cdc42, and substrate

101 c, Cdc42, Rap, and R-Ras but only the former glucosylates RhoA.

102 The glucosylated and non-glucosylated samples adopt a random-coil conformation in

103 sistant and susceptible types of B. vulgaris glucosylate sapogenins and are not located in the known

104 73C11 have neofunctionalized to specifically glucosylate sapogenins at the C3 position and demonstrat

105 2E1-E3, encode glycosyltransferases shown to glucosylate several phenylpropanoids in vitro, including

106 TcdB from Clostridium difficile glucosylates small GTPases (Rho, Rac, and Cdc42) and is

107 nds to cells and enters the cytosol where it glucosylates small GTPases.

108 This toxin acts by glucosylating small GTPases in the Rho/Ras families, but

109 tides mimicking viral mannosylated antigens, glucosylated species and precursors of complex and hybri

110 ts and leaves on media supplemented with the glucosylated sphingosine glucopsychosine, which was read

111 Sensory analysis of the alpha-glucosylated stevioside products by a trained panel reve

112 luding unmodified T4 cytosine (C) DNA or non-glucosylated T4 HMC DNA.

113 omycin pseudoaglycone (GtfC and GtfD) or the glucosylated teicoplanin scaffold, 7 (GtfD).

114 UGGT selectively glucosylates the N-linked glycan of misfolded proteins s

115 strate that recombinant UGT74B1 specifically glucosylates the thiohydroximate functional group.

116 , UGT73C44 and UGT73C45, that are capable of glucosylating the aglycone cardenolide digitoxigenin as

117 Here, we show that the glucosylated thymine DNA base (beta-d-glucosyl-hydroxyme

118 drolase (PH) and mandelonitirile lyase or be glucosylated to form amygdalin.

119 This intermediate (HOMedU) is then glucosylated to form base J.

120 TpeL is a glucosylating toxin, which modifies Ras and induces apop

121 infection (CDI) are primarily due to the Rho-glucosylating toxins A and B.

122 eudomembranous colitis by the actions of Rho-glucosylating toxins A and B.

123 peL is a member of the family of clostridial glucosylating toxins produced by Clostridium perfringens

124 socomial disease in which the two large, Rho-glucosylating toxins TcdA and TcdB are the main virulenc

125 toxin that is conserved in large clostridial glucosylating toxins TcdB, TcdA, TcnA, and TcsL; putativ

126 se, neuraminidase, and two large clostridial glucosylating toxins, TcsL and TcsH.

127 rofound clinical significance of clostridial glucosylating toxins.

128 at is conserved across the large clostridial glucosylating toxins.

129 GtfB efficiently glucosylates vancomycin aglycone using UDP-glucose as th