ライフサイエンスコーパス: glucosylation

1 sult of differences in OAg O-acetylation and glucosylation.

2 on inactivation of host small G-proteins by glucosylation.

3 residues in the reaction mechanism for self-glucosylation.

4 carbon nucleophile in this novel enzymatic C-glucosylation.

5 ding to substrates, independent of substrate glucosylation.

6 ycoproteins for transient, calcium-dependent glucosylation.

7 ication within 2 h, as shown by differential glucosylation.

8 /beta peptide) blocked toxin A-mediated RhoA glucosylation.

9 GNIP2 was shown to stimulate glycogenin self-glucosylation 3-4-fold.

10 either serine or asparagine eliminated self-glucosylation activity and reduced UDP-glucose hydrolyti

11 minated self-glucosylation and reduced trans-glucosylation activity by at least 260-fold but only red

12 le G433A/I434V mutation led to enhanced HDMF glucosylation activity compared to the wild-type enzymes

13 e recombinant yeast confirms the presence of glucosylation activity on sterol and hydroxy fatty acid

14 with k(cat) of 17 min(-1), but has very low glucosylation activity, < or = 0.3 min(-1), for an alter

15 ased stability compared to 3 and position of glucosylation affected the stability of the xanthones wi

16 ns of these strains identified gtr-dependent glucosylation and acetylation.

17 elial T84 cells by mechanisms involving RhoA glucosylation and actin depolymerization.

18 Stabilization by glucosylation and activation by hydrolysis is essential

19 tionalized according to B-ring substitution, glucosylation and esterification.

20 Glucosylation and galactosylation of a panel of represen

21 of approximately 10 min(-1) for the first C-glucosylation and is distributive, with sequential conve

22 MAP kinase activation appears to precede Rho glucosylation and is required for IL-8 transcription and

23 either serine or asparagine eliminated self-glucosylation and reduced trans-glucosylation activity b

24 De(acetylation), glucosylation and sulfonation were the main metabolic pa

25 rase (beta-GT)-mediated protection of 5-hmC (glucosylation) and recombinant mouse Tet1(mTet1)-mediate

26 n, confirming that it directly mediates Skp1 glucosylation, and NMR demonstrated formation of a Glcal

27 ty is regulated by both O-fucosylation and O-glucosylation, and Notch receptors contain multiple pred

28 ar domain of the receptor: O-fucosylation, O-glucosylation, and O-GlcNAcylation.

29 herichia coli or COS cells is active in self-glucosylation assays, and self-glucosylated GN-2 can be

30 Rho glucosylation became evident after 15 minutes.

31 le pAGT activity by 95%, in vivo [(14)C]pABA glucosylation by 77%, and the endogenous pABA-Glc/pABA r

32 We reported previously the intramonomer glucosylation capability of glycogenin without determini

33 hanges arose specifically from the increased glucosylation caused by overexpression of 71B6.

34 the synthesis genes, it possesses a prophage glucosylation cluster, which modifies the GlcNAc residue

35 n cellular ATP levels; cell rounding and Rho glucosylation commenced between 15 and 30 minutes.

36 flammasome by this toxin is dependent on Rho glucosylation, confirming similar findings reported for

37 In this study, we utilized glucosylation-deficient toxin A to show that activation

38 itination is conceptually reminiscent of the glucosylation-deglucosylation occurring in the ER lumen

39 te oligomeric fragments using beta-selective glucosylation followed by gluco to manno epimerization a

40 7:1 ratio represents the published level of glucosylation for S. enteritidis LPS as well as for S. e

41 haracterization of a broad-specificity lipid glucosylation gene from C. bombicola, and the functional

42 plasm, and was eliminated by deletion of the glucosylation genes from the E. coli chromosome, restori

43 To date, glucosylation has only been observed in O-antigens synth

44 arriers for bacteriophage-mediated O-antigen glucosylation in ABC transporter-dependent pathways.

45 hloroaniline (DCA) was rapidly detoxified by glucosylation in Arabidopsis thaliana root cultures, wit

46 The crtX gene was likely involved in C.p.450 glucosylation in Dietzia sp. CQ4.

47 in glucosyltransferase catalysis impairs DNA glucosylation in vitro.

48 ingly, this palladium catalysis directs beta-glucosylations in the absence of classical neighboring g

49 Side chain glucosylation is a common modification strategy found in

50 Protein O-glucosylation is a conserved post-translational modifica

51 O-Glucosylation is stereo-specific: the O-glucosyltransfer

52 Possibly the initial glucosylation is via inter-dimeric catalysis with an int

53 Self-glucosylation leads to the formation of an oligosacchari

54 ccines synthesized from OAg with the highest glucosylation levels, (ii) OAg composed of mixed- or med

55 phila Notch receptor contain the consensus O-glucosylation motif.

56 These results indicate that the LH3-mediated glucosylation occurs at the specific molecular loci in t

57 two-step protocol that consists of enzymatic glucosylation of 5hmC with an azide-modified glucose, fo

58 e product of site-specific enzymatic alpha-d-glucosylation of a lightly protected non-natural disacch

59 Increased glucosylation of ABA led to phenotypic changes in post-g

60 The impact of increased glucosylation of ABA on ABA-related phenotypes has also

61 The results are a clear indication that O-glucosylation of cis-zeatin is a natural metabolic proce

62 From this it was concluded that the glucosylation of DCA may not be as effective in xenobiot

63 hesis of the primer proceeds by intersubunit glucosylation of dimeric glycogenin, even though it has

64 O-Glucosylation of epidermal growth factor-like (EGF) repe

65 GT73B24, UGT71W2, and UGT73B23 catalyzed the glucosylation of HDMF and its structural homolog 2(or 5)

66 to published information suggesting that the glucosylation of HPOs is a viable means of enhancing the

67 dues, and glucose-P-dolichol (GPD)-dependent glucosylation of LLO.

68 The trans-glucosylation of maltose was reduced to undetectable lev

69 c Arabidopsis to determine whether increased glucosylation of monolignols could influence flux throug

70 n conveying them to distinct sites, and that glucosylation of monolignols is necessary for their vacu

71 Taken together, our results indicate that glucosylation of NAE 12:0 by a yet to be determined gluc

72 decrease in Rumi levels results in reduced O-glucosylation of Notch EGF repeats, and that the enzymat

73 Increased glucosylation of other phenylpropanoids also occurred in

74 230 and Tyr232 is necessary to suppress self-glucosylation of purified protein in vitro.

75 antibodies did not affect the TcdA-mediated glucosylation of Rac1 in RAW 264.7 cells, presaturation

76 anoid metabolism and the important role that glucosylation of secondary metabolites can play in cellu

77 sules indicated that cpsF is responsible for glucosylation of serotype C capsular polysaccharide in E

78 We show that bacteriophage-encoded glucosylation of Shigella O antigen, the basis of differ

79 shRNA) directed against SLC11A1 reduced TcdB glucosylation of small Rho GTPases and, consequently, to

80 The glucosylation of T4 phage DNA is part of a phage DNA pro

81 widely in plant tissues, formed either by O-glucosylation of the hydroxylated side chain or N-glucos

82 etoxification occurs predominantly through O-glucosylation of the intermediate BOA-6-OH, most likely

83 559, are responsible for 'form variation' or glucosylation of the O12 antigen galactose (4 position)

84 sylation of the hydroxylated side chain or N-glucosylation of the purine ring structure.

85 lycosyltransferases (UGTs) that catalyze 3-O-glucosylation of the sapogenins oleanolic acid and heder

86 Resistance could be caused by glucosylation of the sapogenins.

87 catecholic siderophore enterobactin (Ent) by glucosylation of three aryl carbon atoms, a process cont

88 O-linked glucosylation of thymine in DNA (base J) is an important

89 We have recently demonstrated that O-linked glucosylation of thymine in trypanosome DNA (base J) reg

90 ansferases) in Fragaria that function in the glucosylation of volatile metabolites by comprehensive b

91 main of TpeL modifies Ras in vitro by mono-O-glucosylation or mono-O-GlcNAcylation.

92 ly, genes encoding enzymes involved in the O-glucosylation pathway have been cloned.

93 evaluated to reach a larger repertoire of O-glucosylation patterns encountered among S. flexneri typ

94 Here we describe a technique termed GLIB (glucosylation, periodate oxidation and biotinylation), w

95 The first approach, termed GLIB (glucosylation, periodate oxidation, biotinylation) uses

96 exploited a heterologous system to study the glucosylation potential of a model O-antigen produced in

97 Thus, LPS glucosylation promotes bacterial invasion and evasion of

98 se that has been suggested to have a role in glucosylation reactions related to the quality control o

99 nt SE6-E21 is identical to the high level of glucosylation reported for S. typhi LPS.

100 4-O-Glucosylation significantly stabilised 1 against degrada

101 e carried out a mutational analysis of these glucosylation sites and determined their effects on Notc

102 This variation may extend the glucosylation spectrum to Ras proteins, as observed prev

103 e a revision of the consensus sequence for O-glucosylation to allow alanine N-terminal to cysteine 2:

104 signaling, but the contribution of protein O-glucosylation to mammalian Notch signaling and embryonic

105 ed glycogenin produced by dimer intrasubunit glucosylation was 16% of that produced by the monomer.

106 he MSAE produced by heterodimer intersubunit glucosylation was 60% of that produced by the wild-type