ライフサイエンスコーパス: glucosylate

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

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

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

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

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

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

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

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

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

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

11 The glucosylated and non-glucosylated samples adopt a random

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

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

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

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

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

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

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

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

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

21 hmU is then glucosylated by a previously unknown glucosyltransferase

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

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

24 In contrast, glucosylated ceramides have profound effects in adipocyt

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

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

27 Other glucosylated compounds of the phenylpropanoid pathway we

28 The major virulence factors are two large glucosylating cytotoxins.

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

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

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

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

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

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

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

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

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

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

39 5 degrees C accumulated SA, particularly in glucosylated form.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

57 18-30-fold reduction in its ability to trans-glucosylate maltose.

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

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

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

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

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

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

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

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

66 Glucosylated oligomannose N-linked oligosaccharides (Glc

67 ecially acetylated>diglucosylated forms than glucosylated ones.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 73C11 have neofunctionalized to specifically glucosylate sapogenins at the C3 position and demonstrat

83 2E1-E3, encode glycosyltransferases shown to glucosylate several phenylpropanoids in vitro, including

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 at is conserved across the large clostridial glucosylating toxins.

101 rofound clinical significance of clostridial glucosylating toxins.

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