ライフサイエンスコーパス: uridine diphosphate

1 are activated by endogenous ATP, UTP, and 5'uridine-diphosphate.

2 bound with uridine diphosphate or with both uridine diphosphate and myricetin were determined at 2.1

3 rase produces efficient galactosylation when uridine diphosphate-galactose is added, affording a pote

4 O-GlcNAcylation requires uridine diphosphate-GlcNAc, a precursor responsive to nu

5 in the glycosyltransferase active site above uridine diphosphate-GlcNAc.

6 for production of the donor nucleotide-sugar uridine-diphosphate-GlcNAc (UDP-GlcNAc) by deletion of t

7 s and was genotyped for the TA repeat at the uridine diphosphate glucononosyltransferase-lA1 promoter

8 46.82 mukat/Kg protein toward phloretin and uridine diphosphate glucose (UDPG) at an optimal tempera

9 ose is produced from glucose 6-phosphate and uridine diphosphate glucose in a two-step process, and r

10 ophosphorylcholine, myo-inositol, imidazole, uridine diphosphate glucose, isocitrate, lactate, and fu

11 On the other hand, flux through the hepatic uridine-diphosphate- glucose pool did not differ between

12 Two uridine diphosphate glucosyltransferases were functional

13 Uridine diphosphate glucunosyltransferases (UGTs) metabo

14 transfers a glucuronic acid moiety from the uridine diphosphate-glucuronic acid (UDP-GlcUA) to the c

15 tabolites produced by cytochrome P450 and/or uridine diphosphate glucuronosyl transferases were simul

16 Uridine diphosphate glucuronosyltransferase (EC 2.4.1.17

17 3A1 and CYP2B1/2, testosterone/4-nitrophenol uridine diphosphate glucuronosyltransferase (UDPGT), and

18 ance of bilirubin requires the expression of uridine diphosphate glucuronosyltransferase (UGT) 1A1; w

19 103-glucuronide (TAS-103-G) predominantly by uridine diphosphate glucuronosyltransferase isoform 1A1

20 (benzoate) can be explained by deletion of a uridine diphosphate glucuronosyltransferase.

21 the linkage region encodes hepatic bilirubin uridine diphosphate-glucuronosyltransferase (UGT1A1).

22 We used rs6742078 located in the uridine diphosphate-glucuronosyltransferase locus as an

23 Uridine diphosphate-glucuronosyltransferase-1A1 deficien

24 Uridine diphosphate-glucuronosyltransferase-1A1 deficien

25 abolite, SN-38, is glucuronidated by hepatic uridine diphosphate glucuronosyltransferases (UGTs).

26 Phase I (cytochromes P-450) and phase II (uridine diphosphate glucuronosyltransferases) drug-metab

27 formiminotransferase cyclodeaminase, and the uridine diphosphate glucuronosyltransferases, whereas al

28 sport proteins as well as other enzymes (eg, uridine diphosphate-glucuronosyltransferases, cytochrome

29 oint LOD score is located 1 cM away from the uridine diphosphate glycosyltransferase 1 (UGT1A1) gene.

30 ome for sequences with similarity to terpene URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASES (UGTs) from Ara

31 d functions, is controlled by specific plant uridine diphosphate glycosyltransferases (UGTs).

32 Four candidate uridine diphosphate glycosyltransferases were expressed

33 iphosphate N-acetylhexosamine (UDP-HexNAc)]/[uridine diphosphate hexose (UDP-hexose)] ratio exhibited

34 ptor with a high affinity for the nucleotide uridine diphosphate, is an important endogenous inhibito

35 lly, and the stereochemistry was assigned as uridine diphosphate N'-diacetylbacillosamine (UDP-diNAcB

36 )-dependent oxidation of the 3'' position of uridine diphosphate N-acetyl-D-glucosamine (UDP-GlcNAc),

37 Purified uridine diphosphate N-acetylenolpyruvylglucosamine reduc

38 uridine diphosphate N-acetylglucosamine and uridine diphosphate N-acetylgalactosamine, leading to th

39 osamine biosynthetic pathway (HBP) generates uridine diphosphate N-acetylglucosamine (UDP-GlcNAc) for

40 Glucose and glutamine are precursors of uridine diphosphate N-acetylglucosamine (UDP-GlcNAc), a

41 e fate of the chitin-biosynthesis precursor, uridine diphosphate N-acetylglucosamine (UDP-GlcNAc), wa

42 nsferase pp-alpha-GanT2 able to utilize both uridine diphosphate N-acetylglucosamine and uridine diph

43 ich catalyzes a key step in the synthesis of uridine diphosphate N-acetylglucosamine, which is requir

44 fect on the biosynthetic reactions involving uridine diphosphate N-acetylglucosamine.

45 pyridyl)-benzimidazole and MurA complexed to uridine diphosphate N-acetylglucosamine.

46 decreased, whereas the distribution of the [uridine diphosphate N-acetylhexosamine (UDP-HexNAc)]/[ur

47 Uridine diphosphate N-acetylmuramate:L-alanine ligase (E

48 ted by decreased enzyme activity and reduced uridine diphosphate-N-acetyl-D-glucosamine, along with d

49 GlcNAc) levels are modulated by two enzymes: uridine diphosphate-N-acetyl-D-glucosamine:polypeptidylt

50 resulting in a 70:30 ratio of UDP-GlcNAc to uridine diphosphate-N-acetylgalactosamine (UDP-GalNAc),

51 cosylation catalyzed by distinct recombinant uridine diphosphate-N-acetylgalactosamine:polypeptide N-

52 With uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc) as

53 nce studies indicated thatlymphostatin binds uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc) but

54 ally characterized to show that it encodes a uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc) C4

55 dramatically reduced intracellular levels of uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc), a

56 mine biosynthetic pathway (HBP), to increase uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc).

57 ltransferase that catalyzes the formation of uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc).

58 the mammalian Golgi membrane transporter for uridine diphosphate-N-acetylglucosamine by phenotypic co

59 ble HeLa cell line that overexpresses murine uridine diphosphate-N-acetylglucosaminyl transferase (OG

60 be the kinetic mechanism of Escherichia coli uridine diphosphate-N-acetylmuramate:L-alanine ligase (U

61 ADP, uridine diphosphate-N-acetylmuramoyl-L-alanine (UNAMA),

62 The structures of UGT78G1 bound with uridine diphosphate or with both uridine diphosphate and

63 e to ADP (e.g., P2Y(1), P2Y(3), P2Y(12)) and uridine diphosphate (P2Y(6)).

64 iphosphate > 5'uridine-triphosphate > or = 5'uridine-diphosphate, supports a P2Y1 receptor (R).

65 Uridine diphosphate (UDP) galactose, a pivotal compound

66 is and then subsequently characterized seven uridine diphosphate (UDP) glycosyltransferases (UGTs) fr

67 zes the reversible conversion of sucrose and uridine diphosphate (UDP) into fructose and UDP-glucose,

68 onse to cysteinyl leukotrienes (cys-LTs) and uridine diphosphate (UDP) that is blocked by cys-LT rece

69 sponse to cys-LTs and the nucleotide ligand, uridine diphosphate (UDP), without increasing their surf

70 o GlcNAc-1-phosphate during the synthesis of uridine diphosphate (UDP)-GlcNAc, a sugar nucleotide cri

71 Microsomal uridine diphosphate (UDP)-glucuronosyltransferase (UGT)

72 ic steps of this pathway involve a series of uridine diphosphate (UDP)-linked peptidoglycan intermedi

73 ltransferase MurU catalyzes the synthesis of uridine diphosphate (UDP)-MurNAc, a crucial precursor of

74 y) are diseases in which the activity of the uridine diphosphate (UDP)-N-acetylglucosamine:lysosomal

75 are responsible for synthesis of an uncommon uridine diphosphate (UDP)-sugar (PglD, PglC, and PglB-ac

76 Unnatural uridine diphosphate (UDP)-sugar donors, UDP-4-deoxy-4-fl

77 ls (hMCs) to stimulation with the nucleotide uridine diphosphate (UDP).

78 ferred by GlmU to afford their corresponding uridine diphosphate(UDP)-sugar nucleotides.

79 Mixtures composed of uridine monophosphate, uridine diphosphate, uridine triphosphate, and their non