ライフサイエンスコーパス: transaldolase

1 clostridia do not contain genes annotated as transaldolase.

2 thesis as an l-threonine:uridine-5'-aldehyde transaldolase.

3 t phosphofructokinase (PP(i)-PFK) instead of transaldolase.

4 ate, changing the chemistry from aldolase to transaldolase.

5 atients with predetermined autoreactivity to transaldolase.

6 s further gene clusters encoding L-threonine transaldolases.

7 e moiety was scrambled via transketolase and transaldolase activities of the pentose phosphate pathwa

8 Mechanistic analysis reveals that transaldolase activity is an intrinsic feature of pyrido

9 ed in Escherichia coli a 45 kDa protein with transaldolase activity was produced.

10 m (Glyceraldehyde 3-phosphate dehydrogenase, transaldolase, alcohol dehydrogenase, and phosphoenolpyr

11 We have isolated a cDNA encoding transaldolase, an enzyme of the pentose-phosphate pathwa

12 Homologies between transaldolase and HSAG-1 break off internally at splice

13 TAREs in both the transaldolase and HSAG-1 genomic loci were surrounded by

14 one structure of the mechanistically similar transaldolase and KDPG aldolase allows the identificatio

15 e in basal and tissue-specific expression of transaldolase and regulation of the metabolic network co

16 an be used to calculate the three individual transaldolase and transketolase extents of reversibility

17 in kinases; (2) metabolic enzymes, including transaldolase and transketolase of the nonoxidative pent

18 fructose-1,6-(bis)phosphate (FBP) aldolase, transaldolase, and 2-keto-3-deoxy-6-phosphogluconate ald

19 ls the importance of glutathione peroxidase, transaldolase, and the concentration of total glutathion

20 of the human transaldolase gene, thus termed transaldolase-associated repetitive elements, TARE, were

21 nant epitopes, 33 peptides overlapping human transaldolase by 5 amino acids were synthesized.

22 We show how a transaldolase can circumvent this limitation, enabling e

23 that ZNF143 initiates transcription from the transaldolase core promoter.

24 enase, 6-phosphogluconate dehydrogenase, and transaldolase, elevated intracellular glutathione levels

25 ZNF143 overexpression also increased transaldolase enzyme activity.

26 acterium leprae, similarity to the conserved transaldolase enzymes from humans, E. coli and Saccharom

27 tibodies binding to the most prominent human transaldolase epitope, between residues 271 and 285, sho

28 The possible effects of transaldolase exchange or selective retention of deuteri

29 C5-to-C3 glucose ratio is <1 indicates that transaldolase exchange, selective retention of deuterium

30 titated using deuterated water corrected for transaldolase exchange.

31 Nase I footprinting with nuclear extracts of transaldolase-expressing cell lines unveiled protection

32 ZNF143 and transaldolase expression correlated in 21 different huma

33 Separate transketolase and transaldolase fluxes could be distinguished in the plast

34 cifically isocitrate lyase, malate synthase, transaldolase, fructose bisphosphatase and phosphoenolpy

35 otide biosynthesis, and the PPP, including a transaldolase gene that is the most prevalent PPP gene i

36 ements flanked by exons 2 and 3 of the human transaldolase gene, thus termed transaldolase-associated

37 to the transcription start site of the human transaldolase gene.

38 ite to the direction of transcription of the transaldolase gene.

39 PfkA of Escherichia coli, which does rely on transaldolase, had a very poor affinity for S7P.

40 While the potato transaldolase has considerable similarity to the enzyme

41 decisive factor in directing autoimmunity to transaldolase in multiple sclerosis patients.

42 The lower efficiency of phage transaldolase may be a tradeoff for other selective adva

43 preliminary data suggesting that L-threonine transaldolases might be useful for the preparation of L-

44 Northern analysis indicated that the transaldolase mRNA accumulated in tubers in response to

45 om various potato tissues indicated that the transaldolase mRNA accumulation to higher levels in the

46 mprove the substrate scope overlap between a transaldolase (ObiH) and a decarboxylase for the product

47 The transaldolase paralogue NQM1 and the transcription facto

48 nserved in the sulfoglycolytic sulfofructose transaldolase pathway, and determine its 3D structure.

49 gar SQ using a sulfoglycolytic sulfofructose transaldolase pathway.

50 of ZNF143 enhanced, maintained, or abolished transaldolase promoter activity, respectively, in HepG2

51 s confirm that ZNF143/73 associates with the transaldolase promoter in vivo.

52 r mutation of the ZNF76/143 motif within the transaldolase promoter.

53 ration by triose phosphate isomerase, or the transaldolase reaction all interact to produce complex (

54 Because the transaldolase reaction and incomplete equilibrium by tri

55 the M. jannaschii MJ0400 gene catalyzes the transaldolase reaction and the protein product of the MJ

56 th unlabeled three-carbon precursors via the transaldolase reaction and/or selective retention of the

57 es a "hydroxyacetone" fragment, which, via a transaldolase reaction, undergoes an aldol condensation

58 of either triose phosphate isomerase or the transaldolase reaction.

59 t the reversibility of the transketolase and transaldolase reactions in the nonoxidative pathway.

60 4, raised against enzymatically active human transaldolase, recognized antigenic determinants corresp

61 Transaldolase regulates redox-dependent apoptosis throug

62 and an L-threonine:4-nitrophenylacetaldehyde transaldolase responsible for (2S,3R)-2-amino-3-hydroxy-

63 Kinetic measurements of phage and host transaldolases revealed that the phage enzymes have k(ca

64 The substitution in transaldolase stabilizes the enamine intermediate requir

65 also encodes fructose bisphosphatase (fbp), transaldolase (tal) and a gene product termed OpcA, whic

66 e responses to oligodendroglial autoantigens transaldolase (TAL) and myelin basic protein (MBP) were

67 ate the evolution of the land plant TAL-type transaldolase (TAL) gene and its potential function in r

68 Transaldolase (TAL) is a key enzyme of the pentose phosp

69 Transaldolase (TAL) is a key enzyme of the reversible no

70 Transaldolase (TAL) is expressed at selectively high lev

71 Transaldolase (TAL) is expressed at selectively high lev

72 Here, we report that male mice lacking transaldolase (TAL)(-/-) are sterile because of defectiv

73 ntose phosphate pathway (PPP), the effect of transaldolase (TAL), a key enzyme of PPP, was investigat

74 hate pathway (PPP), we studied the impact of transaldolase (TAL), a key enzyme of the PPP, on Fas sig

75 n the pentose phosphate pathway (PPP) enzyme transaldolase (TAL; encoded by TALDO1) and liver failure

76 ogue to the pentose phosphate pathway enzyme transaldolase (TAL1), and the transcription factor vitam

77 (psbA), high-light inducible protein (hli), transaldolase (talC) and ribonucleotide reductase (nrd)-

78 is a pyridoxal 5'-phosphate (PLP)-dependent transaldolase that catalyzes a threo-selective aldol-typ

79 Consequently, AprG appears to be a new transaldolase that lacks any apparent sequence similarit

80 h of the pentose phosphate pathway involving transaldolase that places this (13)C-enriched 3-carbon u

81 ite reductase, and metabolic enzymes such as transaldolase, transketolase, malate dehydrogenase, aspa

82 on in T. acidiphilum is accomplished via the transaldolase variant of the CBB cycle, which has not be

83 r to net glycolytic flux, whereas reversible transaldolase velocity was minimal.

84 A three-dimensional model of human transaldolase was developed based on the crystal structu

85 Phage transaldolase was purified to homogeneity from several s

86 Transaldolase, which is expressed in the brain selective

87 fact that Lys146 in aldolase is replaced in transaldolase with Asn35.