ライフサイエンスコーパス: triose

1 (E4P) exclusively by the carboxylation of a triose.

2 ns through gluconeogenesis from the level of trioses.

3 A enters gluconeogenesis at the level of the trioses.

4 henin and barley beta-glucan hydrolysis were triose and tetraose.

5 a variety of amphiphilic alkyl lactates from trioses and long chain alcohols in moderate to high yiel

6 lpha-hydroxy carboxylic acids from tetroses, trioses, and glycolaldehyde, but cannot readily catalyze

7 The triose binds to XI as the unreactive hydrate, but ligand

8 both the nonoxidative pentose phosphate and triose carboxylation pathways or (ii) E4P is formed excl

9 e cannot break a (13)C-(13)C bond within the trioses contributing to glucose, the appearance of [1,2-

10 Thus, the conserved N-linked triose core, ManGlcNAc(2), improves both the kinetics an

11 D-Glyceraldehyde (DGA) is the triose fragment common to the substrates for XI and TIM.

12 wis/Bronsted acidity are able to convert the trioses, glyceraldehyde and dihydroxyacetone, quantitati

13 Triose glycolysis (generation of ATP from glyceraldehyde

14 c and gluconeogenic pathways at the level of triose intermediates could control expression of GR mRNA

15 The obligatory intermediacy of triose intermediates in alginate biosynthesis was proved

16 f deuterium (or tritium) at the level of the triose-isomerase reaction on tracee labeling and tracer

17 e retention of deuterium at the level of the triose-isomerase reaction, or both occur in humans.

18 whole-chain electron transport (J(max)), and triose-P utilization (V(TPU)).

19 R. prowazekii utilizes a second, independent triose phosphate acquisition pathway whereby sn-glycerol

20 of the labeling patterns showed formation of triose phosphate and pyruvate via the Embden-Meyerhof-Pa

21 Cycling between hexose phosphate and triose phosphate and reversible transketolase velocity w

22 sphate pathway are taken into consideration, triose phosphate export in the dark becomes possible by

23 starch degradation to enhance photosynthetic triose phosphate export in the light, but the reactions

24 providing a sustainable flux from starch to triose phosphate in the dark.

25 in the gapA operon encoding five enzymes for triose phosphate interconversion in Bacillus subtilis is

26 molecule HLA-DR1 and an epitope from mutant triose phosphate isomerase (mutTPI).

27 A plastid isoform of triose phosphate isomerase (pdTPI) plays a crucial role

28 The denaturation of triose phosphate isomerase (TIM) from Saccharomyces cere

29 stem, the gene encoding the metabolic enzyme triose phosphate isomerase (tim) was sequenced from a nu

30 architectural elements: a Rossman fold and a triose phosphate isomerase (TIM)-barrel domain for bindi

31 Triose phosphate isomerase (TPI) deficiency glycolytic e

32 m of chromosome 3 is linked with a cytosolic triose phosphate isomerase 4.

33 We have predicted mutations that introduce triose phosphate isomerase activity into ribose-binding

34 , we showed that it is possible to introduce triose phosphate isomerase activity into the ribose-bind

35 und that TpiA2 and RpiB, distant homologs of triose phosphate isomerase and ribose 5-phosphate isomer

36 mobile loop, analogous to those observed in triose phosphate isomerase and tryptophan synthetase.

37 s involved in triose phosphate reduction and triose phosphate isomerase are primarily located in the

38 olase reaction and incomplete equilibrium by triose phosphate isomerase cannot break a (13)C-(13)C bo

39 Given that triose phosphate isomerase is generally assumed to fully

40 le or the PPP but not an influence of either triose phosphate isomerase or the transaldolase reaction

41 rter-like protein 1, p57(Kip2), La, BiP, and triose phosphate isomerase transcripts.

42 ition of His-6 to another expressed protein (triose phosphate isomerase) did not result in stimulatio

43 ropomyosin 1, tropomyosin 2, paramyosin, and triose phosphate isomerase) did not.

44 A, glyceraldehyde 3-phosphate dehydrogenase, triose phosphate isomerase, and enolase 1, are targeted

45 roxyacid oxidase 3, serum albumin precursor, triose phosphate isomerase, and lamin.

46 phosphate dehydrogenase (G3PDH), annexin A2, triose phosphate isomerase, and ubiquitin B precursor.

47 tric acid cycle, incomplete equilibration by triose phosphate isomerase, or the transaldolase reactio

48 used to derive a profile matrix for chicken triose phosphate isomerase, TIM.

49 The TPI1 gene encodes triose phosphate isomerase, which catalyzes the intercon

50 rylation contributes to the heterogeneity of triose phosphate labeling from glycerol in rat liver.

51 In contrast, triose phosphate levels (glyceraldehyde-3-phosphate + di

52 However, enzymes involved in triose phosphate reduction and triose phosphate isomeras

53 hloroplasts, indicating that the M-localized triose phosphate shuttle should be viewed as part of the

54 ic properties compared to well-characterized triose phosphate transport systems from plant plastids.

55 uggest the existence of multiple rickettsial triose phosphate transport systems.

56 amilies as well as the eukaryotic organellar triose phosphate transporter (TPT) and nucleotide-sugar

57 asymmetrical labeling of glucose carbon from triose phosphate.

58 mulation is accompanied by the regulation of triose phosphate/inorganic phosphate transport across th

59 04, and ERF105, were entirely deregulated in triose phosphate/phosphate translocator (tpt) mutants.

60 starting with metabolite export through the triose phosphate/phosphate translocator with subsequent

61 the flux of glycerol and lactate between the triose-phosphate and pyruvate/lactate pools.

62 ng for a deficiency in its ability to export triose-phosphate from the chloroplast.

63 m Clostridium perfringens reveals a modified triose-phosphate isomerase (beta/alpha)8 barrel in which

64 They adopt a partial triose-phosphate isomerase (TIM) barrel fold with N- and

65 Although the enzyme has the anticipated triose-phosphate isomerase (TIM) barrel fold, the cataly

66 c glucoside hydrolase 1 family (alpha/beta)8 triose-phosphate isomerase (TIM) barrel structure with a

67 -fold dimer in head-to-tail arrangement of a triose-phosphate isomerase (TIM) barrel-like alpha/beta

68 y inhibiting the Calvin-Benson cycle enzymes triose-phosphate isomerase and sedoheptulose 1,7-bisphos

69 re of YKL-39 comprises a major (beta/alpha)8 triose-phosphate isomerase barrel domain and a small alp

70 is tilted toward the edge of the PLP binding triose-phosphate isomerase barrel domain.

71 her targets, whereas a single AS ODN against triose-phosphate isomerase did not differ significantly

72 minoaspartate and (ii) the DHAP analogue and triose-phosphate isomerase inhibitor phosphoglycolohydro

73 taalpha) barrel structure, first observed in triose-phosphate isomerase, occurs ubiquitously in natur

74 omerase, heat shock protein 27, cathepsin D, triose-phosphate isomerase, peroxiredoxin 6, and electro

75 The EAL domain exhibits a triose-phosphate isomerase-barrel fold with one antipara

76 s central carbon metabolism by inhibition of triose-phosphate isomerase.

77 dehyde-3-phosphate dehydrogenase (GAPDH) and triose-phosphate isomerase.

78 The double mutants of PGK3 and the triose-phosphate transporter (pgk3.2 tpt3) displayed a d

79 HMG) transcription-factor gene is flanked by triose-phosphate transporter (TPT) and RNA helicase gene

80 The chloroplast envelope triose-phosphate/phosphate translocator (TPT) is respons

81 ized a larger portion of their glycogen from triose phosphates and a smaller portion from tricarboxyl

82 It is produced primarily from triose phosphates and is detoxified to D-lactate (DL) by

83 es were found as follows: (i) glucose versus triose phosphates and phosphoenolpyruvate; (ii) differen

84 e dicarbonyl degradation product formed from triose phosphates during glycolysis.

85 e dicarbonyl degradation product formed from triose phosphates during glycolysis.

86 Fructose bisphosphate was degraded to triose phosphates fairly rapidly, and, as it was degrade

87 viously reported that R. prowazekii acquires triose phosphates for phospholipid biosynthesis via the

88 ariations in f show that the 13C labeling of triose phosphates was not equal in all hepatocytes, even

89 Remarkably, about 10% of the triose phosphates were found to be recycled back to form

90 s of C2 metabolites from hexose, pentose and triose phosphates without carbon loss.

91 and glucose-6-P and between glucose-6-P and triose phosphates, (ii) the release of small excess acet

92 ctures, including phosphate elimination from triose phosphates, carbohydrate degradation under the as

93 yl compound produced by the fragmentation of triose phosphates, forms advanced glycation endproducts

94 rsibly cleaves its ketohexose substrate into triose phosphates.

95 c/gluconeogenic pathways at the level of the triose phosphates.

96 ng made from a homogeneously labeled pool of triose phosphates.

97 way for lipid A biosynthesis; (ii) export of triose-phosphates from rhodoplasts; (iii) and absence of

98 of electron transport as well as the use of triose-phosphates only in wild-type plants during growth

99 on of nine SIL-IS for hexose-, pentose-, and triose-phosphates, UDP-glucose, and adenosine monophosph

100 diphosphates, and hexose-phosphates generate triose-phosphates.

101 EryC and subsequent decarboxylation to yield triose-phosphates.

102 ate pool, resulting in rapid labeling of the triose pool by the administered tracer glycerol.

103 d to fully equilibrate carbon tracers in the triose pool, the marked (13)C asymmetry in glycogen can

104 Entner-Doudoroff (E-D) pathway and that the triose pools are in equilibrium.

105 hat this residue effects the binding of both triose substrates.

106 nt connection between the phosphodianion and triose sugar portions of the substrate by "carving up" G

107 The backflux from triose to hexose phosphate was also found to be substant

108 the first step in the reaction network from triose to lactate.