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 e maintaining a high selectivity towards two trioses (46.4 % to glyceraldehyde and 32.9 % to dihydrox

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

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

7 -phase calculations are reported here on two trioses and three tetroses.

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

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

10 from glucose [(13)C-U], were incorporated as triose (C3), tetrose (C4), pentose (C5) or hexose (C6) m

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

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

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

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

15 In this study, two valuable trioses, glyceraldehyde and dihydroxyacetone, are produc

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

17 Triose glycolysis (generation of ATP from glyceraldehyde

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

35 Triose phosphate isomerase (TPI) deficiency glycolytic e

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

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

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

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

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

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

42 s, we identified the yeast glycolytic enzyme triose phosphate isomerase as being aggregation-prone in

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

44 is exported to the cytosol, where cytosolic triose phosphate isomerase could convert it to dihydroxy

45 Given that triose phosphate isomerase is generally assumed to fully

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

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

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

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

50 osphoglycolate is a competitive inhibitor of triose phosphate isomerase, an enzyme in the Calvin-Bens

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

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

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

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

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

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

57 cytosolic bypass around the block of stromal triose phosphate isomerase.

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

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

60 h and sucrose partitioning, v(o)/v(c) ratio, triose phosphate partitioning, and hexose kinase activit

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

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

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

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

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

66 rocesses: carboxylation, electron transport, triose phosphate use (TPU) and an additional model proce

67 Triose phosphate utilization, although sufficient to sup

68 Hence, the chloroplast malate valve and triose phosphate-3-phosphoglycerate shuttle are predicte

69 asymmetrical labeling of glucose carbon from triose phosphate.

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

71 04, and ERF105, were entirely deregulated in triose phosphate/phosphate translocator (tpt) mutants.

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

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

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

75 We further characterized triose-phosphate isomerase (Asp t 36), one of the domina

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

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

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

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

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

81 ition towards the active site cavity via the triose-phosphate isomerase (TIM) barrel.

82 temperature sensitivity with other reported triose-phosphate isomerase allergens.

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

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

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

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

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

88 ighly conserved with close similarity to the triose-phosphate isomerase protein sequence from Dermato

89 diseased mice reduced 3-nitrotyrosination of triose-phosphate isomerase, an enzyme involved in the fo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 rsibly cleaves its ketohexose substrate into triose phosphates.

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

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

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

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

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

117 EryC and subsequent decarboxylation to yield triose-phosphates.

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

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

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

121 60 to 80% for desired pentose, tetrose, and triose product mixtures and over 20% for hexose.

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

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

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

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