ライフサイエンスコーパス: phosphoglycerate kinase

1 xokinase is functionally open like that of 3-phosphoglycerate kinase.

2 G binding site and in the hinge regions of 3-phosphoglycerate kinase.

3 ting glycolysis, especially by inhibition of phosphoglycerate kinase.

4 n of 1,3-bisphosphoglycerate, a substrate of phosphoglycerate kinase.

5 and the glycolytic phosphotransfer enzyme, 3-phosphoglycerate kinase.

6 xins 1 and 6), and metabolic proteins (e.g., phosphoglycerate kinase 1 (PGK 1), alpha enolase, aldola

7 Since other Hif target genes such phosphoglycerate kinase 1 (Pgk) were Hif-1alpha dependen

8 Phosphoglycerate kinase 1 (PGK1) catalyzes the reversibl

9 The promoter for the phosphoglycerate kinase 1 (PGK1) gene contains an initia

10 8 phosphorylation, leading to ARD1-dependent phosphoglycerate kinase 1 (PGK1) K388 acetylation and su

11 cible in vivo photofootprinting of the human phosphoglycerate kinase 1 (PGK1) promoter, as well as pr

12 Of note, expressions of Phosphoglycerate Kinase 1 (PGK1), Hexokinase 2 (HK2), an

13 ssion and secretion of the glycolytic enzyme phosphoglycerate kinase 1 (PGK1).

14 V600E induce mitochondrial translocation of phosphoglycerate kinase 1 (PGK1); this is mediated by ER

15 ay genes, glucose transporter 1-4 (Glut1-4), phosphoglycerate kinase 1 and Glucokinase but not of pro

16 Elevated levels of phosphoglycerate kinase 1 in the serum were also signifi

17 Hypoxia induces a 10-fold accumulation of phosphoglycerate kinase 1 mRNA in wild type mouse hepato

18 Furthermore, induction of phosphoglycerate kinase 1 mRNA requires Arnt's N-termina

19 Among these candidates, phosphoglycerate kinase 1 was associated with survival i

20 endothelial growth factor (VEGF), Glut1, and phosphoglycerate kinase 1, increased in the Cited2(-/-)

21 HPRTminigene, under the control of the mouse phosphoglycerate kinase-1 gene promoter, was stably expr

22 Here, we used a ubiquitously active phosphoglycerate kinase-1 promoter to drive the expressi

23 Phosphoglycerate kinase 2 (PGK2) is a germ cell-specific

24 ontaining the known, translationally delayed phosphoglycerate kinase 2 (Pgk2) is initially transcribe

25 Both features contrast with the phosphoglycerate kinase 2 retroposon, which is believed

26 dehyde phosphate dehydrogenase (GAPDH) and 3-phosphoglycerate kinase (3-PGK) are enriched in synaptic

27 We studied the role of 3-phosphoglycerate kinase, a glycolytic enzyme, in the met

28 1 mutant exhibited very low but measurable 3-phosphoglycerate kinase activity compared to the wild-ty

29 triphosphate inhibited recombinant T. brucei phosphoglycerate kinase activity in vitro with an IC50 o

30 Phosphoglycerate kinase and 2, 3-diphosphoglycerate muta

31 s illustrated using the N-terminal domain of phosphoglycerate kinase and a synthetic reagent containi

32 ump-induced refolding of two proteins, yeast phosphoglycerate kinase and a ubiquitin mutant.

33 Three loci, coding for the enzymes enolase, phosphoglycerate kinase and alcohol dehydrogenase, have

34 e (glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase and fructose bisphosphate aldola

35 ed to probe the ATP binding sites of yeast 3-phosphoglycerate kinase and glycerol kinase from Candida

36 ubation with bulk ATP or by operation of the phosphoglycerate kinase and pyruvate kinase reactions to

37 ceraldehyde-3-phosphate dehydrogenase), pgk (phosphoglycerate kinase), and tpi (triosephosphate isome

38 gene expression compared with MLV, MSV LTR, phosphoglycerate kinase, and CMV promoters in T-cell lin

39 e, glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase, and enolase were elevated.

40 tion of lactate dehydrogenase A, aldolase-A, phosphoglycerate kinase, and enolase-1 genes.

41 f HIF-1alpha target genes, such as for VEGF, phosphoglycerate kinase, and glucose transporter-1.

42 Therefore, roles of creatine kinase, 3-phosphoglycerate kinase, and pyruvate kinase were evalua

43 Two functional genes encoding phosphoglycerate kinase are differentially expressed dur

44 teomics and stimulation analyses, identified phosphoglycerate kinase as a stimulatory factor for neut

45 ilibrium dynamics of the native state, using phosphoglycerate kinase as model protein.

46 Using yeast phosphoglycerate kinase as model, here we identify the f

47 eviously, we identified that the chloroplast phosphoglycerate kinase (chl-PGK) from Nicotiana bentham

48 Apomyoglobin denaturant unfolding and phosphoglycerate kinase cold denaturation are discussed

49 ompare the folding kinetics of a fluorescent phosphoglycerate kinase construct in 30 mammalian cells

50 sonance energy transfer (FRET) probe-labeled phosphoglycerate kinase construct in two human cell line

51 The two protein domains of phosphoglycerate kinase correspond to two dynamic units,

52 led shRNA upon removal of a floxed reporter (phosphoglycerate kinase-driven enhanced green fluorescen

53 te synthesis from CDV monophosphate, whereas phosphoglycerate kinase (EC 2.7.2.3) and succinyl-CoA sy

54 on, which mapped to pgk, the gene encoding 3-phosphoglycerate kinase, failed to suppress a resD mutat

55 ons of suramin in its free form and bound to phosphoglycerate kinases from T. brucei and S. cerevisae

56 cular-dynamics (MD) simulation of a protein, phosphoglycerate kinase, from which we calculate small-a

57 Fragments of the human phosphoglycerate kinase gene (PGK1) and the plasmid pUC1

58 DNA under the control of the promoter of the phosphoglycerate kinase gene.

59 acetyl-CoA carboxylase) and Pgk-1 (plastid 3-phosphoglycerate kinase) genes to determine phylogenetic

60 atments were identified as adenylate kinase, phosphoglycerate kinase, glyceraldehyde-3-phosphate dehy

61 For the N-terminal domain of phosphoglycerate kinase, hen egg-white lysozyme and BPTI

62 mine whether this was caused by the retained phosphoglycerate kinase I gene promoter (PGK-neo) casset

63 eo, in which a hybrid gene consisting of the phosphoglycerate kinase I promoter drives the neomycin p

64 itro, even though translational diffusion of phosphoglycerate kinase in the cell is slow compared to

65 the stability of the cytoplasmic enzyme PGK (phosphoglycerate kinase) increases in cells, the stabili

66 gen, we propose that plasmin ligands such as phosphoglycerate kinase induce a conformational change i

67 Decrease in the expression of 3-phosphoglycerate kinase led to a corresponding decrease

68 ng intermediates of the N-terminal domain of phosphoglycerate kinase (N-PGK) and a number of conserva

69 he chemically denatured N-terminal domain of phosphoglycerate kinase (N-PGK) has been determined by p

70 n sites around exon 7 of the Gbe1 gene and a phosphoglycerate kinase-Neomycin cassette within intron

71 Phosphoglycerate kinase (PGK) catalyzes a reversible pho

72 The glycolytic enzyme phosphoglycerate kinase (PGK) catalyzes phosphoryl trans

73 Phosphoglycerate kinase (PGK) catalyzes the reversible p

74 In plants, phosphoglycerate kinase (PGK) converts 1,3-bisphosphogly

75 On a dataset of eukaryotic proteins from the phosphoglycerate kinase (PGK) family, interdomain site c

76 the stability and folding relaxation rate of phosphoglycerate kinase (PGK) Forster resonance energy t

77 Previous studies of the N-domain of phosphoglycerate kinase (PGK) from Bacillus stearothermo

78 anidinium-denatured state of the N-domain of phosphoglycerate kinase (PGK) has been characterized usi

79 dues 1-174) of Bacillus stearothermophilus 3-phosphoglycerate kinase (PGK) has been investigated usin

80 ion state analogue (TSA) complexes formed by phosphoglycerate kinase (PGK) have been used to test the

81 y and folding rate of a mutant of the enzyme phosphoglycerate kinase (PGK) inside bone tissue cells a

82 The pneumococcal glycolytic enzyme phosphoglycerate kinase (PGK) is both secreted and bound

83 Escherichia coli phosphoglycerate kinase (PGK) is resistant to proteolyti

84 Incorporation of these fragments upstream of phosphoglycerate kinase (PGK) or cytomegalovirus promote

85 rexpression of PDGFB using a relatively weak phosphoglycerate kinase (PGK) promoter completely avoide

86 Cs transduced by a vector that used a murine phosphoglycerate kinase (PGK) promoter led to a complete

87 cetyl-CoA carboxylase (ACCase) and plastid 3-phosphoglycerate kinase (PGK) to study grass evolution.

88 stigation of the interaction of the enzyme 3-phosphoglycerate kinase (PGK) with aryl and alkyl bispho

89 compaction of the already unfolded state of phosphoglycerate kinase (PGK) with decreasing denaturant

90 ernary complex of the R65Q mutant of yeast 3-phosphoglycerate kinase (PGK) with magnesium 5'-adenylyl

91 Phosphoglycerate kinase (PGK), a downstream protein of h

92 Phosphoglycerate kinase (PGK), a key enzyme in glycolysi

93 The nubian mutant disrupts phosphoglycerate kinase (PGK), an enzyme required for AT

94 We have used phosphoglycerate kinase (PGK), an enzyme that forms its

95 for inhibiting Trypanosoma brucei glycosomal phosphoglycerate kinase (PGK), glyceraldehyde-3-phosphat

96 Phosphoglycerate kinase (PGK), present on the surface of

97 en developed for a two-domain protein, yeast phosphoglycerate kinase (PGK), using Forster resonance e

98 d results for a hinge-bending enzyme, namely phosphoglycerate kinase (PGK), which support and extend

99 factor HIF-1, glucose transporter (GLUT)-1, phosphoglycerate kinase (PGK)-1, and vascular endothelia

100 xpressing the GAL4/VP16 fusion protein (Ad/3-phosphoglycerate kinase (PGK)-GV16) was dose-dependent a

101 ng investigation of the impact of a retained phosphoglycerate kinase (PGK)-neo cassette located betwe

102 ldehyde-3-phosphate dehydrogenase (G3PD) and phosphoglycerate kinase (PGK).

103 and immediately upstream of a gene encoding phosphoglycerate kinase (pgk).

104 tiary structure of the bidomain enzyme yeast phosphoglycerate kinase (PGK).

105 tructure, function, and folding landscape of phosphoglycerate kinase (PGK).

106 mediate state of the large two-domain enzyme phosphoglycerate kinase (PGK).

107 analog diphosphates are phosphorylated by 3-phosphoglycerate kinase (PGK).

108 f proline 204 in the 'hinge' region of yeast phosphoglycerate kinase (PGK).

109 at genes encoding both isoenzymes of tobacco phosphoglycerate kinase (PGK, EC 2.7.2.3) are differenti

110 ng landscape of a FRET-labeled enzyme, yeast phosphoglycerate kinase (PGK-FRET).

111 id, 1,3-BPG,3 and evaluated their binding to phosphoglycerate kinase, PGK (EC 2.7.2.3).

112 e redox features of the Calvin-Benson enzyme phosphoglycerate kinase (PGK1) from the eukaryotic green

113 on nucleosomes present in the human X-linked phosphoglycerate kinase (PGK1) gene.

114 n the transcriptionally active human p53 and phosphoglycerate kinase (pgk1) genes in vivo.

115 dehyde-3-phosphate dehydrogenase (Gap1); and phosphoglycerate kinase (Pgk1).

116 e was confirmed by expressing the glycosomal phosphoglycerate kinase (PGKC) in the Deltappdk/Deltapep

117 reductase, UDP-glucose pyrophosphorylase and phosphoglycerate kinase play a role in heat-stress-media

118 nactivation center XIST and the ATRX, ATP7A, phosphoglycerate kinase, POU3F4, and choroideremia genes

119 hemical shift and hydrogen exchange rates as phosphoglycerate kinase progresses through its catalytic

120 and promoter region of the IRBP gene with a phosphoglycerate kinase-promoted neomycin-resistant gene

121 roviral vector expressing MGMT via the human phosphoglycerate kinase promoter (PGK-MGMT) protects ani

122 ing the human MGMT gene under control of the phosphoglycerate kinase promoter (PGK-MGMT) we increased

123 the neomycin gene under the direction of the phosphoglycerate kinase promoter, and stable transforman

124 F alpha gene is constitutively driven by the phosphoglycerate kinase promoter, or transfected with a

125 ice that overexpress CXCL14 under control of phosphoglycerate kinase promoter.

126 he control of a strong internal constitutive phosphoglycerate kinase promoter.

127 ic enzymes, including lactate dehydrogenase, phosphoglycerate kinase, pyruvate kinase, and acid phosp

128 s in lentiviral vectors (cytomegalovirus and phosphoglycerate kinase) revealed that suppression of vi

129 Inhibition studies of 3-phosphoglycerate kinase show a dramatic decrease in isom

130 ly reported more closely resemble those of 3-phosphoglycerate kinase, suggesting the surprising resul

131 primary spermatocytes to provide a source of phosphoglycerate kinase that is critical to normal motil

132 ed that protein disulfide isomerase-like and phosphoglycerate kinase were required for optimal SCMV r

133 sphates were selectively phosphorylated by 3-phosphoglycerate kinase, whereas, D-deoxynucleoside anal

134 e mesoscopic level, including the pig muscle phosphoglycerate kinase with 416 residues.