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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 nhance the activity of the glycolytic enzyme phosphoglycerate kinase 1 (PGK1) and can increase ATP le
9                                              Phosphoglycerate kinase 1 (PGK1) catalyzes the reversibl
10                         The promoter for the phosphoglycerate kinase 1 (PGK1) gene contains an initia
11                                              Phosphoglycerate kinase 1 (PGK1) is a highly conserved e
12                           Here, we find that phosphoglycerate kinase 1 (PGK1) is recruited to endosom
13 8 phosphorylation, leading to ARD1-dependent phosphoglycerate kinase 1 (PGK1) K388 acetylation and su
14 cible in vivo photofootprinting of the human phosphoglycerate kinase 1 (PGK1) promoter, as well as pr
15 at NogoA-overexpressing muscle cells reduced phosphoglycerate kinase 1 (Pgk1) secretion, resulting in
16                    Here, we demonstrate that phosphoglycerate kinase 1 (PGK1), a gene in the PARK12 s
17                      Of note, expressions of Phosphoglycerate Kinase 1 (PGK1), Hexokinase 2 (HK2), an
18 trate here that PTEN directly interacts with phosphoglycerate kinase 1 (PGK1).
19 ssion and secretion of the glycolytic enzyme phosphoglycerate kinase 1 (PGK1).
20  V600E induce mitochondrial translocation of phosphoglycerate kinase 1 (PGK1); this is mediated by ER
21 ay genes, glucose transporter 1-4 (Glut1-4), phosphoglycerate kinase 1 and Glucokinase but not of pro
22                           Elevated levels of phosphoglycerate kinase 1 in the serum were also signifi
23    Hypoxia induces a 10-fold accumulation of phosphoglycerate kinase 1 mRNA in wild type mouse hepato
24                    Furthermore, induction of phosphoglycerate kinase 1 mRNA requires Arnt's N-termina
25                      Among these candidates, phosphoglycerate kinase 1 was associated with survival i
26 d that two of these proteins, annexin A5 and phosphoglycerate kinase 1, can bind directly with LPA.
27 endothelial growth factor (VEGF), Glut1, and phosphoglycerate kinase 1, increased in the Cited2(-/-)
28  we show that disrupting the glycolytic gene phosphoglycerate kinase-1 (pgk1) impairs Fgf-dependent d
29 HPRTminigene, under the control of the mouse phosphoglycerate kinase-1 gene promoter, was stably expr
30          Here, we used a ubiquitously active phosphoglycerate kinase-1 promoter to drive the expressi
31                                              Phosphoglycerate kinase 2 (PGK2) is a germ cell-specific
32 ontaining the known, translationally delayed phosphoglycerate kinase 2 (Pgk2) is initially transcribe
33              Both features contrast with the phosphoglycerate kinase 2 retroposon, which is believed
34 dehyde phosphate dehydrogenase (GAPDH) and 3-phosphoglycerate kinase (3-PGK) are enriched in synaptic
35                     We studied the role of 3-phosphoglycerate kinase, a glycolytic enzyme, in the met
36 1 mutant exhibited very low but measurable 3-phosphoglycerate kinase activity compared to the wild-ty
37 triphosphate inhibited recombinant T. brucei phosphoglycerate kinase activity in vitro with an IC50 o
38                                              Phosphoglycerate kinase and 2, 3-diphosphoglycerate muta
39 s illustrated using the N-terminal domain of phosphoglycerate kinase and a synthetic reagent containi
40 ump-induced refolding of two proteins, yeast phosphoglycerate kinase and a ubiquitin mutant.
41  Three loci, coding for the enzymes enolase, phosphoglycerate kinase and alcohol dehydrogenase, have
42 e (glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase and fructose bisphosphate aldola
43 was suggested by the increased expression of phosphoglycerate kinase and fructose-bisphosphate aldola
44 ed to probe the ATP binding sites of yeast 3-phosphoglycerate kinase and glycerol kinase from Candida
45 ubation with bulk ATP or by operation of the phosphoglycerate kinase and pyruvate kinase reactions to
46 hosphate dehydrogenase, phosphofructokinase, phosphoglycerate kinase) and DNA-binding proteins [unive
47 ceraldehyde-3-phosphate dehydrogenase), pgk (phosphoglycerate kinase), and tpi (triosephosphate isome
48  gene expression compared with MLV, MSV LTR, phosphoglycerate kinase, and CMV promoters in T-cell lin
49 e, glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase, and enolase were elevated.
50 tion of lactate dehydrogenase A, aldolase-A, phosphoglycerate kinase, and enolase-1 genes.
51 f HIF-1alpha target genes, such as for VEGF, phosphoglycerate kinase, and glucose transporter-1.
52       Therefore, roles of creatine kinase, 3-phosphoglycerate kinase, and pyruvate kinase were evalua
53                Two functional genes encoding phosphoglycerate kinase are differentially expressed dur
54 teomics and stimulation analyses, identified phosphoglycerate kinase as a stimulatory factor for neut
55 ilibrium dynamics of the native state, using phosphoglycerate kinase as model protein.
56                                  Using yeast phosphoglycerate kinase as model, here we identify the f
57 urant-induced unfolding transitions of yeast phosphoglycerate kinase by mapping several inter- and in
58 eviously, we identified that the chloroplast phosphoglycerate kinase (chl-PGK) from Nicotiana bentham
59        Apomyoglobin denaturant unfolding and phosphoglycerate kinase cold denaturation are discussed
60 ompare the folding kinetics of a fluorescent phosphoglycerate kinase construct in 30 mammalian cells
61 sonance energy transfer (FRET) probe-labeled phosphoglycerate kinase construct in two human cell line
62                   The two protein domains of phosphoglycerate kinase correspond to two dynamic units,
63 led shRNA upon removal of a floxed reporter (phosphoglycerate kinase-driven enhanced green fluorescen
64 te synthesis from CDV monophosphate, whereas phosphoglycerate kinase (EC 2.7.2.3) and succinyl-CoA sy
65 on, which mapped to pgk, the gene encoding 3-phosphoglycerate kinase, failed to suppress a resD mutat
66 ons of suramin in its free form and bound to phosphoglycerate kinases from T. brucei and S. cerevisae
67 cular-dynamics (MD) simulation of a protein, phosphoglycerate kinase, from which we calculate small-a
68                       Fragments of the human phosphoglycerate kinase gene (PGK1) and the plasmid pUC1
69  a genome-wide association study uncovered a phosphoglycerate kinase gene that may contribute to the
70 DNA under the control of the promoter of the phosphoglycerate kinase gene.
71 acetyl-CoA carboxylase) and Pgk-1 (plastid 3-phosphoglycerate kinase) genes to determine phylogenetic
72 atments were identified as adenylate kinase, phosphoglycerate kinase, glyceraldehyde-3-phosphate dehy
73                 For the N-terminal domain of phosphoglycerate kinase, hen egg-white lysozyme and BPTI
74 mine whether this was caused by the retained phosphoglycerate kinase I gene promoter (PGK-neo) casset
75 eo, in which a hybrid gene consisting of the phosphoglycerate kinase I promoter drives the neomycin p
76 itro, even though translational diffusion of phosphoglycerate kinase in the cell is slow compared to
77 the stability of the cytoplasmic enzyme PGK (phosphoglycerate kinase) increases in cells, the stabili
78 gen, we propose that plasmin ligands such as phosphoglycerate kinase induce a conformational change i
79              Decrease in the expression of 3-phosphoglycerate kinase led to a corresponding decrease
80 ng intermediates of the N-terminal domain of phosphoglycerate kinase (N-PGK) and a number of conserva
81 he chemically denatured N-terminal domain of phosphoglycerate kinase (N-PGK) has been determined by p
82 n sites around exon 7 of the Gbe1 gene and a phosphoglycerate kinase-Neomycin cassette within intron
83                   Elongation factor iNOS and phosphoglycerate kinase OS were the only proteins presen
84                                              Phosphoglycerate kinase (PGK) catalyzes a reversible pho
85                        The glycolytic enzyme phosphoglycerate kinase (PGK) catalyzes phosphoryl trans
86                                              Phosphoglycerate kinase (PGK) catalyzes the reversible p
87                                   In plants, phosphoglycerate kinase (PGK) converts 1,3-bisphosphogly
88 On a dataset of eukaryotic proteins from the phosphoglycerate kinase (PGK) family, interdomain site c
89 the stability and folding relaxation rate of phosphoglycerate kinase (PGK) Forster resonance energy t
90          Previous studies of the N-domain of phosphoglycerate kinase (PGK) from Bacillus stearothermo
91 anidinium-denatured state of the N-domain of phosphoglycerate kinase (PGK) has been characterized usi
92 dues 1-174) of Bacillus stearothermophilus 3-phosphoglycerate kinase (PGK) has been investigated usin
93 ion state analogue (TSA) complexes formed by phosphoglycerate kinase (PGK) have been used to test the
94 y and folding rate of a mutant of the enzyme phosphoglycerate kinase (PGK) inside bone tissue cells a
95           The pneumococcal glycolytic enzyme phosphoglycerate kinase (PGK) is both secreted and bound
96       We find that binding of an antibody to phosphoglycerate kinase (PGK) is increased twofold under
97                             Escherichia coli phosphoglycerate kinase (PGK) is resistant to proteolyti
98 Incorporation of these fragments upstream of phosphoglycerate kinase (PGK) or cytomegalovirus promote
99 rexpression of PDGFB using a relatively weak phosphoglycerate kinase (PGK) promoter completely avoide
100 Cs transduced by a vector that used a murine phosphoglycerate kinase (PGK) promoter led to a complete
101 cetyl-CoA carboxylase (ACCase) and plastid 3-phosphoglycerate kinase (PGK) to study grass evolution.
102 stigation of the interaction of the enzyme 3-phosphoglycerate kinase (PGK) with aryl and alkyl bispho
103  compaction of the already unfolded state of phosphoglycerate kinase (PGK) with decreasing denaturant
104 ernary complex of the R65Q mutant of yeast 3-phosphoglycerate kinase (PGK) with magnesium 5'-adenylyl
105                                              Phosphoglycerate kinase (PGK), a downstream protein of h
106                                              Phosphoglycerate kinase (PGK), a key enzyme in glycolysi
107                   The nubian mutant disrupts phosphoglycerate kinase (PGK), an enzyme required for AT
108                                 We have used phosphoglycerate kinase (PGK), an enzyme that forms its
109 raldehyde-3-phosphate dehydrogenase (GAPDH), phosphoglycerate kinase (PGK), and phosphoglycerate muta
110 rget genes varied, with the glycolytic gene, Phosphoglycerate kinase (Pgk), being mostly affected.
111 for inhibiting Trypanosoma brucei glycosomal phosphoglycerate kinase (PGK), glyceraldehyde-3-phosphat
112                                              Phosphoglycerate kinase (PGK), present on the surface of
113 3-phosphate dehydrogenase (GAPDH), NG-52 for phosphoglycerate kinase (PGK), shikonin for pyruvate kin
114 en developed for a two-domain protein, yeast phosphoglycerate kinase (PGK), using Forster resonance e
115 d results for a hinge-bending enzyme, namely phosphoglycerate kinase (PGK), which support and extend
116  factor HIF-1, glucose transporter (GLUT)-1, phosphoglycerate kinase (PGK)-1, and vascular endothelia
117 xpressing the GAL4/VP16 fusion protein (Ad/3-phosphoglycerate kinase (PGK)-GV16) was dose-dependent a
118 ng investigation of the impact of a retained phosphoglycerate kinase (PGK)-neo cassette located betwe
119 ldehyde-3-phosphate dehydrogenase (G3PD) and phosphoglycerate kinase (PGK).
120  and immediately upstream of a gene encoding phosphoglycerate kinase (pgk).
121 tiary structure of the bidomain enzyme yeast phosphoglycerate kinase (PGK).
122  mass spectrometry (MS) to study the protein phosphoglycerate kinase (PGK).
123 tructure, function, and folding landscape of phosphoglycerate kinase (PGK).
124 mediate state of the large two-domain enzyme phosphoglycerate kinase (PGK).
125  analog diphosphates are phosphorylated by 3-phosphoglycerate kinase (PGK).
126 f proline 204 in the 'hinge' region of yeast phosphoglycerate kinase (PGK).
127 at genes encoding both isoenzymes of tobacco phosphoglycerate kinase (PGK, EC 2.7.2.3) are differenti
128 ng landscape of a FRET-labeled enzyme, yeast phosphoglycerate kinase (PGK-FRET).
129 id, 1,3-BPG,3 and evaluated their binding to phosphoglycerate kinase, PGK (EC 2.7.2.3).
130 e redox features of the Calvin-Benson enzyme phosphoglycerate kinase (PGK1) from the eukaryotic green
131 on nucleosomes present in the human X-linked phosphoglycerate kinase (PGK1) gene.
132 n the transcriptionally active human p53 and phosphoglycerate kinase (pgk1) genes in vivo.
133 dehyde-3-phosphate dehydrogenase (Gap1); and phosphoglycerate kinase (Pgk1).
134 e was confirmed by expressing the glycosomal phosphoglycerate kinase (PGKC) in the Deltappdk/Deltapep
135 reductase, UDP-glucose pyrophosphorylase and phosphoglycerate kinase play a role in heat-stress-media
136 nactivation center XIST and the ATRX, ATP7A, phosphoglycerate kinase, POU3F4, and choroideremia genes
137 hemical shift and hydrogen exchange rates as phosphoglycerate kinase progresses through its catalytic
138  and promoter region of the IRBP gene with a phosphoglycerate kinase-promoted neomycin-resistant gene
139 roviral vector expressing MGMT via the human phosphoglycerate kinase promoter (PGK-MGMT) protects ani
140 ing the human MGMT gene under control of the phosphoglycerate kinase promoter (PGK-MGMT) we increased
141 the neomycin gene under the direction of the phosphoglycerate kinase promoter, and stable transforman
142 F alpha gene is constitutively driven by the phosphoglycerate kinase promoter, or transfected with a
143 ice that overexpress CXCL14 under control of phosphoglycerate kinase promoter.
144 he control of a strong internal constitutive phosphoglycerate kinase promoter.
145 ic enzymes, including lactate dehydrogenase, phosphoglycerate kinase, pyruvate kinase, and acid phosp
146 s in lentiviral vectors (cytomegalovirus and phosphoglycerate kinase) revealed that suppression of vi
147                      Inhibition studies of 3-phosphoglycerate kinase show a dramatic decrease in isom
148 ly reported more closely resemble those of 3-phosphoglycerate kinase, suggesting the surprising resul
149 primary spermatocytes to provide a source of phosphoglycerate kinase that is critical to normal motil
150 ed that protein disulfide isomerase-like and phosphoglycerate kinase were required for optimal SCMV r
151 sphates were selectively phosphorylated by 3-phosphoglycerate kinase, whereas, D-deoxynucleoside anal
152 e mesoscopic level, including the pig muscle phosphoglycerate kinase with 416 residues.

 
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