ライフサイエンスコーパス: phosphoenolpyruvate

1 an increase in the pyruvate kinase substrate phosphoenolpyruvate.

2 al causes accumulation of Cdc19's substrate, phosphoenolpyruvate.

3 rated via the pentose phosphate pathway, and phosphoenolpyruvate.

4 on, glycogenolysis, and gluconeogenesis from phosphoenolpyruvate.

5 ates FBP-based regulation fail to accumulate phosphoenolpyruvate.

6 ed light-dependent conversion of pyruvate to phosphoenolpyruvate.

7 nce of amino acids derived from pyruvate and phosphoenolpyruvate.

8 nd H2 perturb allosteric activator sites for phosphoenolpyruvate.

9 ere data are available exhibit activation by phosphoenolpyruvate.

10 rresponded to elevated flux from pyruvate to phosphoenolpyruvate.

11 ncident with reduced gluconeogenic flux from phosphoenolpyruvate.

12 carboxylase to oxaloacetate, and via PCK2 to phosphoenolpyruvate.

13 onversion of mitochondrial oxaloacetate into phosphoenolpyruvate.

14 +/- 1 in ZDF-GPI+G, and 24 +/- 2 in ZCL) and phosphoenolpyruvate 260% (4 +/- 2 in ZDF-V, 16 +/- 1 in

15 [2-(13)C]Phosphoenolpyruvate, a key branch point in gluconeogenes

16 At physiologically relevant concentrations, phosphoenolpyruvate and citrate stabilize an active tetr

17 The two most potent activators, phosphoenolpyruvate and citrate, bind to the sulfate ani

18 accumulation of the glycolytic intermediate phosphoenolpyruvate and decreased pyruvate kinase activi

19 e (rM1-PK) which catalyzes the conversion of phosphoenolpyruvate and Mg-ADP to pyruvate and Mg-ATP.

20 Phosphoenolpyruvate and sulfate activate E. coli FBPase

21 y two small molecules, the natural substrate phosphoenolpyruvate and the inhibitor alpha-ketoglutarat

22 ated by signals from both carbon metabolism (phosphoenolpyruvate) and nitrogen metabolism (glutamine)

23 the substrate/product, 2-phospho-D-glycerate/phosphoenolpyruvate, and induces binding of the catalyti

24 e dikinase (PPDK) interconverts pyruvate and phosphoenolpyruvate, and is found in both plastids and t

25 We demonstrate that potassium 1-(13)C-phosphoenolpyruvate becomes hyperpolarized potassium 1-(

26 e strategy to circumvent the competition for phosphoenolpyruvate between 3-deoxy-D-arabino-heptuloson

27 enzyme family: anionic ligands, most likely phosphoenolpyruvate, bind to allosteric activator sites,

28 nding negative trends in kcat and kcat/K0.5 (phosphoenolpyruvate) but not in K0.5 or the Hill coeffic

29 ated HPr, which decreases the PykF Khalf for phosphoenolpyruvate by 10-fold (from 3.5 to 0.36 mm), th

30 transducing protein EIIA(Glc) belongs to the phosphoenolpyruvate carbohydrate phosphotransferase syst

31 The bacterial phosphoenolpyruvate-carbohydrate phosphotransferase syst

32 ions similar to proteins associated with the phosphoenolpyruvate: carbohydrate phosphotransferase sys

33 cted DNA-binding domains (HTH1 and HTH2) and phosphoenolpyruvate: carbohydrate phosphotransferase sys

34 nonphosphomimetic substitutions at conserved phosphoenolpyruvate:carbohydrate phosphotransferase regu

35 nic acid 7-phosphate (DAHP) synthase and the phosphoenolpyruvate:carbohydrate phosphotransferase syst

36 This gene cluster encodes the Aga phosphoenolpyruvate:carbohydrate phosphotransferase syst

37 phosphorylation of glucose catalyzed by the phosphoenolpyruvate:carbohydrate phosphotransferase syst

38 hotransfer protein IIA(Glc) of the bacterial phosphoenolpyruvate:carbohydrate phosphotransferase syst

39 te (PEP) and oxaloacetate (OAA) by cytosolic phosphoenolpyruvate carboxykinase (cPEPCK) were investig

40 , transaldolase, fructose bisphosphatase and phosphoenolpyruvate carboxykinase (encoded by ICL1, MAS1

41 aining a chimeric gene in which the cDNA for phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C) (EC 4.

42 iption of the gene for the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C).

43 e (NAD) phosphate malic enzyme (NADP-ME) and phosphoenolpyruvate carboxykinase (PCK) photosynthetic p

44 intermediates and this relies on the enzyme phosphoenolpyruvate carboxykinase (PCK).

45 pression of the hepatic gluconeogenic genes, phosphoenolpyruvate carboxykinase (PCK1) and glucose-6-p

46 n regulating glucose metabolism by targeting phosphoenolpyruvate carboxykinase (PCK1) and glucose-6-p

47 elates with glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (PCK1) expression, key

48 these, acetylation sites (Lys19 and 514) of phosphoenolpyruvate carboxykinase (Pck1p) were determine

49 Here we show that mitochondrial phosphoenolpyruvate carboxykinase (PCK2), the hub molecu

50 Phosphoenolpyruvate carboxykinase (Pck; EC 4.1.1.32) is

51 d to increased transcriptional expression of phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-

52 pts for archetypical decarboxylation enzymes phosphoenolpyruvate carboxykinase (PEPCK) and malic enzy

53 ncer cells utilize the gluconeogenic enzymes phosphoenolpyruvate carboxykinase (PEPCK) and phosphoeno

54 nvestigate the effect of decreased cytosolic phosphoenolpyruvate carboxykinase (PEPCK) and plastidic

55 transcriptional regulation of Glc-6-Pase and phosphoenolpyruvate carboxykinase (PEPCK) by apoA-IV was

56 Phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the

57 ructural studies of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) demonstrate th

58 Here, we reveal two discrete phosphoenolpyruvate carboxykinase (PEPCK) enzymes in the

59 Phosphoenolpyruvate carboxykinase (PEPCK) expression pla

60 human CYP7A1 gene in bile acid synthesis and phosphoenolpyruvate carboxykinase (PEPCK) gene in glucon

61 ic gluconeogenesis through downregulation of phosphoenolpyruvate carboxykinase (PEPCK) in wild-type (

62 Phosphoenolpyruvate carboxykinase (PEPCK) is an essentia

63 Phosphoenolpyruvate carboxykinase (PEPCK) is well known

64 aling in renal epithelial cells, we used the phosphoenolpyruvate carboxykinase (PEPCK) promoter to ge

65 e structures of the rat cytosolic isoform of phosphoenolpyruvate carboxykinase (PEPCK) reported in th

66 of both glucose-6-phosphatase (Glc-6-P) and phosphoenolpyruvate carboxykinase (Pepck) to an extent s

67 Here we report gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK) transcription

68 utes to TCDD suppression of transcription of phosphoenolpyruvate carboxykinase (PEPCK), a key regulat

69 We provide evidence that phosphoenolpyruvate carboxykinase (PEPCK), an enzyme inv

70 tion, expression of key gluconeogenic genes, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6

71 vestigated the role of glycerol kinase (GK), phosphoenolpyruvate carboxykinase (PEPCK), and pyruvate

72 decarboxylation of [4-(13)C]oxaloacetate via phosphoenolpyruvate carboxykinase (PEPCK), forward TCA c

73 d) could activate p38 and increase levels of phosphoenolpyruvate carboxykinase (PEPCK), glucose-6-pho

74 The key gluconeogenic enzyme, phosphoenolpyruvate carboxykinase (PEPCK), has been show

75 receptor gamma co-activator-1a (PGC-1alpha), phosphoenolpyruvate carboxykinase (PEPCK), pyruvate carb

76 Regulation of phosphoenolpyruvate carboxykinase (PEPCK), the key gene

77 pression of glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (Pepck), two gluconeog

78 In phosphoenolpyruvate carboxykinase (PEPCK)-GFP mice, seri

79 pyruvate dehydrogenase kinase 4 (pdk4), and phosphoenolpyruvate carboxykinase (pepck).

80 duced expression of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase (PEPCK).

81 nic genes glucose-6-phosphatase (G6pase) and phosphoenolpyruvate carboxykinase (Pepck).

82 ME), NAD-dependent malic enzyme (NAD-ME) and phosphoenolpyruvate carboxykinase (PEPCK).

83 nic genes glucose-6-phosphatase (G6Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

84 ces expression of hepatic gluconeogenic gene phosphoenolpyruvate carboxykinase (PEPCK).

85 on of glucose-6-phosphatase (Glc-6-Pase) and phosphoenolpyruvate carboxykinase (PEPCK).

86 to sugar feeding, including both isoforms of phosphoenolpyruvate carboxykinase (pepck).

87 erated in the glycosomes by kinases, such as phosphoenolpyruvate carboxykinase (PEPCK).

88 creased gluconeogenic flux through cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C) and associat

89 tigated whether the mitochondrial isoform of phosphoenolpyruvate carboxykinase (PEPCK-M) is the GTPas

90 Mitochondrial phosphoenolpyruvate carboxykinase (PEPCK-M), encoded by

91 Expression profiles of selected genes (phosphoenolpyruvate carboxykinase - PEPCK, glucocorticoi

92 eased transcription of the gene that encodes phosphoenolpyruvate carboxykinase 1 (a protein involved

93 re detail and indicated that the activity of phosphoenolpyruvate carboxykinase 1 (AT4G37870), a key e

94 nhibited hepatic gluconeogenic genes such as phosphoenolpyruvate carboxykinase 1 (Pck-1) and glucose

95 nic enzymes glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase 1 (PCK1) has negative

96 erosis/cataplerosis via genetic knockdown of phosphoenolpyruvate carboxykinase 1 (Pck1) prevented fat

97 cluding liver glycogen phosphorylase (PYGL), phosphoenolpyruvate carboxykinase 1 (PCK1), and the gluc

98 ing PEP production through overexpression of phosphoenolpyruvate carboxykinase 1 (PCK1), which bolste

99 ticoid regulated kinase 2 (SGK2) to activate phosphoenolpyruvate carboxykinase 1 (PEPCK1) and glucose

100 Phosphoenolpyruvate carboxykinase 1 (PEPCK1) is the crit

101 e-6-phosphatase catalytic subunit (G6Pc) and phosphoenolpyruvate carboxykinase 1 (PEPCK1).

102 We determined MNR effects on fetal liver phosphoenolpyruvate carboxykinase 1 (protein, PEPCK1; ge

103 Furthermore, this treatment normalizes phosphoenolpyruvate carboxykinase 1 contents without aff

104 d dexamethasone-induced transcription of the phosphoenolpyruvate carboxykinase 1 gene was strikingly

105 ith a glucocorticoid response element in the phosphoenolpyruvate carboxykinase 1 promoter in a hormon

106 l hepatic levels of the gluconeogenic enzyme phosphoenolpyruvate carboxykinase 1 were increased in hP

107 the rate-limiting enzyme in gluconeogenesis, phosphoenolpyruvate carboxykinase 1, is regulated throug

108 hosphoenolpyruvate carboxykinase (PEPCK) and phosphoenolpyruvate carboxykinase 2 (PCK2) to reprogram

109 with shizukaol F decreased the expression of phosphoenolpyruvate carboxykinase 2 (PEPCK), glucose-6-p

110 a not only with the rPDK4 gene but also with phosphoenolpyruvate carboxykinase and CPT-1a (carnitine

111 PST administration in KO mice stimulated phosphoenolpyruvate carboxykinase and G6Pase mRNA abunda

112 ssion of two critical gluconeogenic enzymes, phosphoenolpyruvate carboxykinase and glucose-6-phosphat

113 major regulators of hepatic gluconeogenesis, phosphoenolpyruvate carboxykinase and glucose-6-phosphat

114 Suppressed mRNA abundance of phosphoenolpyruvate carboxykinase and glucose-6-phosphat

115 vates expression of gluconeogenic, including phosphoenolpyruvate carboxykinase and glucose-6-phosphat

116 ession of key gluconeogenic genes, including phosphoenolpyruvate carboxykinase and glucose-6-phosphat

117 orrelation between dynamics and catalysis in phosphoenolpyruvate carboxykinase and other enzymes in w

118 malate dehydrogenase, isocitrate lyase, and phosphoenolpyruvate carboxykinase are induced.

119 Phosphoenolpyruvate carboxykinase catalyzes the reversib

120 the nematode analog of the cytosolic form of phosphoenolpyruvate carboxykinase caused a marked extens

121 Transcripts encoding phosphoenolpyruvate carboxykinase did not appear to be r

122 n increase in the liver gluconeogenic enzyme phosphoenolpyruvate carboxykinase expression and activit

123 In addition, increased phosphoenolpyruvate carboxykinase expression in DHet mou

124 orrelated well with the observed increase in phosphoenolpyruvate carboxykinase expression, type IA fi

125 coneogenic enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase in the leptin-infused

126 ts metabolism and discuss the role played by phosphoenolpyruvate carboxykinase in this process.

127 ed cAMP response element binding protein and phosphoenolpyruvate carboxykinase mRNA were profoundly r

128 ge-dependent phosphoenolpyruvate carboxylase/phosphoenolpyruvate carboxykinase process that decreases

129 essing rabbit CRP (CF1-CRP) regulated by the phosphoenolpyruvate carboxykinase promoter such that lev

130 Diabetic mice that expressed the phosphoenolpyruvate carboxykinase promoter-driven BMP-7

131 it CRP (CF1-CRP) under the regulation of the phosphoenolpyruvate carboxykinase promoter.

132 diate complexes of the reaction catalyzed by phosphoenolpyruvate carboxykinase provide direct structu

133 rboxylic acid (TCA) cycle first and then use phosphoenolpyruvate carboxykinase to initiate gluconeoge

134 e, transaldolase, alcohol dehydrogenase, and phosphoenolpyruvate carboxykinase) that indicate the pot

135 decarboxylase systems (NADP-malic enzyme and phosphoenolpyruvate carboxykinase) were critical for mat

136 locomplex and regulates expression of PEPCK (phosphoenolpyruvate carboxykinase), G6P (glucose-6-phosp

137 lectron transfer flavoprotein subunit alpha, phosphoenolpyruvate carboxykinase, aconitate hydratase,

138 gluconeogenic enzymes glucose-6-phosphatase, phosphoenolpyruvate carboxykinase, fructose-1,6-phosphat

139 vity in the liver of L-iNOS-Tg mice, whereas phosphoenolpyruvate carboxykinase, glucose-6-phosphatase

140 oid-regulated hepatic gluconeogenic enzymes, phosphoenolpyruvate carboxykinase, glucose-6-phosphatase

141 glucose production and hepatic expression of phosphoenolpyruvate carboxykinase, glucose-6-phosphatase

142 f ROR target genes, including Glc-6-Pase and phosphoenolpyruvate carboxykinase, in an ROR-dependent m

143 ROP (repressor of phosphoenolpyruvate carboxykinase, PEPCK) is a methanol-

144 colinic acid (3-MPA), a classic inhibitor of phosphoenolpyruvate carboxykinase, photosynthetic O(2) e

145 rget genes such as glucose-6-phosphatase and phosphoenolpyruvate carboxykinase, two key targets for F

146 gluconeogenic enzymes, isocitrate lyase and phosphoenolpyruvate carboxykinase, were also degraded in

147 and the gluconeogenesis controller, hepatic phosphoenolpyruvate carboxykinase, were significantly el

148 egulation of the first gluconeogenic enzyme, phosphoenolpyruvate carboxykinase, when acetate was the

149 sat1 and Psph) and the gluconeogenic enzyme, phosphoenolpyruvate carboxykinase-M (Pck2/PEPCK-M), incr

150 cose-6-phosphatase and the cytosolic form of phosphoenolpyruvate carboxykinase.

151 ls for the enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

152 uconeogenic genes, glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

153 coneogenic enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

154 GLUT-4 translocation and the increased liver phosphoenolpyruvate carboxyl kinase (PEPCK) expression i

155 contribute to the regulation of the model C4 phosphoenolpyruvate carboxylase (C4-Pepc) promoter in ma

156 throughout the dark period revealed changing phosphoenolpyruvate carboxylase (PEPC) capacity.

157 e observed 2- to 4-fold up-regulation of two phosphoenolpyruvate carboxylase (PEPC) gene transcripts

158 Phosphoenolpyruvate carboxylase (PEPC) is a "multifacete

159 Phosphoenolpyruvate carboxylase (PEPC) is a crucial enzy

160 Phosphoenolpyruvate carboxylase (PEPC) is a tightly cont

161 Phosphoenolpyruvate carboxylase (PEPC) is a widely distr

162 The encoded proteins are similar to other phosphoenolpyruvate carboxylase (PEPC) kinases, in that

163 y limited by the enzymatic rates of Rubisco, phosphoenolpyruvate carboxylase (PEPc), and carbonic anh

164 The key enzyme for C4 photosynthesis, Phosphoenolpyruvate Carboxylase (PEPC), evolved from non

165 ogenesis by inhibiting the transcriptions of phosphoenolpyruvate carboxylase (PEPCK) and glucose-6-ph

166 either NAD-ME or PPDK activity, particularly phosphoenolpyruvate carboxylase (PPC) and PPDK in rNAD-M

167 s effect is reduced production of the enzyme phosphoenolpyruvate carboxylase (PPC) and that adventiti

168 e monophosphate (HMP) pathway flux, elevated phosphoenolpyruvate carboxylase (Ppc) flux, and an incre

169 Phosphoenolpyruvate carboxylase (PPC; EC 4.1.1.31) catal

170 lyase, acetate:CoA ligase (AMP forming), and phosphoenolpyruvate carboxylase activities increased in

171 gether with increases of pyruvate kinase and phosphoenolpyruvate carboxylase activities indicate that

172 in the growth medium stimulated flux through phosphoenolpyruvate carboxylase and malic enzyme, altere

173 er respiratory activity and up-regulation of phosphoenolpyruvate carboxylase and NADP-dependent isoci

174 no acids via posttranslational regulation of phosphoenolpyruvate carboxylase and nitrate reductase.

175 ced, whereas the in vitro activities of both phosphoenolpyruvate carboxylase and Rubisco were increas

176 ctron transport (Jmax ), the maximum rate of phosphoenolpyruvate carboxylase carboxylation (Vpmax ),

177 First, the phosphoenolpyruvate carboxylase gene (ppc) from Klebsiel

178 Carbonic anhydrase and phosphoenolpyruvate carboxylase in vitro activity varied

179 esis during fasting through the induction of phosphoenolpyruvate carboxylase kinase (PEPCK), fructose

180 We have examined the complexity of the phosphoenolpyruvate carboxylase kinase (PPCK) gene famil

181 adian clock-controlled protein kinase called phosphoenolpyruvate carboxylase kinase (PPCK).

182 In all plants, PEPC is phosphorylated by Phosphoenolpyruvate Carboxylase Protein Kinase (PPCK).

183 f E. glabrescens accumulated a chloroplastic phosphoenolpyruvate carboxylase protein, albeit at reduc

184 ormation of oxaloacetate exclusively via the phosphoenolpyruvate carboxylase reaction.

185 tivity in the anapleurotic (malic enzyme and phosphoenolpyruvate carboxylase) reactions.

186 stomatal aperture, malic acid inhibition of phosphoenolpyruvate carboxylase, and enzyme kinetics) wa

187 Maize genes encoding phosphoenolpyruvate carboxylase, pyruvate, orthophosphat

188 ctase, and the CO(2)-anaplerotic pathway via phosphoenolpyruvate carboxylase.

189 a few amino acid positions in the key enzyme phosphoenolpyruvate carboxylase.

190 were also found to accumulate chloroplastic phosphoenolpyruvate carboxylase.

191 n enters the TCA cycle via a stage-dependent phosphoenolpyruvate carboxylase/phosphoenolpyruvate carb

192 ecreases in O2 evolution after inhibition of phosphoenolpyruvate carboxylases (PEPCs), and increases

193 Maize had a higher maximum velocity of phosphoenolpyruvate carboxylation, velocity of phosphoen

194 ynthetic protocol for preparation of 1-(13)C-phosphoenolpyruvate-d2, precursor for parahydrogen-induc

195 The phosphoenolpyruvate dehydrogenase complex is also up-reg

196 ulate methyl-alpha-D-glucopyranoside via the phosphoenolpyruvate-dependent glucose:phosphotransferase

197 en demonstrated in GAS, where mutants in the phosphoenolpyruvate-dependent phosphotransferase system

198 A phosphoenolpyruvate-dependent phosphotransferase system

199 een the different phylogenetic kingdoms, the phosphoenolpyruvate-dependent phosphotransferase system

200 bohydrate uptake in microbial species is the phosphoenolpyruvate-dependent phosphotransferase system

201 on upstream of bgaA and in the promoter of a phosphoenolpyruvate-dependent phosphotransferase system

202 Many bacteria express phosphoenolpyruvate-dependent phosphotransferase systems

203 sugar transport protein that is part of the phosphoenolpyruvate-dependent phosphotransferases.

204 uctokinase was linked to a fructose-specific phosphoenolpyruvate-dependent sugar phosphotransferase s

205 peptide represented an EIIA component of the phosphoenolpyruvate-dependent sugar phosphotransferase s

206 A (CcpA) and requires specific components of phosphoenolpyruvate-dependent sugar:phosphotransferase s

207 s of GlpD complexed with substrate analogues phosphoenolpyruvate, glyceric acid 2-phosphate, glyceral

208 he phosphotransfer sequence of the bacterial phosphoenolpyruvate:glycose phosphotransferase system.

209 Glc uptake, the phosphotransfer sequence is: phosphoenolpyruvate --> Enzyme I --> HPr --> IIAGlc -->

210 ws: (i) glucose versus triose phosphates and phosphoenolpyruvate; (ii) differences in the labeling ra

211 hosphatase (FBPase) from Escherichia coli by phosphoenolpyruvate implies rapid feed-forward activatio

212 e dikinase (PPDK), which reversibly converts phosphoenolpyruvate into pyruvate, could also be involve

213 e broader context of the lyase branch of the phosphoenolpyruvate mutase/isocitrate lyase superfamily

214 etate acetylhydrolase (OAH), a member of the phosphoenolpyruvate mutase/isocitrate lyase superfamily,

215 drolase (OAH), an enzyme that belongs to the phosphoenolpyruvate mutase/isocitrate lyase superfamily.

216 Tetramers ligated with either phosphoenolpyruvate or citrate, in contrast to the sulfa

217 is protonating the methylene carbon atom of phosphoenolpyruvate, or EPSP, in the reverse reaction.

218 of pyruvate kinase leads to accumulation of phosphoenolpyruvate (P-enolpyruvate), citrate, and aconi

219 ut maintains high affinity for the substrate phosphoenolpyruvate (PEP) (K(m) = 0.1 mm).

220 horylation by causing a decrease in apparent phosphoenolpyruvate (PEP) affinity.

221 tructure of the Cu(2+) enzyme incubated with phosphoenolpyruvate (PEP) and arabinose 5-phosphate (A5P

222 The mechanisms of molecular recognition of phosphoenolpyruvate (PEP) and oxaloacetate (OAA) by cyto

223 e noted that the affinity of the protein for phosphoenolpyruvate (PEP) becomes reduced several days a

224 permitting in-line phosphoryl transfer from phosphoenolpyruvate (PEP) bound to EIC to His189.

225 ent of Mycobacterium smegmatis GTP-dependent phosphoenolpyruvate (PEP) carboxykinase (GTP-PEPCK) were

226 The energy-conserving phosphoenolpyruvate (PEP) carboxykinase (pck), which nor

227 The activities of phosphoenolpyruvate (PEP) carboxylase (PEPC) and the PEP

228 g evidence indicates important functions for phosphoenolpyruvate (PEP) carboxylase (PEPC) in inorgani

229 , the exclusive formation of oxaloacetate by phosphoenolpyruvate (PEP) carboxylation became evident f

230 ine which chemical moieties of the substrate phosphoenolpyruvate (PEP) contribute to the allosteric i

231 lucose limitation promoted the production of phosphoenolpyruvate (PEP) from glutamine via the activit

232 Synthesis of phosphoenolpyruvate (PEP) from oxaloacetate is an absolu

233 via PEPC2 and PYC, respectively, regenerates phosphoenolpyruvate (PEP) from pyruvate in a pyruvate ph

234 Phosphoenolpyruvate (PEP) generated from pyruvate is req

235 red a new role for the glycolytic metabolite phosphoenolpyruvate (PEP) in sustaining T cell receptor-

236 producers by screening for the gene encoding phosphoenolpyruvate (PEP) mutase, which is required for

237 ate (P-pyr) hydrolase (PPH), a member of the phosphoenolpyruvate (PEP) mutase/isocitrate lyase (PEPM/

238 (13)C(3)-lactate and label enrichment in the phosphoenolpyruvate (PEP) pool was measured.

239 The phosphoenolpyruvate (PEP) synthetase PpsA, which convert

240 densation of arabinose 5-phosphate (A5P) and phosphoenolpyruvate (PEP) to form KDO8P, a key precursor

241 The rearrangement of phosphoenolpyruvate (PEP) to phosphonopyruvate, catalyze

242 a glycolysis enzyme catalyzing conversion of phosphoenolpyruvate (PEP) to pyruvate by transferring a

243 r glycolysis and catalyzes the conversion of phosphoenolpyruvate (PEP) to pyruvate, which supplies ce

244 xylase (Ppc) flux, and an increased ratio of phosphoenolpyruvate (PEP) to pyruvate.

245 ty of sugars to the glycolytic conversion of phosphoenolpyruvate (PEP) to pyruvate.

246 The PTS is initiated by the binding of phosphoenolpyruvate (PEP) to the C-terminal domain (EIC)

247 ys-115 also covalently reacts with substrate phosphoenolpyruvate (PEP) to yield a phospholactoyl addu

248 PTS, phosphoryl groups are transferred from phosphoenolpyruvate (PEP) via the phosphotransferases en

249 sphorylation reaction of pyruvate that forms phosphoenolpyruvate (PEP) via two partial reactions: PPD

250 Using [(32)P]-phosphoenolpyruvate (PEP) we examine the direct substrat

251 tructural model for allosteric inhibition by phosphoenolpyruvate (PEP) wherein a dimer-dimer interfac

252 erol)] and GNG from lactate/amino acids [GNG(phosphoenolpyruvate (PEP))]) or its consequence to hepat

253 ose, [2-(13)C]glycerol 3-phosphate, [2-(13)C]phosphoenolpyruvate (PEP), [2-(13)C]pyruvate, [2-(13)C]a

254 PPDK) catalyzes the reversible conversion of phosphoenolpyruvate (PEP), AMP, and Pi to pyruvate and A

255 on of ATP, pyruvate, and phosphate with AMP, phosphoenolpyruvate (PEP), and pyrophosphate using its c

256 teractions between the allosteric inhibitor, phosphoenolpyruvate (PEP), and the substrate, fructose 6

257 supply of the cytosolic substrate precursor, phosphoenolpyruvate (PEP), into chloroplast as the resul

258 We demonstrate that phosphoenolpyruvate (PEP), the substrate for pyruvate ki

259 homodimer accepts the phosphoryl group from phosphoenolpyruvate (PEP), whereas the monomer does not,

260 tetramer that is allosterically inhibited by phosphoenolpyruvate (PEP), which binds along one dimer-d

261 previously identified as a regulator of the phosphoenolpyruvate (PEP)-dependent:glucose phosphotrans

262 SCS-GTP) to an anaplerotic pathway producing phosphoenolpyruvate (PEP).

263 The bacterial phosphoenolpyruvate (PEP):glycose phosphotransferase sys

264 their phosphorylation, is carried out by the phosphoenolpyruvate (PEP):sugar phosphotransferase syste

265 In the absence of substrate [phosphoenolpyruvate (PEP)], SAXS-monitored conformationa

266 n of a metabolite of interest (in this case, phosphoenolpyruvate, PEP) is established as the objectiv

267 pecific ectopic expression of the plastidial phosphoenolpyruvate/phosphate translocator, displayed a

268 FtsZ, Cdc48), dihydroxyacetone kinase-linked phosphoenolpyruvate phosphotransferase system (EI, DhaK)

269 The phosphoenolpyruvate phosphotransferase system (PEP-PTS)

270 rial sugar phosphorylation utilizes specific phosphoenolpyruvate phosphotransferase system (PTS) enzy

271 The bacterial phosphoenolpyruvate phosphotransferase system (PTS) is a

272 The bacterial phosphoenolpyruvate phosphotransferase system (PTS) is a

273 The phosphoenolpyruvate phosphotransferase system (PTS) is t

274 One such pathway is the phosphoenolpyruvate phosphotransferase system (PTS), a m

275 I (EI) and Hpr components of the V. cholerae phosphoenolpyruvate phosphotransferase system (PTS).

276 Streptococcus mutans is accomplished by the phosphoenolpyruvate-phosphotransferase system (PTS) and

277 The phosphoenolpyruvate-phosphotransferase system (PTS) is a

278 IIAGlc, a component of the glucose-specific phosphoenolpyruvate:phosphotransferase system (PTS) of E

279 olysin A, flagellins (FlaB, FlaC, and FlaD), phosphoenolpyruvate-protein phosphotransferase, and diam

280 ative of a metal-independent subgroup in the phosphoenolpyruvate/pyruvate domain superfamily.

281 yceric acid reduction, starch synthesis, and phosphoenolpyruvate regeneration also vary between BS an

282 osphoenolpyruvate carboxylation, velocity of phosphoenolpyruvate regeneration, light saturated rate o

283 rsion of mitochondrial oxaloacetate (OAA) to phosphoenolpyruvate, regulates glucose carbon flow direc

284 0%) included key responses such as increased phosphoenolpyruvate signaling glucose deprivation and in

285 The Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system (PTS

286 The phosphoenolpyruvate:sugar phosphotransferase system (PTS

287 s inferred by homology, predominantly in the phosphoenolpyruvate:sugar transferase system (PTS).

288 Specifically, transporters of the phosphoenolpyruvate:sugar transferase system were identi

289 ruvate via the transcriptional activation of phosphoenolpyruvate synthase (PpsA).

290 reversibly converts AMP, pyrophosphate, and phosphoenolpyruvate to ATP, orthophosphate, and pyruvate

291 a preferred plastid route from its substrate phosphoenolpyruvate to fatty acids.

292 P-hydrolase (Phy), an enzyme (Ppa) that adds phosphoenolpyruvate to form pseudaminic acid, and finall

293 ing EI, HPr, and assorted EII proteins, uses phosphoenolpyruvate to import and phosphorylate sugars.

294 (PKM2) is an enzyme-catalyzing conversion of phosphoenolpyruvate to pyruvate in the glycolysis pathwa

295 e the transfer of an enolpyruvyl moiety from phosphoenolpyruvate to the 3'-hydroxyl group of UMP.

296 conversion of the glycolytic pathway product phosphoenolpyruvate to the tricarboxylic acid (TCA) cycl

297 ous overexpression of PPC, which facilitates phosphoenolpyruvate utilization and connects the glycoly

298 ncoding components of pathways that generate phosphoenolpyruvate were altered.

299 me that catalyzes 2-phosphoglycerate to form phosphoenolpyruvate, which is also a known plasminogen r

300 step synthesis of oxaloacetate directly from phosphoenolpyruvate without pyruvate as intermediate.