ライフサイエンスコーパス: phosphate

1 onors such as acetyl phosphate and carbamoyl phosphate.

2 protein that binds to phosphatidylinositol 3-phosphate.

3 alkyl-phosphonate moiety replacing the gamma-phosphate.

4 cleaves adenosine into adenine and ribose-1-phosphate.

5 oduce the prosurvival molecule sphingosine-1-phosphate.

6 ing media to permit precipitation of calcium phosphate.

7 o dihydroxyacetone phosphate and erythrose 4-phosphate.

8 plemental diet rich in calcium, lactose, and phosphate.

9 mpatible ceramic nanoparticles of tricalcium phosphate.

10 ibited by its substrate RuBP and other sugar phosphates.

11 ndicate the coexistence of linear and cyclic phosphates.

12 1) within a 5 min incubation with 1-naphthyl phosphate (1-NP) substrate.

13 tion conditions (14 uM Abeta42, 20 mM sodium phosphate, 200 uM EDTA, pH 6.8).

14 t signaling pathways, phosphatidylinositol 5-phosphate 4-kinases (PI5P4Ks) are attractive targets for

15 a member of the rice phosphatidylinositol-4-phosphate 5-kinase family, as a protein that interacts w

16 strate that type Igamma phosphatidylinositol phosphate 5-kinase i5 (PIPKIgammai5), an endosome-locali

17 d adults with COVID-19 receiving chloroquine phosphate, 500 mg once or twice daily, with patients not

18 te homeostasis (PHO) regulon comprises three phosphate acquisition genes - pho1, pho84, and tgp1 - th

19 Phosphate-acquisition genes pho1, pho84 and tgp1 are rep

20 Osteoclast-derived sphingosine-1-phosphate acts in paracrine to promote bone mineralizati

21 Micro-Tom'; the wild type and the GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE [GPAT6] and CUTIN SYNTHASE [CU

22 E)/PPE clusters, responsive to magnesium and phosphate, also showed a phthiocerol dimycocerosate-depe

23 ctive site entailing dislocations of the ATP phosphates, altered contacts to ATP, and variations in t

24 verexpression of Gfat1 (glutamine:fructose-6-phosphate amidotransferase 1), the rate-limiting enzyme

25 we report the design of a series of inositol phosphate analogs as crystallization inhibitors, among w

26 o sub-micromolar concentrations of inorganic phosphate and a range of environmentally abundant P form

27 rticles, and low HDL levels of sphingosine-1-phosphate and apolipoprotein A-I were associated with in

28 ch suggests a regulatory role for testicular phosphate and calcium homeostasis.

29 olecular weight phosphodonors such as acetyl phosphate and carbamoyl phosphate.

30 ences in Raman features corresponding to the phosphate and carbonate bands between the benign and mal

31 e aldolase cleaves SBP into dihydroxyacetone phosphate and erythrose 4-phosphate.

32 ation of Ca phosphates between NaOH-desorbed phosphate and exchangeable Ca(2+) and/or (2) dissolution

33 cantly lower percent tubular reabsorption of phosphate and fibroblast growth factor-23 (FGF23) at all

34 expression of mGPDH, which lowers glycerol 3-phosphate and G6P and also mimics the G6pc repression by

35 Brain phosphocreatine/inorganic phosphate and NTP/exchangeable phosphate were higher at

36 id environments (pH <= 5), particularly when phosphate and other competitors are present in relativel

37 Four samples presented higher phosphate and sulfite concentrations than those permitte

38 cal method for the determination of citrate, phosphate and sulfite in seafood by capillary zone elect

39 oth OW and amended soils (i.e., amorphous Zn-phosphate and Zn sorbed on hydoxylapatite).

40 ron spectroscopy (XPS) confirmed the role of phosphates and carboxylate groups from the cell envelope

41 ndon release, when the levels of high-energy phosphates and glycerophospholipids were lowered.

42 active site constituents that engage the ATP phosphates and the metal cofactors.

43 e presence of close analogs (i.e., glucose-6-phosphate), and can detect glucose above a threshold con

44 hate, pyruvate, lactate, alanine, glycerol-3 phosphate, and isocitrate were significantly associated

45 High iPTH, phosphate, and low 1,25D, but not FGF23, levels predicte

46 ies, including radioligand binding, inositol phosphate, and toxicity assays, proved that we have a se

47 The stable isotopes of sulfate, nitrate, and phosphate are frequently used to study geobiological pro

48 of triphenylphosphine selenide and diphenyl phosphate as a catalyst, a wide range of unsaturated ami

49 lective crystallization of disodium hydrogen phosphate as a dodecahydrate.

50 ation, releasing ammonia and D-erythronate-4-phosphate as coproducts.

51 es showed a remarkably high concentration of phosphates at the bacterial cell wall compared to other

52 ly expressed between ecotypes independent of phosphate availability.

53 an iridium(III) photocatalyst and a dialkyl phosphate base.

54 signaling, with phosphatidylinositol (PI) 3-phosphates being the predominant phosphoinositide lipids

55 NaOH), creating new Ca-P via formation of Ca phosphates between NaOH-desorbed phosphate and exchangea

56 ndings do not support the role of intestinal phosphate binders to reduce cardiovascular risk in patie

57 he ubiquity of phospho-ligands suggests that phosphate binding emerged at the earliest stage of prote

58 For many lineages, phosphate binding emerged later as a niche functionality

59 milarities in their overall architecture and phosphate binding motif, a lack of sequence identity and

60 logical P(i)-receptor based on the bacterial phosphate binding protein with the principle of thermoph

61 nality, but for the oldest protein lineages, phosphate binding was the founding function.

62 s and unravel its details, we identified all phosphate-binding protein lineages in the Evolutionary C

63 the feeds of monogastric animals to improve phosphate bioavailability.

64 ent in several enzymes that hydrolyze cyclic phosphate bonds on different substrates, including cycli

65 load-bearing skeleton and bioglass-magnesium phosphate bone cement as the osteoconductive matrix.

66 t CSH C18 column with gradient elution using phosphate buffer and methanol was used for their optimal

67 inetics of murine norovirus (MNV) by PFA, in phosphate buffer and municipal secondary effluent wastew

68 tal microbalance (EQCM) in sulfuric acid and phosphate buffer electrolytes.

69 eved from FAU (SiO(2):Al(2)O(3) = 80:1) into phosphate buffer for 24 h followed by prolonged release

70 OCT was completely released after 300 min in phosphate buffer pH 7.4.

71 n black particle suspension solution (pH 7.0 phosphate buffer) at varying carbon black concentrations

72 y in the simulated river water samples as in phosphate buffer, reflecting its applicability to real s

73 entrations of Immunoglobulin G (IgG) in both phosphate buffered saline (PBS) and spiked in E. coli ce

74 in a complex matrix (bovine serum albumin in phosphate buffered saline) is also demonstrated through

75 aryngeally aspirated 200 ug of WTC-PM(53) or phosphate-buffered saline (PBS) (controls).

76 ignificant reduction of diarrhea compared to phosphate-buffered saline (PBS) controls (PE = 84.1%; P

77 Four groups were studied: sham and SCI plus phosphate-buffered saline (SCI + PBS), human embryonic k

78 iae (1,500 colony-forming units) or vehicle (phosphate-buffered saline) at 3 or 60 days post-injury.

79 D45(+) cells in the prostates of E. coli- or phosphate-buffered saline-treated mice.

80 were intratracheally instilled with sterile phosphate-buffered saline.

81 q of (212)Pb-daratumumab instead of 11 d for phosphate-buffered saline.

82 as an efficient dynamic covalent reaction in phosphate buffers at neutral pH.

83 acquisition or result in overaccumulation of phosphate by S. aureus However, it does reduce the abili

84 Combretastatin A-4 phosphate (CA4P) is a microtubule-disrupting tumour-sele

85 Since phosphate cannot be efficiently removed by dialysis, the

86 ), monophosphoryl lipid A (MPLA) and calcium phosphate (CaP) used less frequently.

87 concentration depends on the beta-glucose 1-phosphate concentration, couples the conformational swit

88 Even higher phosphate concentrations (>1 molal) can form during evap

89 stations were consistent with differences in phosphate concentrations in those regimes.

90 es, prebiotic experiments commonly use molar phosphate concentrations to overcome phosphate's poor re

91 ablished that vancomycin coprecipitated with phosphate containing molecules.

92 onium-boronate hydrogen bonds, which enables phosphate coordination to boron with a concomitant, ster

93 ced microstructural phase changes of calcium phosphate (CP) leading to the formation of brushite, mon

94 s fabricated by 3D-bioprinting of an in situ phosphate crosslinked poly(vinyl alcohol) polymer.

95 n, calcium is frequently bound to the Pb(II) phosphate crystal lattice structure, causing measurable

96 n in a quadratic nonlinear potassium titanyl phosphate crystal.

97 ular calcification, the formation of calcium phosphate crystals in the vessel wall, is mediated by va

98 in the generation of riboflavin cyclic 4',5'-phosphate (cyclic FMN) through an FMN lyase domain.

99 BACKGROUNDGlucose-6-phosphate dehydrogenase (G6PD) deficiency decreases the

100 Glucose 6-phosphate dehydrogenase (G6PD) deficiency is 1 of the co

101 Moreover, higher activities of glucose 6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehy

102 Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a key enzyme involved

103 esin-1, gelsolin, tubulins, glyceraldehyde-3-phosphate dehydrogenase, calmodulin, ATP synthase, sperm

104 sh L-lactate dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, pyruvate kinase, and glucose-6-

105 In the ISC pathway, the pyridoxal 5'-phosphate-dependent cysteine desulfurase enzyme IscS pro

106 hine aminotransferase (hOAT), a pyridoxal 5'-phosphate-dependent enzyme, plays a critical role in the

107 ect, presumably because they generate ribose-phosphate derivatives from products of an unlinked but e

108 proton transfer from tyrosine to a hydrogen phosphate dianion.

109 neutral arylsulfonate monoesters or charged phosphate diesters and fluorophosphates.

110 omer sulfonates, and several polyfluoroalkyl phosphate diesters.

111 vities of carbonic anhydrase (CA), pyruvate, phosphate dikinase (PPDK), ribulose-1,5-bisphosphate car

112 ated in both apical and as bridging sites in phosphate dimers.

113 as expected, but also unexpectedly increased phosphate efflux, whereas PFBC-associated SLC20A2 varian

114 porter, but strongly decreased XPR1-mediated phosphate efflux.

115 somerize fructose-6-phosphate into glucose-6-phosphate even in the presence of equimolar amounts of g

116 Inadequate urinary phosphate excretion can lead to severe hyperphosphatemia

117 Persistently increased urinary phosphate excretion maintains serum phosphate levels wit

118 ers of this family, none exhibits fructose-6-phosphate (F6P) at the active site.

119 r S7P and the canonical substrate fructose 6-phosphate (F6P).

120 However, the glucose-driven phosphate flush occurred despite inositol pyrophosphate

121 disease suggests that they jointly regulate phosphate fluxes and cellular homeostasis, but direct ev

122 atients with and without IBD evaluated serum phosphate for 28 days following intravenous FCM, and ass

123 were chosen for aggregating AgNPs, potassium phosphate for neutralizing the charges and a di-thiol mo

124 er P through FeOOH absorption and authigenic phosphate formation in sediments, and accordingly reduce

125 viciae 3841 transfers phosphate from PEP via PtsP and NPr to two output regula

126 Renal vein glycerol-3-phosphate (G-3-P) had the strongest correlation with cir

127 the Escherichia coli periplasmic glycerol-3-phosphate (G3P)-binding protein UgpB can serve, in the a

128 (hGGT1) with glutathione (a substrate) and a phosphate-glutathione analog (an irreversible inhibitor)

129 in kinases (EPKs) catalyze the transfer of a phosphate group onto another protein in response to appr

130 etermined that both the bromine atom and the phosphate group were successfully substituted by means o

131 nd in soft source conditions, the protonated phosphate groups are fully back-exchanged in the source,

132 dictated by the number and positions of the phosphate groups in the inositol ring (with seven differ

133 the contribution of the different inositide phosphate groups to catalysis, these structures provide

134 m intercept to identify significant Cytosine-phosphate-Guanine (CpG) sites and differentially methyla

135 ng this period at asthma-associated cytosine-phosphate-guanine (CpG) sites and such an association wa

136 with altered DNA methylation at 605 cytosine-phosphate-guanine (CpG) sites, which were associated wit

137 4 and rs2299007 risk alleles create cytosine-phosphate-guanine sites, which are highly methylated and

138 only demethylation of histones and cytosine-phosphate-guanines (CpGs) in gene promoters and other re

139 , 2-methyl-4-amino-5-hydroxymethylpyrimidine phosphate (HMP-P), has been described to proceed through

140 The fission yeast phosphate homeostasis (PHO) regulon comprises three phos

141 ross-talk between SLC20A2 and XPR1 regulates phosphate homeostasis, and we identified XPR1 as a key i

142 operon encoding a highly conserved inorganic phosphate importer, PstSCAB, increases the sensitivity o

143 3 (FGF23) at all CKD stages, and lower blood phosphate in CKD stages 3-5.

144 Yet, quantifying phosphate in complex aqueous media remains challenging,

145 ould be categorized similarly to nitrate and phosphate in that it originates in part from fertilizer

146 Inversion of the phosphate in these holoenzyme-product complexes supports

147 ples, we found substantial amounts of cyclic phosphates in X. autotrophicus, suggesting that in fresh

148 bited complexes while binding multiple sugar phosphates, including its substrate ribulose 1,5-bisphos

149 dulates the expression of a large set of low-phosphate-induced genes that respond to local and system

150 The analysis of myo-inositol phosphates (InsPs) and myo-inositol pyrophosphates (PP-I

151 alytic cycle after formation of the aspartyl phosphate intermediate (E1~P).

152 erum protein fetuin-A stabilizes calcium and phosphate into 70-100 nm-sized colloidal calciprotein pa

153 To incorporate phosphate into biomolecules, prebiotic experiments commo

154 tion, hGFAT2 is able to isomerize fructose-6-phosphate into glucose-6-phosphate even in the presence

155 of protein and DNA, delivering the scissile phosphate into the rearranged active site.

156 ; however, leaf entry pathways for inorganic phosphate ion (Pi) uptake remain unknown, and it is uncl

157 at the speciation and transport behaviors of phosphate ions are highly influenced by electrolyte pH,

158 Sphingosine 1-phosphate is a bioactive sphingolipid mediator involved

159 Phosphate is central to the origin of life because it is

160 (the TriPPPro approach), in which the gamma-phosphate is covalently modified by two different biodeg

161 However, phosphate is generally limited to micromolar levels in t

162 The recognition of arsenate over phosphate is rare among both proteins and synthetic rece

163 deficiency of the glycolytic enzyme glucose phosphate isomerase (Gpi1) selectively eliminates inflam

164 ature sensitivity with other reported triose-phosphate isomerase allergens.

165 xin-5, secretoglobin family 1D and glucose-6-phosphate isomerase characterized the LF phenotype.

166 onserved with close similarity to the triose-phosphate isomerase protein sequence from Dermatophagoid

167 ehydrogenase, pyruvate kinase, and glucose-6-phosphate isomerase showed IgE-binding for 6%-13% of pat

168 signaling axis comprising phosphoinositide 3-phosphate kinase, Akt Ser/Thr kinase, nitric oxide synth

169 This phosphaturic effect lowered plasma phosphate levels in WT mice and in rats with CKD due to

170 urinary phosphate excretion maintains serum phosphate levels within the normal range, thus protectin

171 dings, we create functional Li||lithium iron phosphate (LFP) batteries in which LFP cathodes with hig

172 moderate to severe hypophosphataemia (serum phosphate < 0.6 mmol/L).

173 include the expansion of genes for inorganic phosphate metabolism, the presence of genes for producti

174 Struvite (magnesium ammonium phosphate-MgNH(4) PO(4) .6H(2) O), which can extensively

175 ke homo-hexacontamer, we conclude that while phosphate moieties present in crRNA and ATP molecules en

176 tions of Hoogsten hydrogen bonds, sugar, and phosphate moieties to the specific G-vacancy fill-in.

177 Building from phosphate monoesters to diesters may have enabled the sy

178 y the glassy structure as primarily isolated phosphate monomers with N incorporated in both apical an

179 ) or the steroid group (topical prednisolone phosphate; n = 57); both regimens were tapered over 10 w

180 rmone-sensitive lipase, and 1-acylglycerol-3-phosphate O-acyltransferase ABHD5.

181 thyleneglycol)-myo-inositol-1,2,3,5-tetrakis(phosphate), (OEG(2))(2)-IP4, displays increased in vitro

182 te (cPyPA) reagent is used to introduce four phosphates on nucleosides regioselectively in a one-flas

183 counteracted by the presence of preadsorbed phosphate or by increasing the BSA coverage, which preve

184 ot prevent the level decrease in high-energy phosphates or protein constituents of mitochondrial resp

185 SD), 0.33; 95% CI, 0.18-0.61), sphingosine-1-phosphate (OR(1SD): 0.60; 95% CI: 0.40-0.89), and apolip

186 s and that nicotinamide adenine dinucleotide phosphate oxidase (NOX)-dependent ROS production might b

187 takes of total energy (p < 0.001), inorganic phosphate (p < 0.001), and phosphate:protein ratio (p =

188 rotein (p = 0.001), and animal-based organic phosphate (p < 0.001), whilst T3-SSB(dp) patients had si

189 the intracellular concentration of inorganic phosphate (P(i) ).

190 A phosphate (P(i))-selective adsorption system featuring i

191 Sorption of nutrients such as phosphate (P) and silicate (Si) by ferric iron (oxyhydr)

192 ous Pb compounds (i.e., carbonate, chloride, phosphate [P], or sulfate) to convert native Pb species

193 The calcium phosphate particles can be used as building blocks for f

194 Namely, tricalcium phosphate particles of equal size and certain porosity a

195 affolds using magnetic levitation of calcium phosphate particles.

196 Survival upon nutrient stress or pentose phosphate pathway (PPP) inhibition depends on compensato

197 glycolysis but increased use of the pentose phosphate pathway (PPP), and an enhanced abundance of th

198 hat may regulate serum urate via the pentose-phosphate pathway and MRPS7 and IDH2 that encode protein

199 d the Krebs cycle, but the levels of pentose phosphate pathway metabolites and of many free amino aci

200 IspH, an enzyme in the methyl erythritol phosphate pathway of isoprenoid synthesis, is essential

201 ssociated cystine metabolism and the pentose phosphate pathway, and uncover an accompanying metabolic

202 ased flux through glycolysis and the pentose phosphate pathway, thereby establishing a critical link

203 phosphorylation is heterogeneous, up to ~20 phosphates per molecule distributed over 51 sites.

204 With high initial ratio of calcium ion to phosphate, periodic precipitation was obtained accompani

205 values corresponding to the relatively short phosphate-phosphate distances through space.

206 Similarly, phosphate (Pi) deficiency inversely affected miR397b and

207 Inorganic phosphate (Pi) is an essential nutrient for human health

208 Low blood phosphate (Pi) reduces muscle function in hypophosphatem

209 The mechanisms regulating phosphate (Pi) uptake are well established, but the func

210 g and accumulation of phosphatidylinositol 4-phosphate (PI4P) on SG membranes.

211 icular, cholesterol and phosphatidylinositol phosphate (PIP) lipids, but the number, location, and es

212 Phosphatidylinositol phosphates (PIPs) are membrane phospholipids that play c

213 status is routinely measured as pyridoxal 5'-phosphate (PLP) in plasma.

214 ate, vitamin B-6 in the form of pyridoxal 5'-phosphate (PLP), and total B-12 with serum TC, LDL-C, HD

215 in LpThi5 is a dimer that binds pyridoxal-5'-phosphate (PLP), apparently without a solvent-exposed Sc

216 Pyridoxal phosphate (PLP)-dependent enzymes can catalyze transform

217 (2AA), an enamine produced by some pyridoxal phosphate (PLP)-dependent enzymes.

218 parallel FCS experiments using p-nitrophenyl phosphate (pNPP) as substrate.

219 nd versus double-strand crossovers, backbone phosphate positions, and single-strand breaks.

220 Intestinal absorption of phosphate proceeds via an active/transcellular route mos

221 luated and describe two new series of cyclic phosphate prodrugs of PPA capable of regenerating excell

222 0.001), inorganic phosphate (p < 0.001), and phosphate:protein ratio (p = 0.001).

223 Simultaneous activation of carboxylates and phosphates provides multiple pathways for the generation

224 hrough stimulation of phosphatidylinositol-3-phosphate (PtdIns(3)P) production and ER membrane curvat

225 Here we use TEM to show that ribose-5-phosphate (R5P) glycation of collagen fibrils - potentia

226 formed dentine comprises equal carbonate to phosphate ratios and mineral to matrix ratios to that of

227 Regulated primarily by the kidneys, phosphate reaches abnormally high blood levels in patien

228 New sphingosine-1-phosphate receptor (S1PR) modulators with more specific

229 le sclerosis, is an agonist of sphingosine-1-phosphate receptor (S1PR), which has been used as a rese

230 Cation-independent mannose-6-phosphate receptor, also called insulin-like growth fact

231 emokine receptor 7 (CCR7) and sphingosine 1- phosphate receptor-1 (S1PR1) expression and glucose meta

232 RORc and an antagonist of the sphingosine-1-phosphate receptor-1-via late-stage methylation from the

233 te, suggesting cation-independent, mannose 6-phosphate receptor-mediated endocytosis from the cell su

234 show that retinal endothelial sphingosine 1-phosphate receptors (S1PRs), which restrain vascular end

235 cence, and nicotinamide adenine dinucleotide phosphate, reduced form oxidases (NOXs) were studied in

236 gs suggest that aging of branch junctions by phosphate release from Arp2/3 complex and mechanical for

237 nes by coupling ATP binding, hydrolysis, and phosphate release to translocation of diverse substrates

238 ich likely promotes ATP hydrolysis and rapid phosphate release.

239 utrient recovery, but their effectiveness on phosphate removal was lower than other charged ions.

240 The PHO regulon is de-repressed in phosphate-replete cells by genetic manipulations that fa

241 , pho84, and tgp1 - that are repressed under phosphate-replete conditions by 5' flanking lncRNAs prt,

242 s reduce the ability of S. aureus to grow in phosphate-replete defined medium.

243 ic, carrying either sialic acid, sulfate, or phosphate residues.

244 regulator GNOM and its suppressor, ADENOSINE PHOSPHATE RIBOSYLATION FACTOR GTPase ACTIVATION PROTEIN

245 s drain areas of extensive agriculture where phosphate-rich fertilizer is applied.

246 e molar phosphate concentrations to overcome phosphate's poor reactivity with organics in water.

247 It is an analog of sphingosine-1-phosphate (S1P) and targets S1P receptors 1, 3, 4, and 5

248 Functional sphingosine-1-phosphate (S1P) receptor 1 (S1PR1) antagonists, such as

249 This leads to reduced sphingosine-1-phosphate (S1P) signaling via the S1P receptor 1 (S1PR1)

250 ingolipid metabolites, such as sphingosine-1-phosphate (S1P), play important roles as second messenge

251 pendent cell proliferation and sphingosine-1-phosphate (S1P)-dependent entosis and apical cell extrus

252 ysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P).

253 rsible pathway, PFK converts sedoheptulose 7-phosphate (S7P) to SBP, after which fructose-bisphosphat

254 in sheep using 3D-printed customized calcium phosphate scaffolds with or without surgical vasculariza

255 Root system configuration in response to phosphate scarcity involved MED16 functioning, which mod

256 However, how low phosphate sensing links to the transcriptional machinery

257 Thus, the loss of the phosphate sensor PstS produced a decrease in A. baumanni

258 S1P (Sphingosine 1-phosphate) signaling coordinates vascular functions in o

259 ually transformed into one containing a lead phosphate solid chemically similar to phosphohedyphane (

260 s after preparation of oversaturated calcium phosphate solutions, PNS with a hydrodynamic radius of R

261 ot tips from these two ecotypes during early phosphate starvation.

262 Arabidopsis thaliana) respond differently to phosphate starvation.

263 l maximum encoded genes related to light and phosphate stress (psbA, psbD and pstS in T4-like and psb

264 ids at endosomes and lysosomes, whereas PI 4-phosphates, such as phosphatidylinositol 4,5-bisphosphat

265 can be competitively inhibited by mannose 6-phosphate, suggesting cation-independent, mannose 6-phos

266 aturally occurring minerals (e.g., silicate, phosphate, sulfate) follows energy-intensive chemical ro

267 Five "competing" co-occurring oxo-anions (phosphate, sulfate, bicarbonate, silicate, and nitrate)

268 Pb is shown to be associated with fatty acid phosphate, sulfate, chloride, and carboxylate ions.

269 al enzyme, 3-deoxy-d-arabino-heptulosonate 7-phosphate synthase (DAH7PS), at the gateway to aromatic

270 ite mutation in the 5-enolpyruvylshikimate 3-phosphate synthase (EPSPS) gene, with minor contribution

271 ical target enzyme 5-enolpyruvyl-shikimate-3-phosphate synthase (EPSPs).

272 on catalyzed by the enzyme indole-3-glycerol phosphate synthase (IGPS) starts with a condensation ste

273 ohol phosphotransferase phosphatidylinositol-phosphate synthase (PIPS), an essential enzyme for mycob

274 te pathway, 3-deoxy-d-arabinoheptulosonate 7-phosphate synthase and chorismate synthase, were also up

275 o up-regulated, as well as indole-3-glycerol phosphate synthase, an enzyme involved in the biosynthes

276 detect the enzyme, 5-enolpyruvulshikimate-3-phosphate synthase, from Agrobacterium sp. strain CP4 (C

277 bidopsis (Arabidopsis thaliana), TREHALOSE-6-PHOSPHATE SYNTHASE1 (TPS1) catalyzes the synthesis of th

278 Tris(1-chloro-2-propyl) phosphate (TCIPP) was the most abundant OPE measured in

279 but patients with CD had greater decline in phosphate than those with UC.

280 ckers that are critical for anchoring the 5'-phosphate to Ago 2 MID domain.

281 ata support a model in which HPr transfers a phosphate to an unidentified downstream transcriptional

282 ase 1 (GFAT1), uses glutamine and fructose 6-phosphate to eventually synthesize uridine diphosphate N

283 necessary for the efficient transfer of acyl-phosphate to PlsY.

284 ries of vinylated analogues of sphingosine-1-phosphate together with their unambiguous configurationa

285 We demonstrated that knockdown of XPR1, a phosphate transporter present in MIN6m9 cells and pancre

286 the sucrose-signaling metabolite trehalose 6-phosphate (Tre6P) and is essential for embryogenesis and

287 olyphosphates are long chains of hundreds of phosphate units.

288 at is consistent with an average size of 3-8 phosphate units.

289 role in citrate-enhanced uptake (additional phosphate uptake due to citrate exudation).

290 r PF-06869206 was previously shown to reduce phosphate uptake in human proximal tubular cells in vitr

291 Conversely, SLC20A2 depletion decreased phosphate uptake only slightly, most likely compensated

292 that overexpression of WT SLC20A2 increased phosphate uptake, as expected, but also unexpectedly inc

293 st from this exudation in terms of increased phosphate uptake, suggesting that root structure plays a

294 entrations were >100 times the average while phosphate was >25 times average.

295 Mean serum phosphate was 1.25 mmol/L (3.87 mg/dl), mean pulse wave

296 ed at the end of the 12-week experiment, and phosphate was found to drive Zn speciation in both OW an

297 ne (Ca(2)Pb(3)(PO(4))(3)(Cl,F,OH)((s))) when phosphate was present.

298 ve been defined, it is unknown if persistent phosphate wasting in nephropathic cystinosis is associat

299 ine/inorganic phosphate and NTP/exchangeable phosphate were higher at 48 h in HT+M versus HT (p = 0.0

300 ards normal, and (2) decreased intracellular phosphate, which down-regulated PRPP synthetase activity