Search results for "phosphate"

showing 10 items of 1874 documents

CCDC 229669: Experimental Crystal Structure Determination

2004

Related Article: M.C.Grunert, J.Schweifer, P.Weinberger, W.Linert, K.Mereiter, G.Hilscher, M.Muller, G.Wiesinger, P.J.van Koningsbruggen|2004|Inorg.Chem.|43|155|doi:10.1021/ic034452z

catena-(tris(mu~2~-14-bis(Tetrazol-1-yl)butane-N^4^N^4'^)-iron(ii) bis(hexafluorophosphate) methanol solvate hydrate)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 229673: Experimental Crystal Structure Determination

2004

Related Article: M.C.Grunert, J.Schweifer, P.Weinberger, W.Linert, K.Mereiter, G.Hilscher, M.Muller, G.Wiesinger, P.J.van Koningsbruggen|2004|Inorg.Chem.|43|155|doi:10.1021/ic034452z

catena-(tris(mu~2~-14-bis(Tetrazol-1-yl)butane-N^4^N^4'^)-iron(ii) bis(hexafluorophosphate) methanol solvate hydrate)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 229672: Experimental Crystal Structure Determination

2004

Related Article: M.C.Grunert, J.Schweifer, P.Weinberger, W.Linert, K.Mereiter, G.Hilscher, M.Muller, G.Wiesinger, P.J.van Koningsbruggen|2004|Inorg.Chem.|43|155|doi:10.1021/ic034452z

catena-(tris(mu~2~-14-bis(Tetrazol-1-yl)butane-N^4^N^4'^)-iron(ii) bis(hexafluorophosphate) methanol solvate hydrate)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 229677: Experimental Crystal Structure Determination

2004

Related Article: M.C.Grunert, J.Schweifer, P.Weinberger, W.Linert, K.Mereiter, G.Hilscher, M.Muller, G.Wiesinger, P.J.van Koningsbruggen|2004|Inorg.Chem.|43|155|doi:10.1021/ic034452z

catena-(tris(mu~2~-14-bis(Tetrazol-1-yl)butane-N^4^N^4'^)-iron(ii) bis(hexafluorophosphate) methanol solvate hydrate)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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RAVITA Technology : new innovation for combined phosphorus and nitrogen recovery

2018

Abstract Present phosphorus (P) recovery technologies mainly contain P recovery from sludge liquor or ash. These types of technologies are suitable for large wastewater treatment plants (WWTPs) with enhanced biological phosphorus removal (EBPR), digestion and/or incineration. In Finland and other Nordic countries, strict P discharge limits require chemical precipitation, thus EBPR alone is not sufficient. Ammonium recovery from wastewater, on the other hand, is not so often discussed. However, recovery from WWTP reject waters would decrease the energy demand of ammonium synthesis by Haber-Bosh technology and the energy demand of the WWTP's biological process. Helsinki Region Environmental S…

chemical precipitationEnvironmental Engineeringwastewater effluentNitrogenAmmonium phosphate0208 environmental biotechnologychemistry.chemical_element02 engineering and technologyjätevesiScandinavian and Nordic Countries010501 environmental sciencesWaste Disposal Fluid01 natural sciencesjätevesilietechemistry.chemical_compoundtyppinutrient recoveryhaitalliset aineetWater Pollutantshazardous substancesAmmoniumta215Phosphoric acidfosforiFinlandta2180105 earth and related environmental sciencesWater Science and Technologyjäteveden käsittelysaostusSewagephosphorus removalPhosphorusPhosphorusPulp and paper industry020801 environmental engineeringIncinerationEnhanced biological phosphorus removalchemistryWastewatertalteenottovaaralliset aineetEnvironmental scienceSewage treatment
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Evidence for essential primary amino groups in a bacterial coupling factor F1ATPase.

1980

Abstract We have found that the binding of pyridoxal-5′-phosphate to 6 primary amino groups leads to the inactivation of the enzyme. A preferential reaction of pyridoxal-5′-phosphate with the α-subunits of this enzyme can be demonstrated. The reactivity of the amino groups is influenced by various effectors. In the presence of ATP the inhibition of the ATPase activity is noncompetitive.

chemistry.chemical_classificationAdenosine TriphosphatasesPrimary (chemistry)Binding SitesChemistryStereochemistryEffectorCell MembraneBiophysicsCell BiologyBiochemistryMicrococcusCoupling (electronics)Structure-Activity RelationshipEnzymeBiochemistrySolubilityPyridoxal PhosphateAtpase activityReactivity (chemistry)Amino AcidsMolecular BiologyBiochemical and biophysical research communications
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Identification and structural characterization of O-beta-ribosyl-(1"----2')-adenosine-5"-phosphate in yeast methionine initiator tRNA.

1990

We report in this paper on the complete structure determination of the modified nucleotide A*, now called Ar(p), that was previously identified in yeast methionine initiator tRNA as an isomeric form of O-ribosyl-adenosine bearing an additional phosphoryl-monoester group on its ribose2 moiety. By using the chemical procedure of periodate oxidation and subsequent beta-elimination with cyclohexylamine on mono- and dinucleotides containing Ar(p), we characterized the location of the phosphate group on the C-5" of the ribose2 moiety, and the linkage between the two riboses as a (1"----2')-glycosidic bond. Since the structural difference between phosphatase treated Ar(p) and authentic O-alpha-rib…

chemistry.chemical_classificationAdenosine monophosphateMethionineRNA Transfer MetStereochemistryChemical structurePhosphataseCyclohexylamineSaccharomyces cerevisiaeBiologyAdenosine Monophosphatechemistry.chemical_compoundchemistryBiochemistryTransfer RNAGeneticsMoietyNucleotideIndicators and ReagentsOxidation-ReductionChromatography High Pressure LiquidNucleic acids research
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The Structure and Metabolism of Carbohydrates

1994

Compared with the variety of carbohydrates in plants, relatively few sugars or sugar derivatives are regularly found in animals either free or as components of more complex compounds. However, it is possible that sugars originating from plants in the diet are transiently retained in animals and distort the normal sugar spectrum. Approximately a dozen sugars and sugar derivatives are regularly found in animals: the pentoses d-ribose and 2-deoxy-d-ribose; the hexoses d-glucose, d-galactose, d-mannose, d-fructose and l-fucose; the uronic acids d-glucuronic acid and l-iduronic acid; and the hexosamines d-glucosamine and d-galactosamine. In addition, d-erythrose, d-ribulose, d-xylulose and d-sed…

chemistry.chemical_classificationAldose reductasebiologyPhosphoric Acid EstersMetabolismPentose phosphate pathwayHexosaminesSialic acidchemistry.chemical_compoundchemistryBiochemistrybiology.proteinSugarAlcohol dehydrogenase
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In vitro effect of organophosphate pesticides, Malathion and chlorpyriphos, on lipid peroxidation and antioxidant enzymes

2008

chemistry.chemical_classificationAntioxidantOrganophosphate pesticidesmedicine.medical_treatmentGeneral MedicineToxicologyIn vitroLipid peroxidationchemistry.chemical_compoundEnzymechemistrymedicineMalathionFood scienceToxicology Letters
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Inhibition of the herpes simplex virus-coded thymidine kinase-complex by 9-?-D-arabinofuranosyladenine 5?-monophosphate (ara-AMP) and 9-(2-hydroxyeth…

1984

The thymidine kinase-complex isolated from herpes simplex virus type 1 and type 2 (HSV-1 and HSV-2) is associated with the following enzyme activities: ATP:dThd (dCyd) deoxypyrimidine kinase, ATP:dTMP thymidylate kinase, ADP:dThd- and AMP:dThd5′-phosphotransferase. In kinetic experiments it is shown that ara-AMP inhibits AMP:dThd- and ADP:dThd phosphotransferase activity, while acyclo-GMP impairs ADP:dThd phosphotransferase reaction only; the inhibition was found to be non-compertitive. The functional subunit ATP:dThd kinase was not affected by either compound.

chemistry.chemical_classificationArabinonucleotidesGuanineKinaseAcyclovirGeneral MedicineBiologyThymidine KinaseThymidylate kinaseVirologyMolecular biologyPhosphotransferaseKineticschemistry.chemical_compoundEnzymechemistryBiochemistryMultienzyme ComplexesThymidine kinaseVirologySimplexvirusNucleotideThymidineVidarabine PhosphateArchives of Virology
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