Search results for "Specificity."

showing 10 items of 2232 documents

Role of hexagonal structure-forming lipids in diadinoxanthin and violaxanthin solubilization and de-epoxidation

2005

In this study, we have examined the influence of different lipids on the solubility of the xanthophyll cycle pigments diadinoxanthin (Ddx) and violaxanthin (Vx) and on the efficiency of Ddx and Vx de-epoxidation by the enzymes Vx de-epoxidase (VDE) from wheat and Ddx de-epoxidase (DDE) from the diatom Cyclotella meneghiniana, respectively. Our results show that the lipids MGDG and PE are able to solubilize both xanthophyll cycle pigments in an aqueous medium. Substrate solubilization is essential for de-epoxidase activity, because in the absence of MGDG or PE Ddx and Vx are present in an aggregated form, with limited accessibility for DDE and VDE. Our results also show that the hexagonal st…

chemistry.chemical_classificationDiatomsBilayerGalactolipidsPhosphatidylethanolaminesLipid BilayersHexagonal phaseDiadinoxanthinSubstrate (chemistry)BiologyXanthophyllsbeta CaroteneBiochemistrySubstrate Specificitychemistry.chemical_compoundEnzymeBiochemistrychemistrySolubilityXanthophyllThylakoidPhosphatidylcholinesOxidoreductasesViolaxanthin
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On the regioselectivity of the Friedländer reaction leading to huprines: stereospecific acid-promoted isomerization of syn-huprines to their anti-reg…

2001

Abstract Racemic 12-amino-6,7,8,11-tetrahydro-7,11-methanocycloocta[ b ]quinoline derivatives ( syn -huprines) substituted at the 9-position with a methyl or ethyl group, and both enantioenriched forms of the 9-ethyl derivative, obtained by chiral MPLC resolution of the racemic mixture, were readily converted to the corresponding anti -isomers (huprines) by stereospecific acid-promoted (AlCl 3 or triflic acid) isomerization of the endocyclic CC double bond from the 9(10)- to the 8(9)-position. These results support the hypothesis that the hitherto unseen syn -huprines are also formed under the usual acidic Friedlander reaction conditions used to prepare the known huprines, but rearrange in…

chemistry.chemical_classificationDouble bondChemistryStereochemistryOrganic ChemistryQuinolineRegioselectivityCatalysisInorganic Chemistrychemistry.chemical_compoundStereospecificityStructural isomerRacemic mixturePhysical and Theoretical ChemistryTriflic acidIsomerizationTetrahedron: Asymmetry
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Protochlorophyllide Reduction: Mechanisms and Evolution¶

2007

Protochlorophyllide (Pchlide) reductases are key enzymes in the process of chlorophyll biosynthesis. In this review, current knowledge on the molecular organization, substrate specificity and assembly of the light-dependent reduced nicotinamide adenine dinucleotide phosphate:Pchlide oxidoreductases are discussed. Characteristics of light-independent enzymes are also described briefly, and the possible reasons for the selection of light-dependent enzymes during the course of evolution are discussed.

chemistry.chemical_classificationEnzymeReduced nicotinamide-adenine dinucleotideProtochlorophyllideBiochemistrychemistrySubstrate specificityGeneral MedicinePhysical and Theoretical ChemistryChlorophyll biosynthesisBiologyBiochemistryPhotochemistry and Photobiology
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Biochemical and Kinetic Analyses of NS5B RNA-Dependent RNA Polymerase of the Hepatitis C Virus

1998

The biochemical properties of the RNA-dependent RNA polymerase (RdRp) of the hepatitis C virus were analyzed. A hexahistidine affinity-tagged NS5B fusion protein was expressed with recombinant baculoviruses in insect cells and purified to near homogeneity. Enzymatic activity of the purified protein was inhibited by KCl or high concentrations of NaCl and was absolutely dependent on Mg2+, which could be replaced by Mn2+. NS5B was found to be processive and able to copy long heteropolymeric templates with an elongation rate of 150-200 nucleotides/min at 22 degreesC. Kinetic constants were determined for all four nucleoside triphosphates and different templates. In case of a heteropolymeric RNA…

chemistry.chemical_classificationHepatitis C virusvirusesRNARNA-dependent RNA polymeraseHepacivirusBiologyViral Nonstructural ProteinsRibonucleosidemedicine.disease_causeRNA-Dependent RNA PolymeraseMolecular biologySubstrate Specificitychemistry.chemical_compoundKineticsBiochemistrychemistryRNA polymeraseVirologymedicineHumansNucleotideNS5BNucleosideVirology
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Stereospecific CC-bond formation with rabbit muscle aldolase - A chemoenzymatic synthesis of (+)-exo-brevicomin

1990

Abstract (+)-(1S,5R,7S)-Exo-brevicomin 9, a sex pheromone of the western pine bark beetle, is synthesized using an aldol reaction catalyzed by fructose-1,6-diphosphate aldolase (EC 4.1.2.13) from rabbit muscle as the key step by which the absolute configuration of the target is established.

chemistry.chemical_classificationKetonebiologyStereochemistryOrganic ChemistryAldolase AAbsolute configurationFructose-bisphosphate aldolasecomplex mixturesBiochemistryEnzyme catalysisStereospecificitychemistryAldol reactionDrug Discoverybiology.proteinAldol condensationTetrahedron Letters
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Stereoselective synthesis of carane-based chiral β- and γ-amino acid derivatives via conjugate addition

2015

Abstract Michael addition of dibenzylamine to (−)-tert-butyl isochaminate, prepared in three steps from (−)-perillaldehyde, furnished a carane-based β-amino acid derivative in a highly stereospecific reaction. The resulting amino ester was transformed to the bicyclic amino acid, a promising building block for the synthesis of 1,3-heterocycles and peptidomimetics. The conjugate addition of nitromethane to α,β-unsaturated methyl ester likewise resulted in nitro esters in stereospecific reactions. Catalytic reduction of the nitro group yielded a γ-amino ester. Under acidic conditions, the hydrolysis of the methyl ester resulted in an unexpected aminolactone-type product through rearrangement o…

chemistry.chemical_classificationNitromethaneBicyclic moleculeStereochemistryOrganic ChemistryEnantioselective synthesisBiochemistryAmino acidHydrolysischemistry.chemical_compoundStereospecificitychemistryDrug DiscoveryNitroMichael reactionamino acid derivativesta116stereoselective synthesiscaraneTetrahedron
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Enzyme molecular mechanism as a starting point to design new inhibitors: a theoretical study of O-GlcNAcase.

2011

O-Glycoprotein 2-acetamino-2-deoxy-β-d-glucopyranosidase (O-GlcNAcase) hydrolyzes O-linked 2-acetamido-2-deoxy-β-d-glucopyranoside (O-GlcNAc) residues from post-translationally modified serine/threonine residues of nucleocytoplasmic protein. The chemical process involves substrate-assisted catalysis, where two aspartate residues have been identified as the two key catalytic residues of O-GlcNAcase. In this report, the first step of the catalytic mechanism used by O-GlcNAcase involving substrate-assisted catalysis has been studied using a hybrid quantum mechanical/molecular mechanical (QM/MM) Molecular Dynamics (MD) calculations. The free energy profile shows that the formation of the oxazol…

chemistry.chemical_classificationProtonStereochemistryClostridium perfringensOxazolineMolecular Dynamics Simulationbeta-N-AcetylhexosaminidasesSurfaces Coatings and FilmsCatalysisSubstrate SpecificitySerinechemistry.chemical_compoundHydrolysisMolecular dynamicsEnzymechemistryMaterials ChemistryQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryThreonineEnzyme InhibitorsOxazolesThe journal of physical chemistry. B
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Nucleoside phosphotransferase of chick embryo

1979

This paper describes a purification procedure and some properties of a nonspecific nucleoside phosphotransferase of chick embryo, an activity which catalyzes the transfer of chick embryo, an activity which catalyzes the transfer of the phosphate ester from a deoxyribonucleotide or a pyrimidine ribonucleotide to a deoxyribonucleoside acceptor. The enzyme is very unstable to heat, dilution and dialysis and it is almost entirely inactivated by DEAE-cellulose chromatography or gel filtration. A marked enhancement in its stability is caused by numerous nucleotides. In these experiments at least 920-fold purification was obtained by using dTTP (50 microM) as nucleotide protector. The enzyme, puri…

chemistry.chemical_classificationRibonucleotideClinical BiochemistrySize-exclusion chromatographyChick EmbryoCell BiologyGeneral MedicineHydrogen-Ion ConcentrationThymidine KinaseSubstrate SpecificityMolecular WeightDeoxyribonucleosidechemistry.chemical_compoundDeoxyribonucleotideEnzymeIsoelectric pointchemistryBiochemistryNucleoside phosphotransferaseChromatography GelAnimalsNucleotideMolecular BiologyMolecular and Cellular Biochemistry
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Relationships between kinetic constants and the amino acid composition of enzymes from the yeast Saccharomyces cerevisiae glycolysis pathway

2012

The kinetic models of metabolic pathways represent a system of biochemical reactions in terms of metabolic fluxes and enzyme kinetics. Therefore, the apparent differences of metabolic fluxes might reflect distinctive kinetic characteristics, as well as sequence-dependent properties of the employed enzymes. This study aims to examine possible linkages between kinetic constants and the amino acid (AA) composition (AAC) for enzymes from the yeast Saccharomyces cerevisiae glycolytic pathway. The values of Michaelis-Menten constant (K M), turnover number (k cat), and specificity constant (k sp = k cat/K M) were taken from BRENDA (15, 17, and 16 values, respectively) and protein sequences of nine…

chemistry.chemical_classificationSpecificity constantbiologyResearchSaccharomyces cerevisiaeMichaelis-Menten constantTurnover numberbiology.organism_classificationMichaelis–Menten kineticsGeneral Biochemistry Genetics and Molecular BiologyYeastComputer Science ApplicationsAmino acidSequence-dependent propertiesComputational MathematicsMetabolic pathwayEnzymechemistryBiochemistryGlycolytic enzymesMultivariate relationshipsEnzyme kineticsSpecificity constantEURASIP Journal on Bioinformatics and Systems Biology
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Stereoselective synthesis of perillaldehyde-based chiral β-amino acid derivatives through conjugate addition of lithium amides.

2014

The Michael addition of dibenzylamine to (+)-tert-butyl perillate (3) and to (+)-tert-butyl phellandrate (6), derived from (S)-(−)-perillaldehyde (1), resulted in diastereomeric β-amino esters 7A–D in a moderately stereospecific reaction in a ratio of 76:17:6:1. After separation of the diastereoisomers, the major product, cis isomer 7A, was quantitatively isomerized to the minor component, trans-amino ester 7D. All four isomers were transformed to the corresponding β-amino acids 10A–D, which are promising building blocks for the synthesis of β-peptides and 1,3-heterocycles in three steps. The steric effects of the isopropyl group at position 4 and of the α-methyl substituent of (R)-N-benzyl…

chemistry.chemical_classificationStereochemistryOrganic Chemistryasymmetric synthesisDiastereomerSubstituentEnantioselective synthesisFull Research PaperAmino acidlcsh:QD241-441chiralchemistry.chemical_compoundChemistryStereospecificitylcsh:Organic chemistrychemistryMichael additionβ-amino acidMichael reactionlcsh:QStereoselectivitylcsh:Scienceta116IsopropylmonoterpeneBeilstein journal of organic chemistry
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