Search results for " Specificity"

showing 10 items of 2170 documents

Structure–activity relationship of sphingomyelin analogs with sphingomyelinase from Bacillus cereus

2012

AbstractThe aim of this study was to examine how structural properties of different sphingomyelin (SM) analogs affected their substrate properties with sphingomyelinase (SMase) from Bacillus cereus. Using molecular docking and dynamics simulations (for SMase–SM complex), we then attempted to explain the relationship between SM structure and enzyme activity. With both micellar and monolayer substrates, 3O-methylated SM was found not to be degraded by the SMase. 2N-methylated SM was a substrate, but was degraded at about half the rate of its 2NH–SM control. PhytoPSM was readily hydrolyzed by the enzyme. PSM lacking one methyl in the phosphocholine head group was a good substrate, but PSM lack…

StereochemistryBiophysicsSphingomyelin phosphodiesteraseBiochemistryCatalysisSubstrate Specificitychemistry.chemical_compoundStructure-Activity RelationshipBacillus cereusBacterial ProteinsCatalytic DomainStructure–activity relationshipMagnesiumPhosphocholinechemistry.chemical_classificationbiologyMolecular StructureActive siteHead group methyl analogCell Biology2N-methylated sphingomyelinEnzyme assaySphingomyelinsEnzymeSphingomyelin PhosphodiesterasechemistryDocking (molecular)biology.proteinPhytosphingomyelinta11813O-methylated sphingomyelinSphingomyelinBiochimica et Biophysica Acta (BBA) - Biomembranes
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Differential Enantioselectivity of Murine GlutathioneS-Transferase Isoenzymes in the Glutathione Conjugation ofTrans-3,4-dihydroxy-1,2-oxy- 1,2,3,4-t…

1998

Abstract The kinetics of the glutathione (GSH) conjugation of (+)- and (−)-enantiomers ofanti- as well assyn-3,4-dihydroxy-1,2-oxy-1,2,3,4-tetrahydrobenzo[c]phenanthrene (B[c]PDE) catalyzed by murine GSHS-transferase (GST) isoenzymes has been investigated. Murine GSTs exhibited significant differences in their enantioselectivity toward B[c]PDE stereoisomers. For example, while pi class isoenzyme mGSTP1-1 was virtually inactive toward stereoisomers with 1Sconfiguration [(−)-syn-and (+)-anti-B[c]PDE], these stereoisomers were good substrates for alpha class isoenzyme mGSTA1-2. When GST activity was measured as a function of varying B[c]PDE concentration (10–320 μM) at a fixed saturating conce…

StereochemistryKineticsBiophysicsAlpha (ethology)BiochemistryIsozymeCatalysisSubstrate SpecificityMicechemistry.chemical_compoundPiAnimalsheterocyclic compoundsMolecular BiologyCarcinogenGlutathione TransferaseStereoisomerismGlutathionePhenanthrenesPhenanthrenemusculoskeletal systemGlutathioneCarcinogens EnvironmentalIsoenzymesKineticschemistrysense organsEnantiomerArchives of Biochemistry and Biophysics
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Solanum incanum and S. heteracanthum as sources of biologically active steroid glycosides: Confirmation of their synonymy

2012

A new spirostanol saponin (1), along with four known saponins, dioscin (2), protodioscin (3), methyl-protodioscin (4), and indioside D (5), and one known steroid glycoalkaloid solamargine (6) were isolated from the two synonymous species, Solanum incanum and S. heteracanthum. The structure of the new saponin was established as (23S,25R)-spirost-5-en-3β,23-diol 3-O-{β-D-xylopyranosyl-(1→2)-O-α-L-rhamnopyranosyl-(1→4)-[O-α-L-rhamnopyranosyl-(1→2)]-β-D-glucopyranoside}, by using a combination of 1D and 2D NMR techniques including (1)H, (13)C, COSY, TOCSY, NOESY, HSQC and HMBC experiments and by mass spectrometry. The compounds 1, 3, 4 and 5 were evaluated for cytotoxicity against five cancer c…

StereochemistryProtodioscinSaponinDiosgeninSolanumSolanaceous AlkaloidsAntioxidantsMicechemistry.chemical_compoundSpecies SpecificityGlycoalkaloidCell Line TumorNeoplasmsDrug DiscoverySpirostansAnimalsHumansSolanum incanumGlycosidesPharmacologychemistry.chemical_classificationSolamargineMolecular StructurebiologyPlant ExtractsGlycosideGeneral MedicineDiosgeninSaponinsbiology.organism_classificationAntineoplastic Agents PhytogenicchemistrySteroidsSolanumPhytotherapyFitoterapia
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Stereoselective synthesis and determination of the cytotoxic properties of spicigerolide and three of its stereoisomers.

2003

Stereoselective syntheses of the naturally occurring, cytotoxic lactone spicigerolide and three nonnatural stereoisomers thereof are described. The commercially available sugar l-rhamnose was in all cases the chiral starting material. Key steps in each of these syntheses were asymmetric Brown allylations and ring-closing metatheses. The cytotoxic activities of the four lactones against a range of tumoral lines were then determined.

StereochemistryRhamnoseStereoisomerismAntineoplastic AgentsMetathesisChemical synthesisRhamnosechemistry.chemical_compoundLactonesStructure-Activity RelationshipCell Line TumorCytotoxic T cellStructure–activity relationshipOrganic chemistryHumanschemistry.chemical_classificationCell DeathChemistryorganic chemicalsOrganic ChemistryStereoisomerismGeneral MedicineSpicigerolideAldoseCyclizationOrgan SpecificityStereoselectivityLactoneThe Journal of organic chemistry
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Structural Basis and Enzymatic Mechanism of the Biosynthesis of C9- from C10-Monoterpenoid Indole Alkaloids

2009

Cutting carbons: The three-dimensional structure of polyneuridine aldehyde esterase (PNAE) gives insight into the enzymatic mechanism of the biosynthesis of C(9)- from C(10)-monoterpenoid indole alkaloids (see scheme). PNAE is a very substrate-specific serine esterase. It harbors the catalytic triad S87-D216-H244, and is a new member of the alpha/beta-fold hydrolase superfamily. Its novel function leads to the diversification of alkaloid structures.

Stereochemistrychemistry [Secologanin Tryptamine Alkaloids]polyneuridine aldehyde esterasePolyneuridine-aldehyde esteraseCatalysisSubstrate SpecificityEnzyme catalysischemistry.chemical_compoundProtein structureBiosynthesisHydrolaseCatalytic triadmetabolism [Mutant Proteins]Indole testchemistry.chemical_classificationGeneral ChemistrySecologanin Tryptamine AlkaloidsProtein Structure Tertiarymetabolism [Carboxylic Ester Hydrolases]metabolism [Secologanin Tryptamine Alkaloids]EnzymeAmino Acid SubstitutionchemistryBiochemistryddc:540BiocatalysisMutant ProteinsCarboxylic Ester HydrolasesAngewandte Chemie International Edition
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Detection of Single Oxygen Molecules with Fluorescence-Labeled Hemocyanins

2005

This study introduces a method to detect individual oxygen molecules by fluorescence microscopy of single hemocyanins. These respiratory proteins from a tarantula bind oxygen with high affinity. A spectrometric signature of the oxygenated protein is transferred to an attached fluorescence label, which can be detected at the single-molecule level. This technique opens new perspectives for the development of small and sensitive oxygen sensors as well as for the investigation of cooperative oxygen binding in respiratory proteins.

Stereochemistrymedicine.medical_treatmentchemistry.chemical_elementBiochemistryOxygenCatalysisColloid and Surface ChemistrySpecies SpecificityChemical affinitymedicineFluorescence microscopeAnimalsMoleculeFluorescent DyesChemistrySpidersHemocyaninGeneral ChemistryFluorescenceOxygenSpectrometry FluorescenceHemocyaninsBiophysicsOxygen sensorCopperOxygen bindingJournal of the American Chemical Society
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Direct High-Performance Liquid Chromatographic Separation of Peptide Enantiomers:  Study on Chiral Recognition by Systematic Evaluation of the Influe…

2002

All-R/all-S enantiomers of oligoalanines (Ala(n), n = 1-10) with N-terminal protection group have been separated by HPLC on chiral stationary phases based on various cinchona alkaloid selectors. Structure-enantioselectivity relationships derived by extensive selector structure optimization provided insights into binding mechanisms and chiral recognition. Their interpretation was supported by X-ray crystal structures of amino acid and dipeptide, respectively, in complex with chiral selector. Optimized selectors have bulky elements representing steric barriers and deep binding pockets that afforded very high enantioselectivities; e.g., for the all-R and all-S enantiomers of N-(3,5-dinitrobenz…

Steric effectsDipeptidebiologyChemistryStereochemistryCinchona AlkaloidsMolecular ConformationCinchonaStereoisomerismStereoisomerismbiology.organism_classificationSensitivity and SpecificityCombinatorial chemistryAnalytical ChemistryChiral column chromatographyStructure-Activity Relationshipchemistry.chemical_compoundEnantiomerPeptidesPhthalazineChiral derivatizing agentChromatography High Pressure LiquidProtein BindingAnalytical Chemistry
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US-Elastography for Breast Lesion Characterization: Prospective Comparison of US BIRADS, Strain Elastography and Shear wave Elastography

2020

 To evaluate the diagnostic performance of strain elastography (SE) and 2 D shear wave elastography (SWE) and SE/SWE combination in comparison with conventional multiparametric ultrasound (US) with respect to improving BI-RADS classification results and differentiating benign and malignant breast lesions using a qualitative and quantitative assessment. In this prospective study, 130 histologically proven breast masses were evaluated with baseline US, color Doppler ultrasound (CDUS), SE and SWE (Toshiba Aplio 500 with a 7-15 MHz wide-band linear transducer). Each lesion was classified according to the BIRADS lexicon by evaluating the size, the B-mode and color Doppler features, the SE qualit…

Strain elastographybreast lesions; characterization; shear wave elastography; strain elastography; BIRADSTransducersBreast lesionBreast NeoplasmsPhysical examinationbreast lesionsSensitivity and Specificity030218 nuclear medicine & medical imagingDiagnosis Differential03 medical and health sciences0302 clinical medicineQuantitative assessmentHumansMedicinecharacterizationRadiology Nuclear Medicine and imagingBreastProspective StudiesUltrasonographyshear wave elastographyShear wave elastography030219 obstetrics & reproductive medicinemedicine.diagnostic_testbusiness.industryUltrasoundReproducibility of ResultsColor doppler ultrasoundBIRADSstrain elastographyElasticity Imaging TechniquesFemaleUltrasonography MammaryElastographybusinessNuclear medicineUltraschall in der Medizin - European Journal of Ultrasound
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Characterization of Streptomyces venezuelae ATCC 10595 rRNA gene clusters and cloning of rrnA

1996

Streptomyces venezuelae ATCC 10595 harbors seven rRNA gene clusters which can be distinguished by BglII digestion. The three rRNA genes present in each set are closely linked with the general structure 16S-23S-5S. We cloned rrnA and sequenced the 16S-23S spacer region and the region downstream of the 5S rRNA gene. No tRNA gene was found in these regions.

Streptomyces venezuelaeMolecular Sequence Data5.8S ribosomal RNADNA RibosomalMicrobiology18S ribosomal RNA5S ribosomal RNASpecies SpecificityRibosomal protein23S ribosomal RNARNA Ribosomal 16SCloning MolecularInternal transcribed spacerMolecular BiologyGeneticsbiologyRNA Ribosomal 5SNucleic Acid HybridizationRNA ProbesRibosomal RNAbiology.organism_classificationMolecular biologyStreptomycesRNA Ribosomal 23SGenes BacterialRNA RibosomalMultigene FamilyResearch ArticleJournal of Bacteriology
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Morphological and molecular redescription of the myxozoanUnicapsula pflugfelderiSchubert, Sprague & Reinboth 1975 from two teleost hosts in the M…

2009

Elongate plasmodia with myxosporean spores belonging to the genus Unicapsula, Davis, 1924 were found in the skeletal muscle of the striped seabream, Lithognathus mormyrus (L.), a candidate for the mediterranean aquaculture. The only species of Unicapsula described from the Mediterranean is Unicapsula pflugfelderi Schubert et al. 1975, which occurs in the picarel, Spicara smaris (L.). For morphological and molecular comparison of U. pflugfelderi from S. smaris with Unicapsula sp. from L. mormyrus measurements of plasmodia and spores, ultrastructural details and 18S and 28S rDNA sequences were analysed. Whereas plasmodia were 2-3 times larger in S. smaris than in L. mormyrus (length 2.47-0.81…

Striped seabreamParasitic Diseases AnimalVeterinary (miscellaneous)ZoologyAquatic ScienceBiologyFish DiseasesMicroscopy Electron TransmissionSpecies SpecificityRNA Ribosomal 28SMediterranean SeaRNA Ribosomal 18SAnimalsSpicara smarisMyxozoaMuscle SkeletalRibosomal DNAPhylogenyMormyrusSporoplasmfungibiology.organism_classificationSea BreamPerciformesSporeDNA GyraseMicroscopy Electron ScanningUltrastructureTaxonomy (biology)Journal of Fish Diseases
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