Search results for "dimer"

showing 10 items of 558 documents

Mutation of a critical tryptophan to lysine in avidin or streptavidin may explain why sea urchin fibropellin adopts an avidin-like domain

1999

Sea urchin fibropellins are epidermal growth factor homologues that harbor a C-terminal domain, similar in sequence to hen egg-white avidin and bacterial streptavidin. The fibropellin sequence was used as a conceptual template for mutation of designated conserved tryptophan residues in the biotin-binding sites of the tetrameric proteins, avidin and streptavidin. Three different mutations of avidin, Trp-110-Lys, Trp-70-Arg and the double mutant, were expressed in a baculovirus-infected insect cell system. A mutant of streptavidin, Trp-120-Lys, was similarly expressed. The homologous tryptophan to lysine (W--K) mutations of avidin and streptavidin were both capable of binding biotin and bioti…

StreptavidinBiotin bindingTime FactorsFunctional dimerLysineMutantBiophysicsBiotinEnzyme-Linked Immunosorbent AssayBiologyBiochemistrychemistry.chemical_compoundBiotinTetramerStructural BiologyGeneticsAnimalsMolecular BiologyExtracellular Matrix ProteinsBinding SitesEpidermal Growth FactorLysineAvidin-biotin technologyTemperatureTryptophanCell BiologyAvidinRecombinant ProteinsKineticsReversiblechemistryBiochemistryBiotinylationSea UrchinsMutationbiology.proteinRecombinant avidin and streptavidinStreptavidinBiotin-bindingAvidinChromatography LiquidProtein BindingFEBS Letters
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Dimer-tetramer transition between solution and crystalline states of streptavidin and avidin mutants.

2003

ABSTRACT The biotin-binding tetrameric proteins, streptavidin from Streptomyces avidinii and chicken egg white avidin, are excellent models for the study of subunit-subunit interactions of a multimeric protein. Efforts are thus being made to prepare mutated forms of streptavidin and avidin, which would form monomers or dimers, in order to examine their effect on quaternary structure and assembly. In the present communication, we compared the crystal structures of binding site W→K mutations in streptavidin and avidin. In solution, both mutant proteins are known to form dimers, but upon crystallization, both formed tetramers with the same parameters as the native proteins. All of the intersub…

StreptavidinModels MolecularStereochemistryProtein ConformationDimerBiotinCrystallography X-RayMicrobiologychemistry.chemical_compoundProtein structureBiotinTetramerEgg WhiteStructural BiologyAnimalsProtein Structure QuaternaryMolecular BiologyBinding SitesbiologyAvidinStreptomycesSolutionschemistryBiochemistryBiotinylationMutationbiology.proteinProtein quaternary structureStreptavidinCarrier ProteinsCrystallizationChickensDimerizationAvidinJournal of bacteriology
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Prospects of in vivo 31P NMR method in glyphosate degradation studies in whole cell system

2009

Abstract The degradation of the phosphonate herbicide glyphosate ( N -phosphonomethylglycine) by four taxonomically distinct microorganisms was studied in vivo in whole cell system using phosphorus nuclear magnetic spectroscopy ( 31 P NMR). The time-course of glyphosate metabolization in dense cell cultures was followed by means of 31 P NMR up to 21 days after the addition. The results obtained by this non-invasive way confirmed that the cells of Spirulina platensis and Streptomyces lusitanus biodegrade herbicide. Moreover, phosphorus starvation influenced the rate of glyphosate degradation by S. platensis . On the other hand, the results of similar measurements in the cultures of green alg…

Streptomyces lusitanusMicroorganismChlorella vulgarischemistry.chemical_elementBioengineeringBiologyApplied Microbiology and BiotechnologyBiochemistrybiodegradationchemistry.chemical_compoundglyphosatein vivo31P NMRBotanyFusarium dimerumspirulina platensisPhosphorusBiodegradationbiology.organism_classificationStreptomyces lusitanusPhosphonatexenobiotic metabolismchemistryBiochemistryGlyphosateGreen algaeChlorella vulgarisBiotechnologyEnzyme and Microbial Technology
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Dual-Mode Chiral Self-Assembly of Cone-Shaped Subphthalocyanine Aromatics

2020

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/jacs.0c07291

SubphthalocyanineChemistryThermodynamic equilibriumDimerStackingSupramolecular chemistryPorphyrinoidsSelf-assemblyQuímicaGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryEnantiopure drugPolymerizationChemical physicsLiquid crystalSupramolecular PolymersSelf-assembly
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Exploring reactivity of a bis-sulfonium zirconocene-ate dimer: synthesis of various zwitterionic phosphonium anionic zirconocene complexes

2007

Abstract Formal [3+2] cycloaddition reactions between the bis-sulfonium zirconocene-ate dimer 1a and methylpropiolate, benzaldehyde and carbon disulfide afforded stable zwitterionic phosphonium zirconocene-ate complexes 2–4, respectively, with two orthocondensed five-membered heterocycles. X-ray crystal structure of 4 has been determined. Elemental chalcogens (S, Se, Te) gave rise also to a new variety of five-coordinate zirconium(IV) complexes (5–7) by a formal [3+1] cycloaddition reaction. In these bicyclic zirconates, sulfur is included in a five-membered ring while the second chalcogen is in a four-membered one.

SulfoniumDimer010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryInorganic ChemistryBenzaldehydechemistry.chemical_compoundChalcogenanionic zirconoceneMaterials ChemistryOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)PhosphoniumPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSBicyclic molecule010405 organic chemistrysulfoniumOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryzirconocene-atephosphoniumCycloaddition3. Good health0104 chemical scienceschemistrychalcogenszwitterionic complexes
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Isolation, dynamic NMR study and X-ray characterisation of a bis sulfonium zirconocene-ate dimer.

2004

The novel dimer [Cp(2)Zr[upper bond start]([minus sign in circle])S([plus sign in circle])CH(Ph)CH[double bond]C[upper bond end]PPh(2)](2), the first example of a structurally characterised sulfur-bridged binuclear zirconathiolane complex, was prepared, characterised by NMR spectroscopy and X-ray crystallography, and some aspects of its solution behaviour were studied.

SulfoniumStereochemistryDimerMetals and AlloysX-rayGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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Ein neuer Syntheseweg zu Offenkettigen und cyclischen Oligoetherketonen

1998

A Novel Synthetic Route to Open-Chained and Cyclic Oligoetherketones Oligoetherketones of the structure 2a,b can be generated by repetitive insertion reactions of terminal biscarbenoids 4a,b, into the OH bonds of diols like 5. The formation of the corresponding ring systems 7a and the involved carbene dimerization leading to 8b are processes which compete with the linear polyinsertion. A related one-component reaction can be performed with ω-hydroxy-1-diazo-2-alkanones (13a–c 14a–c).

Terminal (electronics)ChemistryStereochemistryCarbene dimerizationRing (chemistry)Journal f�r Praktische Chemie/Chemiker-Zeitung
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Synthesis, characterization, crystal structures and magnetic exchange in dinuclear copper complexes with 3-amino-1-propanol as terminal and bridging …

1990

Abstract The synthesis, X-ray structures and spectroscopic and magnetic properties are described for two groups of dinuclear Cu(II) compounds with the ligand 3-amino-1-propanol (Hap). The formulae of the compounds are for group A: [Cu(ap)(anion)]2, in which ap is the dehydronated Hap and the anions are formate, nitrate, chloride and bromide and for group B: [Cu(ap)(Hap)]2(anion)2, with anion = iodide, bromide, chloride, nitrate and tetrafluoroborate. The structure of group A compounds consists of dinuclear units with the co-planar centrosymmetric chromophore ANCuOO′CuNA, in which the A ligands (anions) bridge to neighbouring units as axial ligands, thereby forming infinite chains. Dimer Cu……

TetrafluoroborateCoordination sphereChemistryHydrogen bondStereochemistryLigandDimerBridging ligandCrystal structureSquare pyramidal molecular geometryInorganic Chemistrychemistry.chemical_compoundCrystallographyMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Through-space spin-spin coupling in acetylenic systems. Ab initio and DFT calculations

2003

Abstract: We have investigated, by means of ab initio and DFT calculations, the magnitude of through-space spin-spin couplings ( J CH and J HH ) in CH/π bonded van der Waals dimers involving acetylene, and in a structurally related covalent compound (4-ethynylphenanthrene). Within regions where the interaction is stabilizing J HH couplings are very small (< 0.1 Hz) for all complexes. In the acetylene-methane complex J CH is also very small, whereas in the acetylene-benzene complex and the acetylene dimer it shows a relatively large dependence on the tilt angle from the T-shaped arrangement, for which the smallest values are calculated, to a parallel slipped arrangement where J CH is ca. 0.5…

Through-space couplingDimerAb initioDFTCatalysisspin-spin couplinglcsh:ChemistryInorganic Chemistrychemistry.chemical_compoundsymbols.namesakeNMR spectroscopyComputational chemistryThrough-space coupling / NMR / ab initio / DFTPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryNMR spectroscopy; computational chemistry; spin-spin couplingSpin (physics)lcsh:QH301-705.5Molecular BiologySpectroscopyCouplingab initioChemistryOrganic ChemistryGeneral MedicineNuclear magnetic resonance spectroscopycomputational chemistryNMRComputer Science ApplicationsCrystallographylcsh:Biology (General)lcsh:QD1-999AcetyleneCovalent bondsymbolsCondensed Matter::Strongly Correlated ElectronsComputingMethodologies_GENERALvan der Waals force
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First-principles simulations of hydrogen peroxide formation catalyzed by small neutral gold clusters.

2009

Energetics and dynamical pathways for hydrogen peroxide formation from H(2) and O(2) bound to neutral gold dimers and tetramers have been investigated by applying several strategies: T = 0 K geometry optimizations, constrained Car-Parrinello molecular dynamics simulations at T = 300 K and metadynamics at T = 300 K. The competing reaction channels for water and hydrogen peroxide formation have been found and characterized. In each case, the reaction barriers for Au cluster catalyzed proton transfer are less than 1 eV. Water formation is a competitive reaction channel, and the relative weight of H(2)O and H(2)O(2) products may depend on the chosen Au cluster size. Dynamic simulations demonstr…

Time FactorsProtonDimerGeneral Physics and AstronomyCatalysisCatalysischemistry.chemical_compoundMolecular dynamicsTransition metalComputational chemistryCluster (physics)Computer SimulationPhysical and Theoretical ChemistryHydrogen peroxideModels StatisticalChemistryChemistry PhysicalMetadynamicsTemperatureWaterHydrogen PeroxideChemical physicsEnvironmental PollutantsGoldProtonsDimerizationPhysical chemistry chemical physics : PCCP
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