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showing 10 items of 1641 documents

Low temperature optical spectroscopy of cobalt-substituted hemocyanin from Carcinus maenas

1993

In this work we report the optical absorption spectra of three cobalt-substituted derivatives of hemocyanin (He) from Carcinus maenas, in the temperature range 300–20 K. The derivatives studied are the mononuclear (Co2+)-He with a single cobalt ion in the “CuA” site, the binuclear (Co2+)2-He and the binuclear mixed metal (Co2+-Cu1+)-He. At low temperature three main bands are clearly resolved; the temperature dependence of their zeroth, first and second moments sheds light on the stereodynamic properties in the surroundings of the chromophore. Within the limits of the reported analysis, in the binuclear derivatives the motions coupled to the chromophore appear to be “essentially harmonic” i…

biologyLigandMetal ions in aqueous solutionBiophysicsAnalytical chemistryActive sitechemistry.chemical_elementGeneral MedicineChromophoreAtmospheric temperature rangeCrystallographychemistrybiology.proteinSpectroscopyRotational–vibrational couplingCobaltEuropean Biophysics Journal
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Selektivit�tsstudien: OH-, NH- und SH-gruppenspezifische Reagentien - ihre Anwendung in der organischen Analytik und als Schutzgruppen in der Synthese

1992

Selectivity: OH-, NH- and SH-Groupspecific Reagents. The Application in Organic Analysis and as Protective Groups Phosphylhalides and -pseudohalides R1R2P(O)X (X = Cl, F, CN, N3, OC6H4NO2(p)) reactdepending on X- with a different selectivity with OHNH- and SH-groups. Vinylsulfones ArSO2CH = CH2 are SH-selective. Silanes R3SiH are OH-selective. By exchange of one ligand bound on P, SO2 or Si by the 5-dimethylamino resp. the 5-methoxynaphthalinogroup reagents are formed, which combine group selectivity with fluorescence. The fluorescence is quenched if a ligand or the leaving group is substituted by a NO2-group. The fluorescence appears again if after the group selective fixation the ligand w…

biologyLigandStereochemistryChemistryLeaving groupActive siteTrypsinFluorescenceSerineReagentmedicinebiology.proteinSelectivitymedicine.drugJournal f�r Praktische Chemie/Chemiker-Zeitung
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Theoretical studies of HIV-1 reverse transcriptase inhibition

2012

Computational methods for accurately calculating the binding affinity of a ligand for a protein play a pivotal role in rational drug design. We herein present a theoretical study of the binding of five different ligands to one of the proteins responsible for the human immunodeficiency virus type 1 (HIV-1) cycle replication; the HIV-1 reverse transcriptase (RT). Two types of approaches are used based on molecular dynamics (MD) simulations within hybrid QM/MM potentials: the alchemical free energy perturbation method, FEP, and the pathway method, in which the ligand is physically pulled away from the binding site, thus rendering a potential of mean force (PMF) for the binding process. Our com…

biologyMolecular StructureStereochemistryChemistryRational designGeneral Physics and AstronomyActive siteDrug designMolecular Dynamics SimulationLigand (biochemistry)HIV Reverse TranscriptaseFree energy perturbationMolecular dynamicsStructure-Activity Relationshipbiology.proteinQuantum TheoryReverse Transcriptase InhibitorsPhysical and Theoretical ChemistryBinding siteRNase H
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Computational Modeling of Biological Systems: The LDH Story

2010

Lactate dehydrogenases, LDH, catalyzed reaction has been used in this chapter as a conductor wire to present the evolution and difficulties on computing methods to model chemical reactions in enzymes, since the early calculations based at semiempirical level carried out in gas phase to the recent sophisticated simulations based on hybrid Quantum Mechanical/Molecular Mechanics Dynamics (QM/MM MD) schemes. LDH catalyzes the reversible transformation of pyruvate into lactate. The chemical step consists in a hydride and a proton transfer from the cofactor (NADH) and a protonated histidine (His195), respectively. This fact has generated a lot of controversy about the timing of both transfers in …

biologyProtonChemistryHydridebiology.proteinActive siteThermodynamicsProtonationPotential of mean forceChemical reactionQuantumEnzyme catalysis
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Dehydrochlorination of Hexachlorocyclohexanes Catalyzed by the LinA Dehydrohalogenase. A QM/MM Study

2015

The elucidation of the catalytic role of LinA dehydrohalogenase in the degradation processes of hexachlorocyclohexane (HCH) isomers is extremely important to further studies on the bioremediation of HCH polluted areas. Herein, QM/MM free energy simulations are employed to provide the details of the dehydrochlorination reaction of two HCH isomers (γ and β). In particular, the role of the protonation state of one of the catalytic residues-His73-is explored. Based on our calculations, two distinct minimum free energy pathways (concerted and stepwise) were found for γ-HCH and β-HCH. The choice of the reaction channel for the dehydrochlorination reactions of γ- and β-HCH was shown to depend on t…

biologyProtonConcerted reactionStereochemistryHexachlorocyclohexaneActive siteProtonationSurfaces Coatings and FilmsCatalysisQM/MMchemistry.chemical_compoundchemistryComputational chemistryMaterials Chemistrybiology.proteinDegradation (geology)Physical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Lactobacillus tucceti sp. nov., a new lactic acid bacterium isolated from sausage

2006

Abstract Following the application of several molecular techniques strain R 19c, isolated from sausage by Reuter in 1970 and deposited at the DSMZ as Lactobacillus sp., has been identified as pertaining to a new species. It showed singular ISR- Dde I and ISR- Hae III profiles that allowed its differentiation from 68 lactic acid bacteria reference strains analyzed. Phylogenetic analysis based on 16S rRNA gene sequences places this strain in the genus Lactobacillus within the Lactobacillus alimentarius group. Species L. versmoldensis is the closest phylogenetic neighbor with 96.3% sequence similarity. DNA–DNA hybridization experiments confirmed the independent status at species level of this …

biologyRhamnoseNucleic Acid Hybridizationfood and beveragesbiology.organism_classification16S ribosomal RNADNA RibosomalPolymerase Chain ReactionApplied Microbiology and BiotechnologyMicrobiologyLactic acidMicrobiologyMeat ProductsLactobacilluschemistry.chemical_compoundPhenotypechemistryLactobacillusPeptidoglycanDeoxyribonucleases Type II Site-SpecificMelibioseRibosomal DNAPhylogenyEcology Evolution Behavior and SystematicsBacteriaSystematic and Applied Microbiology
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Cu/P(4-PVP) stereochemistry in tetralin liquid-phase oxidation

2007

Abstract Cu/P(4-PVP) catalyst was used as catalyst for oxidation of tetralin in liquid phase. The catalyst was prepared by reaction of a Cu(II) salt with a 4-vinylpyridine-co-divinylbenzene polymer receptor and characterized by solid 1 H and 13 C NMR, XPS, FTIR, ESR spectroscopies, and by chemical reaction with pure tetralin. That information was used to gain insight into the stereochemistry of the active site needed to orient the reaction toward tetralone production. It was found that the Cu coordination with the pyridine was critical in influencing the peroxy-radical catalytic reaction, and that polyvinylpyridine was able to limit the autothermal oxidation. The active center is postulated…

biologyStereochemistryActive siteHeterogeneous catalysisChemical reactionCatalysisCatalysisActive centerchemistry.chemical_compoundchemistryPyridinebiology.proteinTetraloneTetralinPhysical and Theoretical ChemistryJournal of Catalysis
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An ab initio conformational study on captopril

2003

Abstract Captopril can interact regio- and stereo-specifically with various functional groups present at the active site of angiotensin converting enzyme (ACE). Since no X-ray structure of ACE is available, Captopril, as an ACE inhibitor may be used as a ‘molecular caliper’, to estimate upper and lower bound values for separation d, where the mercaptidic terminal group of the molecule is linked to the enzyme Zn2+ cofactor, while the carboxylate links via an hydrogen bond to the guanidine moiety of an arginine side chain. As the results of this Ab Initio study, the conformations of the dianionic form of the full captopril molecule are reported here.

biologyStereochemistryHydrogen bondAb initioActive siteCaptoprilAngiotensin-converting enzymeCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundchemistryACE inhibitorbiology.proteinmedicineMoietyPhysical and Theoretical ChemistryGuanidinemedicine.drugJournal of Molecular Structure: THEOCHEM
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Chemoselektive Fluoreszenzstudien am Subtilisin und “Thiosubtilisin”

1985

Chemoselective Fluorescence Studies with Subtilisin and “Thiosubtilisin” The serine hydroxy group in the active site of subtilisin is selectively “phosphylated”3). This is demonstrated using the fluorescent phosphinic fluoride 1. “Thiosubtilisin” does not react with 1 but with the SH-selective and fluorescent vinyl sulfone 2.

biologyStereochemistryfungiOrganic ChemistryHydroxy groupSubtilisinActive siteVinyl sulfoneFluorescenceSerineenzymes and coenzymes (carbohydrates)chemistry.chemical_compoundchemistrybiology.proteinOrganic chemistryPhysical and Theoretical ChemistryFluorideLiebigs Annalen der Chemie
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Metal specificity of the Ni(II) and Zn(II) binding sites of the N-terminal and G-domain of E. coli HypB

2021

HypB is one of the chaperones required for proper nickel insertion into [NiFe]-hydrogenase. Escherichia coli HypB has two potential Ni(II) and Zn(II) binding sites—the N-terminal one and the so-called GTPase one. The metal-loaded HypB–SlyD metallochaperone complex activates nickel release from the N-terminal HypB site. In this work, we focus on the metal selectivity of the two HypB metal binding sites and show that (i) the N-terminal region binds Zn(II) and Ni(II) ions with higher affinity than the G-domain and (ii) the lower affinity G domain binds Zn(II) more effectively than Ni(II). In addition, the high affinity N-terminal domain, both in water and membrane mimicking SDS solution, has a…

biologychemistry.chemical_elementZincmedicine.disease_causeInorganic ChemistryMetalCrystallographyNickelchemistryG-domainChaperone (protein)visual_artbiology.proteinvisual_art.visual_art_mediummedicineMetallochaperone complexBinding siteEscherichia coliDalton Transactions
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