Search results for "acids"

showing 10 items of 3520 documents

Toward very potent, non-covalent organophosphonate inhibitors of cathepsin C and related enzymes by 2-amino-1-hydroxy-alkanephosphonates dipeptides

2013

Cathepsins play an important role in several human disorders and therefore the design and synthesis of their inhibitors attracts considerable interest in current medicinal chemistry approaches. Due to the presence of a strong sulphydryl nucleophile in the active center of the cysteine type cathepsins, most strategies to date have yielded covalent inhibitors. Here we present a series of non-covalent β-amino-α-hydroxyalkanephosphonate dipeptidic inhibitors of cathepsin C, ranking amongst the best low-molecular weight inhibitors of this enzyme. Their binding modes determined by molecular modelling indicate that the hydroxymethyl fragment of the molecule, not the phosphonate moiety, acts as a t…

Models MolecularStereochemistryhydroxyphosphonateBiochemistryCathepsin CCathepsin BCathepsin CInhibitory Concentration 50chemistry.chemical_compoundCathepsin OTransition state analogCathepsin KHumanscysteine proteasePeptide bondcathepsinAminesEnzyme InhibitorsCathepsinDipeptideChemistryMolecular MimicryDipeptidesGeneral MedicineOrganophosphatesEnzyme ActivationinhibitorBiochemistryHydroxy AcidsBiochimie
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String kernels and high-quality data set for improved prediction of kinked helices in α-helical membrane proteins.

2011

The reasons for distortions from optimal α-helical geometry are widely unknown, but their influences on structural changes of proteins are significant. Hence, their prediction is a crucial problem in structural bioinformatics. For the particular case of kink prediction, we generated a data set of 132 membrane proteins containing 1014 manually labeled helices and examined the environment of kinks. Our sequence analysis confirms the great relevance of proline and reveals disproportionately high occurrences of glycine and serine at kink positions. The structural analysis shows significantly different solvent accessible surface area mean values for kinked and nonkinked helices. More important, …

Models MolecularSupport Vector MachineProlineGeneral Chemical EngineeringGlycineLibrary and Information SciencesProtein Structure SecondaryAccessible surface areaSet (abstract data type)Structural bioinformaticsC++ string handlingSerineAnimalsHumansDatabases ProteinQuantitative Biology::BiomoleculesModels StatisticalChemistryComputational BiologyMembrane ProteinsGeneral ChemistryComputer Science ApplicationsData setCrystallographyMembrane proteinα helicalResearch Designlipids (amino acids peptides and proteins)Biological systemJournal of chemical information and modeling
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Functional competition within a membrane: Lipid recognition vs. transmembrane helix oligomerization

2015

Abstract Binding of specific lipids to large, polytopic membrane proteins is well described, and it is clear that such lipids are crucial for protein stability and activity. In contrast, binding of defined lipid species to individual transmembrane helices and regulation of transmembrane helix monomer–oligomer equilibria by binding of distinct lipids is a concept, which has emerged only lately. Lipids bind to single-span membrane proteins, both in the juxta-membrane region as well as in the hydrophobic membrane core. While some interactions counteract transmembrane helix oligomerization, in other cases lipid binding appears to enhance oligomerization. As reversible oligomerization is involve…

Models MolecularSyntaxin 1AMembrane lipidsLipid BilayersBiophysicsBiologyBinding CompetitiveBiochemistryProtein Structure SecondaryMembrane LipidsLipid bindingOligomerizationIntegral membrane proteinC99Transmembrane channelsMolecular StructureMembrane transport proteinCell MembranePeripheral membrane proteinMembrane ProteinsCell Biologyp24Transmembrane proteinProtein Structure TertiaryCell biologyTransmembrane domainMembrane proteinMembrane proteinbiology.proteinlipids (amino acids peptides and proteins)Protein BindingBiochimica et Biophysica Acta (BBA) - Biomembranes
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Exploiting a list of protein sequences

2007

Abstract: We describe a software program to help exploit a database of aligned protein sequences. In addition to the classical lists of sequences, a graphical representation is used to get a better overview of the information. As natural parameters, the type of amino acid and sequence position are used. Various plots or 3D representations are then updated. Examples are shown based on globin sequences from various species and on the abnormal human hemoglobins. The software should be of interest to protein engineers who need to know what variants are already known.

Models MolecularTheoretical computer scienceExploitProtein ConformationBiologyHemoglobinsSoftwareNeed to knowComputer GraphicsGeneticsAnimalsHumansAmino Acid SequenceAmino AcidsDatabases ProteinRepresentation (mathematics)BiologyGeneticsSequencebusiness.industryGeneral MedicineProtein Structure TertiaryMutationHuman medicinebusinessSoftwareGene
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Quenching of fluorescein-conjugated lipids by antibodies. Quantitative recognition and binding of lipid-bound haptens in biomembrane models, formatio…

1992

Three model biomembrane systems, monolayers, micelles, and vesicles, have been used to study the influence of chemical and physical variables of hapten presentation at membrane interfaces on antibody binding. Hapten recognition and binding were monitored for the anti-fluorescein monoclonal antibody 4–4-20 generated against the hapten, fluorescein, in these membrane models as a function of fluorescein-conjugated lipid architecture. Specific recognition and binding in this system are conveniently monitored by quenching of fluorescein emission upon penetration of fluorescein into the antibody's active site. Lipid structure was shown to play a large role in affecting antibody quenching. Interes…

Models MolecularTime FactorsProtein ConformationStereochemistry030303 biophysicsMolecular ConformationBiophysicsModels BiologicalMice03 medical and health scienceschemistry.chemical_compoundAnimalsFluoresceinBinding siteLipid bilayerMicellesPhospholipids030304 developmental biologyPhosphatidylethanolamine0303 health sciencesLiposomeVesicleCell MembraneAntibodies MonoclonalMembranes ArtificialBiological membraneFluoresceinsKineticsSpectrometry FluorescencechemistryLiposomeslipids (amino acids peptides and proteins)Binding Sites AntibodyHaptensHaptenResearch ArticleBiophysical Journal
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Multifaceted Palladium Catalysts Towards the Tandem Diboration-Arylation Reactions of Alkenes

2008

Novel Pd(2) (6+) compounds have been synthesized in high yield. These compounds and their Pd(2) (4+) counterparts as synthetic precursors mediate the diboration of vinylarenes and aliphatic 1-alkenes, and under mild and basic reaction conditions they produce a variety of 1,2-diboronate esters with excellent conversions and chemoselectivities. The presence of bis(catecholato)diboron (B(2)cat(2)) favours the reduction of Pd(III) to Pd(II), while the catalytic precursor of Pd(II) is transformed into Pd(0)-nanoparticles. An "in situ" catalytic tandem reaction has been designed to transform the diboronate intermediates into the monoarylated product, which after oxidative workup, provides the car…

Models MolecularTime Factorschemistry.chemical_elementStereoisomerismAlkenesCrystallography X-RayCatalysisAdductCatalysisCascade reactionOrganometallic CompoundsOrganic chemistryParticle SizeChemoselectivitychemistry.chemical_classificationMolecular StructureChemistryAlkeneOrganic ChemistryStereoisomerismGeneral ChemistryBoronic AcidsCombinatorial chemistryAlcoholsYield (chemistry)PalladiumPalladiumChemistry - A European Journal
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Substituted phosphonic analogues of phenylglycine as inhibitors of phenylalanine ammonia lyase from potatoes.

2018

A series of phosphonic acid analogues of phenylglycine variously substituted in phenyl ring have been synthesized and evaluated for their inhibitory activity towards potato l-phenylalanine ammonia lyase. Most of the compounds appeared to act as moderate (micromolar) inhibitors of the enzyme. Analysis of their binding performed using molecular modeling have shown that they might be bound either in active site of the enzyme or in the non-physiologic site. The latter one is located in adjoining deep site nearby the to the entrance channel for substrate into active site.

Models MolecularaminophosphonatesMolecular modelStereochemistryPhosphorous AcidsGlycinePhenylalanine ammonia-lyase010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryAmmoniachemistry.chemical_compoundStructure-Activity RelationshipPAL inhibitorsEnzyme InhibitorsPhenylalanine Ammonia-LyaseSolanum tuberosumchemistry.chemical_classificationbiologymolecular modeling010405 organic chemistryActive siteSubstrate (chemistry)General MedicineLyase0104 chemical sciencesEnzymechemistrybiology.proteinBiochimie
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Density functional theory fragment descriptors to quantify the reactivity of a molecular family: Application to amino acids

2007

By using the exact density functional theory, one demonstrates that the value of the local electronic softness of a molecular fragment is directly related to the polarization charge (Coulomb hole) induced by a test electron removed (or added) from (at) the fragment. Our finding generalizes to a chemical group a formal relation between these molecular descriptors recently obtained for an atom in a molecule using an approximate atomistic model [P. Senet and M. Yang, J. Chem. Sci. 117, 411 (2005)]. In addition, a practical ab initio computational scheme of the Coulomb hole and related local descriptors of reactivity of a molecular family having in common a similar fragment is presented. As a b…

Models Molecularchemistry.chemical_classificationQuantitative Biology::BiomoleculesQuantitative structure–activity relationshipBinding SitesChemistryAb initioGeneral Physics and AstronomyAmino acidModels ChemicalAb initio quantum chemistry methodsComputational chemistryMolecular descriptorMoleculeComputer SimulationDensity functional theoryAmino AcidsPhysical and Theoretical ChemistryAlgorithmsFragment molecular orbitalProtein BindingThe Journal of Chemical Physics
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Conformational investigation of α,β-dehydropeptides. X. Molecular and crystal structure of Ac-ΔAla-NMe2 compared with those of Ac-L-Ala-NMe2, Ac-DL-A…

2002

A series of three homologous dimethyldiamides Ac-DeltaAla-NMe2, Ac-L-Ala-NMe2 and Ac-DL-Ala-NMe2 has been synthesized and the structures of these amides determined from single-crystal X-ray diffraction data. To learn more about the conformational preferences of compounds studied, the fully relaxed (phi-psi) conformational energy maps in vacuo (AM1) of Ac-DeltaAla-NMe2 and Ac-L-Ala-NMe2 were obtained, and the calculated minima reoptimized with the DFT/B3LYP/6-31G** method. The crystal-state results have been compared with the literature data. Ac-DeltaAla-NMe2 and other alpha,beta-dehydroamino acid dimethyldiamides, Ac-DeltaXaa-NMe2 adopt the conservative conformation of the torsion angles ph…

Models Moleculardehydroalanine derivativeProtein ConformationStereochemistryαPeptidedimethylamidesCrystal structureX‐ray crystallographyCrystallography X-RayBiochemistryEndocrinologyProtein structureMoleculeBeta (finance)crystal and molecular structuresalanine derivativesβ‐dehydroamino acidstheoretical calculationschemistry.chemical_classificationAlanineamino acid amidesAmino acidCrystallographydehydropeptideschemistryX-ray crystallographyPeptidesRamachandran plotJOURNAL OF PEPTIDE RESEARCH
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Formation of irreversibly bound annexin A1 protein domains on POPC/POPS solid supported membranes

2008

AbstractThe specific interaction of annexin A1 with phospholipid bilayers is scrutinized by means of scanning force and fluorescence microscopy, quartz crystal microbalance, ellipsometry, and modeled by dynamic Monte Carlo simulations. It was found that POPC/POPS bilayers exhibit phase separation in POPC- and POPS-enriched domains as a function of Ca2+ concentration. Annexin A1 interacts with POPC/POPS bilayers by forming irreversibly bound protein domains with monolayer thickness on POPS-enriched nanodomains, while the attachment of proteins to the POPC-enriched regions is fully reversible. A thorough kinetic analysis of the process reveals that both, the binding constant of annexin A1 at …

Models Moleculargenetic structuresLipid BilayersBiophysicsPhospholipidAnalytical chemistryPhosphatidylserines02 engineering and technologyMicroscopy Atomic ForceBiochemistryBiophysical PhenomenaMembrane Lipids03 medical and health scienceschemistry.chemical_compoundProtein structureSFMMonolayerMicropatterned membranesAnimalsHumansPOPCMonte Carlo simulationAnnexin A1030304 developmental biologyFluorescence microscopy0303 health sciencesEllipsometrytechnology industry and agricultureCell BiologyQuartz crystal microbalanceSurface Plasmon Resonance021001 nanoscience & nanotechnologyBinding constantProtein Structure TertiaryMembraneMicroscopy FluorescencechemistryQCMPhosphatidylcholinesBiophysicsCalciumlipids (amino acids peptides and proteins)Adsorption0210 nano-technologyMonte Carlo MethodProtein BindingAnnexin A1Biochimica et Biophysica Acta (BBA) - Biomembranes
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