Search results for "Protein structure"

showing 10 items of 757 documents

Influence of the hydrophilic face on the folding ability and stability of α-helix bundles: relevance to the peptide catalytic activity

2000

Although not the sole feature responsible, the packing of amino acid side chains in the interior of proteins is known to contribute to protein conformational specificity. While a number of amphipathic peptide sequences with optimized hydrophobic domains has been designed to fold into a desired aggregation state, the contribution of the amino acids located on the hydrophilic side of such peptides to the final packing has not been investigated thoroughly. A set of self-aggregating 18-mer peptides designed previously to adopt a high level of alpha-helical conformation in benign buffer is used here to evaluate the effect of the nature of the amino acids located on the hydrophilic face on the pa…

chemistry.chemical_classificationCrystallographyEndocrinologyProtein structurechemistryProtein designProtein foldingPeptideBiochemistryPeptide sequenceProtein tertiary structureAlpha helixAmino acidThe Journal of Peptide Research
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Sulfated and Non-Sulfated Glycopeptide Recognition Domains of P-Selectin Glycoprotein Ligand 1 and their Binding to P- and E-Selectin

2009

Total synthesis through block glycosylation and selective chemical O-sulfation of tyrosine residues yielded the glycopeptide recognition domain A (X=SO(3) (-)) of the P-selectin glycoprotein ligand 1, in which the terminal sialic acid of the complex hexasaccharide side chain was replaced by (S)-cyclohexyl lactic acid. In binding assays the O-sulfated structure A showed high affinity towards P-selectin, the non-sulfated towards E-selectin.

chemistry.chemical_classificationGlycosylationMembrane GlycoproteinsGlycosylationSulfatesStereochemistryGlycopeptidesGeneral ChemistryLigand (biochemistry)CatalysisGlycopeptideProtein Structure TertiarySialic acidMiceP-Selectinchemistry.chemical_compoundProtein structurechemistryBiochemistryAnimalsHumansP-selectin glycoprotein ligand-1TyrosineE-SelectinGlycoproteinAngewandte Chemie International Edition
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Competing salt effects on phase behavior of protein solutions: tailoring of protein interaction by the binding of multivalent ions and charge screeni…

2014

The phase behavior of protein solutions is affected by additives such as crowder molecules or salts. In particular, upon addition of multivalent counterions, a reentrant condensation can occur; i.e., protein solutions are stable for low and high multivalent ion concentrations but aggregating at intermediate salt concentrations. The addition of monovalent ions shifts the phase boundaries to higher multivalent ion concentrations. This effect is found to be reflected in the protein interactions, as accessed via small-angle X-ray scattering. Two simulation schemes (a Monte Carlo sampling of the counterion binding configurations using the detailed protein structure and an analytical coarse-grain…

chemistry.chemical_classificationIonsCondensationOsmolar ConcentrationSurfaces Coatings and FilmsIonProtein–protein interactionProtein structurechemistryX-Ray DiffractionIonic strengthComputational chemistryPhase (matter)Scattering Small AngleMaterials ChemistryMoleculeHumansSaltsPhysical and Theoretical ChemistryCounterionSerum AlbuminThe journal of physical chemistry. B
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Conformational studies of hexapeptides containing two dehydroamino acid residues in positions 2 and 5 in peptide chain

2008

Conformational preferences of a group of hexapeptides containing two dehydroamino acid residues in Positions 2 and 5 in peptide chain were investigated by means of spectroscopic methods (NMR and CD) and theoretical calculations. In the case of dimethylsulfoxide (DMSO) solution, only peptide with free N-termini adopted rigid 310-helical conformation, for the rest of examined peptides extended and “zig-zag” conformers were predominant. CD measurements showed that only in chloroform solution the conformational freedom of investigated peptides was restricted. © 2008 Wiley Periodicals, Inc. Biopolymers 89: 691–699, 2008. This article was originally published online as an accepted preprint. The “…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyProtein ConformationStereochemistryCircular DichroismMolecular Sequence DataOrganic ChemistryTemperatureBiophysicsPeptideGeneral MedicineAmidesBiochemistryProtein Structure SecondaryBiomaterialschemistry.chemical_compoundChain (algebraic topology)chemistryDehydroalanineAmino Acid SequenceAmino AcidsProtonsPeptidesConformational isomerismBiopolymers
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Structure-based statistical analysis of transmembrane helices

2012

Recent advances in determination of the high-resolution structure of membrane proteins now enable analysis of the main features of amino acids in transmembrane (TM) segments in comparison with amino acids in water-soluble helices. In this work, we conducted a large-scale analysis of the prevalent locations of amino acids by using a data set of 170 structures of integral membrane proteins obtained from the MPtopo database and 930 structures of water-soluble helical proteins obtained from the protein data bank. Large hydrophobic amino acids (Leu, Val, Ile, and Phe) plus Gly were clearly prevalent in TM helices whereas polar amino acids (Glu, Lys, Asp, Arg, and Gln) were less frequent in this …

chemistry.chemical_classificationModels MolecularChemistryCell MembraneBiophysicsComputational BiologyMembrane ProteinsWaterHelix-turn-helixGeneral MedicineBiofísicaProtein Structure SecondaryAmino acidTransmembrane domainCrystallographyMembrane proteinSolubilitySeqüència d'aminoàcidsHelixChou–Fasman methodThermodynamicsDatabases ProteinIntegral membrane proteinHydrophobicity scales
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Orientation and Dynamics of Peptides in Membranes Calculated from 2H-NMR Data

2009

Solid-state (2)H-NMR is routinely used to determine the alignment of membrane-bound peptides. Here we demonstrate that it can also provide a quantitative measure of the fluctuations around the distinct molecular axes. Using several dynamic models with increasing complexity, we reanalyzed published (2)H-NMR data on two representative alpha-helical peptides: 1), the amphiphilic antimicrobial peptide PGLa, which permeabilizes membranes by going from a monomeric surface-bound to a dimeric tilted state and finally inserting as an oligomeric pore; and 2), the hydrophobic WALP23, which is a typical transmembrane segment, although previous analysis had yielded helix tilt angles much smaller than ex…

chemistry.chemical_classificationModels MolecularChemistryProtein ConformationCell MembraneMembraneBiophysicsPeptideRotationProtein Structure SecondaryMolecular dynamicsHydrophobic mismatchCrystallographyTransmembrane domainMembraneChemical physicsOrientation (geometry)HelixPeptidesNuclear Magnetic Resonance BiomolecularAntimicrobial Cationic PeptidesBiophysical Journal
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Crystal structure of the bifunctional soybean Bowman-Birk inhibitor at 0.28-nm resolution. Structural peculiarities in a folded protein conformation.

1996

The Bowman-Birk inhibitor from soybean is a small protein that contains a binary arrangement of trypsin-reactive and chymotrypsin-reactive subdomains. In this report, the crystal structure of this anticarcinogenic protein has been determined to 0.28-nm resolution by molecular replacement from crystals grown at neutral pH. The crystal structure differs from a previously determined NMR structure [Werner, M. H. & Wemmer, D. E. (1992) Biochemistry 31, 999-1010] in the relative orientation of the two enzyme-insertion loops, in some details of the main chain trace, in the presence of favourable contacts in the trypsin-insertion loop, and in the orientation of several amino acid side chains. The p…

chemistry.chemical_classificationModels MolecularMagnetic Resonance SpectroscopyStereochemistryProtein ConformationMolecular Sequence DataWaterCrystal structureCrystallography X-RayBiochemistryProtein tertiary structureProtein Structure SecondaryAmino acidCrystallographychemistry.chemical_compoundKineticsProtein structurechemistrySide chainChymotrypsinProtein foldingMolecular replacementAmino Acid SequenceBifunctionalTrypsin Inhibitor Bowman-Birk SoybeanEuropean journal of biochemistry
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The dynamic orientation of membrane-bound peptides: bridging simulations and experiments.

2007

AbstractThe structural organization in a peptide/membrane supramolecular complex is best described by knowledge of the peptide orientation plus its time-dependent and spatial fluctuations. The static orientation, defined by the peptide tilt and a rotation about its molecular axis, is accessible through a number of spectroscopic methods. However, peptide dynamics, although relevant to understand the functionality of these systems, remains largely unexplored. Here, we describe the orientation and dynamics of Trp-flanked and Lys-flanked hydrophobic peptides in a lipid bilayer from molecular dynamics simulations. A novel view is revealed, where collective nontrivial distributions of time-evolvi…

chemistry.chemical_classificationModels MolecularMembranesProtein ConformationLipid BilayersBiophysicsSupramolecular chemistryAnchoringMembrane ProteinsPeptideOrientation (graph theory)CrystallographyMolecular dynamicsMembraneProtein structurechemistryModels ChemicalChemical physicsComputer SimulationLipid bilayerDimyristoylphosphatidylcholinePeptidesBiophysical journal
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Two penta­de­hydro­peptides with different configurations of the ΔPhe residues

2009

Comparison of the crystal structures of two pentadehydropeptides containing DeltaPhe residues, namely (Z,Z)-N-(tert-butoxycarbonyl)glycyl-alpha,beta-phenylalanylglycyl-alpha,beta-phenylalanylglycine (or Boc(0)-Gly(1)-Delta(Z)Phe(2)-Gly(3)-Delta(Z)Phe(4)-Gly(5)-OH) methanol solvate, C(29)H(33)N(5)O(8) x CH(4)O, (I), and (E,E)-N-(tert-butoxycarbonyl)glycyl-alpha,beta-phenylalanylglycyl-alpha,beta-phenylalanylglycine (or Boc(0)-Gly(1)-Delta(E)Phe(2)-Gly(3)-Delta(E)Phe(4)-Gly(5)-OH), C(29)H(33)N(5)O(8), (II), indicates that the Delta(Z)Phe residue is a more effective inducer of folded structures than the Delta(E)Phe residue. The values of the torsion angles phi and psi show the presence of two …

chemistry.chemical_classificationMolecular StructureProtein ConformationOrganic CompoundsStereochemistryHydrogen bondPhenylalanineMolecular Sequence DataHydrogen BondingPhenylalanineGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyAmino acidCrystallographyResidue (chemistry)Protein structurechemistryIntramolecular forceMoleculeAmino Acid SequenceOligopeptidesProtein BindingActa Crystallographica Section C-Crystal Structure Communications
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Combinatorial chemistry of  -hairpins

2000

Combinatorial chemistry is expanding rapidly both in terms of chemistry development and application to the synthesis of compound libraries for lead discovery and optimization. Combinatorial technologies continue evolving and developing, in fact they are being used as basic research tools in different fields that include peptide/protein folding. This review examines the use of combinatorial chemistry in the design of peptides and protein domains that adopt beta-sheet conformations. In particular, the use of conformationally restricted peptide libraries has allowed the identification of linear peptides that are folded in a beta-hairpin structure in plain aqueous solutions.

chemistry.chemical_classificationPeptidomimeticChemistryOrganic ChemistryProtein domainPeptideGeneral MedicineCombinatorial chemistryCatalysisPeptide ConformationInorganic ChemistryProtein structureBasic researchDrug DiscoveryProtein foldingPhysical and Theoretical ChemistryPeptide libraryMolecular BiologyInformation SystemsMolecular Diversity
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