Literatura académica sobre el tema "Sulfur Peptide"
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Artículos de revistas sobre el tema "Sulfur Peptide"
Rademann, Jörg, Ahsanullah Ahsanullah, Abbas Hassan y Farzana L. Ansari. "Integration of C-Acylation in the Solid-Phase Synthesis of Peptides and Peptidomimetics Employing Meldrum’s Acid, Phosphorus, and Sulfur Ylides". Synthesis 54, n.º 06 (12 de octubre de 2021): 1503–17. http://dx.doi.org/10.1055/a-1667-3648.
Texto completoNeugebauer, W. J. y E. Escher. "Peptide labelling with sulfur-35". International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes 39, n.º 6 (enero de 1988): 539. http://dx.doi.org/10.1016/0883-2889(88)90255-9.
Texto completoAdams, Michael W. W., James F. Holden, Angeli Lal Menon, Gerrit J. Schut, Amy M. Grunden, Chun Hou, Andrea M. Hutchins et al. "Key Role for Sulfur in Peptide Metabolism and in Regulation of Three Hydrogenases in the Hyperthermophilic ArchaeonPyrococcus furiosus". Journal of Bacteriology 183, n.º 2 (15 de enero de 2001): 716–24. http://dx.doi.org/10.1128/jb.183.2.716-724.2001.
Texto completoKaufmann, Christine y Margret Sauter. "Sulfated plant peptide hormones". Journal of Experimental Botany 70, n.º 16 (20 de junio de 2019): 4267–77. http://dx.doi.org/10.1093/jxb/erz292.
Texto completoFrancioso, Antonio, Alessia Baseggio Conrado, Carla Blarzino, Cesira Foppoli, Elita Montanari, Simone Dinarelli, Alessandra Giorgi, Luciana Mosca y Mario Fontana. "One- and Two-Electron Oxidations of β-Amyloid25-35 by Carbonate Radical Anion (CO3•−) and Peroxymonocarbonate (HCO4−): Role of Sulfur in Radical Reactions and Peptide Aggregation". Molecules 25, n.º 4 (20 de febrero de 2020): 961. http://dx.doi.org/10.3390/molecules25040961.
Texto completoPrütz, Walter A., John Butler, Edward J. Land y A. John Swallow. "Unpaired Electron Migration between Aromatic and Sulfur Peptide Units". Free Radical Research Communications 2, n.º 1-2 (enero de 1986): 69–75. http://dx.doi.org/10.3109/10715768609088056.
Texto completoKosted, Paula J., Shirley A. Gerhardt y John E. Sherwood. "Pheromone-Related Inhibitors of Ustilago hordei Mating and Tilletia tritici Teliospore Germination". Phytopathology® 92, n.º 2 (febrero de 2002): 210–16. http://dx.doi.org/10.1094/phyto.2002.92.2.210.
Texto completoAbe, Tomoko, Yoshiteru Hashimoto, Ye Zhuang, Yin Ge, Takuto Kumano y Michihiko Kobayashi. "Peptide Bond Synthesis by a Mechanism Involving an Enzymatic Reaction and a Subsequent Chemical Reaction". Journal of Biological Chemistry 291, n.º 4 (19 de noviembre de 2015): 1735–50. http://dx.doi.org/10.1074/jbc.m115.700989.
Texto completoKeegan, Brenna C., Daniel Ocampo y Jason Shearer. "pH Dependent Reversible Formation of a Binuclear Ni2 Metal-Center within a Peptide Scaffold". Inorganics 7, n.º 7 (16 de julio de 2019): 90. http://dx.doi.org/10.3390/inorganics7070090.
Texto completoZeng, Xiang, Xiaobo Zhang y Zongze Shao. "Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341T from Deep-Sea Hydrothermal Sediments". International Journal of Molecular Sciences 21, n.º 1 (6 de enero de 2020): 368. http://dx.doi.org/10.3390/ijms21010368.
Texto completoTesis sobre el tema "Sulfur Peptide"
Hippauf, Felix. "Tailoring Pore Size and Polarity for Liquid Phase Adsorption by Porous Carbons". Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-223482.
Texto completoChappell, Paul Elliott. "Structural studies of peptide binding to chicken class I MHC molecules, the CD6-CD166 interaction and enzymes involved in bacterial sulfur metabolism". Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:d4fa5a1b-530b-4a10-8184-02742cfa34f6.
Texto completoYamamoto, Masaru. "Synthesis and oxidation studies of sulfur containing inhibitors for human leukocyte elastase : (2) synthesis of cyclic peptide analogs for tissue factor pathway inhibitor (TFPI) : Part 2 synthesis and evaluation of aziridinecarboxylic acid analogs as a new family of cysteine proteinase inhibitors". Diss., Georgia Institute of Technology, 1993. http://hdl.handle.net/1853/25953.
Texto completoValer, Luca. "Histidine ligated Iron-Sulfur Proteins and Peptides". Doctoral thesis, Università degli studi di Trento, 2022. https://hdl.handle.net/11572/355641.
Texto completoMatteucci, Mizio. "Solid phase synthesis and applications of sulfur bridged peptides". Thesis, University of Southampton, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274652.
Texto completoHautier, Alexandre. "Synthesis and characterization of copper-peptide systems for oxidation catalysis". Thesis, Aix-Marseille, 2018. http://www.theses.fr/2018AIXM0758.
Texto completoCatalysis gives access to efficient transformations at a lower cost in energy and generally offers possibilities to reduce or eliminate the need for and the generation of hazardous compounds . The development of a catalyst is often inspired by Nature that performs challenging chemical transformations with high rates and high selectivity under mild conditions and aqueous media. For example, copper dependent proteins can react to oxidize a broad range of substrates. Inspired by biological systems, metallopeptides have recently emerged as reliable platforms to evolve new catalysts because they are chemically accessible, easy to handle and fine-tune.In this work we synthetized a family of bioinspired decapeptides containing His and Asp residues as metal ion coordinating amino acids. Their copper coordination properties were studied using pH potentiometry, and different spectroscopic techniques (UV-Vis, CD, EPR, NMR). The data indicates that all the peptides bind copper and form similar major copper(II) species at a pH close to neutrality where copper (II) is coordinated by the side-chains of His and Asp residues. Finally, the capabilities of these metallopeptides to perform a variety of oxidative transformations in aqueous solution at room temperature, using H2O2 as the oxidant were evaluated in parallel with that of amyloid-β peptides copper (II) complexes. This study revealed that i) the scaffold of the designed peptides had an impact on the catalytic efficiencies and enantiomeric excess and ii) the amyloid-β peptides copper (II) complexes are less active than our designed copper(II) peptide systems
Srour, Batoul. "Emerging roles for natural and artificial lipids in shaping the catalytic function, stability and oligomeric state of membrane proteins". Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAF068/document.
Texto completoThe study of biological membranes involves the examination of the different properties of its main components: as lipids and proteins. In this manuscript, the lipid-lipid interaction and the lipid-protein interaction were monitored by vibrational spectroscopy (Raman and Infrared). We have been interested in the first part in studying the structure and organization of phospholipids in the gel phase and the liquid crystalline phase using mid infrared spectroscopy. In addition, the effect of the head group composition on the hydrogen bonding behaviour of lipid mixtures was probed using far infrared spectroscopy. In the second part, the interaction of the NADH ubiquinone oxidoreductase protein and NuoL mutant (D563N) with zinc was investigated through FTIR difference spectroscopy where the conformational changes upon zinc binding were monitored. Finally, the metal-ligand vibrations of the iron- sulfur clusters in NuoB mutants (C64A G100C) at different pH were analysed using Raman spectroscopy
Rossetto, Daniele. "Emergence, survival, and selection of metal-binding peptides in the prebiotic environment". Doctoral thesis, Università degli studi di Trento, 2022. https://hdl.handle.net/11572/355344.
Texto completoImani, Zeynab. "Le rôle d’interactions N-H···S proximales dans des peptides". Thesis, université Paris-Saclay, 2021. http://www.theses.fr/2021UPASF015.
Texto completoNon-covalent interactions play a key role in chemical biology phenomena such as the stabilization of protein tertiary and quaternary structure or protein-protein and protein-substrate recognition. Among these interactions, the classical amide-type NH···O=C hydrogen bond has been thoroughly studied. The study of other types of non-covalent interactions implicating peptide backbone NH groups is much rarer. This work focused on the impact of NH···S hydrogen bonding on the conformational preferences of thioether amino acid residues and their short oligomers. A panel of capped derivatives of the following non-canonical sulfur-containing amino acids was prepared: Cys(Me) (acyclic), Attc (thietane), Atlc (thiolane), Atc (thiane). These derivatives were characterized computationally, by IR/UV double resonance laser spectroscopy in the gas phase, by IR and NMR spectroscopy in solution, and in the solid state. We demonstrated the concomitant existence of inter-residue C6ˠ NH···S hydrogen bonds and C5 NH···O=C interactions in each of these four compounds. This combined stabilizing feature was also prevalent in Attc oligomers. A different intra-residue C5ˠ NH···S hydrogen bond was characterized in short oligomers of Atlc and Atc, in some cases associated with a ˠ-turn NH···O=C interaction. The significance of NH···S bonding in the combined C5-C6ˠ structural feature of Attc was evaluated by comparison with capped derivatives of other four-membered ring amino acids: Ac4c (cyclobutane), Aatc(Me) (azetidine), Aotc (oxetane). The C5–C6ˠ feature was present in the three heterocyclic residues: comparison of their IR spectra in gas phase and in solution, aided by theoretical calculations, allowed us to identify an increasing strength of NH···X hydrogen bonding from X=O to X=S to X=N
Hadjidakis, I. "Studies relating to the ferrodoxins : The influence of synthetic peptides on the assembly of iron-sulphur clusters". Thesis, University of Exeter, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353046.
Texto completoCapítulos de libros sobre el tema "Sulfur Peptide"
Prütz, Walter A. "Free Radical Transfer Involving Sulphur Peptide Functions". En Sulfur-Centered Reactive Intermediates in Chemistry and Biology, 389–99. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5874-9_34.
Texto completoNakamura, Akira y Norikazu Ueyama. "Importance of Peptide Sequence in Electron-Transfer Reactions of Iron—Sulfur Clusters". En ACS Symposium Series, 292–301. Washington, DC: American Chemical Society, 1988. http://dx.doi.org/10.1021/bk-1988-0372.ch014.
Texto completoNakamura, Akira y Norikazu Ueyama. "Chemical Functions of Single and Double NH---S Hydrogen Bond in Iron-Sulfur Metalloproteins; Model Ligands with Cys-containing Peptide and Simple Acylaminobenzenethiolate". En Nuclear Magnetic Resonance of Paramagnetic Macromolecules, 265–79. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8573-6_12.
Texto completoSpaltenstein, A., J. Leban, E. S. Furfine y K. D. Stewart. "Synthesis of C2-symmetric HIV-protease inhibitors with sulfur-containing central units". En Peptides 1992, 933–35. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1470-7_428.
Texto completoGreiner, Georg y Peter Hermann. "Application of penicillin amidohydrolase (PAH) for sulphur and amino deprotection in peptide synthesis". En Peptides 1990, 277–78. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3034-9_117.
Texto completoGazal, Sharon, Gary Gellerman, Ofer Ziv, Olga Karpov, Pninit Litman, Moshe Bracha, Michel Afargan y Chaim Gilon. "Human Somatostatin Receptor Specificity of Backbone-Cyclic Analogs Containing Novel Sulfur Building Units". En Peptides: The Wave of the Future, 626–27. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_291.
Texto completoAbraham, E. P. y G. G. F. Newton. "Structure and Function of Some Sulphur-Containing Peptides". En Ciba Foundation Symposium - Amino Acids and Peptides with Antimetabolic Activity, 205–25. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719114.ch16.
Texto completoAppleton, Trevor G. "Diammine- and Diamineplatinum Complexes with Non-Sulfur-Containing Amino Acids and Peptides". En Cisplatin, 363–76. Zürich: Verlag Helvetica Chimica Acta, 2006. http://dx.doi.org/10.1002/9783906390420.ch14.
Texto completoLee, Sang-Hyeup, Juyoung Yoon, Kensuke Nakamura y Yoon-Sik Lee. "Preparation of β-Amino-α-mercapto Acids and Amides: Stereocontrolled Syntheses of 2′-Sulfur Analogues of the Taxol C-13 Side Chain, Both syn and and S-Acetyl-N-benzoyl-3-phenylisocysteine". En Peptides: The Wave of the Future, 50–51. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_19.
Texto completoWecker, Matt y Drew Smith. "[16] Selection for RNA: Peptide recognition through sulfur alkylation chemistry". En Methods in Enzymology, 229–37. Elsevier, 2000. http://dx.doi.org/10.1016/s0076-6879(00)18055-3.
Texto completoActas de conferencias sobre el tema "Sulfur Peptide"
Mansy, Sheref. "Prebiotic iron-sulfur peptides as precursors of enzymes". En Goldschmidt2021. France: European Association of Geochemistry, 2021. http://dx.doi.org/10.7185/gold2021.7211.
Texto completoInformes sobre el tema "Sulfur Peptide"
Cytryn, Eddie, Mark R. Liles y Omer Frenkel. Mining multidrug-resistant desert soil bacteria for biocontrol activity and biologically-active compounds. United States Department of Agriculture, enero de 2014. http://dx.doi.org/10.32747/2014.7598174.bard.
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