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المؤلفون: Mir, Fatemeh M., Crisma, Marco, Toniolo, Claudio, Lubell, William D.

المصدر: Chemical science (Camb. 2010. Print) 10 (2019): 6908–6914. doi:10.1039/c9sc01683j
info:cnr-pdr/source/autori:Mir, Fatemeh M.; Crisma, Marco; Toniolo, Claudio; Lubell, William D./titolo:Isolated alpha-turn and incipient gamma-helix/doi:10.1039%2Fc9sc01683j/rivista:Chemical science (Camb. 2010. Print)/anno:2019/pagina_da:6908/pagina_a:6914/intervallo_pagine:6908–6914/volume:10

مصطلحات موضوعية: peptide conformation, linear oligopeptides, X-ray diffraction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=cnr_________::49b5b10032336c7a1c6d36ab3577a5ed

المؤلفون: Marco Crisma, Alessandro Moretto, Jonathan Clayden, Giulia Marafon, Matteo De Poli, Cristina Peggion, Daniela Mazzier

المصدر: Mazzier, D, Crisma, M, De Poli, M, Marafon, G, Peggion, C, Clayden, J & Moretto, A 2016, ' Helical foldamers incorporating photoswitchable residues for light-mediated modulation of conformational preference ', Journal of the American Chemical Society, vol. 138, no. 25, pp. 8007-8018 . https://doi.org/10.1021/jacs.6b04435
Journal of the American Chemical Society
138 (2016): 8007–8018. doi:10.1021/jacs.6b04435
info:cnr-pdr/source/autori:Mazzier, Daniela; Crisma, Marco; De Poli, Matteo; Marafon, Giulia; Peggion, Cristina; Clayden, Jonathan; Moretto, Alessandro/titolo:Helical Foldamers Incorporating Photoswitchable Residues for Light-Mediated Modulation of Conformational Preference/doi:10.1021%2Fjacs.6b04435/rivista:Journal of the American Chemical Society (Print)/anno:2016/pagina_da:8007/pagina_a:8018/intervallo_pagine:8007–8018/volume:138

مصطلحات موضوعية: chemistry.chemical_classification, Photoisomerization, 010405 organic chemistry, Stereochemistry, Hydrogen bond, Chemistry (all), Foldamer, Peptide, General Chemistry, 010402 general chemistry, Catalysis, Biochemistry, Colloid and Surface Chemistry, 01 natural sciences, 0104 chemical sciences, chemistry, SCREW-SENSE PREFERENCE, ACHIRAL PEPTIDE-CHAIN, ALPHA-AMINO-ACIDS, LINEAR OLIGOPEPTIDES, CRYSTAL-STRUCTURE, COMMUNICATION, OXAZOL-5(4H)-ONE, PHOTOISOMERIZATION, INFORMATION, Linker, Fumaramide

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::206a3e84a01522a1b4f9cc26c16026f8
https://doi.org/10.1021/jacs.6b04435

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المؤلفون: Giulia Marafon, Alessandro Moretto, Marco Crisma, Marta De Zotti, Ileana Menegazzo, Claudio Toniolo

المصدر: Soft matter
13 (2017): 4231–4240. doi:10.1039/c7sm00764g
info:cnr-pdr/source/autori:Marafon, Giulia; Menegazzo, Ileana; De Zotti, Marta; Crisma, Marco; Toniolo, Claudio; Moretto, Alessandro/titolo:Tuning morphological architectures generated through living supramolecular assembly of a helical foldamer end-capped with two complementary nucleobases/doi:10.1039%2Fc7sm00764g/rivista:Soft matter (Print)/anno:2017/pagina_da:4231/pagina_a:4240/intervallo_pagine:4231–4240/volume:13

مصطلحات موضوعية: Circular dichroism, Stereochemistry, Base pair, Chemistry (all), Condensed Matter Physics, Supramolecular chemistry, MOLECULAR RECOGNITION, 010402 general chemistry, 01 natural sciences, Supramolecular assembly, Nucleobase, Turn (biochemistry), chemistry.chemical_compound, LINEAR OLIGOPEPTIDES, VIBRATIONAL CIRCULAR-DICHROISM, 010405 organic chemistry, Foldamer, General Chemistry, self-assembly, 0104 chemical sciences, Thymine, X-ray diffraction, Crystallography, PEPTIDE NUCLEIC-ACIDS, chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85bb1175d505cd3e556b44f62c195901
http://hdl.handle.net/11577/3251959

المؤلفون: Padmanabhan Balaram, Alessandro Moretto, Carlos Cativiela, Carlos Alemán, Chandrasekharan Ramakrishnan, Cristina Peggion, Fernando Formaggio, Marco Crisma, Claudio Toniolo

المساهمون: Ministerio de Economía y Competitividad (España), Gobierno de Aragón, Centro de Supercomputación de Cataluña, European Commission, Universitat Politècnica de Catalunya. Departament d'Enginyeria Química, Universitat Politècnica de Catalunya. IMEM - Innovació, Modelització i Enginyeria en (BIO) Materials

المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instname
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Recercat. Dipósit de la Recerca de Catalunya
Chemistry-A European Journal 21 (2015): 13866–13877. doi:10.1002/chem.201501467
info:cnr-pdr/source/autori:Toniolo, Claudio; Crisma, Marco; Moretto, Alessandro; Peggion, Cristina; Formaggio, Fernando; Aleman, Carlos; Cativiela, Carlos; Ramakrishnan, Chandrasekharan; Balaram, Padmanabhan/titolo:Peptide delta-Turn: Literature Survey and Recent Progress/doi:10.1002%2Fchem.201501467/rivista:Chemistry-A European Journal/anno:2015/pagina_da:13866/pagina_a:13877/intervallo_pagine:13866–13877/volume:21

مصطلحات موضوعية: Protein Conformation, Peptide, LINEAR OLIGOPEPTIDES, conformational-analysis, Protein structure, Author Keywords:cis-amide, conformational analysis, peptides, statistical analysis, X-ray diffractionNUCLEAR-MAGNETIC-RESONANCE, HYDROGEN-BOND DISTANCES, CYSTEINYL-L-CYSTEINE, ALPHA-AMINO-ACIDS, CONFORMATIONAL-ANALYSIS, CRYSTAL-STRUCTURE, CYCLIC PENTAPEPTIDE, ENERGY MINIMIZATION, FOLDED CONFORMATION, Surveys and Questionnaires, Conformational energy, cysteinyl-l-cysteine, hydrogen-bond distances, Topology (chemistry), alpha-amino-acids, chemistry.chemical_classification, Chemistry, Temperature, Folding (chemistry), nuclear-magnetic-resonance, Statistical analysis, Cyclic pentapeptide, Pèptids, Stereochemistry, energy minimization, cyclic pentapeptide, Computational biology, Peptides, Cyclic, Catalysis, Turn (biochemistry), Enginyeria química [Àrees temàtiques de la UPC], cis-amide, linear oligopeptides, folded conformation, Organic Chemistry, Proteins, crystal-structure, General Chemistry, Protein Structure, Tertiary, X-ray diffraction, Conformational analysis, Literature survey, Peptides

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b0a332f1efd0a4fb112ddcd6493cd59
http://hdl.handle.net/10261/154770

المؤلفون: Gareth A. Morris, Juan A. Aguilar, Matteo De Poli, James Raftery, Marta De Zotti, Jonathan Clayden

المصدر: De Poli, M, De Zotti, M, Raftery, J, Aguilar, J A, Morris, G A & Clayden, J 2013, ' Left-handed helical preference in an achiral peptide chain is induced by an l-amino acid in an N-terminal type II β-turn ', Journal of Organic Chemistry, vol. 78, no. 6, pp. 2248-2255 . https://doi.org/10.1021/jo302705k

مصطلحات موضوعية: Models, Molecular, Aminoisobutyric Acids, Magnetic Resonance Spectroscopy, Protein Conformation, Stereochemistry, Solid-state, Peptide, Crystallography, X-Ray, Protein Structure, Secondary, SCREW-SENSE PREFERENCE, α-aminoisobutyric acid, LINEAR OLIGOPEPTIDES, STEREOCHEMICAL CRITERIA, NUCLEAR MAGNETIC-RESONANCE, SOLUTION CONFORMATIONAL-ANALYSIS, Residue (chemistry), Amino Acids, chemistry.chemical_classification, Left handed, Chemistry, Circular Dichroism, Organic Chemistry, Stereoisomerism, Valine, Amino acid, N-terminus, Oligopeptides

وصف الملف: application/octet-stream

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a46a2fbe183a70820f06c85250170551
https://doi.org/10.1021/jo302705k

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