Use of natural-abundance15N-nmr spectroscopy to investigate the secondary structure of peptides: Gramicidin S
Author:
Publisher
Wiley
Subject
Organic Chemistry,Biomaterials,Biochemistry,General Medicine,Biophysics
Reference21 articles.
1. Theory and practice for studies of peptides by 15N nuclear magnetic resonance at natural abundance: gramicidin S
2. Qualitative aspects of hydrogen-deuterium exchange in the proton, carbon-13, and nitrogen-15 nuclear magnetic resonance spectra of viomycin in aqueous solution
3. Applications of natural-abundance nitrogen-15 nuclear magnetic resonance to large biochemically important molecules.
4. Nitrogen-15 nuclear magnetic resonance spectrum of alumichrome. Detection by a double resonance Fourier transform technique
5. Hydrogen-deuterium substitution and solvent effects on the nitrogen-15 nuclear magnetic resonance of gramicidin S: evaluation of secondary structure
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1. Solvent Effects on Nitrogen Chemical Shifts;Annual Reports on NMR Spectroscopy;2015
2. Design, synthesis and structural analysis of mixed α/β-peptides that adopt stable cyclic hairpin-like conformations;Tetrahedron;2012-03
3. Konformation und biologische Wirkung von cyclischen Peptiden;Angewandte Chemie;2006-01-20
4. Mixed micelle formation between gramicidin-S and a nonionic detergent: a nuclear magnetic resonance model study of peptide/detergent aggregation;European Biophysics Journal;1999-01-22
5. Heteronuclear NMR studies of cobalt corrinoids. 14. Amide proton and nitrogen-15 NMR studies of base-on cobalamins;Inorganic Chemistry;1993-05
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