15N NMR spectroscopy 31†—preliminary study on the insulin-a chain (bunte salt form)
暂无分享,去创建一个
[1] H. Kricheldorf. 15N NMR spectroscopy. 30—structure/shift relationships of oligopeptides and copolypeptides, including gramicidin S , 1981 .
[2] W. Hull,et al. Use of natural‐abundance 15N‐nmr spectroscopy to investigate the secondary structure of peptides: Gramicidin S , 1980 .
[3] W. Hull,et al. 15N NMR spectroscopy. 23—Shift effects of protecting groups in oligopeptides of glycine and alanine , 1980 .
[4] W. Hull,et al. 15N NMR spectroscopy 14. Neighboring residue effects in glycine-containing polypeptides† , 1979 .
[5] W. Hull,et al. Qualitative aspects of hydrogen-deuterium exchange in the 1H, 13C, and 15N nuclear magnetic resonance spectra of viomycin in aqueous solution. , 1978, Biochemistry.
[6] D. Urry,et al. Hydrogen-deuterium substitution and solvent effects on the nitrogen-15 nuclear magnetic resonance of gramicidin S: evaluation of secondary structure. , 1978, Biochemistry.
[7] R. B. Moon,et al. Applications of natural-abundance nitrogen-15 nuclear magnetic resonance to large biochemically important molecules. , 1975, Proceedings of the National Academy of Sciences of the United States of America.
[8] G. Hawkes,et al. Theory and practice for studies of peptides by 15N nuclear magnetic resonance at natural abundance: gramicidin S , 1975, Nature.
[9] H. Kricheldorf. 15N NMR spectroscopy. 19—spectroscopic characterization of cyclodipeptides (2,5‐dioxopiperazines) , 1980 .
[10] W. Hull,et al. 15N NMR Spectroscopy. 21. Copolymerization of Glycine N-Carboxyanhydride with γ-Methyl Glutamate N-Carboxyanhydride, S-Benzylcysteine N-Carboxyanhydride, Leucine N-Carboxyanhydride, and Valine N-Carboxyanhydride , 1980 .
[11] John D. Roberts,et al. Conformational analysis by nuclear magnetic resonance spectroscopy: Nitrogen-15 NMR of a cyclic pentapeptide , 1979 .
[12] H. Gattner,et al. [A21-Asparaginimide] insulin. Saponification of insulin hexamethyl ester, I. , 1977, Hoppe-Seyler´s Zeitschrift für physiologische Chemie.