The stereochemistry and dynamics of natural products and biopolymers from proton relaxation spectroscopy: spin-label delineation of inner and outer protons of gramicidin S including hydrogen bonds
- 1 March 1982
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 104 (6), 1534-1537
- https://doi.org/10.1021/ja00370a014
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- The quantitation of nuclear Overhauser effect methods for total conformational analysis of peptides in solution. Application to gramicidin SBiophysical Journal, 1978
- Individual residue correlation times of peptides from proton relaxation parameters: Application to gramicidin SBiochemical and Biophysical Research Communications, 1978
- Conformation of cyclic peptides. 9. Cyclodimerization of a hexapeptide unit at high concentration. Rationalization in terms of the conformation of the cyclic dodecapeptideJournal of the American Chemical Society, 1977
- Peptide hydrogen bonding. Conformation dependence of the carbonyl carbon-13 nuclear magnetic resonance chemical shifts in ferrichrome. A study by carbon-13-{nitrogen-15} Fourier double resonance spectroscopyJournal of the American Chemical Society, 1977
- Nuclear overhauser effects and the conformation of gramicidin SBiochemical and Biophysical Research Communications, 1977