Conformational Interconversions of the Cyclic Hexapeptide Cyclo(Pro-Gly)(3)
A cyclic hexapeptide, cyclo(Pro-Gly-Pro-Gly-Pro-Gly), has been synthesized; its solution conformations were examined by 220-MHz nuclear magnetic resonance spectroscopy. The solution structures have been deduced, and shown to vary as a function of solvent polarity. In addition, it has been found that...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1972
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC426811/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4505660/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.69.7.1825 |
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