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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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Bibliografische gegevens
Hoofdauteurs: Deber, Charles M., Torchia, Dennis A., Wong, Simon C. K., Blout, Elkan R.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1972
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC426811/
https://ncbi.nlm.nih.gov/pubmed/4505660
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