Conformation of the cyclic pentapeptide Gly-L-Pro-L-Ser-D-Ala-L-Pro in the crystalline state and an example of rotational "isomerism" between analogs
- 1 January 1979
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 101 (1) , 181-184
- https://doi.org/10.1021/ja00495a030
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Solution conformation of cyclo-(Gly-Pro-Ser-D-Ala-Pro). Hydrogen-bonded reverse turns in cyclic pentapeptidesJournal of the American Chemical Society, 1979
- Conformational and ion binding studies of a cyclic pentapeptide. Evidence for .beta. and .gamma. turns in solutionJournal of the American Chemical Society, 1978