Synthesis and Properties of Gramicidin S Analogs Containing d-Phe–l-Pro–d-Val or l-Phe–l-Pro–d-Val Sequences in Place of d-Phe–l-Pro–l-Val Sequence in the β-Turn Part of the Antibiotic
- 1 February 1985
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 58 (2) , 531-535
- https://doi.org/10.1246/bcsj.58.531
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- Studies on the β-Turn of Peptides. VII. Syntheses and Antibiotic Activities of Gramicidin S Analogs with l-Pro-l-Asn or l-Pro-d-Ala Sequence at the β-Turn PartBulletin of the Chemical Society of Japan, 1983
- Comparison of conformation and antimicrobial activity of synthetic analogs of gramicidin S: Stereochemical consideration of the role of D‐phenylalanine in the antibioticBiopolymers, 1978
- Appendix 2—Possible molecular models for gramicidin S and their relationship to present ideas of protein structureBiochemical Journal, 1957