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Structure of cyclic peptides: the crystal and solution conformation of cyclo(Phe-Phe-Aib-Leu-Pro)

✍ Scribed by ZANOTTI, GIANCARLO ;SAVIANO, MICHELE ;SAVIANO, GABRIELLA ;TANCREDI, TEODORICO ;ROSSI, FILOMENA ;PEDONE, CARLO ;BENEDETTI, ETTORE


Book ID
110893671
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
679 KB
Volume
51
Category
Article
ISSN
1397-002X

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Synthesis and conformation of the cyclic
✍ Shunsaku Kimura; Yukio Imanishi πŸ“‚ Article πŸ“… 1983 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 779 KB

Cyclic octapeptides, cyclo(X-Pro)4, where X represents Phe, Leu, or Lys(Z), were synthesized and their conformations investigated. A Cz-symmetric conformer containing two cis peptide bonds was found in all of these cyclic octapeptides. The numbers of available conformations due to the cis-trans isom

Conformations of cyclic peptides V. A pr
✍ Kenneth D. Kopple πŸ“‚ Article πŸ“… 1971 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 697 KB

## Abstract The 220 MHz proton magnetic resonance spectrum of the cyclic heptapeptide evoli‐dine, __cyclo__‐Ser‐Phe‐Leu‐Pro‐Val‐Asn‐Leu, has been analyzed. From the temperature dependence of chemical shift of the peptide protons in dimethyl sulfoxide, it is concluded that the peptide protons of the