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Nuclear magnetic resonance studies on the structure of the tetrapeptide tuftsin L-threonyl-L-lysyl-L-prolyl-L-arginine, and its pentapeptide analog L-threonyl-L-lysyl-L-prolyl-L-prolyl-L-arginine

✍ Scribed by Blumenstein, Michael; Layne, Porter P.; Najjar, Victor A.

Book ID: 127263718
Publisher: American Chemical Society
Year: 1979
Tongue: English
Weight: 822 KB
Volume: 18
Category: Article
ISSN: 0006-2960
DOI: 10.1021/bi00590a032

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## Abstract The ^13^C chemical shifts and spin‐lattice relaxation times are reported for __cyclo__(L‐Pro‐L‐Leu) and __cyclo__(L‐Pro‐D‐Leu). The chemical shifts of the D and L leucyl residues in the cyclic peptides differ from each other by 1.8 and 3.6 parts per million for the α and β carbons, resp