CONFORMATIONS OF CYCLIC OCTAPEPTIDES. 5. CRYSTAL STRUCTURE OF CYCLO(Cys-Gly-Pro-Phe)2 AND ROTATING FRAME RELAXATION (T1 rho ) NMR STUDIES OF INTERNAL MOBILITY IN CYCLIC OCTAPEPTIDES.

DOI: 10.1021/ja00221a012

Source and publish data:

Journal of the American Chemical Society p. 4168 - 4176 (1988)

Update date:2022-07-30

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Authors:

Kopple Kopple

Wang Wang

Cheng Cheng

Bhandary

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Article abstract of DOI:10.1021/ja00221a012

The disulfide-bridged cyclic octapeptide cyclo(Cys-Gly-Pro-Phe)//2 (I) was synthesized, a crystal structure was determined, and studies of proton spin-lattice relaxation in the rotating frame were made to probe its internal mobility in solution. Cyclo(Cys

Full text of DOI:10.1021/ja00221a012

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