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- W2518587527 abstract "Conformational energy calculations were carried out on H-Pro-Leu-Gly-NH2, the factor that in- hibits the release of melanocyte stimulating hormone, and its biologically active analog, H-Pro-Ala-Gly-NH2. Both peptides were found to be relatively compact mole- cules that retain, however, some degree of flexibility. After structure refinement, H-Pro-Leu-Gly-NH2 possesses at least three preferred compact conformations. Two of these conformations occupy rather broad and flat energy troughs, while a third occupies a narrow and deep poten- tial energy well. This third structure, which consists of a 10-membered 3-turn closed by a (4 -- 1) hydrogen bond between the proton of the trans carboxamide of Gly and the C=O of Pro, is the one that was proposed for H-Pro- Leu-Gly-NH2 in dimethylsulfoxide and was also found by x-ray analysis." @default.
- W2518587527 created "2016-09-16" @default.
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- W2518587527 date "2016-01-01" @default.
- W2518587527 modified "2023-09-23" @default.
- W2518587527 title "Tertiary Structure of H-Pro-Leu-Gly-NH2, of Melanocyte Stimulating Hormone, Deri Energy Calculations (conformation/conformation-activity relationship/hypol" @default.
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