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- W2076421764 abstract "Two-dimensional 1H-nmr spectra of the α-mating factor [in dimethyl sulfoxide-d6 (DMSO) and in water] and several dodecapeptide analogues (in DMSO) were obtained. Homonuclear correlated spectroscopy resulted in the complete and unequivocal assignment of all backbone and side-chain resonances of the peptides. The solution conformation of the pheromones was probed using two-dimensional (2D) nuclear Overhauser effect spectroscopy (NOESY) and rotating frame nuclear Overhauer effect spectroscopy (ROESY). The 2D NOE results, and results of complementary one-dimensional experiments, suggest that a type II β-turn is assumed by the central portion of active pheromones in both DMSO and water. Inactive analogues of the α-factor do not exhibit this structural feature. Except for this one β-turn, the nmr parameters for α-factor are indicative of a conformationally flexible molecule in both solvents. This conclusion is in contrast to that of other researchers who have proposed a highly structured conformation of α-factor in aqueous solution." @default.
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- W2076421764 date "1988-03-01" @default.
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- W2076421764 title "A type II ?-turn in a flexible peptide: Proton assignment and conformational analysis of the ?-factor fromsaccharomyces cerevisiae in solution" @default.
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- W2076421764 doi "https://doi.org/10.1002/bip.360270307" @default.
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