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• W2122331034 startingPage "135" @default.
• W2122331034 abstract "The conformations of the phytotoxic cyclic tetrapeptide tentoxin [cyclo-(L-MeAla1-L-Leu2-MePhe[(Z)Δ]3-Gly4 )] have been studied in aqueous solution by two-dimensional proton nmr at various temperatures. Contrary to what is observed in chloroform, tentoxin exhibits multiple exchanging conformations in water. Aggregation phenomena were also observed. Four conformations with different proportions (51, 37, 8, and 4%) were observed at −5°C. Models were constructed from nmr parameters and restrained molecular dynamics simulations. All the models exhibit cis-trans-cis-trans conformation of the amide bond sequence. The conversion from one form to another is accomplished by a conformational peptide flip consisting of a 180° rotation of a nonmethylated peptide bond. © 1995 John Wiley & Sons, Inc." @default.
• W2122331034 created "2016-06-24" @default.
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• W2122331034 date "1995-08-01" @default.
• W2122331034 modified "2023-09-25" @default.
• W2122331034 title "Multiple interconverting conformers of the cyclic tetrapeptide tentoxin, [<i>cyclo</i>-(<scp>L</scp>-MeAla¹-<scp>L</scp>-Leu²-MePhe[(Z)Δ]³-Gly⁴)], as seen by two-dimensional¹H-nmr spectroscopy" @default.
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• W2122331034 doi "https://doi.org/10.1002/bip.360360204" @default.
• W2122331034 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/7492742" @default.
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