Solution structures by NMR of a novel antifungal drug: Petriellin A |
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Authors: | Dang Jason Aurelio Luigi Hughes Andrew B Brownlee Robert T C |
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Affiliation: | Department of Chemistry, La Trobe University, VIC 3086, Australia. r.brownlee@latrobe.edu.au |
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Abstract: | ![]() Petriellin A is a novel cyclic depsipeptide antifungal compound consisting of nine l-configured residues, one d-phenyllactic acid (PhLac) and three unknown chiral centres: two N-methyl-threonines (MeThr1 & MeThr2) and one N-methyl-isoleucine (MeIle). NMR experiments including 2D ROESY, NOESY along with structural and energy calculations predicted that the unknown chiral centres were all l-configured, which was later verified chemically. Simulated annealing, dynamics calculations and minimisation processes showed Petriellin A to have a folded "C-shaped" structure. |
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