Relationship between the conformation of the cyclopeptides isolated from the fungus Amanita phalloides (Vaill. Ex Fr.) Secr. and its toxicity

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The electronic structures and conformational studies of the cyclopeptides, O-methyl-α-amanitin, phalloidin and antamanide, were obtained from molecular parameters on the basis of semiempiric and ab initio methods.

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Detalles Bibliográficos
Autores principales:	Battista, M.E., Vitale, A.A., Pomilio, A.B.
Formato:	Artículo publishedVersion
Publicado:	2000
Materias:	cyclopeptide fungal protein toxic substance ab initio calculation Amanita phalloides carbon nuclear magnetic resonance conference paper empiricism hydrogen bond molecular interaction nonhuman protein conformation protein isolation protein structure stereochemistry structure activity relation structure analysis toxicity
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p489_Battista https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14203049_v5_n3_p489_Battista_oai
Aporte de:	Repositorio Digital de la Universidad de Buenos Aires (UBA) de Universidad de Buenos Aires

Descripción
Sumario:	The electronic structures and conformational studies of the cyclopeptides, O-methyl-α-amanitin, phalloidin and antamanide, were obtained from molecular parameters on the basis of semiempiric and ab initio methods.