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Alamethicine synthesis

Remarkably, nearly half of the amino acid components are L-a-amino-isobutyric acid residues (Aib), an amino acid not present in ribosome-manufactured proteins (p. 8). Peptides containing Aib-residues have been recognized to form a-helices particularly readily, an explanation of the pore forming properties of alamethicins and of similar natural and artificial polypeptides. In the natural analogs alanine or valine is found to be replaced by Aib closely related natural compounds are among others, suzukacillin, trichotoxin (mould products), and less similar, a component of bee venom, the 25-peptide mellitin. In the synthesis of peptides containing a-amino-isobutyric acid certain difficulties are encountered due to the poor steric accessibility of the amino—as well as of the carboxyl group. [Pg.210]


See other pages where Alamethicine synthesis is mentioned: [Pg.203]    [Pg.167]    [Pg.297]    [Pg.379]    [Pg.162]    [Pg.310]    [Pg.485]    [Pg.487]    [Pg.483]    [Pg.300]    [Pg.15]    [Pg.263]    [Pg.14]    [Pg.190]   
See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.1096 ]

See also in sourсe #XX -- [ Pg.1096 ]

See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.1096 ]




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Alamethicin

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