Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/73592
Type: Artigo de periódico
Title: The lack of intramolecular hydrogen bonding and the side chain effect in alanine conformers
Author: Cormanich, RA
Ducati, LC
Rittner, R
Abstract: Although amino acids are considered one of the most important classes of compounds found in Nature, the literature has few reports that have been made to understand the intramolecular interactions that govern their conformational energies and geometries. Actually, it has been arbitrarily assigned that possible intramolecular hydrogen bonding is the responsible force that dictates amino acid conformational preferences. In this paper, calculations at B3LYP/aug-cc-pVDZ level of theory within the NBO and QTAIM frameworks have shown that hyperconjugation and steric effects interplay, not H-bonding, are the intramolecular interactions that govern alanine conformational preferences. It is also shown that the steric interactions between the alanine methyl group side chain and its main chain influences its energies and geometries. (C) 2012 Elsevier B.V. All rights reserved.
Subject: Conformational analysis
Amino acids
Alanine
Hydrogen bonding
Intramolecular interactions
Country: Holanda
Editor: Elsevier Science Bv
Rights: fechado
Identifier DOI: 10.1016/j.molstruc.2012.01.047
Date Issue: 2012
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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