A comprehensive conformational analysis of tryptophan, its ionic and dimeric forms

Purushotham, Uppula ; Sastry, G. Narahari (2014) A comprehensive conformational analysis of tryptophan, its ionic and dimeric forms Journal of Computational Chemistry, 35 (8). pp. 595-610. ISSN 0192-8651

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/jcc.234...

Related URL: http://dx.doi.org/10.1002/jcc.23482

Abstract

Tryptophan is an essential amino acid, and understanding the conformational preferences of monomer and dimer is a subject of outstanding relevance in biological systems. An exhaustive first principles investigation of tryptophan (W) and its ionized counterparts cations (WC), anions (WA), and zwitterions (WZ) has been carried out. A comprehensive and systematic study of tryptophan dimer (WD) conformations resulted in about 62 distinct minima on the potential energy surface. The hydrogen bonds and a variety of noncovalent interactions such as OH-π, NH-π, CH-π, CH-O, and π-π interactions stabilized different forms of tryptophan and its dimers. Over all in monomeric conformers which have NH-O, hydrogen bonds showed higher stability than other conformers. A cursory analysis reveal that the most stable dimers stabilized by hydrogen bonding interactions while the less stable dimers showed aromatic side chain interactions. Protein Data Bank analysis of tryptophan dimers reveals that at a larger distance greater than 5 Å, T-shaped orientations (CH-π interactions) are more prevalent, while stacked orientations (π-π interactions) are predominant at a smaller distance.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons, Inc.
Keywords:Tryptophan Dimer; Conformational Analysis; PDB Analysis; Noncovalent Interactions; DFT
ID Code:108627
Deposited On:27 Jul 2017 12:42
Last Modified:27 Jul 2017 12:42

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