Synthesis and conformational studies of a hybrid cyclic peptide based on cis-β-furanoid sugar amino acid (FSAA) and ornithine

Chandrasekhar, Srivari ; Saritha, Birudaraju ; Naresh, Police ; Udayakiran, Marelli ; Raji Reddy, Chada ; Jagadeesh, Bharatam (2008) Synthesis and conformational studies of a hybrid cyclic peptide based on cis-β-furanoid sugar amino acid (FSAA) and ornithine Helvetica Chimica Acta, 91 (7). pp. 1267-1276. ISSN 0018-019X

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/hlca.20...

Related URL: http://dx.doi.org/10.1002/hlca.200890138

Abstract

The conformational control of a 14-helix nucleating template, cis-β-furanoid sugar amino acid (FSAA), over a flexible δ-amino acid, ornithine is studied in a FSAA-ornithine cyclic tetrapeptide. Extensive NMR and MD studies reveal that the cyclic peptide adopts a three-dimentional bowl-shape cavity, which promotes six- and seven-membered intra- and inter-residue H-bonding, in polar and non-polar solvents, respectively.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Peptides; Cis-β-furanoid Sugar Amino Acid (FSAA); Hydrogen Bonds; Ornithine
ID Code:62362
Deposited On:22 Sep 2011 03:34
Last Modified:22 Sep 2011 03:34

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