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Peptide models XXIV: An ab initio study on N-formyl-L-prolinamide with trans peptide bond. The existence or non-existence of αL and ϵL conformations

✍ Scribed by Hector A. Baldoni; Ana M. Rodriguez; Miguel A. Zamora; Graciela N. Zamarbide; Ricardo D. Enriz; Ödön Farkas; Pal Csàszàr; Ladislaus L. Torday; Carlos P. Sosa; Imre Jàkli; Andràs Perzel; Julius Gy. Papp; Miklos Hollosi; Imre G. Csizmadia

Book ID
114143461
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
555 KB
Volume
465
Category
Article
ISSN
0166-1280

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Peptide models XXXI. Conformational prop
Peptide models XXXI. Conformational properties of hydrophobic residues shaping the core of proteins. An ab initio study of N-formyl-L-valinamide and N-formyl-L-phenylalaninamide
✍ Péter Hudáky; Imre Jákli; Attila G. Császár; András Perczel 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 349 KB

## Abstract Employing introductory (3‐21G RHF) and medium‐size (6‐311++G\*\* B3LYP) __ab initio__ calculations, complete conformational libraries, containing as many as 27 conformers, have been determined for diamide model systems incorporating the amino acids valine (Val) and phenylalanine (Phe).