Theoretical investigation of the conformations of the methylamide of N-acetyl-L-phenylalanine

Autor: Lipkind, G. M., Arkhipova, S. F., Popov, E. M.
Zdroj: Russian Chemical Bulletin; February 1970, Vol. 19 Issue: 2 p265-271, 7p
Abstrakt: 1.In the methylamide of N-acetyl-L-phenylalanine there is a substantial interrelationship of the conformational states of the basic and side chains.2.The most energetically preferential conformations of the basic and side chains in folded and unfolded forms of N-acetyl-L-phenylalanine were determined.3.The conformations of the residues phen, tyr, and try in myoglobin are close to the optimum in this molecule.
Databáze: Supplemental Index