The Journal of Organic Chemistry · 2013 · 51 citations · 46 references
Life SciencesBiochemistryProtein FoldingStructural BiochemistryStructural BiologyAmino Acid ChemistryMacromolecular AssemblyProtein ConformationProtein StructureSecondary StructureSecondary Structure FormationAmino Acid Sequence EffectsBeta Turn ConformationBeta TurnsBeta-turn FormationChirality Of Amino AcidsHelical ConformationResidue-residue Interactions
Oligomers of the achiral amino acid Aib adopt helical conformations in which the screw-sense may be controlled by a single N-terminal residue. Using crystallographic and NMR techniques, we show that the left- or right-handed sense of helical induction arises from the nature of the β-turn at the N terminus: the tertiary amino acid L-Val induces a left-handed type II β-turn in both the solid state and in solution, while the corresponding quaternary amino acid L-α-methylvaline induces a right-handed type III β-turn.
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