Cyclopropane analogue of valine: influence of side chain orientation on peptide folding
作者:Ana I. Jiménez、Michel Marraud、Carlos Cativiela
DOI:10.1016/s0040-4039(03)00514-8
日期:2003.4
The cyclopropane analogue of valine (1-amino-2,2-dimethylcyclopropanecarboxylic acid, c3Val) has been synthesised and incorporated into the model peptides tBuCO-l-Pro-l-c3Val-NHiPr and tBuCO-l-Pro-d-c3Val-NHiPr. In the solid state, both dipeptides accommodate a type II β-turn stabilised by an NHiPr to tBuCO hydrogen bond. Remarkably, the peptide incorporating l-c3Val also exhibits a distorted γ-turn
已合成缬氨酸的环丙烷类似物(1-氨基-2,2-二甲基环丙烷羧酸,c 3 Val)并将其掺入模型肽t BuCO-1-Pro-lc 3 Val-NH i Pr和t BuCO-1- Pro-dc 3 Val-NH i Pr。在固态下,两个二肽都具有通过NH i Pr到t BuCO氢键稳定的II型β-转角。引人注目的是,掺有lc 3 Val的肽在环丙烷残基周围也表现出扭曲的γ转角,Pro-CO和NH i Pr分子内氢键。