首页> 外文会议>American Peptide Symposium >Introduction of N-alkyl Residues in Proline-rich Peptides: Effect on SH3 Binding Affinity and Peptide Conformation
【24h】

Introduction of N-alkyl Residues in Proline-rich Peptides: Effect on SH3 Binding Affinity and Peptide Conformation

机译:富含富含脯氨酸肽中的N-烷基残基的引入:对SH3结合亲和力和肽构象的影响

获取原文

摘要

Proline-rich peptides are involved in the interactions with SH3 domains. The analysis of these interactions emphasizes that the peculiar role of the proline residue can be explained by its direct involvement in the domain recognition, rather than by the increased structural stability of the peptide-ligand. In particular, the N-alkyl substitution of the proline residue is to be regarded as the main responsible for the ligand specificity, and the removal of this moiety has a deleterious effect on the binding affinity mainly because of the loss of van der Waals contact, rather than the destabilization of the PPII helix conformation [1].
机译:富含脯氨酸的肽参与与SH3结构域的相互作用。对这些相互作用的分析强调脯氨酸残基的特殊作用可以通过其直接参与域识别,而不是通过肽 - 配体的增加的结构稳定性来解释。特别地,脯氨酸残基的N-烷基取代将被视为负责配体特异性的主要负责,并且该部分的除去对结合亲和力具有有害影响,主要是由于van der Waals接触的损失,而不是PPII螺旋​​构象的稳定化[1]。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号