European Biophysics Journal

, Volume 36, Issue 3, pp 213–224 | Cite as

A molecular dynamics study of Cyclophilin A free and in complex with the Ala-Pro dipeptide

Original Paper

Abstract

Six different molecular dynamics simulations of Cyclophilin A, three with the protein free in water and three with the Ala-Pro dipeptide bound to the protein, have been performed, and analysed with respect to structure and hydration of the active site. The water structure in the binding pocket of the free Cyclophilin A was found to mimic the experimentally obtained binding cis conformation of the dipeptide. Cyclophilin A is a peptidyl–prolyl cis–trans isomerase (PPIase), but the mechanism of the cis/trans isomerization is not exactly clear. This study was performed to understand better the binding between dipeptide and Cyclophilin A, but also two previously proposed isomerization mechanisms are discussed.

Supplementary material

249_2006_121_MOESM1_ESM.pdf (160 kb)
Supplementary data (PDF 161 kb)

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Copyright information

© EBSA 2007

Authors and Affiliations

  1. 1.Department of Biosciences and NutritionKarolinska InstitutetHuddingeSweden
  2. 2.School of Biotechnology, The Department of Theoretical ChemistryRoyal Institute of Technology, AlbaNova University CenterStockholmSweden

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