Modelling and study of cyclosporin A and related compounds in complexes with a Trypanosoma cruzi cyclophilin.
@article{Carraro2007ModellingAS, title={Modelling and study of cyclosporin A and related compounds in complexes with a Trypanosoma cruzi cyclophilin.}, author={R. Carraro and J. Bua and A. Ru{\'i}z and M. Paulino}, journal={Journal of molecular graphics & modelling}, year={2007}, volume={26 1}, pages={ 48-61 } }
Cyclophilins (CyPs) are enzymes involved in protein folding, catalyzing the isomerisation of peptidyl prolyl bonds in proteins and peptides between the cis- and trans-conformations. They are also the major cellular target for the immunosuppressive drug Cyclosporin A (CsA). In Trypanosoma cruzi, the most abundantly expressed CyP is an isoform of 19 kDa, TcCyP19, in which the enzymatic activity is inhibited by CsA. Among a reported set of CsA analogues, two non-immunosuppressive compounds, H-7-94… CONTINUE READING
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