1990/10/31 by Horst Kessler, Matthias Köck, Thomas Wein +1 · 8 citations
Biochemistry, Genetics and Molecular Biology · Medicine · Materials Science · #DNA and Nucleic Acid Chemistry #Metal complexes synthesis and properties #Enzyme Structure and Function
paper · doi:10.1002/hlca.19900730703
Abstract New investigations of cyclosporin A in CDCl 3 have been performed to obtain additional and more accurate distance restraints than utilized in our previous studies of cyclosporin A. Build‐up rates at 600 MHz using 6 different mixing times at low temperatures (252.5 K) were determined and transformed into distances using the two‐spin approximation. With the new distance restraints in the MD simulations using the GROMOS package, we can unambiguously conclude the presence of a βII′‐turn. The new structure resembles the X‐ray structure more than the structure previously determined, especially regarding the orientation of the MeBmt side chain. In the new structure and in the solid state, the side chain is folded over the backbone (although there are substantial differences in the χ 1 torsion), in contrast to the old structure, where the side chain is extended away from the backbone.