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Updated: Jul 14, 2026

Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy
Published on: September 17, 2017
Solid-state NMR and rigid body molecular dynamics to determine domain orientations of monomeric phospholamban
Alessandro Mascioni1, Christine Karim, Jamillah Zamoon
1Department of Chemistry, University of Minnesota, Minneapolis 55455, USA.
Abstract:
Solid-state NMR spectroscopy, in conjunction with rigid body molecular dynamics calculations, shows that monomeric phospholamban in lipid bilayers has two distinct helical domains, with an interhelical angle within 60-100 degrees, ruling out the possibility of a continuous alpha-helical structure for this protein.
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