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An investigation into the origin of the dramatically reduced reactivity of peptide-prolyl-thioesters in native chemical ligation
Authors:Pollock Samuel B  Kent Stephen B H
Affiliation:Department of Chemistry, Institute for Biophysical Dynamics, The University of Chicago, Chicago, Illinois 60637, USA.
Abstract:The low reactivity of peptide-prolyl-thioesters in native chemical ligation is not due to steric effects at the β-carbon, but rather to the presence of a carbonyl moiety on the nitrogen atom of the proline.
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