Crystallographic studies on the binding modes of P2-P3 butanediamide renin inhibitors

Abstract

The binding modes of three peptidomimetic P2-P3 butanediamide renin inhibitors have been determined by x-ray crystallography. The inhibitors are bound with their backbones in an extended conformation, and their side chains occupying the S5 to S1' pockets. A (2-amino-4-thiazolyl)methyl side chain at the P2 position shows stronger hydrogen-bonding and van der Waals interactions with renin than the His side chain, which is present in the natural substrate. The ACHPA-γ-lactam transition state analog has similar interactions with renin as the dihydroxyethylene transition state analog.