2p59

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Image:2p59.jpg

2p59, resolution 2.900Å

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Crystal Structure of Hepatitis C Virus NS3.4A protease

Overview

Reversible tetrapeptide-based compounds have been shown to effectively, inhibit the hepatitis C virus NS3.4A protease. Inhibition of viral, replicon RNA production in Huh-7 cells has also been demonstrated. We show, herein that the inclusion of hydrogen bond donors on the P4 capping group, of tetrapeptide-based inhibitors result in increased binding potency to, the NS3.4A protease. The capping groups also impart significant effects on, the pharmacokinetic profile of these inhibitors.

About this Structure

2P59 is a Single protein structure of sequence from Gb virus c with as ligand. Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

Inhibitors of hepatitis C virus NS3.4A protease. Effect of P4 capping groups on inhibitory potency and pharmacokinetics., Perni RB, Chandorkar G, Cottrell KM, Gates CA, Lin C, Lin K, Luong YP, Maxwell JP, Murcko MA, Pitlik J, Rao G, Schairer WC, Van Drie J, Wei Y, Bioorg Med Chem Lett. 2007 Jun 15;17(12):3406-11. Epub 2007 Apr 3. PMID:17482818

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