This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


1w3c

From Proteopedia

Revision as of 14:18, 30 October 2007 by OCA (Talk | contribs)
Jump to: navigation, search

1w3c, resolution 2.3Å

Drag the structure with the mouse to rotate

CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS3 PROTEASE IN COMPLEX WITH A PEPTIDOMIMETIC INHIBITOR

Overview

The design of a series of peptidomimetic inhibitors of the hepatitis C, virus NS3 protease is described. These inhibitors feature an, indoline-2-carboxamide as a novel heterocyclic replacement for the P3, amino acid residue and N-terminal capping group of tripeptide based, inhibitors. The crystal structure of the ternary NS3/NS4A/inhibitor, complex for the most active molecule in this series highlights its, suitability as an N-terminal capping group of a dipeptide inhibitor of the, NS3 protease.

About this Structure

1W3C is a [Single protein] structure of sequence from [Viruses] with DN1 and DN2 as [ligands]. Structure known Active Site: AC1. Full crystallographic information is available from [OCA].

Reference

The design and enzyme-bound crystal structure of indoline based peptidomimetic inhibitors of hepatitis C virus NS3 protease., Ontoria JM, Di Marco S, Conte I, Di Francesco ME, Gardelli C, Koch U, Matassa VG, Poma M, Steinkuhler C, Volpari C, Harper S, J Med Chem. 2004 Dec 16;47(26):6443-6. PMID:15588076

Page seeded by OCA on Tue Oct 30 16:23:41 2007

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools