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1w3c

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==Overview==
==Overview==
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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.
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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==
==About this Structure==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Viruses]]
[[Category: Viruses]]
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[[Category: Marco, S.Di.]]
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[[Category: Marco, S Di.]]
[[Category: Volpari, C.]]
[[Category: Volpari, C.]]
[[Category: DN1]]
[[Category: DN1]]
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[[Category: serine protease]]
[[Category: serine protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:18:48 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:40:02 2008''

Revision as of 13:40, 21 February 2008


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 and as ligands. Known structural/functional Site: . 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 Thu Feb 21 15:40:02 2008

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