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1bt7

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[[Image:1bt7.gif|left|200px]]
[[Image:1bt7.gif|left|200px]]
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{{Structure
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|PDB= 1bt7 |SIZE=350|CAPTION= <scene name='initialview01'>1bt7</scene>
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|SITE= <scene name='pdbsite=CTS:Catalytic+Site'>CTS</scene> and <scene name='pdbsite=ZNB:Zn+Binding+Site'>ZNB</scene>
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{{STRUCTURE_1bt7| PDB=1bt7 | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1bt7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1bt7 OCA], [http://www.ebi.ac.uk/pdbsum/1bt7 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1bt7 RCSB]</span>
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'''THE SOLUTION NMR STRUCTURE OF THE N-TERMINAL PROTEASE DOMAIN OF THE HEPATITIS C VIRUS (HCV) NS3-PROTEIN, FROM BK STRAIN, 20 STRUCTURES'''
'''THE SOLUTION NMR STRUCTURE OF THE N-TERMINAL PROTEASE DOMAIN OF THE HEPATITIS C VIRUS (HCV) NS3-PROTEIN, FROM BK STRAIN, 20 STRUCTURES'''
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[[Category: Nardi, M C.]]
[[Category: Nardi, M C.]]
[[Category: Steinkuhler, C.]]
[[Category: Steinkuhler, C.]]
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[[Category: hydrolase]]
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[[Category: Hydrolase]]
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[[Category: serine protease]]
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[[Category: Serine protease]]
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[[Category: viral non-structural protein]]
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[[Category: Viral non-structural protein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 11:55:48 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:07:46 2008''
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Revision as of 08:55, 2 May 2008

Template:STRUCTURE 1bt7

THE SOLUTION NMR STRUCTURE OF THE N-TERMINAL PROTEASE DOMAIN OF THE HEPATITIS C VIRUS (HCV) NS3-PROTEIN, FROM BK STRAIN, 20 STRUCTURES


Overview

The solution structure of the hepatitis C virus (BK strain) NS3 protein N-terminal domain (186 residues) has been solved by NMR spectroscopy. The protein is a serine protease with a chymotrypsin-type fold, and is involved in the maturation of the viral polyprotein. Despite the knowledge that its activity is enhanced by the action of a viral protein cofactor, NS4A, the mechanism of activation is not yet clear. The analysis of the folding in solution and the differences from the crystallographic structures allow the formulation of a model in which, in addition to the NS4A cofactor, the substrate plays an important role in the activation of the catalytic mechanism. A unique structural feature is the presence of a zinc-binding site exposed on the surface, subject to a slow conformational exchange process.

About this Structure

1BT7 is a Single protein structure of sequence from Hepatitis c virus. Full crystallographic information is available from OCA.

Reference

The solution structure of the N-terminal proteinase domain of the hepatitis C virus (HCV) NS3 protein provides new insights into its activation and catalytic mechanism., Barbato G, Cicero DO, Nardi MC, Steinkuhler C, Cortese R, De Francesco R, Bazzo R, J Mol Biol. 1999 Jun 4;289(2):371-84. PMID:10366511 Page seeded by OCA on Fri May 2 11:55:48 2008

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