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1jxp

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(New page: 200px<br /><applet load="1jxp" size="450" color="white" frame="true" align="right" spinBox="true" caption="1jxp, resolution 2.2&Aring;" /> '''BK STRAIN HEPATITIS C...)
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'''BK STRAIN HEPATITIS C VIRUS (HCV) NS3-NS4A'''<br />
'''BK STRAIN HEPATITIS C VIRUS (HCV) NS3-NS4A'''<br />
==Overview==
==Overview==
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The crystal structure of the NS3 protease of the hepatitis C virus (BK, strain) has been determined in the space group P6(3)22 to a resolution of, 2.2 A. This protease is bound with a 14-mer peptide representing the, central region of the NS4A protein. There are two molecules of the, NS3(1-180)-NS4A(21'-34') complex per asymmetric unit. Each displays a, familiar chymotrypsin-like fold that includes two beta-barrel domains and, four short alpha-helices. The catalytic triad (Ser-139, His-57, and, Asp-81) is located in the crevice between the beta-barrel domains. The, NS4A peptide forms an almost completely enclosed peptide surface, association with the protease. In contrast to the reported H strain, complex of NS3 protease-NS4A peptide in a trigonal crystal form (Kim JL et, al., 1996, Cell 87:343-355), the N-terminus of the NS3 protease is, well-ordered in both molecules in the asymmetric unit of our hexagonal, crystal form. The folding of the N-terminal region of the NS3 protease is, due to the formation of a three-helix bundle as a result of crystal, packing. When compared with the unbound structure (Love RA et al., 1996, Cell 87:331-342), the binding of the NS4A peptide leads to the ordering of, the N-terminal 28 residues of the NS3 protease into a beta-strand and an, alpha-helix and also causes local rearrangements important for a, catalytically favorable conformation at the active site. Our analysis, provides experimental support for the proposal that binding of an, NS4A-mimicking peptide, which increases catalytic rates, is necessary but, not sufficient for formation of a well-ordered, compact and, hence, highly, active protease molecule.
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The crystal structure of the NS3 protease of the hepatitis C virus (BK strain) has been determined in the space group P6(3)22 to a resolution of 2.2 A. This protease is bound with a 14-mer peptide representing the central region of the NS4A protein. There are two molecules of the NS3(1-180)-NS4A(21'-34') complex per asymmetric unit. Each displays a familiar chymotrypsin-like fold that includes two beta-barrel domains and four short alpha-helices. The catalytic triad (Ser-139, His-57, and Asp-81) is located in the crevice between the beta-barrel domains. The NS4A peptide forms an almost completely enclosed peptide surface association with the protease. In contrast to the reported H strain complex of NS3 protease-NS4A peptide in a trigonal crystal form (Kim JL et al., 1996, Cell 87:343-355), the N-terminus of the NS3 protease is well-ordered in both molecules in the asymmetric unit of our hexagonal crystal form. The folding of the N-terminal region of the NS3 protease is due to the formation of a three-helix bundle as a result of crystal packing. When compared with the unbound structure (Love RA et al., 1996, Cell 87:331-342), the binding of the NS4A peptide leads to the ordering of the N-terminal 28 residues of the NS3 protease into a beta-strand and an alpha-helix and also causes local rearrangements important for a catalytically favorable conformation at the active site. Our analysis provides experimental support for the proposal that binding of an NS4A-mimicking peptide, which increases catalytic rates, is necessary but not sufficient for formation of a well-ordered, compact and, hence, highly active protease molecule.
==About this Structure==
==About this Structure==
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1JXP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Hepatitis_c_virus_genotype_1b_(isolate_bk) Hepatitis c virus genotype 1b (isolate bk)] with ZN as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1JXP OCA].
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1JXP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Hepatitis_c_virus_genotype_1b_(isolate_bk) Hepatitis c virus genotype 1b (isolate bk)] with <scene name='pdbligand=ZN:'>ZN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JXP OCA].
==Reference==
==Reference==
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[[Category: serine proteinase]]
[[Category: serine proteinase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 18:40:23 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:27:55 2008''

Revision as of 11:27, 21 February 2008


1jxp, resolution 2.2Å

Drag the structure with the mouse to rotate

BK STRAIN HEPATITIS C VIRUS (HCV) NS3-NS4A

Overview

The crystal structure of the NS3 protease of the hepatitis C virus (BK strain) has been determined in the space group P6(3)22 to a resolution of 2.2 A. This protease is bound with a 14-mer peptide representing the central region of the NS4A protein. There are two molecules of the NS3(1-180)-NS4A(21'-34') complex per asymmetric unit. Each displays a familiar chymotrypsin-like fold that includes two beta-barrel domains and four short alpha-helices. The catalytic triad (Ser-139, His-57, and Asp-81) is located in the crevice between the beta-barrel domains. The NS4A peptide forms an almost completely enclosed peptide surface association with the protease. In contrast to the reported H strain complex of NS3 protease-NS4A peptide in a trigonal crystal form (Kim JL et al., 1996, Cell 87:343-355), the N-terminus of the NS3 protease is well-ordered in both molecules in the asymmetric unit of our hexagonal crystal form. The folding of the N-terminal region of the NS3 protease is due to the formation of a three-helix bundle as a result of crystal packing. When compared with the unbound structure (Love RA et al., 1996, Cell 87:331-342), the binding of the NS4A peptide leads to the ordering of the N-terminal 28 residues of the NS3 protease into a beta-strand and an alpha-helix and also causes local rearrangements important for a catalytically favorable conformation at the active site. Our analysis provides experimental support for the proposal that binding of an NS4A-mimicking peptide, which increases catalytic rates, is necessary but not sufficient for formation of a well-ordered, compact and, hence, highly active protease molecule.

About this Structure

1JXP is a Protein complex structure of sequences from Hepatitis c virus genotype 1b (isolate bk) with as ligand. Full crystallographic information is available from OCA.

Reference

Complex of NS3 protease and NS4A peptide of BK strain hepatitis C virus: a 2.2 A resolution structure in a hexagonal crystal form., Yan Y, Li Y, Munshi S, Sardana V, Cole JL, Sardana M, Steinkuehler C, Tomei L, De Francesco R, Kuo LC, Chen Z, Protein Sci. 1998 Apr;7(4):837-47. PMID:9568891

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