1cu1
From Proteopedia
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{{STRUCTURE_1cu1| PDB=1cu1 | SCENE= }} | {{STRUCTURE_1cu1| PDB=1cu1 | SCENE= }} | ||
===CRYSTAL STRUCTURE OF AN ENZYME COMPLEX FROM HEPATITIS C VIRUS=== | ===CRYSTAL STRUCTURE OF AN ENZYME COMPLEX FROM HEPATITIS C VIRUS=== | ||
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{{ABSTRACT_PUBMED_10574797}} | {{ABSTRACT_PUBMED_10574797}} | ||
==About this Structure== | ==About this Structure== | ||
- | + | [[1cu1]] is a 2 chain structure of [[Helicase]] with sequence from [http://en.wikipedia.org/wiki/Hepatitis_c_virus Hepatitis c virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CU1 OCA]. | |
+ | |||
+ | ==See Also== | ||
+ | *[[Helicase|Helicase]] | ||
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:010574797</ref><ref group="xtra">PMID:016008349</ref><ref group="xtra">PMID:019119853</ref><references group="xtra"/> | |
[[Category: Hepatitis c virus]] | [[Category: Hepatitis c virus]] | ||
- | [[Category: Single protein]] | ||
[[Category: Weber, P C.]] | [[Category: Weber, P C.]] | ||
[[Category: Yao, N.]] | [[Category: Yao, N.]] | ||
- | [[Category: Bifunctional | + | [[Category: Bifunctional]] |
[[Category: Hepatitis c virus]] | [[Category: Hepatitis c virus]] | ||
- | + | [[Category: Hydrolase]] | |
- | + | [[Category: Protease-helicase]] |
Revision as of 22:41, 26 July 2012
Contents |
CRYSTAL STRUCTURE OF AN ENZYME COMPLEX FROM HEPATITIS C VIRUS
Template:ABSTRACT PUBMED 10574797
About this Structure
1cu1 is a 2 chain structure of Helicase with sequence from Hepatitis c virus. Full crystallographic information is available from OCA.
See Also
Reference
- Yao N, Reichert P, Taremi SS, Prosise WW, Weber PC. Molecular views of viral polyprotein processing revealed by the crystal structure of the hepatitis C virus bifunctional protease-helicase. Structure. 1999 Nov 15;7(11):1353-63. PMID:10574797
- Maga G, Gemma S, Fattorusso C, Locatelli GA, Butini S, Persico M, Kukreja G, Romano MP, Chiasserini L, Savini L, Novellino E, Nacci V, Spadari S, Campiani G. Specific targeting of hepatitis C virus NS3 RNA helicase. Discovery of the potent and selective competitive nucleotide-mimicking inhibitor QU663. Biochemistry. 2005 Jul 19;44(28):9637-44. PMID:16008349 doi:10.1021/bi047437u
- Thibeault D, Massariol MJ, Zhao S, Welchner E, Goudreau N, Gingras R, Llinas-Brunet M, White PW. Use of the fused NS4A peptide-NS3 protease domain to study the importance of the helicase domain for protease inhibitor binding to hepatitis C virus NS3-NS4A. Biochemistry. 2009 Feb 3;48(4):744-53. PMID:19119853 doi:10.1021/bi801931e