4b6e

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[[Image:4b6e.png|left|200px]]
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==Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function==
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<StructureSection load='4b6e' size='340' side='right' caption='[[4b6e]], [[Resolution|resolution]] 2.46&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4b6e]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Hepatitis_c_virus_(isolate_bk) Hepatitis c virus (isolate bk)]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4B6E OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4B6E FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=10L:1H-INDAZOL-7-AMINE'>10L</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1a1q|1a1q]], [[1bt7|1bt7]], [[1c2p|1c2p]], [[1csj|1csj]], [[1cu1|1cu1]], [[1gx5|1gx5]], [[1gx6|1gx6]], [[1jxp|1jxp]], [[1nhu|1nhu]], [[1nhv|1nhv]], [[1ns3|1ns3]], [[1os5|1os5]], [[1quv|1quv]], [[2awz|2awz]], [[2ax0|2ax0]], [[2ax1|2ax1]], [[2brk|2brk]], [[2brl|2brl]], [[2i1r|2i1r]], [[2jc0|2jc0]], [[2jc1|2jc1]], [[2wcx|2wcx]], [[2who|2who]], [[2xwy|2xwy]], [[4a92|4a92]], [[8ohm|8ohm]], [[4b6f|4b6f]]</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4b6e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4b6e OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4b6e RCSB], [http://www.ebi.ac.uk/pdbsum/4b6e PDBsum]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Here we report a highly conserved new binding site located at the interface between the protease and helicase domains of the hepatitis C virus (HCV) NS3 protein. Using a chemical lead, identified by fragment screening and structure-guided design, we demonstrate that this site has a regulatory function on the protease activity via an allosteric mechanism. We propose that compounds binding at this allosteric site inhibit the function of the NS3 protein by stabilizing an inactive conformation and thus represent a new class of direct-acting antiviral agents.
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{{STRUCTURE_4b6e| PDB=4b6e | SCENE= }}
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Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function.,Saalau-Bethell SM, Woodhead AJ, Chessari G, Carr MG, Coyle J, Graham B, Hiscock SD, Murray CW, Pathuri P, Rich SJ, Richardson CJ, Williams PA, Jhoti H Nat Chem Biol. 2012 Sep 30. doi: 10.1038/nchembio.1081. PMID:23023261<ref>PMID:23023261</ref>
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===Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function===
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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{{ABSTRACT_PUBMED_23023261}}
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== References ==
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<references/>
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==About this Structure==
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__TOC__
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[[4b6e]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Hepatitis_c_virus_(isolate_bk) Hepatitis c virus (isolate bk)]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4B6E OCA].
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</StructureSection>
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[[Category: Carr, M G.]]
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[[Category: Carr, M G]]
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[[Category: Chessari, G.]]
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[[Category: Chessari, G]]
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[[Category: Coyle, J.]]
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[[Category: Coyle, J]]
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[[Category: Graham, B.]]
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[[Category: Graham, B]]
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[[Category: Hiscock, S D.]]
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[[Category: Hiscock, S D]]
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[[Category: Jhoti, H.]]
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[[Category: Jhoti, H]]
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[[Category: Murray, C W.]]
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[[Category: Murray, C W]]
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[[Category: Pathuri, P.]]
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[[Category: Pathuri, P]]
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[[Category: Rich, S J.]]
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[[Category: Rich, S J]]
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[[Category: Richardson, C J.]]
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[[Category: Richardson, C J]]
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[[Category: Saalau-Bethell, S M.]]
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[[Category: Saalau-Bethell, S M]]
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[[Category: Williams, P A.]]
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[[Category: Williams, P A]]
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[[Category: Woodhead, A J.]]
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[[Category: Woodhead, A J]]
[[Category: Allosteric pocket]]
[[Category: Allosteric pocket]]
[[Category: Fusion protein]]
[[Category: Fusion protein]]
[[Category: Helicase-protease]]
[[Category: Helicase-protease]]
[[Category: Hydrolase]]
[[Category: Hydrolase]]

Revision as of 14:34, 9 December 2014

Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function

4b6e, resolution 2.46Å

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