5wys

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'''Unreleased structure'''
 
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The entry 5wys is ON HOLD until Paper Publication
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==luciferase with inhibitor 3i==
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<StructureSection load='5wys' size='340' side='right' caption='[[5wys]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5wys]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5WYS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5WYS 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=7V6:5-[(3R)-3-(4-boranylphenyl)-3-oxidanyl-propyl]-2-oxidanyl-benzoic+acid'>7V6</scene></td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Photinus-luciferin_4-monooxygenase_(ATP-hydrolyzing) Photinus-luciferin 4-monooxygenase (ATP-hydrolyzing)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.13.12.7 1.13.12.7] </span></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=5wys FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5wys OCA], [http://pdbe.org/5wys PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5wys RCSB], [http://www.ebi.ac.uk/pdbsum/5wys PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5wys ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/LUCI_PHOPY LUCI_PHOPY]] Produces green light with a wavelength of 562 nm.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Chalcone refers to an aromatic ketone and an enone that constitutes the central core for various important biological compounds in drug discovery. Moreover, the firefly luciferase (Fluc) as the bioluminescent reporter has been widely used in life science research and high-throughput screening (HTS). However, Fluc might suffer from direct inhibition by HTS compounds resulting in the occurrence of "false positives." In the current research, we discovered a series of chalcone compounds as Fluc inhibitors with favorable potency both in vitro and in vivo. Moreover, our compound 3i showed remarkable systemic inhibition in transgenic mice. Both enzymatic kinetics study and cocrystal structure demonstrated that compound 3i is competitive for substrate aminoluciferin, while noncompetitive for ATP. Besides, compound 3i exhibited excellent selectivity as a promising quenching agent in a simulated dual-luciferase reporter assay. We believed that our research would contribute to improving scientists' awareness of the Fluc inhibitors, pay attention to the bias results, and even expand the utilization of bioluminescence in life science research.
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Authors: Gu, L., Su, J., Wang, F.
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Inhibiting Firefly Bioluminescence by Chalcones.,Zhang H, Su J, Lin Y, Bai H, Liu J, Chen H, Du L, Gu L, Li M Anal Chem. 2017 Jun 6;89(11):6099-6105. doi: 10.1021/acs.analchem.7b00813. Epub, 2017 May 23. PMID:28492074<ref>PMID:28492074</ref>
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Description: luciferase with inhibitor 3i
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 5wys" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Gu, L]]
[[Category: Gu, L]]
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[[Category: Wang, F]]
 
[[Category: Su, J]]
[[Category: Su, J]]
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[[Category: Wang, F]]
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[[Category: Inhibitor]]
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[[Category: Luciferase]]
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[[Category: Oxidoreductase-oxidoreductase inhibitor complex]]

Revision as of 08:30, 27 December 2017

luciferase with inhibitor 3i

5wys, resolution 3.00Å

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