4xwk

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==P-glycoprotein co-crystallized with BDE-100==
==P-glycoprotein co-crystallized with BDE-100==
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<StructureSection load='4xwk' size='340' side='right' caption='[[4xwk]], [[Resolution|resolution]] 3.50&Aring;' scene=''>
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<StructureSection load='4xwk' size='340' side='right'caption='[[4xwk]], [[Resolution|resolution]] 3.50&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[4xwk]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4XWK OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4XWK FirstGlance]. <br>
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<table><tr><td colspan='2'>[[4xwk]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4XWK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4XWK 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=4C8:2,4-DIBROMOPHENYL+2,4,6-TRIBROMOPHENYL+ETHER'>4C8</scene></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.5&#8491;</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/Xenobiotic-transporting_ATPase Xenobiotic-transporting ATPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.3.44 3.6.3.44] </span></td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=4C8:2,4-DIBROMOPHENYL+2,4,6-TRIBROMOPHENYL+ETHER'>4C8</scene></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=4xwk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4xwk OCA], [http://pdbe.org/4xwk PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4xwk RCSB], [http://www.ebi.ac.uk/pdbsum/4xwk PDBsum]</span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4xwk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4xwk OCA], [https://pdbe.org/4xwk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4xwk RCSB], [https://www.ebi.ac.uk/pdbsum/4xwk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4xwk ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
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[[http://www.uniprot.org/uniprot/MDR1A_MOUSE MDR1A_MOUSE]] Energy-dependent efflux pump responsible for decreased drug accumulation in multidrug-resistant cells.<ref>PMID:19325113</ref>
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[https://www.uniprot.org/uniprot/MDR1A_MOUSE MDR1A_MOUSE] Energy-dependent efflux pump responsible for decreased drug accumulation in multidrug-resistant cells.<ref>PMID:19325113</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The world's oceans are a global reservoir of persistent organic pollutants to which humans and other animals are exposed. Although it is well known that these pollutants are potentially hazardous to human and environmental health, their impacts remain incompletely understood. We examined how persistent organic pollutants interact with the drug efflux transporter P-glycoprotein (P-gp), an evolutionarily conserved defense protein that is essential for protection against environmental toxicants. We identified specific congeners of organochlorine pesticides, polychlorinated biphenyls, and polybrominated diphenyl ethers that inhibit mouse and human P-gp, and determined their environmental levels in yellowfin tuna from the Gulf of Mexico. In addition, we solved the cocrystal structure of P-gp bound to one of these inhibitory pollutants, PBDE (polybrominated diphenyl ether)-100, providing the first view of pollutant binding to a drug transporter. The results demonstrate the potential for specific binding and inhibition of mammalian P-gp by ubiquitous congeners of persistent organic pollutants present in fish and other foods, and argue for further consideration of transporter inhibition in the assessment of the risk of exposure to these chemicals.
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Global marine pollutants inhibit P-glycoprotein: Environmental levels, inhibitory effects, and cocrystal structure.,Nicklisch SC, Rees SD, McGrath AP, Gokirmak T, Bonito LT, Vermeer LM, Cregger C, Loewen G, Sandin S, Chang G, Hamdoun A Sci Adv. 2016 Apr 15;2(4):e1600001. doi: 10.1126/sciadv.1600001. eCollection 2016, Apr. PMID:27152359<ref>PMID:27152359</ref>
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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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<div class="pdbe-citations 4xwk" style="background-color:#fffaf0;"></div>
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Xenobiotic-transporting ATPase]]
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[[Category: Large Structures]]
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[[Category: Chang, G]]
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[[Category: Mus musculus]]
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[[Category: McGrath, A P]]
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[[Category: Chang G]]
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[[Category: Rees, S D]]
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[[Category: McGrath AP]]
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[[Category: Hydrolase]]
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[[Category: Rees SD]]
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[[Category: Membrane protein]]
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[[Category: Transporter]]
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Current revision

P-glycoprotein co-crystallized with BDE-100

PDB ID 4xwk

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