5ng5

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m (Protected "5ng5" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5ng5 is ON HOLD
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==multi-drug efflux; membrane transport; RND superfamily; Drug resistance==
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<StructureSection load='5ng5' size='340' side='right' caption='[[5ng5]], [[Resolution|resolution]] 6.50&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5ng5]] is a 15 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5NG5 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5NG5 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=5QF:6-[2-(3,4-DIMETHOXYPHENYL)ETHYLSULFANYL]-8-[4-(2-METHOXYETHYL)PIPERAZIN-1-YL]-3,3-DIMETHYL-1,4-DIHYDROPYRANO[3,4-C]PYRIDINE-5-CARBONITRILE'>5QF</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=5ng5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ng5 OCA], [http://pdbe.org/5ng5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5ng5 RCSB], [http://www.ebi.ac.uk/pdbsum/5ng5 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5ng5 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/ACRZ_ECOLI ACRZ_ECOLI]] AcrA-AcrB-AcrZ-TolC is a drug efflux protein complex with a broad substrate specificity. This protein binds to AcrB and is required for efflux of some but not all substrates, suggesting it may influence the specificity of drug export.<ref>PMID:23010927</ref> [[http://www.uniprot.org/uniprot/ACRA_ECOLI ACRA_ECOLI]] AcrA-AcrB-AcrZ-TolC is a drug efflux protein complex with broad substrate specificity that uses the proton motive force to export substrates. This subunit may act as an adapter protein that links AcrB and TolC stably together. It is elongated in shape, being long enough to span the periplasm.<ref>PMID:9878415</ref> [[http://www.uniprot.org/uniprot/ACRB_ECOLI ACRB_ECOLI]] AcrAB is a drug efflux protein with a broad substrate specificity.<ref>PMID:16915237</ref> <ref>PMID:16946072</ref> <ref>PMID:17194213</ref> [[http://www.uniprot.org/uniprot/TOLC_ECOLI TOLC_ECOLI]] Outer membrane channel, which is required for the function of several efflux systems such as AcrAB-TolC, AcrEF-TolC, EmrAB-TolC and MacAB-TolC. These systems are involved in export of antibiotics and other toxic compounds from the cell. TolC is also involved in import of colicin E1 into the cells.<ref>PMID:6337123</ref> <ref>PMID:11274125</ref> <ref>PMID:15228545</ref> <ref>PMID:18955484</ref> <ref>PMID:23176499</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Bacterial efflux pumps confer multidrug resistance by transporting diverse antibiotics from the cell. In Gram-negative bacteria, some of these pumps form multi-protein assemblies that span the cell envelope. Here we report the near-atomic resolution cryoEM structures of the Escherichia coli AcrAB-TolC multidrug efflux pump in resting and drug transport states, revealing a quaternary structural switch that allosterically couples and synchronizes initial ligand binding with channel opening. Within the transport-activated state, the channel remains open even though the pump cycles through three distinct conformations. Collectively, our data provide a dynamic mechanism for the assembly and operation of the AcrAB-TolC pump.
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Authors: Wang, Z., Fan, G., Hryc, C.F., Blaza, J.N., Serysheva, I.I., Schmid, M.F., Chiu, W., Luisi, B.F., Du, D.
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An allosteric transport mechanism for the AcrAB-TolC Multidrug Efflux Pump.,Wang Z, Fan G, Hryc CF, Blaza JN, Serysheva II, Schmid MF, Chiu W, Luisi BF, Du D Elife. 2017 Mar 29;6. pii: e24905. doi: 10.7554/eLife.24905. PMID:28355133<ref>PMID:28355133</ref>
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Description: multi-drug efflux; membrane transport; RND superfamily; Drug resistance
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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 5ng5" 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>
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[[Category: Blaza, J N]]
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[[Category: Chiu, W]]
[[Category: Du, D]]
[[Category: Du, D]]
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[[Category: Luisi, B.F]]
 
[[Category: Fan, G]]
[[Category: Fan, G]]
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[[Category: Chiu, W]]
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[[Category: Hryc, C F]]
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[[Category: Blaza, J.N]]
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[[Category: Luisi, B F]]
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[[Category: Hryc, C.F]]
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[[Category: Schmid, M F]]
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[[Category: Schmid, M.F]]
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[[Category: Serysheva, I I]]
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[[Category: Serysheva, I.I]]
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[[Category: Wang, Z]]
[[Category: Wang, Z]]
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[[Category: Drug resistance]]
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[[Category: Membrane protein]]
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[[Category: Membrane transport]]
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[[Category: Multi-drug efflux]]
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[[Category: Rnd superfamily]]

Revision as of 13:01, 19 April 2017

multi-drug efflux; membrane transport; RND superfamily; Drug resistance

5ng5, resolution 6.50Å

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