7rit

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==Drug-free A. baumannii MsbA==
==Drug-free A. baumannii MsbA==
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<StructureSection load='7rit' size='340' side='right'caption='[[7rit]]' scene=''>
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<StructureSection load='7rit' size='340' side='right'caption='[[7rit]], [[Resolution|resolution]] 5.20&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7RIT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7RIT FirstGlance]. <br>
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7RIT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7RIT FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7rit FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7rit OCA], [https://pdbe.org/7rit PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7rit RCSB], [https://www.ebi.ac.uk/pdbsum/7rit PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7rit ProSAT]</span></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">Electron Microscopy, [[Resolution|Resolution]] 5.2&#8491;</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=7rit FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7rit OCA], [https://pdbe.org/7rit PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7rit RCSB], [https://www.ebi.ac.uk/pdbsum/7rit PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7rit ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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ATP-binding cassette (ABC) transporters couple ATP hydrolysis to substrate transport across biological membranes. Although many are promising drug targets, their mechanisms of modulation by small molecule inhibitors remain largely unknown. Intriguingly, two first-generation inhibitors of the MsbA transporter, TBT1 and G247, induce opposite effects on ATP hydrolysis. Using single-particle cryo-electron microscopy and functional assays, we show that TBT1 and G247 bind adjacent yet separate pockets in the MsbA transmembrane domains. Two TBT1 molecules asymmetrically occupy the substrate binding site, leading to a collapsed inward-facing conformation with decreased distance between the nucleotide-binding domains (NBDs). In contrast, two G247 molecules symmetrically increases NBD distance in a wide inward-open state of MsbA. The divergent mechanisms of action of these MsbA inhibitors provide important insights into ABC transporter pharmacology.
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Distinct allosteric mechanisms of first-generation MsbA inhibitors.,Thelot FA, Zhang W, Song K, Xu C, Huang J, Liao M Science. 2021 Sep 23. doi: 10.1126/science.abi9009. PMID:34554829<ref>PMID:34554829</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 7rit" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>

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Drug-free A. baumannii MsbA

PDB ID 7rit

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