6em8: Difference between revisions
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<StructureSection load='6em8' size='340' side='right' caption='[[6em8]], [[Resolution|resolution]] 8.40Å' scene=''> | <StructureSection load='6em8' size='340' side='right' caption='[[6em8]], [[Resolution|resolution]] 8.40Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6em8]] is a 10 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EM8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EM8 FirstGlance]. <br> | <table><tr><td colspan='2'>[[6em8]] is a 10 chain structure with sequence from [http://en.wikipedia.org/wiki/"micrococcus_aureus"_(rosenbach_1884)_zopf_1885 "micrococcus aureus" (rosenbach 1884) zopf 1885]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EM8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EM8 FirstGlance]. <br> | ||
</td></tr><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=6em8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6em8 OCA], [http://pdbe.org/6em8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6em8 RCSB], [http://www.ebi.ac.uk/pdbsum/6em8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6em8 ProSAT]</span></td></tr> | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">clpC, BER48_000499, CEJ93_12415, ERS072738_00457, ERS072840_00763, ERS073583_01020, ERS074020_00452, HMPREF3211_01370 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1280 "Micrococcus aureus" (Rosenbach 1884) Zopf 1885])</td></tr> | ||
<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=6em8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6em8 OCA], [http://pdbe.org/6em8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6em8 RCSB], [http://www.ebi.ac.uk/pdbsum/6em8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6em8 ProSAT]</span></td></tr> | |||
</table> | </table> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
Revision as of 09:53, 24 October 2018
S.aureus ClpC resting state, C2 symmetrisedS.aureus ClpC resting state, C2 symmetrised
Structural highlights
Publication Abstract from PubMedRing-forming AAA+ chaperones exert ATP-fueled substrate unfolding by threading through a central pore. This activity is potentially harmful requiring mechanisms for tight repression and substrate-specific activation. The AAA+ chaperone ClpC with the peptidase ClpP forms a bacterial protease essential to virulence and stress resistance. The adaptor MecA activates ClpC by targeting substrates and stimulating ClpC ATPase activity. We show how ClpC is repressed in its ground state by determining ClpC cryo-EM structures with and without MecA. ClpC forms large two-helical assemblies that associate via head-to-head contacts between coiled-coil middle domains (MDs). MecA converts this resting state to an active planar ring structure by binding to MD interaction sites. Loss of ClpC repression in MD mutants causes constitutive activation and severe cellular toxicity. These findings unravel an unexpected regulatory concept executed by coiled-coil MDs to tightly control AAA+ chaperone activity. Regulatory coiled-coil domains promote head-to-head assemblies of AAA+ chaperones essential for tunable activity control.,Carroni M, Franke KB, Maurer M, Jager J, Hantke I, Gloge F, Linder D, Gremer S, Turgay K, Bukau B, Mogk A Elife. 2017 Nov 22;6. doi: 10.7554/eLife.30120. PMID:29165246[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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