6mj1
From Proteopedia
(Difference between revisions)
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<StructureSection load='6mj1' size='340' side='right'caption='[[6mj1]], [[Resolution|resolution]] 2.60Å' scene=''> | <StructureSection load='6mj1' size='340' side='right'caption='[[6mj1]], [[Resolution|resolution]] 2.60Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[6mj1]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6MJ1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6MJ1 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6mj1]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Bacsu Bacsu]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6MJ1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6MJ1 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=6mj1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6mj1 OCA], [http://pdbe.org/6mj1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6mj1 RCSB], [http://www.ebi.ac.uk/pdbsum/6mj1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6mj1 ProSAT]</span></td></tr> | + | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">yttP, BSU29630 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=224308 BACSU])</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=6mj1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6mj1 OCA], [http://pdbe.org/6mj1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6mj1 RCSB], [http://www.ebi.ac.uk/pdbsum/6mj1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6mj1 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | Bacillus subtilis is a bacterium capable of differentiating into a spore form more resistant to environmental stress. Early in sporulation, each cell possesses two copies of a circular chromosome. A polar FtsZ ring (Z-ring) directs septation over one of the chromosomes, generating two cell compartments. The smaller "forespore" compartment initially contains only 25-30% of one chromosome, and this transient genetic asymmetry is required for differentiation. Timely assembly of polar Z-rings and precise capture of chromosome in the forespore both require the DNA-binding protein RefZ. To mediate its role in chromosome capture, RefZ must bind to specific DNA motifs (RBMs) that localize near the poles at the time of septation. Cells artificially induced to express RefZ during vegetative growth cannot assemble Z-rings, an effect that also requires DNA-binding. We hypothesized that RefZ-RBM complexes mediate precise chromosome capture by modulating FtsZ function. To investigate, we isolated 10 RefZ loss-of-function (rLOF) variants unable to inhibit cell division, yet still capable of binding RBMs. Sporulating cells expressing the rLOF variants in place of wild-type RefZ phenocopied a DeltarefZ mutant, suggesting that RefZ acts through an FtsZ-dependent mechanism. The crystal structure of RefZ was solved and wild-type RefZ and the rLOF variants were further characterized. Our data suggest that RefZ's oligomerization state and specificity for the RBMs are critical determinants influencing RefZ's ability to affect FtsZ dynamics. We propose that RBM-bound RefZ complexes function as a developmentally regulated nucleoid occlusion system for fine-tuning the position of the septum relative to the chromosome during sporulation.ImportanceThe bacterial nucleoid forms a large, highly organized structure. Thus, in addition to storing the genetic code, the nucleoid harbors positional information that can be leveraged by DNA-binding proteins to spatially constrain cellular activities. During B. subtilis sporulation, the nucleoid undergoes reorganization and the cell division protein FtsZ assembles polarly to direct septation over one chromosome. The TetR-family protein RefZ binds DNA motifs (RBMs) localized near the poles at the time of division, and is required for both timely FtsZ assembly and precise capture of DNA in the future spore compartment. Our data suggest that RefZ exploits nucleoid organization by associating with polarly localized RBMs to modulate the positioning of FtsZ relative to the chromosome during sporulation. | ||
+ | |||
+ | A DNA-binding protein tunes septum placement during Bacillus subtilis sporulation.,Brown EE, Miller AK, Krieger IV, Otto RM, Sacchettini JC, Herman JK J Bacteriol. 2019 Jun 3. pii: JB.00287-19. doi: 10.1128/JB.00287-19. PMID:31160399<ref>PMID:31160399</ref> | ||
+ | |||
+ | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
+ | </div> | ||
+ | <div class="pdbe-citations 6mj1" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
+ | [[Category: Bacsu]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Brown, E E]] | [[Category: Brown, E E]] |
Revision as of 06:31, 19 June 2019
Crystal structure of RefZ (regulator of FtsZ) from Bacillus subtilis
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