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| ==Structural basis for the assembly of the mitotic motor kinesin-5 into bipolar tetramers== | | ==Structural basis for the assembly of the mitotic motor kinesin-5 into bipolar tetramers== |
- | <StructureSection load='4pxt' size='340' side='right' caption='[[4pxt]], [[Resolution|resolution]] 2.90Å' scene=''> | + | <StructureSection load='4pxt' size='340' side='right'caption='[[4pxt]], [[Resolution|resolution]] 2.90Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[4pxt]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Drome Drome]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4PXT OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4PXT FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4pxt]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Drosophila_melanogaster Drosophila melanogaster]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4PXT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4PXT FirstGlance]. <br> |
- | </td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr> |
- | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4pxu|4pxu]]</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=4pxt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4pxt OCA], [https://pdbe.org/4pxt PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4pxt RCSB], [https://www.ebi.ac.uk/pdbsum/4pxt PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4pxt ProSAT]</span></td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CG9191, KLP2, Klp61F, Klp61F or DmKlp61F or CG9191 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=7227 DROME])</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=4pxt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4pxt OCA], [http://pdbe.org/4pxt PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4pxt RCSB], [http://www.ebi.ac.uk/pdbsum/4pxt PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4pxt ProSAT]</span></td></tr> | + | |
| </table> | | </table> |
| == Function == | | == Function == |
- | [[http://www.uniprot.org/uniprot/KL61_DROME KL61_DROME]] Important role in mitotic dividing cells. Microtubule motor required for spindle body separation. Slow plus-end directed microtubule motor capable of cross-linking and sliding apart antiparallel microtubules, thereby pushing apart the associated spindle poles during spindle assembly and function. | + | [https://www.uniprot.org/uniprot/KL61_DROME KL61_DROME] Important role in mitotic dividing cells. Microtubule motor required for spindle body separation. Slow plus-end directed microtubule motor capable of cross-linking and sliding apart antiparallel microtubules, thereby pushing apart the associated spindle poles during spindle assembly and function. |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| </div> | | </div> |
| <div class="pdbe-citations 4pxt" style="background-color:#fffaf0;"></div> | | <div class="pdbe-citations 4pxt" style="background-color:#fffaf0;"></div> |
| + | |
| + | ==See Also== |
| + | *[[Kinesin 3D Structures|Kinesin 3D Structures]] |
| == References == | | == References == |
| <references/> | | <references/> |
| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Drome]] | + | [[Category: Drosophila melanogaster]] |
- | [[Category: Al-Bassam, J]] | + | [[Category: Large Structures]] |
- | [[Category: Nithianantham, S]] | + | [[Category: Al-Bassam J]] |
- | [[Category: Scholey, J E]] | + | [[Category: Nithianantham S]] |
- | [[Category: Scholey, J M]] | + | [[Category: Scholey JE]] |
- | [[Category: Anti-parallel four-helix bundle]]
| + | [[Category: Scholey JM]] |
- | [[Category: Bipolar assembly domain of kinesin-5]]
| + | |
- | [[Category: Bipolar tetramer]]
| + | |
- | [[Category: Cell cycle]]
| + | |
- | [[Category: Coiled-coil]]
| + | |
- | [[Category: Crosslinking adjacent microtubules into bundles throughout the mitotic spindle]]
| + | |
- | [[Category: Kinesin-5 functions via a sliding filament mechanism]]
| + | |
- | [[Category: Microtubule]]
| + | |
| Structural highlights
Function
KL61_DROME Important role in mitotic dividing cells. Microtubule motor required for spindle body separation. Slow plus-end directed microtubule motor capable of cross-linking and sliding apart antiparallel microtubules, thereby pushing apart the associated spindle poles during spindle assembly and function.
Publication Abstract from PubMed
Chromosome segregation during mitosis depends upon Kinesin-5 motors, which display a conserved, bipolar homotetrameric organization consisting of two motor dimers at opposite ends of a central rod. Kinesin-5 motors crosslink adjacent microtubules to drive or constrain their sliding apart, but the structural basis of their organization is unknown. In this study, we report the atomic structure of the bipolar assembly (BASS) domain that directs four Kinesin-5 subunits to form a bipolar minifilament. BASS is a novel 26-nm four-helix bundle, consisting of two anti-parallel coiled-coils at its center, stabilized by alternating hydrophobic and ionic four-helical interfaces, which based on mutagenesis experiments, are critical for tetramerization. Strikingly, N-terminal BASS helices bend as they emerge from the central bundle, swapping partner helices, to form dimeric parallel coiled-coils at both ends, which are offset by 90 degrees . We propose that BASS is a mechanically stable, plectonemically-coiled junction, transmitting forces between Kinesin-5 motor dimers during microtubule sliding. DOI: http://dx.doi.org/10.7554/eLife.02217.001.
Structural basis for the assembly of the mitotic motor Kinesin-5 into bipolar tetramers.,Scholey JE, Nithianantham S, Scholey JM, Al-Bassam J Elife. 2014 Apr 8;3:e02217. doi: 10.7554/eLife.02217. PMID:24714498[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Scholey JE, Nithianantham S, Scholey JM, Al-Bassam J. Structural basis for the assembly of the mitotic motor Kinesin-5 into bipolar tetramers. Elife. 2014 Apr 8;3:e02217. doi: 10.7554/eLife.02217. PMID:24714498
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