4gkq

</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=4gkq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gkq OCA], [https://pdbe.org/4gkq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4gkq RCSB], [https://www.ebi.ac.uk/pdbsum/4gkq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4gkq ProSAT]</span></td></tr>

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== Publication Abstract from PubMed ==

It is widely accepted that movement of kinesin motor proteins is accomplished by coupling ATP binding, hydrolysis, and product release to conformational changes in the microtubule-binding and force-generating elements of their motor domain. Therefore, understanding how the Saccharomyces cerevisiae proteins Cik1 and Vik1 are able to function as direct participants in movement of Kar3Cik1 and Kar3Vik1 kinesin complexes presents an interesting challenge given that their motor homology domain (MHD) cannot bind ATP. Our crystal structures of the Vik1 ortholog from Candida glabrata may provide insight into this mechanism by showing that its neck and neck mimic-like element can adopt several different conformations reminiscent of those observed in catalytic kinesins. We found that when the neck is alpha-helical and interacting with the MHD core, the C-terminus of CgVik1 docks onto the central beta-sheet similarly to the ATP-bound form of Ncd. Alternatively, when neck-core interactions are broken, the C-terminus is disordered. Mutations designed to impair neck rotation, or some of the neck-MHD interactions, decreased microtubule gliding velocity and steady-state ATPase rate of CgKar3Vik1 complexes significantly. These results strongly suggest that neck rotation and neck mimic docking in Vik1 and Cik1 may be a structural mechanism for communication with Kar3.

Neck rotation and neck mimic docking in the non-catalytic Kar3-associated protein Vik1.,Duan D, Jia Z, Joshi M, Brunton J, Chan M, Drew D, Davis D, Allingham JS J Biol Chem. 2012 Oct 7. PMID:23043140<ref>PMID:23043140</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>

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== References ==

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