6f1v

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m (Protected "6f1v" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6f1v is ON HOLD
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==C terminal region of the dynein heavy chains in the dynein tail/dynactin/BICDR1 complex==
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<StructureSection load='6f1v' size='340' side='right' caption='[[6f1v]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
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Authors: Urnavicius, L., Lau, C.K., Elshenawy, M.M., Morales-Rios, E., Motz, C., Yildiz, A., Carter, A.P.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6f1v]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6F1V OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6F1V FirstGlance]. <br>
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Description: C terminal region of the dynein heavy chains in the dynein tail/dynactin/BICDR1 complex
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6f1t|6f1t]], [[6f1u|6f1u]]</td></tr>
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[[Category: Unreleased Structures]]
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<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=6f1v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6f1v OCA], [http://pdbe.org/6f1v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6f1v RCSB], [http://www.ebi.ac.uk/pdbsum/6f1v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6f1v ProSAT]</span></td></tr>
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[[Category: Lau, C.K]]
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</table>
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== Disease ==
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[[http://www.uniprot.org/uniprot/DYHC1_HUMAN DYHC1_HUMAN]] Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures;Autosomal dominant non-syndromic intellectual disability;Autosomal dominant Charcot-Marie-Tooth disease type 2O. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
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== Function ==
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[[http://www.uniprot.org/uniprot/DYHC1_HUMAN DYHC1_HUMAN]] Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Plays a role in mitotic spindle assembly and metaphase plate congression (PubMed:27462074).<ref>PMID:27462074</ref>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Carter, A P]]
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[[Category: Elshenawy, M M]]
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[[Category: Lau, C K]]
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[[Category: Morales-Rios, E]]
[[Category: Motz, C]]
[[Category: Motz, C]]
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[[Category: Carter, A.P]]
 
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[[Category: Elshenawy, M.M]]
 
[[Category: Urnavicius, L]]
[[Category: Urnavicius, L]]
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[[Category: Morales-Rios, E]]
 
[[Category: Yildiz, A]]
[[Category: Yildiz, A]]
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[[Category: Complex]]
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[[Category: Cryo-em]]
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[[Category: Motor protein]]

Revision as of 07:08, 17 January 2018

C terminal region of the dynein heavy chains in the dynein tail/dynactin/BICDR1 complex

6f1v, resolution 3.40Å

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