5nfd: Difference between revisions
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==Antiparallel monomeric coiled coil of Kif21A== | |||
<StructureSection load='5nfd' size='340' side='right' caption='[[5nfd]], [[Resolution|resolution]] 2.18Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[5nfd]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5NFD OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5NFD 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=5nfd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5nfd OCA], [http://pdbe.org/5nfd PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5nfd RCSB], [http://www.ebi.ac.uk/pdbsum/5nfd PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5nfd ProSAT]</span></td></tr> | |||
[[ | </table> | ||
[[ | == Disease == | ||
[[http://www.uniprot.org/uniprot/KI21A_HUMAN KI21A_HUMAN]] Congenital fibrosis of extraocular muscles. The disease is caused by mutations affecting the gene represented in this entry. | |||
== Function == | |||
[[http://www.uniprot.org/uniprot/KI21A_HUMAN KI21A_HUMAN]] Microtubule-binding motor protein probably involved in neuronal axonal transport. In vitro, has a plus-end directed motor activity (By similarity). | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Bianchi, S]] | [[Category: Bianchi, S]] | ||
[[Category: Steinmetz, M | [[Category: Kraatz, S H.W]] | ||
[[Category: Steinmetz, M O]] | |||
[[Category: Coiled coil]] | |||
[[Category: Kinesin]] | |||
[[Category: Motor protein]] | |||
Revision as of 07:56, 2 May 2018
Antiparallel monomeric coiled coil of Kif21A
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