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5nfd
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==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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