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5d3a
From Proteopedia
(Difference between revisions)
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<StructureSection load='5d3a' size='340' side='right'caption='[[5d3a]], [[Resolution|resolution]] 2.50Å' scene=''> | <StructureSection load='5d3a' size='340' side='right'caption='[[5d3a]], [[Resolution|resolution]] 2.50Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[5d3a]] is a 2 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[5d3a]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D3A OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D3A FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></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=5d3a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d3a OCA], [https://pdbe.org/5d3a PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d3a RCSB], [https://www.ebi.ac.uk/pdbsum/5d3a PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d3a ProSAT]</span></td></tr> | |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [ | + | [https://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 == | == Function == | ||
| - | [ | + | [https://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). |
==See Also== | ==See Also== | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Bianchi | + | [[Category: Bianchi S]] |
| - | [[Category: Kammerer | + | [[Category: Kammerer AR]] |
| - | [[Category: Kraatz | + | [[Category: Kraatz S]] |
| - | [[Category: Steinmetz | + | [[Category: Steinmetz MO]] |
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Revision as of 10:19, 21 June 2023
KIF21A regulatory coiled coil
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