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2ycu
From Proteopedia
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| - | + | ==Crystal Structure of Human Non Muscle Myosin 2C in Pre-power stroke state== | |
| - | + | <StructureSection load='2ycu' size='340' side='right' caption='[[2ycu]], [[Resolution|resolution]] 2.25Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[2ycu]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2YCU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2YCU FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=AOV:ADP+ORTHOVANADATE'>AOV</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr> | |
| - | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1g8x|1g8x]]</td></tr> | |
| - | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Myosin_ATPase Myosin ATPase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.6.4.1 3.6.4.1] </span></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=2ycu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ycu OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2ycu RCSB], [http://www.ebi.ac.uk/pdbsum/2ycu PDBsum]</span></td></tr> |
| - | [[2ycu]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2YCU OCA]. | + | </table> |
| + | == Disease == | ||
| + | [[http://www.uniprot.org/uniprot/MYH14_HUMAN MYH14_HUMAN]] Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome;Autosomal dominant non-syndromic sensorineural deafness type DFNA. 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. | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/MYH14_HUMAN MYH14_HUMAN]] Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Myosin ATPase]] | [[Category: Myosin ATPase]] | ||
| - | [[Category: Chinthalapudi, K | + | [[Category: Chinthalapudi, K]] |
| - | [[Category: Heissler, S M | + | [[Category: Heissler, S M]] |
| - | [[Category: Manstein, D J | + | [[Category: Manstein, D J]] |
[[Category: Motor protein]] | [[Category: Motor protein]] | ||
Revision as of 13:30, 19 November 2014
Crystal Structure of Human Non Muscle Myosin 2C in Pre-power stroke state
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