9mxd: Difference between revisions

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New page: '''Unreleased structure''' The entry 9mxd is ON HOLD Authors: Brunzelle, J.S., Shuvalova, L., Watterson, D.M. Description: Human E104A calmodulin:MLCK RM20 complex [[Category: Unreleas...
 
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'''Unreleased structure'''


The entry 9mxd is ON HOLD
==Human E104A calmodulin:MLCK RM20 complex==
 
<StructureSection load='9mxd' size='340' side='right'caption='[[9mxd]], [[Resolution|resolution]] 1.17&Aring;' scene=''>
Authors: Brunzelle, J.S., Shuvalova, L., Watterson, D.M.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9mxd]] 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=9MXD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9MXD FirstGlance]. <br>
Description: Human E104A calmodulin:MLCK RM20 complex
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.17&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene></td></tr>
[[Category: Brunzelle, J.S]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9mxd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9mxd OCA], [https://pdbe.org/9mxd PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9mxd RCSB], [https://www.ebi.ac.uk/pdbsum/9mxd PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9mxd ProSAT]</span></td></tr>
[[Category: Shuvalova, L]]
</table>
[[Category: Watterson, D.M]]
== Disease ==
[https://www.uniprot.org/uniprot/CALM1_HUMAN CALM1_HUMAN] The disease is caused by mutations affecting the gene represented in this entry. Mutations in CALM1 are the cause of CPVT4.  The disease is caused by mutations affecting the gene represented in this entry. Mutations in CALM1 are the cause of LQT14.
== Function ==
[https://www.uniprot.org/uniprot/CALM1_HUMAN CALM1_HUMAN] Calmodulin mediates the control of a large number of enzymes, ion channels, aquaporins and other proteins through calcium-binding. Among the enzymes to be stimulated by the calmodulin-calcium complex are a number of protein kinases and phosphatases. Together with CCP110 and centrin, is involved in a genetic pathway that regulates the centrosome cycle and progression through cytokinesis (PubMed:16760425). Mediates calcium-dependent inactivation of CACNA1C (PubMed:26969752). Positively regulates calcium-activated potassium channel activity of KCNN2 (PubMed:27165696).<ref>PMID:16760425</ref> <ref>PMID:23893133</ref> <ref>PMID:26969752</ref> <ref>PMID:27165696</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Brunzelle JS]]
[[Category: Shuvalova L]]
[[Category: Watterson DM]]
Retrieved from "https://proteopedia.org/9mxd"