6gdk: Difference between revisions

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'''Unreleased structure'''


The entry 6gdk is ON HOLD
==Calcium bound form of human calmodulin mutant F141L==
 
<StructureSection load='6gdk' size='340' side='right' caption='[[6gdk]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
Authors: Grachov, O., Holt, C., Overgaard, M.T., Wimmer, R.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[6gdk]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6GDK OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6GDK FirstGlance]. <br>
Description: Calcium bound form of human calmodulin mutant F141L
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene></td></tr>
[[Category: Unreleased Structures]]
<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=6gdk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6gdk OCA], [http://pdbe.org/6gdk PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6gdk RCSB], [http://www.ebi.ac.uk/pdbsum/6gdk PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6gdk ProSAT]</span></td></tr>
</table>
== Disease ==
[[http://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 ==
[[http://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: Grachov, O]]
[[Category: Holt, C]]
[[Category: Holt, C]]
[[Category: Grachov, O]]
[[Category: Overgaard, M T]]
[[Category: Wimmer, R]]
[[Category: Wimmer, R]]
[[Category: Overgaard, M.T]]
[[Category: Calmodulin]]
[[Category: Signaling protein]]

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