8bfg: Difference between revisions

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-'''Unreleased structure'''
-The entry 8bfg is ON HOLD  until Paper Publication
+==Solution structure of human apo/Calmodulin G113R (G114R)==
+<StructureSection load='8bfg' size='340' side='right'caption='[[8bfg]]' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8bfg]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8BFG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8BFG FirstGlance]. <br>
-Description:
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8bfg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8bfg OCA], [https://pdbe.org/8bfg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8bfg RCSB], [https://www.ebi.ac.uk/pdbsum/8bfg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8bfg ProSAT]</span></td></tr>
+</table>
+== 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: Brohus MB]]
+[[Category: Holler CV]]
+[[Category: Iwai H]]
+[[Category: Niemelae M]]
+[[Category: Overgaard MT]]
+[[Category: Petersson NM]]
+[[Category: Wimmer R]]