8ahs

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(New page: '''Unreleased structure''' The entry 8ahs is ON HOLD until Paper Publication Authors: Durvanger, Z., Harmat, V. Description: Crystal structure of human Ca2+/Calmodulin in complex with ...)
Current revision (08:11, 7 February 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8ahs is ON HOLD until Paper Publication
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==Crystal structure of human Ca2+/Calmodulin in complex with melittin==
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<StructureSection load='8ahs' size='340' side='right'caption='[[8ahs]], [[Resolution|resolution]] 2.48&Aring;' scene=''>
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Authors: Durvanger, Z., Harmat, V.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8ahs]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Apis_mellifera Apis mellifera] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8AHS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8AHS FirstGlance]. <br>
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Description: Crystal structure of human Ca2+/Calmodulin in complex with melittin
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.48&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<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>
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[[Category: Durvanger, Z]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8ahs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8ahs OCA], [https://pdbe.org/8ahs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8ahs RCSB], [https://www.ebi.ac.uk/pdbsum/8ahs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8ahs ProSAT]</span></td></tr>
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[[Category: Harmat, V]]
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</table>
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== Disease ==
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[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.
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== Function ==
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[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>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Apis mellifera]]
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Durvanger Z]]
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[[Category: Harmat V]]

Current revision

Crystal structure of human Ca2+/Calmodulin in complex with melittin

PDB ID 8ahs

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