4okh: Difference between revisions
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<StructureSection load='4okh' size='340' side='right'caption='[[4okh]], [[Resolution|resolution]] 2.45Å' scene=''> | <StructureSection load='4okh' size='340' side='right'caption='[[4okh]], [[Resolution|resolution]] 2.45Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4okh]] is a 3 chain structure with sequence from [ | <table><tr><td colspan='2'>[[4okh]] is a 3 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=4OKH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4OKH FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=PEU:2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,68,71,74,77,80-HEPTACOSAOXADOOCTACONTAN-82-OL'>PEU</scene | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=PEU:2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,68,71,74,77,80-HEPTACOSAOXADOOCTACONTAN-82-OL'>PEU</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4okh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4okh OCA], [https://pdbe.org/4okh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4okh RCSB], [https://www.ebi.ac.uk/pdbsum/4okh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4okh ProSAT]</span></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/CAN3_HUMAN CAN3_HUMAN] Autosomal recessive limb girdle muscular dystrophy type 2A. The disease is caused by mutations affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/CAN3_HUMAN CAN3_HUMAN] Calcium-regulated non-lysosomal thiol-protease. | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Allingham | [[Category: Allingham JS]] | ||
[[Category: Campbell | [[Category: Campbell RL]] | ||
[[Category: Davies | [[Category: Davies PL]] | ||
[[Category: Partha | [[Category: Karunan Partha S]] | ||
[[Category: Ravulapalli | [[Category: Ravulapalli R]] | ||
Revision as of 07:30, 25 January 2023
Crystal structure of calpain-3 penta-EF-hand domain
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