4n6v: Difference between revisions
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<StructureSection load='4n6v' size='340' side='right'caption='[[4n6v]], [[Resolution|resolution]] 1.80Å' scene=''> | <StructureSection load='4n6v' size='340' side='right'caption='[[4n6v]], [[Resolution|resolution]] 1.80Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4n6v]] is a 10 chain structure with sequence from [ | <table><tr><td colspan='2'>[[4n6v]] is a 10 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=4N6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4N6V FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</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=4n6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4n6v OCA], [https://pdbe.org/4n6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4n6v RCSB], [https://www.ebi.ac.uk/pdbsum/4n6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4n6v 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/CYTB_HUMAN CYTB_HUMAN] Defects in CSTB are the cause of progressive myoclonic epilepsy type 1 (EPM1) [MIM:[https://omim.org/entry/254800 254800]. EPM1 is an autosomal recessive disorder characterized by severe, stimulus-sensitive myoclonus and tonic-clonic seizures. The onset, occurring between 6 and 13 years of age, is characterized by convulsions. Myoclonus begins 1 to 5 years later. The twitchings occur predominantly in the proximal muscles of the extremities and are bilaterally symmetrical, although asynchronous. At first small, they become late in the clinical course so violent that the victim is thrown to the floor. Mental deterioration and eventually dementia develop.<ref>PMID:9012407</ref> | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/CYTB_HUMAN CYTB_HUMAN] This is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor of cathepsins L, H and B. | ||
<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: Mihelic | [[Category: Mihelic M]] | ||
[[Category: Renko | [[Category: Renko M]] | ||
[[Category: Taler-Vercic | [[Category: Taler-Vercic A]] | ||
[[Category: Turk | [[Category: Turk D]] | ||
[[Category: Zerovnik | [[Category: Zerovnik E]] | ||
Revision as of 08:12, 11 January 2023
Partial rotational order disorder structure of human stefin B
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