3oy6: Difference between revisions
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<StructureSection load='3oy6' size='340' side='right'caption='[[3oy6]], [[Resolution|resolution]] 2.31Å' scene=''> | <StructureSection load='3oy6' size='340' side='right'caption='[[3oy6]], [[Resolution|resolution]] 2.31Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[3oy6]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[3oy6]] is a 2 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=3OY6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3OY6 FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.31Å</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=3oy6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3oy6 OCA], [https://pdbe.org/3oy6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3oy6 RCSB], [https://www.ebi.ac.uk/pdbsum/3oy6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3oy6 ProSAT]</span></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=3oy6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3oy6 OCA], [https://pdbe.org/3oy6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3oy6 RCSB], [https://www.ebi.ac.uk/pdbsum/3oy6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3oy6 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/UROK_HUMAN UROK_HUMAN] Defects in PLAU are the cause of Quebec platelet disorder (QPD) [MIM:[https://omim.org/entry/601709 601709]. QPD is an autosomal dominant bleeding disorder due to a gain-of-function defect in fibrinolysis. Although affected individuals do not exhibit systemic fibrinolysis, they show delayed onset bleeding after challenge, such as surgery. The hallmark of the disorder is markedly increased PLAU levels within platelets, which causes intraplatelet plasmin generation and secondary degradation of alpha-granule proteins.<ref>PMID:20007542</ref> | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/UROK_HUMAN UROK_HUMAN] Specifically cleaves the zymogen plasminogen to form the active enzyme plasmin. | |||
<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: Andreasen PA]] | |||
[[Category: Andreasen | [[Category: Huang MD]] | ||
[[Category: Huang | [[Category: Jiang LG]] | ||
[[Category: Jiang | |||
Latest revision as of 16:59, 1 November 2023
The crystal structure of uPA complex with peptide inhibitor MH036 at pH4.6
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