4zks: Difference between revisions

<table><tr><td colspan='2'>[[4zks]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ZKS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4ZKS FirstGlance]. <br>

</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=4zks FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4zks OCA], [https://pdbe.org/4zks PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4zks RCSB], [https://www.ebi.ac.uk/pdbsum/4zks PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4zks ProSAT]</span></td></tr>

[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>  

[https://www.uniprot.org/uniprot/UROK_HUMAN UROK_HUMAN] Specifically cleaves the zymogen plasminogen to form the active enzyme plasmin.

*[[Urokinase 3D Structures|Urokinase 3D Structures]]

[[Category: Homo sapiens]]

[[Category: Synthetic construct]]

[[Category: Andreasen PA]]

[[Category: Huang M]]

[[Category: Jiang L]]