3m61
From Proteopedia
(Difference between revisions)
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<StructureSection load='3m61' size='340' side='right'caption='[[3m61]], [[Resolution|resolution]] 1.68Å' scene=''> | <StructureSection load='3m61' size='340' side='right'caption='[[3m61]], [[Resolution|resolution]] 1.68Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[3m61]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[3m61]] 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=3M61 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3M61 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]] 1.68Å</td></tr> |
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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=3m61 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3m61 OCA], [https://pdbe.org/3m61 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3m61 RCSB], [https://www.ebi.ac.uk/pdbsum/3m61 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3m61 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=3m61 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3m61 OCA], [https://pdbe.org/3m61 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3m61 RCSB], [https://www.ebi.ac.uk/pdbsum/3m61 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3m61 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. | |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | + | [[Category: Andreasen PA]] | |
- | [[Category: Andreasen | + | [[Category: Chen L]] |
- | [[Category: Chen | + | [[Category: Huang M]] |
- | [[Category: Huang | + | [[Category: Jiang L]] |
- | [[Category: Jiang | + | [[Category: Meehan EJ]] |
- | [[Category: Meehan | + | [[Category: Wind T]] |
- | [[Category: Wind | + | [[Category: Yuan C]] |
- | [[Category: Yuan | + | |
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Current revision
Crystal structure of complex of urokinase and a upain-1 variant(W3A) in pH4.6 condition
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Categories: Homo sapiens | Large Structures | Andreasen PA | Chen L | Huang M | Jiang L | Meehan EJ | Wind T | Yuan C