4xsk
From Proteopedia
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| - | ''' | + | ==Structure of PAItrap, an uPA mutant== |
| - | + | <StructureSection load='4xsk' size='340' side='right' caption='[[4xsk]], [[Resolution|resolution]] 1.50Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[4xsk]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4XSK OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4XSK FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PGE:TRIETHYLENE+GLYCOL'>PGE</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | |
| - | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/U-plasminogen_activator U-plasminogen activator], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.73 3.4.21.73] </span></td></tr> | |
| - | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4xsk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4xsk OCA], [http://pdbe.org/4xsk PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4xsk RCSB], [http://www.ebi.ac.uk/pdbsum/4xsk PDBsum]</span></td></tr> | |
| - | [[Category: | + | </table> |
| + | == Disease == | ||
| + | [[http://www.uniprot.org/uniprot/UROK_HUMAN UROK_HUMAN]] Defects in PLAU are the cause of Quebec platelet disorder (QPD) [MIM:[http://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 == | ||
| + | [[http://www.uniprot.org/uniprot/UROK_HUMAN UROK_HUMAN]] Specifically cleaves the zymogen plasminogen to form the active enzyme plasmin. | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: U-plasminogen activator]] | ||
| + | [[Category: Andreasen, P]] | ||
| + | [[Category: Flaumenhaft, R]] | ||
| + | [[Category: Furie, B]] | ||
| + | [[Category: Gong, L]] | ||
| + | [[Category: Hong, Z]] | ||
[[Category: Huang, M]] | [[Category: Huang, M]] | ||
[[Category: Lin, L]] | [[Category: Lin, L]] | ||
| + | [[Category: Lin, Z]] | ||
[[Category: Liu, M]] | [[Category: Liu, M]] | ||
[[Category: Proulle, V]] | [[Category: Proulle, V]] | ||
[[Category: Yuan, C]] | [[Category: Yuan, C]] | ||
| - | [[Category: | + | [[Category: Antagonist]] |
| - | [[Category: | + | [[Category: Blood clotting]] |
| - | [[Category: | + | [[Category: Pai-1]] |
| - | [[Category: | + | [[Category: Upa]] |
| - | + | ||
| - | + | ||
Revision as of 15:50, 3 February 2016
Structure of PAItrap, an uPA mutant
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Categories: U-plasminogen activator | Andreasen, P | Flaumenhaft, R | Furie, B | Gong, L | Hong, Z | Huang, M | Lin, L | Lin, Z | Liu, M | Proulle, V | Yuan, C | Antagonist | Blood clotting | Pai-1 | Upa
