7pck: Difference between revisions
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{{STRUCTURE_7pck| PDB=7pck | SCENE= }} | {{STRUCTURE_7pck| PDB=7pck | SCENE= }} | ||
===CRYSTAL STRUCTURE OF WILD TYPE HUMAN PROCATHEPSIN K=== | ===CRYSTAL STRUCTURE OF WILD TYPE HUMAN PROCATHEPSIN K=== | ||
{{ABSTRACT_PUBMED_10048321}} | |||
==Disease== | |||
[[http://www.uniprot.org/uniprot/CATK_HUMAN CATK_HUMAN]] Defects in CTSK are the cause of pycnodysostosis (PKND) [MIM:[http://omim.org/entry/265800 265800]]. PKND is an autosomal recessive osteochondrodysplasia characterized by osteosclerosis and short stature.<ref>PMID:8703060</ref><ref>PMID:9529353</ref><ref>PMID:10491211</ref><ref>PMID:10878663</ref> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/CATK_HUMAN CATK_HUMAN]] Closely involved in osteoclastic bone resorption and may participate partially in the disorder of bone remodeling. Displays potent endoprotease activity against fibrinogen at acid pH. May play an important role in extracellular matrix degradation. | |||
==About this Structure== | ==About this Structure== | ||
[[7pck]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7PCK OCA]. | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:010048321</ref><references group="xtra"/><references/> | ||
[[Category: Cathepsin K]] | [[Category: Cathepsin K]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Sivaraman, J.]] | [[Category: Sivaraman, J.]] | ||
[[Category: Cysteine protease]] | [[Category: Cysteine protease]] | ||
[[Category: Hydrolase]] | |||
[[Category: Procathepsin k]] | [[Category: Procathepsin k]] | ||
[[Category: Proregion]] | [[Category: Proregion]] | ||