3h7d: Difference between revisions

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{{STRUCTURE_3h7d|  PDB=3h7d  |  SCENE=  }}  
{{STRUCTURE_3h7d|  PDB=3h7d  |  SCENE=  }}  
===The crystal structure of the cathepsin K Variant M5 in complex with chondroitin-4-sulfate===
===The crystal structure of the cathepsin K Variant M5 in complex with chondroitin-4-sulfate===
{{ABSTRACT_PUBMED_021193413}}
{{ABSTRACT_PUBMED_21193413}}


==Disease==
==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>  
[[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==
==Function==
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==About this Structure==
==About this Structure==
[[3h7d]] is a 2 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=3H7D OCA].  
[[3h7d]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3H7D OCA].  


==See Also==
==See Also==
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<ref group="xtra">PMID:021193413</ref><references group="xtra"/><references/>
<ref group="xtra">PMID:021193413</ref><references group="xtra"/><references/>
[[Category: Cathepsin K]]
[[Category: Cathepsin K]]
[[Category: Homo sapiens]]
[[Category: Human]]
[[Category: Bromme, D.]]
[[Category: Bromme, D.]]
[[Category: Cherney, M M.]]
[[Category: Cherney, M M.]]