1by8: Difference between revisions
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<StructureSection load='1by8' size='340' side='right'caption='[[1by8]], [[Resolution|resolution]] 2.60Å' scene=''> | <StructureSection load='1by8' size='340' side='right'caption='[[1by8]], [[Resolution|resolution]] 2.60Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1by8]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[1by8]] is a 1 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=1BY8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1BY8 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]] 2.6Å</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=1by8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1by8 OCA], [https://pdbe.org/1by8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1by8 RCSB], [https://www.ebi.ac.uk/pdbsum/1by8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1by8 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=1by8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1by8 OCA], [https://pdbe.org/1by8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1by8 RCSB], [https://www.ebi.ac.uk/pdbsum/1by8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1by8 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/CATK_HUMAN CATK_HUMAN] Defects in CTSK are the cause of pycnodysostosis (PKND) [MIM:[https://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 == | ||
[https://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. | |||
== 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: Abdel-Mequid | [[Category: Abdel-Mequid SS]] | ||
[[Category: Carr | [[Category: Carr TJ]] | ||
[[Category: Desjarlais | [[Category: Desjarlais RL]] | ||
[[Category: Janson | [[Category: Janson CA]] | ||
[[Category: Lalonde | [[Category: Lalonde JM]] | ||
[[Category: Smith | [[Category: Smith WW]] | ||
[[Category: Thompson | [[Category: Thompson SK]] | ||
[[Category: Tomaszek | [[Category: Tomaszek TA]] | ||
[[Category: Veber | [[Category: Veber DF]] | ||
[[Category: Yamashita | [[Category: Yamashita DS]] | ||
[[Category: Zhao | [[Category: Zhao B]] | ||