4tkn: Difference between revisions
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4tkn]] is a 6 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4TKN OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4TKN FirstGlance]. <br> | <table><tr><td colspan='2'>[[4tkn]] is a 6 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4TKN OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4TKN FirstGlance]. <br> | ||
</td></tr><tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4tkn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4tkn OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4tkn RCSB], [http://www.ebi.ac.uk/pdbsum/4tkn PDBsum]</span></td></tr> | </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=4tkn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4tkn OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4tkn RCSB], [http://www.ebi.ac.uk/pdbsum/4tkn PDBsum]</span></td></tr> | ||
<table> | </table> | ||
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/KRIT1_HUMAN KRIT1_HUMAN]] Hereditary cerebral cavernous malformation. Cerebral cavernous malformations 1 (CCM1) [MIM:[http://omim.org/entry/116860 116860]]: A congenital vascular anomaly of the central nervous system that can result in hemorrhagic stroke, seizures, recurrent headaches, and focal neurologic deficits. The lesions are characterized by grossly enlarged blood vessels consisting of a single layer of endothelium and without any intervening neural tissue, ranging in diameter from a few millimeters to several centimeters. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:12172908</ref> | [[http://www.uniprot.org/uniprot/KRIT1_HUMAN KRIT1_HUMAN]] Hereditary cerebral cavernous malformation. Cerebral cavernous malformations 1 (CCM1) [MIM:[http://omim.org/entry/116860 116860]]: A congenital vascular anomaly of the central nervous system that can result in hemorrhagic stroke, seizures, recurrent headaches, and focal neurologic deficits. The lesions are characterized by grossly enlarged blood vessels consisting of a single layer of endothelium and without any intervening neural tissue, ranging in diameter from a few millimeters to several centimeters. Note=The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:12172908</ref> | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Boggon, T J | [[Category: Boggon, T J]] | ||
[[Category: Liu, W | [[Category: Liu, W]] | ||
[[Category: Stiegler, A L | [[Category: Stiegler, A L]] | ||
[[Category: Zhang, R | [[Category: Zhang, R]] | ||
[[Category: Ferm domain]] | [[Category: Ferm domain]] | ||
[[Category: Npxf motif]] | [[Category: Npxf motif]] | ||
[[Category: Npxy motif]] | [[Category: Npxy motif]] | ||
[[Category: Protein transport-signaling protein complex]] | [[Category: Protein transport-signaling protein complex]] | ||
