1i4o: Difference between revisions
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1i4o]] 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=1I4O OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1I4O FirstGlance]. <br> | <table><tr><td colspan='2'>[[1i4o]] 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=1I4O OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1I4O 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=1i4o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1i4o OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1i4o RCSB], [http://www.ebi.ac.uk/pdbsum/1i4o 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=1i4o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1i4o OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1i4o RCSB], [http://www.ebi.ac.uk/pdbsum/1i4o PDBsum]</span></td></tr> | ||
<table> | </table> | ||
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/XIAP_HUMAN XIAP_HUMAN]] Defects in XIAP are the cause of lymphoproliferative syndrome X-linked type 2 (XLP2) [MIM:[http://omim.org/entry/300635 300635]]. XLP is a rare immunodeficiency characterized by extreme susceptibility to infection with Epstein-Barr virus (EBV). Symptoms include severe or fatal mononucleosis, acquired hypogammaglobulinemia, pancytopenia and malignant lymphoma.<ref>PMID:17080092</ref> | [[http://www.uniprot.org/uniprot/XIAP_HUMAN XIAP_HUMAN]] Defects in XIAP are the cause of lymphoproliferative syndrome X-linked type 2 (XLP2) [MIM:[http://omim.org/entry/300635 300635]]. XLP is a rare immunodeficiency characterized by extreme susceptibility to infection with Epstein-Barr virus (EBV). Symptoms include severe or fatal mononucleosis, acquired hypogammaglobulinemia, pancytopenia and malignant lymphoma.<ref>PMID:17080092</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Huang, Y | [[Category: Huang, Y]] | ||
[[Category: Myszka, D G | [[Category: Myszka, D G]] | ||
[[Category: Park, Y C | [[Category: Park, Y C]] | ||
[[Category: Rich, R L | [[Category: Rich, R L]] | ||
[[Category: Segal, D | [[Category: Segal, D]] | ||
[[Category: Wu, H | [[Category: Wu, H]] | ||
[[Category: Apoptosis-hydrolase complex]] | [[Category: Apoptosis-hydrolase complex]] | ||
[[Category: Protease-inhibitor]] | [[Category: Protease-inhibitor]] | ||
