1kmc

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1kmc]] 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=1KMC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1KMC FirstGlance]. <br>
<table><tr><td colspan='2'>[[1kmc]] 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=1KMC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1KMC FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1i4o|1i4o]], [[1i51|1i51]], [[1i3o|1i3o]]</td></tr>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1i4o|1i4o]], [[1i51|1i51]], [[1i3o|1i3o]]</td></tr>
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<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=1kmc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1kmc OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1kmc RCSB], [http://www.ebi.ac.uk/pdbsum/1kmc PDBsum]</span></td></tr>
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<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=1kmc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1kmc OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1kmc RCSB], [http://www.ebi.ac.uk/pdbsum/1kmc PDBsum]</span></td></tr>
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<table>
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</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]]
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[[Category: Bode, W.]]
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[[Category: Bode, W]]
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[[Category: Riedl, S J.]]
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[[Category: Riedl, S J]]
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[[Category: Salvesen, G S.]]
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[[Category: Salvesen, G S]]
[[Category: Apoptosis]]
[[Category: Apoptosis]]
[[Category: Apoptosis-hydrolase complex]]
[[Category: Apoptosis-hydrolase complex]]

Revision as of 16:07, 5 January 2015

Crystal Structure of the Caspase-7 / XIAP-BIR2 Complex

1kmc, resolution 2.90Å

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