9lq2: Difference between revisions
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The entry | ==Structure of human dimeric NLRP7-TCL1A complex== | ||
<StructureSection load='9lq2' size='340' side='right'caption='[[9lq2]], [[Resolution|resolution]] 3.58Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[9lq2]] is a 6 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=9LQ2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9LQ2 FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.58Å</td></tr> | |||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9lq2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9lq2 OCA], [https://pdbe.org/9lq2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9lq2 RCSB], [https://www.ebi.ac.uk/pdbsum/9lq2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9lq2 ProSAT]</span></td></tr> | ||
</table> | |||
== Disease == | |||
[https://www.uniprot.org/uniprot/NALP7_HUMAN NALP7_HUMAN] Partial hydatidiform mole;Complete hydatidiform mole. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:16462743</ref> <ref>PMID:19246479</ref> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/NALP7_HUMAN NALP7_HUMAN] Inhibits CASP1/caspase-1-dependent IL1B secretion.<ref>PMID:15817483</ref> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Li JH]] | |||
[[Category: Liu QT]] | |||
Latest revision as of 08:11, 11 December 2025
Structure of human dimeric NLRP7-TCL1A complex
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