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2km6

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[2km6]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KM6 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2KM6 FirstGlance]. <br>
<table><tr><td colspan='2'>[[2km6]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KM6 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2KM6 FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">NLRP7, NALP7, NOD12, PYPAF3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr>
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</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">NLRP7, NALP7, NOD12, PYPAF3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</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=2km6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2km6 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2km6 RCSB], [http://www.ebi.ac.uk/pdbsum/2km6 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=2km6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2km6 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2km6 RCSB], [http://www.ebi.ac.uk/pdbsum/2km6 PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://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>
[[http://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>
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Peti, W.]]
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[[Category: Peti, W]]
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[[Category: Pinheiro, A.]]
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[[Category: Pinheiro, A]]
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[[Category: Proell, M.]]
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[[Category: Proell, M]]
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[[Category: Schwarzenbacher, R.]]
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[[Category: Schwarzenbacher, R]]
[[Category: Atp-binding]]
[[Category: Atp-binding]]
[[Category: Disease mutation]]
[[Category: Disease mutation]]

Revision as of 17:30, 19 January 2015

NMR structure of the NLRP7 Pyrin domain

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