3v42

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[3v42]] is a 2 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=3V42 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3V42 FirstGlance]. <br>
<table><tr><td colspan='2'>[[3v42]] is a 2 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=3V42 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3V42 FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">BHD, FLCN ([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">BHD, FLCN ([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=3v42 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3v42 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3v42 RCSB], [http://www.ebi.ac.uk/pdbsum/3v42 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=3v42 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3v42 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3v42 RCSB], [http://www.ebi.ac.uk/pdbsum/3v42 PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/FLCN_HUMAN FLCN_HUMAN]] Familial spontaneous pneumothorax;Birt-Hogg-Dube syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The gene represented in this entry may be involved in disease pathogenesis.
[[http://www.uniprot.org/uniprot/FLCN_HUMAN FLCN_HUMAN]] Familial spontaneous pneumothorax;Birt-Hogg-Dube syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The gene represented in this entry may be involved in disease pathogenesis.
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Blundell, T L.]]
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[[Category: Blundell, T L]]
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[[Category: Chirgadze, D Y.]]
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[[Category: Chirgadze, D Y]]
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[[Category: Nookala, R K.]]
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[[Category: Nookala, R K]]
[[Category: Folliculin]]
[[Category: Folliculin]]
[[Category: Protein binding]]
[[Category: Protein binding]]
[[Category: Tumor suppressor]]
[[Category: Tumor suppressor]]

Revision as of 11:05, 4 January 2015

Crystal structure of renal tumor suppressor protein, folliculin

3v42, resolution 2.00Å

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