4euw

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[4euw]] is a 3 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=4EUW OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4EUW FirstGlance]. <br>
<table><tr><td colspan='2'>[[4euw]] is a 3 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=4EUW OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4EUW FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">SGT82680, SOX9 ([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">SGT82680, SOX9 ([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=4euw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4euw OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4euw RCSB], [http://www.ebi.ac.uk/pdbsum/4euw 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=4euw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4euw OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4euw RCSB], [http://www.ebi.ac.uk/pdbsum/4euw PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/SOX9_HUMAN SOX9_HUMAN]] Campomelic dysplasia;46,XX testicular disorder of sex development;46,XX ovotesticular disorder of sex development. 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.
[[http://www.uniprot.org/uniprot/SOX9_HUMAN SOX9_HUMAN]] Campomelic dysplasia;46,XX testicular disorder of sex development;46,XX ovotesticular disorder of sex development. 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.
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: JCSG, Joint Center for Structural Genomics.]]
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[[Category: Structural genomic]]
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[[Category: STEMCELL, Partnership for Stem Cell Biology.]]
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[[Category: STEMCELL, Partnership for Stem Cell Biology]]
[[Category: Activator]]
[[Category: Activator]]
[[Category: Dna-binding]]
[[Category: Dna-binding]]
[[Category: Hmg domain]]
[[Category: Hmg domain]]
[[Category: Jcsg]]
[[Category: Jcsg]]
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[[Category: Joint center for structural genomic]]
 
[[Category: Nucleus]]
[[Category: Nucleus]]
[[Category: Partnership for stem cell biology]]
[[Category: Partnership for stem cell biology]]
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[[Category: Protein structure initiative]]
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[[Category: PSI, Protein structure initiative]]
[[Category: Protein-dna complex]]
[[Category: Protein-dna complex]]
[[Category: Psi-biology]]
[[Category: Psi-biology]]
[[Category: Stemcell]]
[[Category: Stemcell]]
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[[Category: Structural genomic]]
 
[[Category: Transcription]]
[[Category: Transcription]]
[[Category: Transcription regulation]]
[[Category: Transcription regulation]]
[[Category: Transcription-dna complex]]
[[Category: Transcription-dna complex]]

Revision as of 12:16, 4 January 2015

Crystal structure of a HMG domain of transcription factor SOX-9 bound to DNA (SOX-9/DNA) from Homo sapiens at 2.77 A resolution

4euw, resolution 2.77Å

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