2os6: Difference between revisions

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[2os6]] is a 2 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=2OS6 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2OS6 FirstGlance]. <br>
<table><tr><td colspan='2'>[[2os6]] is a 2 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=2OS6 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2OS6 FirstGlance]. <br>
</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2omj|2omj]]</td></tr>
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2omj|2omj]]</td></tr>
<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=2os6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2os6 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2os6 RCSB], [http://www.ebi.ac.uk/pdbsum/2os6 PDBsum]</span></td></tr>
<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=2os6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2os6 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2os6 RCSB], [http://www.ebi.ac.uk/pdbsum/2os6 PDBsum]</span></td></tr>
<table>
</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/ARHGC_HUMAN ARHGC_HUMAN]] Note=A chromosomal aberration involving ARHGEF12 may be a cause of acute leukemia. Translocation t(11;11)(q23;23) with MLL.  
[[http://www.uniprot.org/uniprot/ARHGC_HUMAN ARHGC_HUMAN]] Note=A chromosomal aberration involving ARHGEF12 may be a cause of acute leukemia. Translocation t(11;11)(q23;23) with MLL.  
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Huang, H.]]
[[Category: Huang, H]]
[[Category: Liu, J.]]
[[Category: Liu, J]]
[[Category: Yang, Y.]]
[[Category: Yang, Y]]
[[Category: Cell adhesion]]
[[Category: Cell adhesion]]
[[Category: Cytoskeleton rearrangement]]
[[Category: Cytoskeleton rearrangement]]
[[Category: Nerve system development]]
[[Category: Nerve system development]]