2os6
From Proteopedia
(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]] | ||
Revision as of 15:36, 19 January 2015
Solution structure of LARG PDZ domain in complex with C-terminal octa-peptide of Plexin B1
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