2dl8

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[2dl8]] 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=2DL8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2DL8 FirstGlance]. <br>
<table><tr><td colspan='2'>[[2dl8]] 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=2DL8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2DL8 FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">SRGAP2, FNBP2, KIAA0456 ([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">SRGAP2, FNBP2, KIAA0456 ([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=2dl8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2dl8 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2dl8 RCSB], [http://www.ebi.ac.uk/pdbsum/2dl8 PDBsum], [http://www.topsan.org/Proteins/RSGI/2dl8 TOPSAN]</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=2dl8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2dl8 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2dl8 RCSB], [http://www.ebi.ac.uk/pdbsum/2dl8 PDBsum], [http://www.topsan.org/Proteins/RSGI/2dl8 TOPSAN]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/FNBP2_HUMAN FNBP2_HUMAN]] Note=A chromosomal aberration disrupting SRGAP2 has been found in a patient with early infantile epileptic encephalopathy. Balanced translocation t(1;9)(q32;q13).
[[http://www.uniprot.org/uniprot/FNBP2_HUMAN FNBP2_HUMAN]] Note=A chromosomal aberration disrupting SRGAP2 has been found in a patient with early infantile epileptic encephalopathy. Balanced translocation t(1;9)(q32;q13).
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Hayashi, F.]]
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[[Category: Hayashi, F]]
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[[Category: Qin, X R.]]
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[[Category: Qin, X R]]
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[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
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[[Category: Structural genomic]]
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[[Category: Yokoyama, S.]]
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[[Category: Yokoyama, S]]
[[Category: Formin-binding protein 2]]
[[Category: Formin-binding protein 2]]
[[Category: National project on protein structural and functional analyse]]
[[Category: National project on protein structural and functional analyse]]
[[Category: Nppsfa]]
[[Category: Nppsfa]]
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[[Category: Riken structural genomics/proteomics initiative]]
 
[[Category: Rsgi]]
[[Category: Rsgi]]
[[Category: Sh3 domain]]
[[Category: Sh3 domain]]
[[Category: Signaling protein]]
[[Category: Signaling protein]]
[[Category: Slit-robo rho gtpase activating protein 2]]
[[Category: Slit-robo rho gtpase activating protein 2]]
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[[Category: Structural genomic]]
 

Revision as of 17:33, 15 January 2015

Solution structure of the SH3 domain of human SLIT-ROBO Rho GTPase-activating protein 2

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