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{{STRUCTURE_2cr4|  PDB=2cr4  |  SCENE=  }}
===Solution structure of the SH2 domain of human SH3BP2 protein===


==Disease==
==Solution structure of the SH2 domain of human SH3BP2 protein==
[[http://www.uniprot.org/uniprot/3BP2_HUMAN 3BP2_HUMAN]] Defects in SH3BP2 are the cause of cherubism (CRBM) [MIM:[http://omim.org/entry/118400 118400]]. CRBM is an autosomal dominant inherited syndrome characterized by excessive bone degradation of the upper and lower jaws, which often begins around three years of age. It is followed by development of fibrous tissue masses, which causes a characteristic facial swelling.<ref>PMID:11381256</ref><ref>PMID:12900899</ref><ref>PMID:14577811</ref>  
<StructureSection load='2cr4' size='340' side='right'caption='[[2cr4]]' scene=''>
 
== Structural highlights ==
==Function==
<table><tr><td colspan='2'>[[2cr4]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CR4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2CR4 FirstGlance]. <br>
[[http://www.uniprot.org/uniprot/3BP2_HUMAN 3BP2_HUMAN]] Binds differentially to the SH3 domains of certain proteins of signal transduction pathways. Binds to phosphatidylinositols; linking the hemopoietic tyrosine kinase fes to the cytoplasmic membrane in a phosphorylation dependent mechanism.  
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
 
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2cr4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cr4 OCA], [https://pdbe.org/2cr4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2cr4 RCSB], [https://www.ebi.ac.uk/pdbsum/2cr4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2cr4 ProSAT], [https://www.topsan.org/Proteins/RSGI/2cr4 TOPSAN]</span></td></tr>
==About this Structure==
</table>
[[2cr4]] 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=2CR4 OCA].
== Disease ==
 
[https://www.uniprot.org/uniprot/3BP2_HUMAN 3BP2_HUMAN] Defects in SH3BP2 are the cause of cherubism (CRBM) [MIM:[https://omim.org/entry/118400 118400]. CRBM is an autosomal dominant inherited syndrome characterized by excessive bone degradation of the upper and lower jaws, which often begins around three years of age. It is followed by development of fibrous tissue masses, which causes a characteristic facial swelling.<ref>PMID:11381256</ref> <ref>PMID:12900899</ref> <ref>PMID:14577811</ref>  
==Reference==
== Function ==
<references group="xtra"/><references/>
[https://www.uniprot.org/uniprot/3BP2_HUMAN 3BP2_HUMAN] Binds differentially to the SH3 domains of certain proteins of signal transduction pathways. Binds to phosphatidylinositols; linking the hemopoietic tyrosine kinase fes to the cytoplasmic membrane in a phosphorylation dependent mechanism.
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Hatta, R.]]
[[Category: Large Structures]]
[[Category: Hayashi, F.]]
[[Category: Hatta R]]
[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Hayashi F]]
[[Category: Tomizawa, T.]]
[[Category: Tomizawa T]]
[[Category: Yokoyama, S.]]
[[Category: Yokoyama S]]
[[Category: Yoshida, M.]]
[[Category: Yoshida M]]
[[Category: 3bp-2]]
[[Category: National project on protein structural and functional analyse]]
[[Category: Nppsfa]]
[[Category: Riken structural genomics/proteomics initiative]]
[[Category: Rsgi]]
[[Category: Sh2 domain]]
[[Category: Signaling protein]]
[[Category: Structural genomic]]
Retrieved from "https://proteopedia.org/2cr4"