3syx

<StructureSection load='3syx' size='340' side='right' caption='[[3syx]], [[Resolution|resolution]] 2.45&Aring;' scene=''>

<table><tr><td colspan='2'>[[3syx]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SYX OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3SYX FirstGlance]. <br>

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=YT3:YTTRIUM+(III)+ION'>YT3</scene></td></tr>

<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">SPRED1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=3syx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3syx OCA], [http://pdbe.org/3syx PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3syx RCSB], [http://www.ebi.ac.uk/pdbsum/3syx PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=3syx ProSAT]</span></td></tr>

[[http://www.uniprot.org/uniprot/SPRE1_HUMAN SPRE1_HUMAN]] Legius syndrome. The disease is caused by mutations affecting the gene represented in this entry.

[[http://www.uniprot.org/uniprot/SPRE1_HUMAN SPRE1_HUMAN]] Tyrosine kinase substrate that inhibits growth-factor-mediated activation of MAP kinase. Negatively regulates hematopoiesis of bone marrow (By similarity).