8a6h
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Small molecule stabilizer (compound 7) for C-RAF and 14-3-3== | |
- | + | <StructureSection load='8a6h' size='340' side='right'caption='[[8a6h]], [[Resolution|resolution]] 1.60Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8a6h]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8A6H OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8A6H FirstGlance]. <br> | |
- | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.6Å</td></tr> | |
- | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=L6L:3-[2-(dimethylamino)ethyldisulfanyl]-1-[4-oxidanyl-4-[3-(trifluoromethyl)phenyl]piperidin-1-yl]propan-1-one'>L6L</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=NH2:AMINO+GROUP'>NH2</scene>, <scene name='pdbligand=SEP:PHOSPHOSERINE'>SEP</scene></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=8a6h FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8a6h OCA], [https://pdbe.org/8a6h PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8a6h RCSB], [https://www.ebi.ac.uk/pdbsum/8a6h PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8a6h ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/1433S_HUMAN 1433S_HUMAN] Adapter protein implicated in the regulation of a large spectrum of both general and specialized signaling pathways. Binds to a large number of partners, usually by recognition of a phosphoserine or phosphothreonine motif. Binding generally results in the modulation of the activity of the binding partner. When bound to KRT17, regulates protein synthesis and epithelial cell growth by stimulating Akt/mTOR pathway (By similarity). p53-regulated inhibitor of G2/M progression. | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Arkin MR]] | ||
+ | [[Category: Brunsveld L]] | ||
+ | [[Category: Centorrino F]] | ||
+ | [[Category: Kenanova DN]] | ||
+ | [[Category: Neitz J]] | ||
+ | [[Category: Ottmann C]] | ||
+ | [[Category: Sijbesma E]] | ||
+ | [[Category: Vickery H]] | ||
+ | [[Category: Virta J]] | ||
+ | [[Category: Visser EJ]] | ||
+ | [[Category: Zhong M]] |
Current revision
Small molecule stabilizer (compound 7) for C-RAF and 14-3-3
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Categories: Homo sapiens | Large Structures | Arkin MR | Brunsveld L | Centorrino F | Kenanova DN | Neitz J | Ottmann C | Sijbesma E | Vickery H | Virta J | Visser EJ | Zhong M