4dhn
From Proteopedia
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| - | {{STRUCTURE_4dhn| PDB=4dhn | SCENE= }} | ||
| - | ===Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening=== | ||
| - | {{ABSTRACT_PUBMED_23939230}} | ||
| - | == | + | ==Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening== |
| - | [[http://www.uniprot.org/uniprot/1433S_HUMAN 1433S_HUMAN | + | <StructureSection load='4dhn' size='340' side='right'caption='[[4dhn]], [[Resolution|resolution]] 1.80Å' scene=''> |
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[4dhn]] is a 1 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=4DHN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4DHN 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]] 1.8Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0KC:{2-[2-(CYCLOPENTYLAMINO)-2-OXOETHOXY]PHENYL}PHOSPHONIC+ACID'>0KC</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</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=4dhn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4dhn OCA], [https://pdbe.org/4dhn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4dhn RCSB], [https://www.ebi.ac.uk/pdbsum/4dhn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4dhn 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. | ||
| - | == | + | ==See Also== |
| - | [[ | + | *[[14-3-3 protein 3D structures|14-3-3 protein 3D structures]] |
| - | + | __TOC__ | |
| - | + | </StructureSection> | |
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Kohlbacher | + | [[Category: Large Structures]] |
| - | [[Category: Ottmann | + | [[Category: Kohlbacher O]] |
| - | [[Category: Roeglin | + | [[Category: Ottmann C]] |
| - | [[Category: Thiel | + | [[Category: Roeglin L]] |
| - | + | [[Category: Thiel P]] | |
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Current revision
Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening
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