4afj
From Proteopedia
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- | [[ | + | ==5-aryl-4-carboxamide-1,3-oxazoles: potent and selective GSK-3 inhibitors== |
+ | <StructureSection load='4afj' size='340' side='right' caption='[[4afj]], [[Resolution|resolution]] 1.98Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[4afj]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4AFJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4AFJ FirstGlance]. <br> | ||
+ | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=SJJ:5-(4-METHOXYPHENYL)-N-(PYRIDIN-4-YLMETHYL)-1,3-OXAZOLE-4-CARBOXAMIDE'>SJJ</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene><br> | ||
+ | <tr><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=PTR:O-PHOSPHOTYROSINE'>PTR</scene></td></tr> | ||
+ | <tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2uw9|2uw9]], [[1o6k|1o6k]], [[1gng|1gng]], [[1h8f|1h8f]], [[1q3w|1q3w]], [[3zrk|3zrk]], [[1i09|1i09]], [[1o9u|1o9u]], [[2x37|2x37]], [[3zrm|3zrm]], [[4acg|4acg]], [[2jdr|2jdr]], [[1o6l|1o6l]], [[1j1b|1j1b]], [[1r0e|1r0e]], [[1q41|1q41]], [[2x39|2x39]], [[4ach|4ach]], [[3zrl|3zrl]], [[2jld|2jld]], [[1q3d|1q3d]], [[4acc|4acc]], [[1q5k|1q5k]], [[2jdo|2jdo]], [[4acd|4acd]], [[1pyx|1pyx]], [[1q4l|1q4l]], [[1j1c|1j1c]], [[1uv5|1uv5]], [[2xh5|2xh5]]</td></tr> | ||
+ | <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=4afj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4afj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4afj RCSB], [http://www.ebi.ac.uk/pdbsum/4afj PDBsum]</span></td></tr> | ||
+ | <table> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | 5-Aryl-4-carboxamide-1,3-oxazoles are a novel, potent and selective series of GSK-3 inhibitors. The optimization of the series to yield compounds with cell activity and brain permeability is described. | ||
- | + | 5-Aryl-4-carboxamide-1,3-oxazoles: Potent and selective GSK-3 inhibitors.,Gentile G, Merlo G, Pozzan A, Bernasconi G, Bax B, Bamborough P, Bridges A, Carter P, Neu M, Yao G, Brough C, Cutler G, Coffin A, Belyanskaya S Bioorg Med Chem Lett. 2012 Mar 1;22(5):1989-94. Epub 2012 Jan 21. PMID:22310227<ref>PMID:22310227</ref> | |
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- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
+ | </div> | ||
- | + | ==See Also== | |
- | + | *[[Glycogen synthase kinase 3|Glycogen synthase kinase 3]] | |
- | + | == References == | |
- | + | <references/> | |
- | + | __TOC__ | |
- | + | </StructureSection> | |
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- | == | + | |
- | [[ | + | |
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- | == | + | |
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Bamborough, P.]] | [[Category: Bamborough, P.]] |
Revision as of 08:12, 5 June 2014
5-aryl-4-carboxamide-1,3-oxazoles: potent and selective GSK-3 inhibitors
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Categories: Homo sapiens | Bamborough, P. | Bax, B. | Belyanskaya, S. | Bernasconi, G. | Bridges, A. | Brough, C. | Carter, P. | Coffin, A. | Cutler, G. | Gentile, G. | Merlo, G. | Neu, M. | Pozzan, A. | Yao, G. | Kinase | Transferase-peptide complex