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3rcj
From Proteopedia
(Difference between revisions)
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| - | [[ | + | ==Rapid preparation of triazolyl substituted NH-heterocyclic kinase inhibitors via one-pot Sonogashira coupling TMS-deprotection CuAAC sequence== |
| + | <StructureSection load='3rcj' size='340' side='right' caption='[[3rcj]], [[Resolution|resolution]] 1.70Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[3rcj]] is a 1 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=3RCJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3RCJ FirstGlance]. <br> | ||
| + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=3RC:3-(1-BENZYL-1H-1,2,3-TRIAZOL-4-YL)-1H-PYRROLO[2,3-B]PYRIDINE'>3RC</scene></td></tr> | ||
| + | <tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=SEP:PHOSPHOSERINE'>SEP</scene></td></tr> | ||
| + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3hrc|3hrc]]</td></tr> | ||
| + | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">PDPK1, PDK1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr> | ||
| + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Non-specific_serine/threonine_protein_kinase Non-specific serine/threonine protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.1 2.7.11.1] </span></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=3rcj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3rcj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3rcj RCSB], [http://www.ebi.ac.uk/pdbsum/3rcj PDBsum]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | The one-pot, three-component Sonogashira coupling-TMS-deprotection-CuAAC ("click") sequence is the key reaction for the rapid synthesis of triazolyl substituted N-Boc protected NH-heterocycles, such as indole, indazole, 4-, 5-, 6-, and 7-azaindoles, 4,7-diazaindole, 7-deazapurines, pyrrole, pyrazole, and imidazole. Subsequently, the protective group was readily removed to give the corresponding triazolyl derivatives of these tremendously important NH-heterocycles. All compounds have been tested in a broad panel of kinase assays. Several compounds, 8f, 8h, 8k, and 8l, have been shown to inhibit the kinase PDK1, a target with high oncology relevance, and thus they are promising lead structures for the development of more active derivatives. The X-ray structure analysis of compound 8f in complex with PDK1 has revealed the detailed binding mode of the molecule in the kinase. | ||
| - | + | Rapid preparation of triazolyl substituted NH-heterocyclic kinase inhibitors via one-pot Sonogashira coupling-TMS-deprotection-CuAAC sequence.,Merkul E, Klukas F, Dorsch D, Gradler U, Greiner HE, Muller TJ Org Biomol Chem. 2011 May 31. PMID:21625704<ref>PMID:21625704</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| + | </div> | ||
| - | + | ==See Also== | |
| - | + | *[[3-phosphoinositide-dependent protein kinase 1|3-phosphoinositide-dependent protein kinase 1]] | |
| - | == | + | == References == |
| - | [[ | + | <references/> |
| - | + | __TOC__ | |
| - | == | + | </StructureSection> |
| - | < | + | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
| - | [[Category: Dorsch, D | + | [[Category: Dorsch, D]] |
| - | [[Category: Graedler, U | + | [[Category: Graedler, U]] |
| - | [[Category: Greiner, H E | + | [[Category: Greiner, H E]] |
| - | [[Category: Klukas, F | + | [[Category: Klukas, F]] |
| - | [[Category: Merkul, E | + | [[Category: Merkul, E]] |
| - | [[Category: Mueller, T J.J | + | [[Category: Mueller, T J.J]] |
| - | [[Category: Sirrenberg, C | + | [[Category: Sirrenberg, C]] |
[[Category: Agc kinase]] | [[Category: Agc kinase]] | ||
[[Category: Atp binding]] | [[Category: Atp binding]] | ||
Revision as of 12:47, 9 December 2014
Rapid preparation of triazolyl substituted NH-heterocyclic kinase inhibitors via one-pot Sonogashira coupling TMS-deprotection CuAAC sequence
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Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Dorsch, D | Graedler, U | Greiner, H E | Klukas, F | Merkul, E | Mueller, T J.J | Sirrenberg, C | Agc kinase | Atp binding | Phosphorylation | Serine/threonine-protein kinase | Transferase | Transferase-transferase inhibitor complex
