6mum
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Murine PI3K delta kinsae domain - cpd 3== | |
+ | <StructureSection load='6mum' size='340' side='right'caption='[[6mum]], [[Resolution|resolution]] 3.06Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[6mum]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6MUM OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6MUM FirstGlance]. <br> | ||
+ | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=K47:[(3S)-3-{[8-(1-ethyl-5-methyl-1H-pyrazol-4-yl)-9-methyl-9H-purin-6-yl]oxy}pyrrolidin-1-yl](oxan-4-yl)methanone'>K47</scene></td></tr> | ||
+ | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Phosphatidylinositol-4,5-bisphosphate_3-kinase Phosphatidylinositol-4,5-bisphosphate 3-kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.153 2.7.1.153] </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=6mum FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6mum OCA], [http://pdbe.org/6mum PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6mum RCSB], [http://www.ebi.ac.uk/pdbsum/6mum PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6mum ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | PI3Kdelta catalytic activity is required for immune cell activation, and has been implicated in inflammatory diseases as well as hematological malignancies in which the AKT pathway is overactive. A purine PI3Kdelta inhibitor bearing a benzimidazolone-piperidine motif was found to be poorly tolerated in dog, which was attributed to diffuse vascular injury. Several strategies were implemented to mitigate this finding, including reconstruction of the benzimidazolone-piperidine selectivity motif. Structure-based design led to the identification of O- and N-linked heterocycloalkyls, with pyrrolidines being particularly ligand efficient and kinome selective, and having an improved safety pharmacology profile. A representative was advanced into a dog tolerability study where it was found to be well tolerated, with no histopathological evidence of vascular injury. | ||
- | + | Structure Overhaul Affords a Potent Purine PI3Kdelta Inhibitor with Improved Tolerability.,Methot JL, Zhou H, Kattar SD, McGowan MA, Wilson K, Garcia Y, Deng Y, Altman M, Fradera X, Lesburg C, Fischmann T, Li C, Alves S, Shah S, Fernandez R, Goldenblatt P, Hill A, Shaffer L, Chen D, Tong V, McLeod RL, Yu H, Bass A, Kemper R, Gatto NT, LaFranco-Scheuch L, Trotter BW, Guzi T, Katz JD J Med Chem. 2019 Apr 22. doi: 10.1021/acs.jmedchem.8b01818. PMID:30986068<ref>PMID:30986068</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | [[Category: | + | </div> |
- | [[Category: Fischmann, T | + | <div class="pdbe-citations 6mum" style="background-color:#fffaf0;"></div> |
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Phosphatidylinositol-4,5-bisphosphate 3-kinase]] | ||
+ | [[Category: Fischmann, T O]] | ||
+ | [[Category: Inflammatory disorder]] | ||
+ | [[Category: Isoform-specific inhibitor]] | ||
+ | [[Category: Phosphoinositide 3-kinase]] | ||
+ | [[Category: Transferase]] |
Revision as of 08:53, 1 May 2019
Murine PI3K delta kinsae domain - cpd 3
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