7qpf
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 7qpf is ON HOLD until Paper Publication Authors: Leonard, P.M., Langgard, M. Description: Discovery of Lu AF11167, a Phosphodiesterase 10A inhibito...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate== | |
| - | + | <StructureSection load='7qpf' size='340' side='right'caption='[[7qpf]], [[Resolution|resolution]] 1.70Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[7qpf]] 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=7QPF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7QPF 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]] 1.7Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EFJ:2-(1~{H}-benzimidazol-2-ylsulfanylmethyl)-3-bromanyl-5,7-dimethyl-imidazo[1,2-a]pyrimidine'>EFJ</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> |
| - | [[Category: Langgard | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7qpf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7qpf OCA], [https://pdbe.org/7qpf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7qpf RCSB], [https://www.ebi.ac.uk/pdbsum/7qpf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7qpf ProSAT]</span></td></tr> |
| - | [[Category: Leonard | + | </table> |
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/PDE10_HUMAN PDE10_HUMAN] Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. Can hydrolyze both cAMP and cGMP, but has higher affinity for cAMP and is more efficient with cAMP as substrate.<ref>PMID:17389385</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Langgard M]] | ||
| + | [[Category: Leonard PM]] | ||
Current revision
Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
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