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4tpm

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<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=4tpm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4tpm OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4tpm RCSB], [http://www.ebi.ac.uk/pdbsum/4tpm PDBsum]</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=4tpm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4tpm OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4tpm RCSB], [http://www.ebi.ac.uk/pdbsum/4tpm PDBsum]</span></td></tr>
</table>
</table>
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== Function ==
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[[http://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>
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== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==

Revision as of 11:18, 25 December 2014

Crystal structure of 2-(3-alkoxy-1-azetidinyl) quinolines as PDE10A Inhibitors

4tpm, resolution 2.77Å

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