4muw

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m (Protected "4muw" [edit=sysop:move=sysop])
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'''Unreleased structure'''
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{{STRUCTURE_4muw| PDB=4muw | SCENE= }}
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===Crystal Structure of PDE10A with Novel Keto-Benzimidazole Inhibitor===
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{{ABSTRACT_PUBMED_24102193}}
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The entry 4muw is ON HOLD
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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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Authors: Chmait, S., Jordan, S.
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==About this Structure==
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[[4muw]] is a 2 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=4MUW OCA].
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Description: Crystal Structure of PDE10A with Novel Keto-Benzimidazole Inhibitor
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==Reference==
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<ref group="xtra">PMID:024102193</ref><references group="xtra"/><references/>
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[[Category: Homo sapiens]]
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[[Category: Chmait, S.]]
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[[Category: Jordan, S.]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]
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[[Category: Inhibitor]]
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[[Category: Keto-benzimidazole]]
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[[Category: Pde10a]]
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[[Category: Phosphodiesterase 10a]]

Revision as of 06:41, 23 October 2013

Template:STRUCTURE 4muw

Contents

Crystal Structure of PDE10A with Novel Keto-Benzimidazole Inhibitor

Template:ABSTRACT PUBMED 24102193

Function

[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.[1]

About this Structure

4muw is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Hu E, Kunz RK, Chen N, Rumfelt S, Siegmund A, Andrews K, Chmait S, Zhao S, Davis C, Chen H, Lester-Zeiner D, Ma J, Biorn C, Shi J, Porter A, Treanor J, Allen JR. Design, Optimization, and Biological Evaluation of Novel Keto-Benzimidazoles as Potent and Selective Inhibitors of Phosphodiesterase 10A (PDE10A). J Med Chem. 2013 Oct 8. PMID:24102193 doi:http://dx.doi.org/10.1021/jm401234w
  1. ↑ Wang H, Liu Y, Hou J, Zheng M, Robinson H, Ke H. Structural insight into substrate specificity of phosphodiesterase 10. Proc Natl Acad Sci U S A. 2007 Apr 3;104(14):5782-7. Epub 2007 Mar 26. PMID:17389385

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