4ia0
From Proteopedia
(Difference between revisions)
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- | + | {{STRUCTURE_4ia0| PDB=4ia0 | SCENE= }} | |
+ | ===Crystal structure of the PDE5A1 catalytic domain in complex with novel inhibitors=== | ||
+ | {{ABSTRACT_PUBMED_23867165}} | ||
- | + | ==Function== | |
+ | [[http://www.uniprot.org/uniprot/PDE5A_HUMAN PDE5A_HUMAN]] Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. This phosphodiesterase catalyzes the specific hydrolysis of cGMP to 5'-GMP. | ||
- | + | ==About this Structure== | |
+ | [[4ia0]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4IA0 OCA]. | ||
- | + | ==Reference== | |
+ | <ref group="xtra">PMID:023867165</ref><references group="xtra"/><references/> | ||
+ | [[Category: 3',5'-cyclic-GMP phosphodiesterase]] | ||
+ | [[Category: Chen, T.]] | ||
+ | [[Category: Ren, J.]] | ||
+ | [[Category: Xu, Y.]] | ||
+ | [[Category: Hydrolase]] | ||
+ | [[Category: Hydrolase-hydrolase inhibitor complex]] |
Revision as of 12:08, 1 January 2014
Contents |
Crystal structure of the PDE5A1 catalytic domain in complex with novel inhibitors
Template:ABSTRACT PUBMED 23867165
Function
[PDE5A_HUMAN] Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. This phosphodiesterase catalyzes the specific hydrolysis of cGMP to 5'-GMP.
About this Structure
4ia0 is a 1 chain structure. Full crystallographic information is available from OCA.
Reference
- Gong X, Wang G, Ren J, Liu Z, Wang Z, Chen T, Yang X, Jiang X, Shen J, Jiang H, Aisa HA, Xu Y, Li J. Exploration of the 5-bromopyrimidin-4(3H)-ones as potent inhibitors of PDE5. Bioorg Med Chem Lett. 2013 Sep 1;23(17):4944-7. doi: 10.1016/j.bmcl.2013.06.062. , Epub 2013 Jun 29. PMID:23867165 doi:http://dx.doi.org/10.1016/j.bmcl.2013.06.062