1soj: Difference between revisions

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~~'''~~CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B IN COMPLEX WITH IBMX~~'''~~

===CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B IN COMPLEX WITH IBMX===

~~==Overview==~~

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~~Phosphodiesterases (PDEs) are enzymes that modulate cyclic nucleotide signaling and as such are clinical targets for a range of disorders including congestive heart failure~~, ~~erectile dysfunction~~, and inflammation. The PDE3 family comprises two highly homologous subtypes expressed in different tissues, and inhibitors of this family have been shown to increase lipolysis in adipocytes. A specific PDE3B (the ~~lipocyte-localized subtype) inhibitor would be a very useful tool~~ to ~~evaluate~~ the ~~effects of PDE3 inhibition~~ on ~~lipolysis and metabolic rate and might become a novel tool for treatment of obesity~~. ~~We report here the three-dimensional structures of the catalytic domain of human PDE3B in complex with a generic PDE inhibitor and a novel PDE3 selective inhibitor~~. ~~These structures explain the dual cAMP/cGMP binding capabilities of PDE3, provide the molecular basis for inhibitor specificity~~, ~~and can supply a valid platform for~~ the ~~design of improved compounds~~.

The line below this paragraph, {{ABSTRACT_PUBMED_15147193}}, adds the Publication Abstract to the page

(as it appears on PubMed at http://www.pubmed.gov), where 15147193 is the PubMed ID number.

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==About this Structure==

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[[Category: Varnerin, J P.]]

[[Category: Pde3b phosphodiesterase]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on ~~Sat May 3 08~~:57:16 2008''

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 23:12:38 2008''

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-[[Image:1soj.gif|left|200px]]
+{{Seed}}
+[[Image:1soj.png|left|200px]]
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 {{STRUCTURE_1soj|  PDB=1soj  |  SCENE=  }}
-'''CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B IN COMPLEX WITH IBMX'''
+===CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B IN COMPLEX WITH IBMX===
-==Overview==
+<!--
-Phosphodiesterases (PDEs) are enzymes that modulate cyclic nucleotide signaling and as such are clinical targets for a range of disorders including congestive heart failure, erectile dysfunction, and inflammation. The PDE3 family comprises two highly homologous subtypes expressed in different tissues, and inhibitors of this family have been shown to increase lipolysis in adipocytes. A specific PDE3B (the lipocyte-localized subtype) inhibitor would be a very useful tool to evaluate the effects of PDE3 inhibition on lipolysis and metabolic rate and might become a novel tool for treatment of obesity. We report here the three-dimensional structures of the catalytic domain of human PDE3B in complex with a generic PDE inhibitor and a novel PDE3 selective inhibitor. These structures explain the dual cAMP/cGMP binding capabilities of PDE3, provide the molecular basis for inhibitor specificity, and can supply a valid platform for the design of improved compounds.
+The line below this paragraph, {{ABSTRACT_PUBMED_15147193}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 15147193 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_15147193}}
 ==About this Structure==
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 [[Category: Varnerin, J P.]]
 [[Category: Pde3b phosphodiesterase]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 08:57:16 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 23:12:38 2008''