This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
4g2j
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | + | {{STRUCTURE_4g2j| PDB=4g2j | SCENE= }} | |
| + | ===Human pde9 in complex with selective compound=== | ||
| + | {{ABSTRACT_PUBMED_23025719}} | ||
| - | + | ==Function== | |
| + | [[http://www.uniprot.org/uniprot/PDE9A_HUMAN PDE9A_HUMAN]] Hydrolyzes the second messenger cGMP, which is a key regulator of many important physiological processes.<ref>PMID:18757755</ref> | ||
| - | + | ==About this Structure== | |
| + | [[4g2j]] 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=4G2J OCA]. | ||
| - | + | ==Reference== | |
| + | <ref group="xtra">PMID:023025719</ref><references group="xtra"/><references/> | ||
| + | [[Category: 3',5'-cyclic-GMP phosphodiesterase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Liu, S.]] | ||
| + | [[Category: Cgmp->gmp]] | ||
| + | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
| + | [[Category: Inhibitor]] | ||
| + | [[Category: Phosphodiesterase]] | ||
Revision as of 16:19, 19 June 2013
Contents |
Human pde9 in complex with selective compound
Template:ABSTRACT PUBMED 23025719
Function
[PDE9A_HUMAN] Hydrolyzes the second messenger cGMP, which is a key regulator of many important physiological processes.[1]
About this Structure
4g2j is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Claffey MM, Helal CJ, Verhoest PR, Kang Z, Fors KS, Jung S, Zhong J, Bundesmann MW, Hou X, Lui S, Kleiman RJ, Vanase-Frawley M, Schmidt AW, Menniti F, Schmidt CJ, Hoffman WE, Hajos M, McDowell L, O'Connor RE, Macdougall-Murphy M, Fonseca KR, Becker SL, Nelson FR, Liras S. Application of structure-based drug design and parallel chemistry to identify selective, brain penetrant, in vivo active phosphodiesterase 9A inhibitors. J Med Chem. 2012 Nov 8;55(21):9055-68. doi: 10.1021/jm3009635. Epub 2012 Oct 12. PMID:23025719 doi:10.1021/jm3009635
