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6A3N

Crystal structure of the PDE9 catalytic domain in complex with inhibitor 2

Summary for 6A3N
Entry DOI10.2210/pdb6a3n/pdb
DescriptorHigh affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, ZINC ION, MAGNESIUM ION, ... (5 entities in total)
Functional Keywordspde9 inhibitor complex, hydrolase
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight77080.37
Authors
Wu, Y.N.,Zhou, Q.,Chen, Y.P.,Luo, H.B. (deposition date: 2018-06-15, release date: 2019-04-10, Last modification date: 2023-11-22)
Primary citationWu, Y.,Zhou, Q.,Zhang, T.,Li, Z.,Chen, Y.P.,Zhang, P.,Yu, Y.F.,Geng, H.,Tian, Y.J.,Zhang, C.,Wang, Y.,Chen, J.W.,Chen, Y.,Luo, H.B.
Discovery of Potent, Selective, and Orally Bioavailable Inhibitors against Phosphodiesterase-9, a Novel Target for the Treatment of Vascular Dementia.
J. Med. Chem., 62:4218-4224, 2019
Cited by
PubMed: 30916555
DOI: 10.1021/acs.jmedchem.8b01041
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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