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Ligands
Code Name Style Show Link
0H3 7-(6-methoxypyridin-3-yl)-4-{[2-(propan-2-yloxy)ethyl]amino}-1-(2-propoxyethyl)pyrido[4,3-D]pyrimidin-2(1h)-one
MG Magnesium ion
ZN Zinc ion
Non-standard Residues
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Code : 3TGG   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/HYDROLASE INHIBITOR
Title : A novel series of potent and selective PDE5 inhibitor2
Release Data : 2012-01-25
Compound :
mol_id molecule chains synonym
1 cGMP-specific 3',5'-cyclic phosphodiesterase A cGMP-binding cGMP-specific phosphodiesterase, CGB-PDE
ec: 3.1.4.35
fragment: Catalytic residues 534-858
mutation: R658P, N662Q, S663F, Y664L, Q666T, R667N, Q674L, L675M, C677D, H678E, I680V, M681L, Q751E
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human SPODOPTERA FRUGIPERDA  (taxid:7108)
gene: PDE5A, PDE5
expression_system_common: FALL ARMYWORM
expression_system_vector_type: Baculovirus
Authors : Han, S.
Keywords : phosphodiesterase, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.91 Å )
Citation :

Investigation of the pyrazinones as PDE5 inhibitors: evaluation of regioisomeric projections into the solvent region.

Hughes, R.O.,Maddux, T.,Joseph Rogier, D.  et al.
(2011)  Bioorg.Med.Chem.Lett.  21 : 6348 - 6352

PubMed: 21955943
DOI: 10.1016/j.bmcl.2011.08.106

Chain : A
UniProt : O76074 (PDE5A_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
3',5'-cyclic GMP + H2O = GMP + H(+) 3.1.4.35 PubMed:15260978, PubMed:9714779
left-to-right PubMed:15260978