PDB 4phw
PDB Information
PDB | 4PHW |
Method | X-RAY DIFFRACTION |
Host Organism | Escherichia coli |
Gene Source | Homo sapiens |
Primary Citation | Discovery of Clinical Candidate 1-(4-(3-(4-(1H-Benzo[d]imidazole-2-carbonyl)phenoxy)pyrazin-2-yl)piperidin-1-yl)ethanone (AMG 579), A Potent, Selective, and Efficacious Inhibitor of Phosphodiesterase 10A (PDE10A).
J.Med.Chem.
|
Header | Hydrolase/Hydrolase Inhibitor |
Released | 2014-05-07 |
Resolution | 2.500 |
CATH Insert Date | 24 Aug, 2014 |
PDB Images (5)
PDB Prints
PDB Chains (2)
Chain ID | Date inserted into CATH | CATH Status |
---|---|---|
A | 25 Aug, 2014 | Chopped |
B | 25 Aug, 2014 | Chopped |
CATH Domains (2)
Domain ID | Date inserted into CATH | Superfamily | CATH Status |
---|---|---|---|
4phwA00 | 27 Aug, 2014 | 1.10.1300.10 | Assigned |
4phwB00 | 27 Aug, 2014 | 1.10.1300.10 | Assigned |
UniProtKB Entries (2)
Accession | Gene ID | Taxon | Description |
---|---|---|---|
Q9Y233 | PDE10_HUMAN | Homo sapiens | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A |
Q9Y233 | PDE10_HUMAN | Homo sapiens | cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A |