4NPW
Crystal structure of human PDE1B bound to inhibitor 19A (7,8-dimethoxy-N-[(2S)-1-(3-methyl-1H-pyrazol-5-yl)propan-2-yl]quinazolin-4-amine)
Functional Information from GO Data
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE ZN A 1001 |
Chain | Residue |
A | HIS227 |
A | HIS263 |
A | ASP264 |
A | ASP370 |
A | HOH1112 |
A | HOH1116 |
site_id | AC2 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE MG A 1002 |
Chain | Residue |
A | HOH1113 |
A | HOH1114 |
A | HOH1115 |
A | ASP264 |
A | HOH1111 |
A | HOH1112 |
site_id | AC3 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE 0NY A 1003 |
Chain | Residue |
A | TYR222 |
A | HIS223 |
A | HIS373 |
A | LEU388 |
A | PHE392 |
A | LEU409 |
A | GLN421 |
A | PHE424 |
A | HOH1101 |
A | HOH1102 |
A | HOH1104 |
Functional Information from PROSITE/UniProt
site_id | PS00126 |
Number of Residues | 12 |
Details | PDEASE_I_1 3'5'-cyclic nucleotide phosphodiesterase domain signature. HDYeHtGttNsF |
Chain | Residue | Details |
A | HIS263-PHE274 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 1 |
Details | Active site: {"description":"Proton donor","evidences":[{"source":"UniProtKB","id":"O76083","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 4 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"15260978","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1TAZ","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4NPV","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4NPW","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |