6C7I
Crystal structure of human phosphodiesterase 2A with 1-(2-chloro-5-methoxy-phenyl)-N-isobutyl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline-8-carboxamide
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004114 | molecular_function | 3',5'-cyclic-nucleotide phosphodiesterase activity |
A | 0007165 | biological_process | signal transduction |
A | 0008081 | molecular_function | phosphoric diester hydrolase activity |
B | 0004114 | molecular_function | 3',5'-cyclic-nucleotide phosphodiesterase activity |
B | 0007165 | biological_process | signal transduction |
B | 0008081 | molecular_function | phosphoric diester hydrolase activity |
C | 0004114 | molecular_function | 3',5'-cyclic-nucleotide phosphodiesterase activity |
C | 0007165 | biological_process | signal transduction |
C | 0008081 | molecular_function | phosphoric diester hydrolase activity |
D | 0004114 | molecular_function | 3',5'-cyclic-nucleotide phosphodiesterase activity |
D | 0007165 | biological_process | signal transduction |
D | 0008081 | molecular_function | phosphoric diester hydrolase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 16 |
Details | binding site for residue EP7 A 1001 |
Chain | Residue |
A | THR768 |
A | HOH1119 |
A | HOH1128 |
A | HOH1142 |
A | HOH1219 |
A | HOH1237 |
A | HOH1270 |
D | LYS584 |
A | LEU770 |
A | ASP808 |
A | LEU809 |
A | GLN812 |
A | ILE826 |
A | PHE830 |
A | GLN859 |
A | PHE862 |
site_id | AC2 |
Number of Residues | 6 |
Details | binding site for residue ZN A 1002 |
Chain | Residue |
A | HIS660 |
A | HIS696 |
A | ASP697 |
A | ASP808 |
A | HOH1136 |
A | HOH1249 |
site_id | AC3 |
Number of Residues | 6 |
Details | binding site for residue MG A 1003 |
Chain | Residue |
A | ASP697 |
A | HOH1134 |
A | HOH1136 |
A | HOH1176 |
A | HOH1191 |
A | HOH1265 |
site_id | AC4 |
Number of Residues | 18 |
Details | binding site for residue EP7 B 1001 |
Chain | Residue |
B | HIS656 |
B | THR768 |
B | LEU770 |
B | ASP808 |
B | LEU809 |
B | GLN812 |
B | ILE826 |
B | PHE830 |
B | GLN859 |
B | PHE862 |
B | ILE866 |
B | HOH1106 |
B | HOH1149 |
B | HOH1151 |
B | HOH1225 |
B | HOH1248 |
B | HOH1264 |
B | HOH1343 |
site_id | AC5 |
Number of Residues | 6 |
Details | binding site for residue ZN B 1002 |
Chain | Residue |
B | HIS660 |
B | HIS696 |
B | ASP697 |
B | ASP808 |
B | HOH1110 |
B | HOH1254 |
site_id | AC6 |
Number of Residues | 6 |
Details | binding site for residue MG B 1003 |
Chain | Residue |
B | ASP697 |
B | HOH1110 |
B | HOH1119 |
B | HOH1154 |
B | HOH1165 |
B | HOH1260 |
site_id | AC7 |
Number of Residues | 12 |
Details | binding site for residue EP7 C 1001 |
Chain | Residue |
C | THR768 |
C | LEU770 |
C | ASP808 |
C | GLN812 |
C | ILE826 |
C | PHE830 |
C | PHE862 |
C | HOH1113 |
C | HOH1120 |
C | HOH1169 |
C | HOH1199 |
C | HOH1222 |
site_id | AC8 |
Number of Residues | 6 |
Details | binding site for residue ZN C 1002 |
Chain | Residue |
C | HIS660 |
C | HIS696 |
C | ASP697 |
C | ASP808 |
C | HOH1103 |
C | HOH1193 |
site_id | AC9 |
Number of Residues | 6 |
Details | binding site for residue MG C 1003 |
Chain | Residue |
C | ASP697 |
C | HOH1103 |
C | HOH1134 |
C | HOH1147 |
C | HOH1192 |
C | HOH1246 |
site_id | AD1 |
Number of Residues | 15 |
Details | binding site for residue EP7 D 1001 |
Chain | Residue |
A | ASP588 |
A | GLN591 |
D | THR768 |
D | LEU770 |
D | ASP808 |
D | LEU809 |
D | GLN812 |
D | ILE826 |
D | PHE830 |
D | PHE862 |
D | HOH1118 |
D | HOH1175 |
D | HOH1223 |
D | HOH1253 |
D | HOH1294 |
site_id | AD2 |
Number of Residues | 6 |
Details | binding site for residue ZN D 1002 |
Chain | Residue |
D | ASP697 |
D | ASP808 |
D | HOH1144 |
D | HOH1184 |
D | HIS660 |
D | HIS696 |
site_id | AD3 |
Number of Residues | 6 |
Details | binding site for residue MG D 1003 |
Chain | Residue |
D | ASP697 |
D | HOH1140 |
D | HOH1144 |
D | HOH1168 |
D | HOH1169 |
D | HOH1251 |
Functional Information from PROSITE/UniProt
site_id | PS00126 |
Number of Residues | 12 |
Details | PDEASE_I_1 3'5'-cyclic nucleotide phosphodiesterase domain signature. HDLdHrGtnNsF |
Chain | Residue | Details |
A | HIS696-PHE707 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 4 |
Details | ACT_SITE: Proton donor => ECO:0000250|UniProtKB:O76083 |
Chain | Residue | Details |
A | SER912 | |
B | SER912 | |
C | SER912 | |
D | SER912 |
site_id | SWS_FT_FI2 |
Number of Residues | 20 |
Details | BINDING: BINDING => ECO:0000250|UniProtKB:Q922S4 |
Chain | Residue | Details |
A | PHE687 | |
B | GLN755 | |
C | PHE687 | |
C | GLY702 | |
C | SER721 | |
C | ASN744 | |
C | GLN755 | |
D | PHE687 | |
D | GLY702 | |
D | SER721 | |
D | ASN744 | |
A | GLY702 | |
D | GLN755 | |
A | SER721 | |
A | ASN744 | |
A | GLN755 | |
B | PHE687 | |
B | GLY702 | |
B | SER721 | |
B | ASN744 |
site_id | SWS_FT_FI3 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000269|PubMed:15938621, ECO:0000269|PubMed:19828435, ECO:0000269|PubMed:23899287, ECO:0007744|PDB:1Z1L, ECO:0007744|PDB:3IBJ, ECO:0007744|PDB:3ITM, ECO:0007744|PDB:3ITU, ECO:0007744|PDB:4HTX, ECO:0007744|PDB:4HTZ, ECO:0007744|PDB:4JIB |
Chain | Residue | Details |
A | LEU916 | |
B | LEU916 | |
C | LEU916 | |
D | LEU916 |