1PGF
PROSTAGLANDIN H2 SYNTHASE-1 COMPLEXED WITH 1-(4-IODOBENZOYL)-5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID (IODOINDOMETHACIN), CIS MODEL
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0001516 | biological_process | prostaglandin biosynthetic process |
A | 0004601 | molecular_function | peroxidase activity |
A | 0004666 | molecular_function | prostaglandin-endoperoxide synthase activity |
A | 0005737 | cellular_component | cytoplasm |
A | 0005783 | cellular_component | endoplasmic reticulum |
A | 0005789 | cellular_component | endoplasmic reticulum membrane |
A | 0006979 | biological_process | response to oxidative stress |
A | 0008217 | biological_process | regulation of blood pressure |
A | 0016020 | cellular_component | membrane |
A | 0016702 | molecular_function | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen |
A | 0019371 | biological_process | cyclooxygenase pathway |
A | 0020037 | molecular_function | heme binding |
A | 0042803 | molecular_function | protein homodimerization activity |
A | 0043005 | cellular_component | neuron projection |
A | 0043231 | cellular_component | intracellular membrane-bounded organelle |
A | 0046872 | molecular_function | metal ion binding |
A | 0051213 | molecular_function | dioxygenase activity |
A | 0098869 | biological_process | cellular oxidant detoxification |
B | 0001516 | biological_process | prostaglandin biosynthetic process |
B | 0004601 | molecular_function | peroxidase activity |
B | 0004666 | molecular_function | prostaglandin-endoperoxide synthase activity |
B | 0005737 | cellular_component | cytoplasm |
B | 0005783 | cellular_component | endoplasmic reticulum |
B | 0005789 | cellular_component | endoplasmic reticulum membrane |
B | 0006979 | biological_process | response to oxidative stress |
B | 0008217 | biological_process | regulation of blood pressure |
B | 0016020 | cellular_component | membrane |
B | 0016702 | molecular_function | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen |
B | 0019371 | biological_process | cyclooxygenase pathway |
B | 0020037 | molecular_function | heme binding |
B | 0042803 | molecular_function | protein homodimerization activity |
B | 0043005 | cellular_component | neuron projection |
B | 0043231 | cellular_component | intracellular membrane-bounded organelle |
B | 0046872 | molecular_function | metal ion binding |
B | 0051213 | molecular_function | dioxygenase activity |
B | 0098869 | biological_process | cellular oxidant detoxification |
Functional Information from PDB Data
site_id | COB |
Number of Residues | 4 |
Details | THE CYCLOOXYGENASE ACTIVE SITE IS LOCATED WITHIN A LONG HYDROPHOBIC CHANNEL AT A REGION DEFINED BY RESIDUES ARG 120, SER 530 (SITE OF ASPIRIN ACETYLATION), TYR 385, AND GLU 524. (B CHAIN) |
Chain | Residue |
B | SER530 |
B | TYR385 |
B | GLU524 |
B | ARG120 |
site_id | COX |
Number of Residues | 4 |
Details | THE CYCLOOXYGENASE ACTIVE SITE IS LOCATED WITHIN A LONG HYDROPHOBIC CHANNEL AT A REGION DEFINED BY RESIDUES ARG 120, SER 530 (SITE OF ASPIRIN ACETYLATION), TYR 385, AND GLU 524. (A CHAIN) |
Chain | Residue |
A | ARG120 |
A | SER530 |
A | TYR385 |
A | GLU524 |
site_id | PEB |
Number of Residues | 4 |
Details | THE PEROXIDASE ACTIVE SITE IS AT THE HEME (HEM 601) SITE. HIS 388 IS THE PROXIMAL HEME LIGAND. (B CHAIN) |
Chain | Residue |
B | GLN203 |
B | HIS207 |
B | HIS388 |
B | HEM601 |
site_id | PER |
Number of Residues | 4 |
Details | THE PEROXIDASE ACTIVE SITE IS AT THE HEME (HEM 601) SITE. HIS 388 IS THE PROXIMAL HEME LIGAND. (A CHAIN) |
Chain | Residue |
A | GLN203 |
A | HIS207 |
A | HIS388 |
A | HEM601 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 72 |
Details | TRANSMEM: Helical |
Chain | Residue | Details |
A | ILE74-LEU82 | |
A | PRO86-LEU92 | |
A | ARG97-ALA105 | |
A | ILE108-ASN122 | |
B | ILE74-LEU82 | |
B | PRO86-LEU92 | |
B | ARG97-ALA105 | |
B | ILE108-ASN122 |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | ACT_SITE: Proton acceptor |
Chain | Residue | Details |
A | HIS207 | |
B | HIS207 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | ACT_SITE: For cyclooxygenase activity => ECO:0000269|PubMed:2122967 |
Chain | Residue | Details |
A | TYR385 | |
B | TYR385 |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | BINDING: axial binding residue |
Chain | Residue | Details |
A | HIS388 | |
B | HIS388 |
site_id | SWS_FT_FI5 |
Number of Residues | 2 |
Details | SITE: Not glycosylated => ECO:0000269|PubMed:8349699 |
Chain | Residue | Details |
A | ASN104 | |
B | ASN104 |
site_id | SWS_FT_FI6 |
Number of Residues | 2 |
Details | SITE: Aspirin-acetylated serine |
Chain | Residue | Details |
A | SER530 | |
B | SER530 |
site_id | SWS_FT_FI7 |
Number of Residues | 6 |
Details | CARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000269|PubMed:8349699 |
Chain | Residue | Details |
A | ASN68 | |
A | ASN144 | |
A | ASN410 | |
B | ASN68 | |
B | ASN144 | |
B | ASN410 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1mhl |
Chain | Residue | Details |
A | VAL291 |
site_id | CSA2 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1mhl |
Chain | Residue | Details |
B | VAL291 |
site_id | CSA3 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1mhl |
Chain | Residue | Details |
A | HIS207 | |
A | TYR385 | |
A | GLN203 |
site_id | CSA4 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1mhl |
Chain | Residue | Details |
B | HIS207 | |
B | TYR385 | |
B | GLN203 |