2X7Y
P450 BM3 F87A in complex with DMSO
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004497 | molecular_function | monooxygenase activity |
A | 0005506 | molecular_function | iron ion binding |
A | 0016705 | molecular_function | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen |
A | 0020037 | molecular_function | heme binding |
B | 0004497 | molecular_function | monooxygenase activity |
B | 0005506 | molecular_function | iron ion binding |
B | 0016705 | molecular_function | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen |
B | 0020037 | molecular_function | heme binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 28 |
Details | BINDING SITE FOR RESIDUE HEM A 1456 |
Chain | Residue |
A | LYS69 |
A | THR268 |
A | THR269 |
A | PHE331 |
A | PRO392 |
A | PHE393 |
A | GLY394 |
A | ARG398 |
A | CYS400 |
A | ILE401 |
A | GLY402 |
A | LEU75 |
A | ALA406 |
A | DMS1460 |
A | HOH2272 |
A | HOH2273 |
A | HOH2274 |
A | HOH2275 |
A | HOH2276 |
A | HOH2277 |
A | HOH2279 |
A | LEU86 |
A | ALA87 |
A | TRP96 |
A | PHE107 |
A | PHE261 |
A | ALA264 |
A | GLY265 |
site_id | AC2 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN A 1457 |
Chain | Residue |
A | ASP231 |
A | HIS236 |
A | HIS285 |
A | HOH2278 |
site_id | AC3 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE ZN A 1458 |
Chain | Residue |
A | HIS92 |
A | LYS336 |
B | GLU373 |
site_id | AC4 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE ZN A 1459 |
Chain | Residue |
A | ASP338 |
A | GLU348 |
B | HIS285 |
site_id | AC5 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE DMS A 1460 |
Chain | Residue |
A | ALA264 |
A | HEM1456 |
A | HOH2279 |
site_id | AC6 |
Number of Residues | 26 |
Details | BINDING SITE FOR RESIDUE HEM B 1456 |
Chain | Residue |
B | LYS69 |
B | LEU86 |
B | ALA87 |
B | TRP96 |
B | PHE107 |
B | PHE261 |
B | ALA264 |
B | GLY265 |
B | THR268 |
B | THR269 |
B | ALA328 |
B | PHE331 |
B | PRO392 |
B | PHE393 |
B | GLY394 |
B | ARG398 |
B | ALA399 |
B | CYS400 |
B | ILE401 |
B | GLY402 |
B | DMS1458 |
B | HOH2194 |
B | HOH2268 |
B | HOH2269 |
B | HOH2270 |
B | HOH2272 |
site_id | AC7 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE ZN B 1457 |
Chain | Residue |
B | ASP231 |
B | HIS236 |
B | GLU430 |
site_id | AC8 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE DMS B 1458 |
Chain | Residue |
B | HEM1456 |
B | HOH2273 |
Functional Information from PROSITE/UniProt
site_id | PS00086 |
Number of Residues | 10 |
Details | CYTOCHROME_P450 Cytochrome P450 cysteine heme-iron ligand signature. FGnGQRACIG |
Chain | Residue | Details |
A | PHE393-GLY402 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:15020590, ECO:0007744|PDB:1SMJ |
Chain | Residue | Details |
A | TYR51 | |
B | TYR51 |
Chain | Residue | Details |
A | CYS400 | |
B | CYS400 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | SITE: Important for catalytic activity => ECO:0000305|PubMed:16403573, ECO:0000305|PubMed:7578081 |
Chain | Residue | Details |
A | THR268 | |
B | THR268 |
Catalytic Information from CSA
site_id | MCSA1 |
Number of Residues | 3 |
Details | M-CSA 699 |
Chain | Residue | Details |
A | THR268 | electrostatic stabiliser, steric role |
A | PHE393 | electrostatic stabiliser, steric role |
A | CYS400 | electrostatic stabiliser |
site_id | MCSA2 |
Number of Residues | 3 |
Details | M-CSA 699 |
Chain | Residue | Details |
B | THR268 | electrostatic stabiliser, steric role |
B | PHE393 | electrostatic stabiliser, steric role |
B | CYS400 | electrostatic stabiliser |