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Crystal Structure of Human Microsomal P450 3A4[OXIDOREDUCTASE]
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Crystal structure of human cytochrome P4503A4 bound to an inhibitor ritonavir[OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR]
Crystal structure of human P450 3A4 in complex with ketoconazole[OXIDOREDUCTASE]
Crystal structure of human P450 3A4 in complex with erythromycin[OXIDOREDUCTASE]
Crystal structure of human cytochrome P450 3A4[OXIDOREDUCTASE]
Clotrimazole complex of Cytochrome P450 46A1[OXIDOREDUCTASE]
Voriconazole complex of Cytochrome P450 46A1[OXIDOREDUCTASE]
Tranylcypromine complex of Cytochrome P450 46A1[OXIDOREDUCTASE]
Thioperamide complex of Cytochrome P450 46A1[OXIDOREDUCTASE]
Crystal structure of human cytochrome P450 46A1[OXIDOREDUCTASE]
Crystal structure of human cytochrome P450 46A1 in complex with cholesterol-3-sulphate[OXIDOREDUCTASE]
Structure of the A264E mutant of cytochrome P450 BM3 complexed with palmitoleate[OXIDOREDUCTASE]
A single mutation of P450 BM3 induces the conformational rearrangement seen upon substrate-binding in wild-type enzyme[OXIDOREDUCTASE]
Distinct Monooxygenase and Farnesene Synthase Active Sites in Cytochrome P450 170A1[OXIDOREDUCTASE]
Crystal structure of Cytochrome P450 170A1 (CYP170A1) from Streptomyces coelicolor[OXIDOREDUCTASE]
Crystal structure of the A264Q heme domain of cytochrome P450 BM3[OXIDOREDUCTASE]
Structure of the A264K mutant of cytochrome P450 BM3[OXIDOREDUCTASE]
Structure of N-(12-imidazolyl-dodecanoyl)-L-leucine inhibitor bound to the heme domain of Cytochrome P450-BM3[OXIDOREDUCTASE]
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