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Crystal structure of human prostacyclin synthase in complex with inhibitor minoxidil[ISOMERASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
Crystal structure of human prostacyclin synthase[ISOMERASE]
Crystal structure of zebrafish prostacyclin synthase (cytochrome P450 8A1) in complex with substrate analog U51605[ISOMERASE]
Crystal structure of zebrafish prostacyclin synthase (cytochrome P450 8A1)[ISOMERASE]
Crystal structure of human CYP7A1[OXIDOREDUCTASE]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
Crystal structure of human lanosterol 14alpha-demethylase (CYP51)[OXIDOREDUCTASE]
Crystal structure of human lanosterol 14alpha-demethylase (CYP51) in complex with econazole[OXIDOREDUCTASE]
Crystal structure of human lanosterol 14alpha-demethylase (CYP51) in complex with ketoconazole[OXIDOREDUCTASE]
X-ray structure of cyp51 from trypanosoma brucei in complex with posaconazole in two different conformations[OXIDOREDUCTASE]
X-ray structure of CYP51 from the human pathogen Trypanosoma brucei in complex with fluconazole[OXIDOREDUCTASE]
Crystal structure of sterol 14-alpha demethylase (CYP51) from Trypanosoma brucei bound to an inhibitor N-(1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethyl)-4-(5-phenyl-1,3,4-oxaziazol-2-yl)benzamide[O...
Crystal structure of sterol 14-alpha demethylase (CYP51) from Trypanosoma brucei in ligand free state[OXIDOREDUCTASE]
Crystal structure of sterol 14alpha-demethylase (CYP51) from Trypanosoma cruzi in complex with an inhibitor VNF ((4-(4-chlorophenyl)-N-[2-(1H-imidazol-1-yl)-1-phenylethyl]benzamide)[OXIDOREDUCTASE]
Crystal structure of sterol 14alpha-demethylase (CYP51) from Trypanosoma cruzi in complex with inhibitor fluconazole[OXIDOREDUCTASE]
Crystal structure of sterol 14-alpha demethylase (CYP51) from Trypanosoma cruzi in complex with a potential antichagasic drug, posaconazole[OXIDOREDUCTASE]
Crystal structure of sterol 14-alpha demethylase (CYP51) from Leishmania infantum in complex with fluconazole[OXIDOREDUCTASE]
Crystal structure analysis of the C37L/C151T/C442A-triple mutant of CYP51 from Mycobacterium tuberculosis[OXIDOREDUCTASE]
CYP51 of M. tuberculosis bound to an inhibitor N-[(1S)-2-METHYL-1-(PYRIDIN-4-YLCARBAMOYL)PROPYL]CYCLOHEXANECARBOXAMIDE[OXIDOREDUCTASE]
CYP51 OF M. TUBERCULOSIS BOUND TO AN INHIBITOR 3-{[(4-METHYLPHENYL)SULFONYL]AMINO}PROPYL PYRIDIN-4-YLCARBAMATE[OXIDOREDUCTASE]
View in iCn3D PubMedProteinsConserved DomainsPubChem Compound
CYP51 OF M. TUBERCULOSIS BOUND TO AN INHIBITOR CIS-4-METHYL-N-[(1S)-3-(METHYLSULFANYL)-1-(PYRIDIN-4-YLCARBAMOYL)PROPYL]CYCLOHEXANECARBOXAMIDE[OXIDOREDUCTASE]
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