Abstract
Molecular modelling of human cytochrome P450 (CYP) isoforms is described, based on amino acid sequence homology with a unique bacterial P450 (CYP102) of known crystal structure. It is found that for the human hepatic P450s involved in the metabolism of xenobiotics, ie. CYPIA2, CYP 1A6, CYP2B6, CYP2C9, CYP2C 19, CYP2D6, CYP2E1 and CYP3A4, there is a satisfactory agreement between specific substrate characteristics and topographical features of the putative active sites, including complementarity with key amino acid residues in the P450 haem environments. A combination of homology model interactions with substrates and certain molecular properties of the compounds themselves provides a methodology for the evaluation of potential P450 selectivity in new chemical entities (NCEs).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Aryl Hydrocarbon Hydroxylases*
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Bacteria / enzymology
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Binding Sites
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Cytochrome P-450 CYP1A2 / chemistry
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Cytochrome P-450 CYP2A6
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Cytochrome P-450 CYP2C19
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Cytochrome P-450 CYP2C9
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Cytochrome P-450 CYP2D6 / chemistry
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Cytochrome P-450 CYP2E1 / chemistry
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Cytochrome P-450 CYP3A
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Cytochrome P-450 Enzyme System / chemistry*
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Cytochrome P-450 Enzyme System / metabolism*
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Humans
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Liver / enzymology
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Mixed Function Oxygenases / chemistry
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Models, Molecular
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Sequence Homology*
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Steroid 16-alpha-Hydroxylase*
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Steroid Hydroxylases / chemistry
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Substrate Specificity
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Xenobiotics / metabolism*
Substances
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Xenobiotics
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Cytochrome P-450 Enzyme System
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Mixed Function Oxygenases
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Steroid Hydroxylases
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CYP2C9 protein, human
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Cytochrome P-450 CYP2C9
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Cytochrome P-450 CYP2E1
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Aryl Hydrocarbon Hydroxylases
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CYP1A2 protein, human
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CYP2C19 protein, human
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CYP3A protein, human
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Cytochrome P-450 CYP1A2
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Cytochrome P-450 CYP2A6
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Cytochrome P-450 CYP2C19
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Cytochrome P-450 CYP2D6
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Cytochrome P-450 CYP3A
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Steroid 16-alpha-Hydroxylase
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CYP3A4 protein, human