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Membrane-attached mammalian cytochromes P450: An overview of the membrane's effects on structure, drug binding, and interactions with redox partners

期刊

JOURNAL OF INORGANIC BIOCHEMISTRY
卷 183, 期 -, 页码 117-136

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2018.03.002

关键词

CYP; Drug metabolism; Protein-membrane interactions; Ligand passage

资金

  1. Czech Grant Agency [P208/12/G016]
  2. Palacky University Olomouc [IGA_PrF_2018_032]
  3. Ministry of Education, Youth and Sports of the Czech Republic [LO1305, CZ.02.2.69/0.0/0.0/16]

向作者/读者索取更多资源

Mammalian cytochromes P450 are an important class of enzymes involved in the biotransformation of many endo- and exogenous compounds. Cytochrome P450 isoforms are attached to the membrane of the endoplasmic reticulum or mitochondria, and their catalytic domains move along the membrane surface while being partially immersed in the membrane environment. Their active sites are connected to both the membrane and cytosolic environments via a complex network of access channels. Consequently, they can accept substrates from both environments. The membrane also supports the interactions of cytochromes P450 with their redox partners. In this review, we provide an overview of current knowledge of the structure, flexibility, and interactions with substrates and redox partners of cytochrome P450 on membranes, amalgamating information derived from both experiments and simulations.

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