CYP3A5
Cytochrome P450 3A5 | |||||||||
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Identifiers | |||||||||
EC number | 1.14.14.1 | ||||||||
CAS number | 120831-25-4 | ||||||||
Databases | |||||||||
IntEnz | IntEnz view | ||||||||
BRENDA | BRENDA entry | ||||||||
ExPASy | NiceZyme view | ||||||||
KEGG | KEGG entry | ||||||||
MetaCyc | metabolic pathway | ||||||||
PRIAM | profile | ||||||||
PDB structures | RCSB PDB PDBe PDBsum | ||||||||
Gene Ontology | AmiGO / QuickGO | ||||||||
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Cytochrome P450 3A5 (CYP3A5) is an enzyme that belongs to the cytochrome P450 family. It is involved in the metabolism of various substances in the body, including drugs, steroids, and carcinogens. The enzyme is encoded by the CYP3A5 gene, which is located on chromosome 7.
Function[edit | edit source]
CYP3A5 is primarily expressed in the liver and intestine, where it plays a crucial role in the oxidation of small organic molecules. This enzyme is responsible for the metabolism of approximately 50% of all drugs used in clinical practice, making it a significant player in pharmacokinetics.
Genetic Variability[edit | edit source]
The expression of CYP3A5 varies significantly among individuals due to genetic polymorphisms. The most common polymorphism is the CYP3A5*3 allele, which results in a splicing defect and reduced enzyme activity. Individuals with the CYP3A5*1 allele, on the other hand, have higher enzyme activity. This genetic variability can influence drug metabolism and efficacy, leading to personalized medicine approaches.
Clinical Significance[edit | edit source]
CYP3A5 is involved in the metabolism of several important drugs, including tacrolimus, cyclosporine, and midazolam. Variations in CYP3A5 activity can affect drug levels and therapeutic outcomes. For example, individuals with the CYP3A5*1 allele may require higher doses of tacrolimus to achieve therapeutic levels.
Related Enzymes[edit | edit source]
CYP3A5 is part of the CYP3A subfamily, which also includes CYP3A4, CYP3A7, and CYP3A43. These enzymes share similar substrate specificities but differ in their expression patterns and regulatory mechanisms.
See Also[edit | edit source]
References[edit | edit source]
External Links[edit | edit source]
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Contributors: Prab R. Tumpati, MD