CYP3A5

Ideogram human chromosome 7

Cytochrome P450 3A5
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
Search PMC articles PubMed articles NCBI proteins

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

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

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

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

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

• Cytochrome P450
• CYP3A4
• Pharmacogenomics
• Drug metabolism
• Liver enzyme

External Links

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