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Enzyme Polymorphism: History
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Contributor: Yu Peng

Enzyme polymorphism is the occurrence of inherited variation in enzyme structure, abundance, or activity within a population. Alternative alleles can encode molecular forms with different biochemical properties or alter the amount of enzyme produced [1]. Such genetic variation contributes to differences in metabolic phenotypes among individuals [2]. In methyltransferases, sequence variation can change enzyme properties and the rate at which particular compounds undergo methylation [3]. Regulatory variants, coding substitutions, and differences in gene copy number can contribute through distinct molecular routes. The observed phenotype also incorporates the cellular environment and the substrate being examined [4]. Characterization links the frequency and identity of inherited variants to measurements of expression or catalytic function, while distinguishing variants with demonstrated functional effects from those without established biochemical consequences [5].

  • genetic variation
  • enzyme activity
  • alleles
  • pharmacogenetics

Enzyme function and inhibition·Molecular Biology·Biochemistry, Genetics and Molecular Biology·Life Sciences

References

  1. Allan E. Rettie; Jeffrey P. Jones; CLINICAL AND TOXICOLOGICAL RELEVANCE OF CYP2C9: Drug-Drug Interactions and Pharmacogenetics. Annu. Rev. Pharmacol. Toxicol. 2005, 45, 477-494, 10.1146/annurev.pharmtox.45.120403.095821.
  2. Allen D. Roses; Pharmacogenetics and the practice of medicine. Nature 2000, 405, 857-865, 10.1038/35015728.
  3. Richard M. Weinshilboum; Diane M. Otterness; Carol L. Szumlanski; METHYLATION PHARMACOGENETICS: Catechol O-Methyltransferase, Thiopurine Methyltransferase, and Histamine N-Methyltransferase. Annu. Rev. Pharmacol. Toxicol. 1999, 39, 19-52, 10.1146/annurev.pharmtox.39.1.19.
  4. Urs A. Meyer; Pharmacogenetics – five decades of therapeutic lessons from genetic diversity. Nat. Rev. Genet. 2004, 5, 669-676, 10.1038/nrg1428.
  5. Rafał Prost; Wojciech Płaziński; Natural Polymorphic Variants in the CYP450 Superfamily: A Review of Potential Structural Mechanisms and Functional Consequences. Int. J. Mol. Sci. 2025, 26, 7797, 10.3390/ijms26167797.
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