arylamine N-acetyltransferase 1; arylamide acetylase 1; monomorphic arylamine N-acetyltransferase; MNAT; N-acetyltransferase type 1; NAT-1 (NAT1 AAC1)
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Function
- role in the detoxification of a plethora of hydrazine & arylamine drugs
- catalyzes the N- or O-acetylation of various arylamine & heterocyclic amine substrates
acetyl-CoA + an arylamine = CoA + an N-acetylarylamine
Structure
- belongs to the arylamine N-acetyltransferase family
Compartment
Pathology
- bioactivates several known carcinogens
Polymorphism
- N-acetylation polymorphism is determined by a low or high NAT activity in liver
- implicated in the action & toxicity of amine-containing drugs
- candidate risk factor for susceptibility to neural tube defects
- slow acetylation genotypes have been associated with lung cancer risk
- the NAT1*10 allele has been associated with increased risk of colon cancer & urinary bladder cancers & with higher levels of N-acetyltransferase activity & DNA adducts in aromatic amine tumor target organs such as colon & urinary bladder
Notes
- NAT1 was historically considered to be monomorphic in nature; NAT2 historically polymorphic NAT
- the allelic variation Ile-149 designated as NAT1*17 is part of the NAT1*11 allelic variation
More general terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/P18440.html
- ↑ NAT alleles http://www.louisville.edu/medschool/pharmacology/NAT.html
- ↑ NIEHS-SNPs http://egp.gs.washington.edu/data/nat1/
- ↑ SHMPD; The singapore human mutation and polymorphism database http://shmpd.bii.a-star.edu.sg/gene.php?genestart=A&genename=NAT1