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芳胺N-乙酰基转移酶I

Arylamine N-acetyltransferase I.

作者信息

Minchin Rodney F, Hanna Patrick E, Dupret Jean-Marie, Wagner Carston R, Rodrigues-Lima Fernando, Butcher Neville J

机构信息

School of Biomedical Sciences, University of Queensland, Queensland, Australia.

出版信息

Int J Biochem Cell Biol. 2007;39(11):1999-2005. doi: 10.1016/j.biocel.2006.12.006. Epub 2007 Jan 20.


DOI:10.1016/j.biocel.2006.12.006
PMID:17392017
Abstract

Arylamine N-acetyltransferase I (NAT1) is a phase II enzyme that acetylates a wide range of arylamine and hydrazine substrates. The NAT1 gene is located on chromosome 8 and shares homology to NAT genes found in most mammalian species. Gene expression occurs from at least two promoters and a number of tissue-specific transcripts have been identified. The gene is polymorphic with most mutations identified to date producing an unstable protein that is subject to polyubiquitination. The NAT1 protein contains a catalytic triad similar to a number of cysteine proteases and transglutaminases. NAT1 is widely distributed in the body, but the only endogenous substrate identified to date is the folate catabolite p-aminobenzoylglutamate. Recent links between NAT1 genotypes and susceptibility to spina bifida suggests that the enzyme has an important role in folate homeostasis.

摘要

芳胺N - 乙酰基转移酶I(NAT1)是一种II期酶,可使多种芳胺和肼类底物乙酰化。NAT1基因位于8号染色体上,与大多数哺乳动物物种中发现的NAT基因具有同源性。基因表达至少来自两个启动子,并且已经鉴定出许多组织特异性转录本。该基因具有多态性,迄今为止鉴定出的大多数突变都会产生不稳定的蛋白质,该蛋白质会被多聚泛素化。NAT1蛋白含有一个与许多半胱氨酸蛋白酶和转谷氨酰胺酶相似的催化三联体。NAT1在体内广泛分布,但迄今为止鉴定出的唯一内源性底物是叶酸分解代谢产物对氨基苯甲酰谷氨酸。NAT1基因型与脊柱裂易感性之间的最新联系表明,该酶在叶酸稳态中具有重要作用。

相似文献

[1]
Arylamine N-acetyltransferase I.

Int J Biochem Cell Biol. 2007

[2]
Arylamine N-acetyltransferases: structural and functional implications of polymorphisms.

Toxicology. 2008-12-30

[3]
NMR-based model reveals the structural determinants of mammalian arylamine N-acetyltransferase substrate specificity.

J Mol Biol. 2006-10-13

[4]
Genomic organization of human arylamine N-acetyltransferase Type I reveals alternative promoters that generate different 5'-UTR splice variants with altered translational activities.

Biochem J. 2005-4-1

[5]
Identification of amino acids imparting acceptor substrate selectivity to human arylamine acetyltransferases NAT1 and NAT2.

Biochem J. 2000-5-15

[6]
Effect of arylamine acetyltransferase Nat3 gene knockout on N-acetylation in the mouse.

Drug Metab Dispos. 2007-7

[7]
Identification of the xenobiotic-metabolizing enzyme arylamine N-acetyltransferase 1 as a new target of cisplatin in breast cancer cells: molecular and cellular mechanisms of inhibition.

Mol Pharmacol. 2008-6

[8]
Arylamine N-acetyltransferase aggregation and constitutive ubiquitylation.

J Mol Biol. 2006-8-18

[9]
Arylamine N-acetyltransferases.

Expert Opin Drug Metab Toxicol. 2007-4

[10]
Description of a novel polymorphic gene encoding for arylamine N-acetyltransferase in the rhesus macaque (Macaca mulatta), a model animal for endometriosis.

Pharmacogenet Genomics. 2007-3

引用本文的文献

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Pharmaceutics. 2023-11-15

[2]
Population variability of rhesus macaque (Macaca mulatta) NAT1 gene for arylamine N-acetyltransferase 1: Functional effects and comparison with human.

Sci Rep. 2019-7-29

[3]
Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models.

Arch Toxicol. 2018-6-18

[4]
Evaluation of -Aminosalicylic Acid as a Substrate of Multiple Solute Carrier Uptake Transporters and Possible Drug Interactions with Nonsteroidal Anti-inflammatory Drugs .

Antimicrob Agents Chemother. 2017-4-24

[5]
Importance of the Evaluation of N-Acetyltransferase Enzyme Activity Prior to 5-Aminosalicylic Acid Medication for Ulcerative Colitis.

Inflamm Bowel Dis. 2016-8

[6]
In-depth analysis of the critical genes and pathways in colorectal cancer.

Int J Mol Med. 2015-10

[7]
N-acetyltransferase genotypes and the pharmacokinetics and tolerability of para-aminosalicylic acid in patients with drug-resistant pulmonary tuberculosis.

Antimicrob Agents Chemother. 2015-7

[8]
Effects of human arylamine N-acetyltransferase I knockdown in triple-negative breast cancer cell lines.

Cancer Med. 2015-4

[9]
Differences between murine arylamine N-acetyltransferase type 1 and human arylamine N-acetyltransferase type 2 defined by substrate specificity and inhibitor binding.

BMC Pharmacol Toxicol. 2014-11-29

[10]
Xenobiotic-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models.

Arch Toxicol. 2014-12

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