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A Gene Cluster Encoding Cholesterol Catabolism in a Soil Actinomycete Provides Insight into Mycobacterium tuberculosis Survival in Macrophages

Proceedings of the National Academy of Sciences - PNAS, 2007-02, Vol.104 (6), p.1947-1952

2007

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Gene expression profiling of primary male breast cancers reveals two unique subgroups and identifies N-acetyltransferase-1 (NAT1) as a novel prognostic biomarker

Breast cancer research : BCR, 2012-02, Vol.14 (1), p.R31-R31, Article R31

2012

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From arylamine N-acetyltransferase to folate-dependent acetyl CoA hydrolase: impact of folic acid on the activity of (HUMAN)NAT1 and its homologue (MOUSE)NAT2

PloS one, 2014-05, Vol.9 (5), p.e96370

2014

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Identification of NAD(P)H quinone oxidoreductase activity in azoreductases from P. aeruginosa: azoreductases and NAD(P)H quinone oxidoreductases belong to the same FMN-dependent superfamily of enzymes

PloS one, 2014-06, Vol.9 (6), p.e98551

2014

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Synthesis of Arabino glycosyl triazoles as potential inhibitors of mycobacterial cell wall biosynthesis

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (23), p.6265-6267

2008

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Characterization of a Carbon-Carbon Hydrolase from Mycobacterium tuberculosis Involved in Cholesterol Metabolism

The Journal of biological chemistry, 2010-01, Vol.285 (1), p.434-443

2010

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Prospective virtual screening with Ultrafast Shape Recognition: the identification of novel inhibitors of arylamine N-acetyltransferases

Journal of the Royal Society interface, 2010-02, Vol.7 (43), p.335

2010

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Membrane Biochemistry

Sim, Edith

1, 1982

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Deletion of a xenobiotic metabolizing gene in mice affects folate metabolism

Biochemical and biophysical research communications, 2007-12, Vol.364 (3), p.556-560

2007

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Selective small molecule inhibitors of the potential breast cancer marker, human arylamine N-acetyltransferase 1, and its murine homologue, mouse arylamine N-acetyltransferase 2

Bioorganic & medicinal chemistry, 2009-01, Vol.17 (2), p.905-918

2009

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Exploration of piperidinols as potential antitubercular agents

Molecules (Basel, Switzerland), 2014-10, Vol.19 (10), p.16274-16290

2014

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Downregulation of Hepatic Acetylation of Drugs in Chronic Renal Failure

Journal of the American Society of Nephrology, 2008-07, Vol.19 (7), p.1352-1359

2008

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Drug metabolism and antibiotic resistance in micro‐organisms

British journal of pharmacology, 2017-07, Vol.174 (14), p.2159-2160

2017

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Divergence of Cofactor Recognition across Evolution: Coenzyme A Binding in a Prokaryotic Arylamine N-Acetyltransferase

Journal of molecular biology, 2008-01, Vol.375 (1), p.178-191

2008

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A novel color change mechanism for breast cancer biomarker detection: naphthoquinones as specific ligands of human arylamine N-acetyltransferase 1

PloS one, 2013-08, Vol.8 (8), p.e70600-e70600

2013

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Update on the pharmacogenetics of NATs: structural considerations

Pharmacogenomics, 2008-11, Vol.9 (11), p.1673-1693

2008

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Cloning and Characterization of Arylamine N -Acetyltransferase Genes from Mycobacterium smegmatis and Mycobacterium tuberculosis: Increased Expression Results in Isoniazid Resistance

Journal of Bacteriology, 1999-02, Vol.181 (4), p.1343-1347

1999

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Pathogenic mycobacteria achieve cellular persistence by inhibiting the Niemann-Pick Type C disease cellular pathway

Wellcome open research, 2017-06, Vol.1, p.18-18

2017

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The COOH Terminus of Arylamine N-Acetyltransferase from Salmonella typhimurium Controls Enzymic Activity

The Journal of biological chemistry, 2002-04, Vol.277 (14), p.12175-12181

2002

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Arylamine N-acetyltransferases in mycobacteria

Current drug metabolism, 2008-07, Vol.9 (6), p.510

2008

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Binding of the anti‐tubercular drug isoniazid to the arylamine N‐acetyltransferase protein from Mycobacterium smegmatis

Protein science, 2005-03, Vol.14 (3), p.775-782

2005

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Pathogenic mycobacteria achieve cellular persistence by inhibiting the Niemann-Pick Type C disease cellular pathway

Wellcome open research, 2017, Vol.1, p.18

2017

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Expression, purification, characterization and structure of Pseudomonas aeruginosa arylamine N-acetyltransferase

Biochemical journal, 2005-01, Vol.385 (Pt 2), p.605-612

2005

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Arylamine N-Acetyltransferase-1 Is Highly Expressed in Breast Cancers and Conveys Enhanced Growth and Resistance to Etoposide in Vitro

Molecular cancer research, 2003-09, Vol.1 (11), p.826-835

2003

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A Gene Cluster Encoding Cholesterol Catabolism in a Soil Actinomycete Provides Insight into Mycobacterium tuberculosis Survival in Macrophages

Gene expression profiling of primary male breast cancers reveals two unique subgroups and identifies N-acetyltransferase-1 (NAT1) as a novel prognostic biomarker

From arylamine N-acetyltransferase to folate-dependent acetyl CoA hydrolase: impact of folic acid on the activity of (HUMAN)NAT1 and its homologue (MOUSE)NAT2

Identification of NAD(P)H quinone oxidoreductase activity in azoreductases from P. aeruginosa: azoreductases and NAD(P)H quinone oxidoreductases belong to the same FMN-dependent superfamily of enzymes

Synthesis of Arabino glycosyl triazoles as potential inhibitors of mycobacterial cell wall biosynthesis

Characterization of a Carbon-Carbon Hydrolase from Mycobacterium tuberculosis Involved in Cholesterol Metabolism

Prospective virtual screening with Ultrafast Shape Recognition: the identification of novel inhibitors of arylamine N-acetyltransferases

Membrane Biochemistry

Deletion of a xenobiotic metabolizing gene in mice affects folate metabolism

Selective small molecule inhibitors of the potential breast cancer marker, human arylamine N-acetyltransferase 1, and its murine homologue, mouse arylamine N-acetyltransferase 2

Exploration of piperidinols as potential antitubercular agents

Downregulation of Hepatic Acetylation of Drugs in Chronic Renal Failure

Drug metabolism and antibiotic resistance in micro‐organisms

Divergence of Cofactor Recognition across Evolution: Coenzyme A Binding in a Prokaryotic Arylamine N-Acetyltransferase

A novel color change mechanism for breast cancer biomarker detection: naphthoquinones as specific ligands of human arylamine N-acetyltransferase 1

Update on the pharmacogenetics of NATs: structural considerations

Cloning and Characterization of Arylamine N -Acetyltransferase Genes from Mycobacterium smegmatis and Mycobacterium tuberculosis: Increased Expression Results in Isoniazid Resistance

Pathogenic mycobacteria achieve cellular persistence by inhibiting the Niemann-Pick Type C disease cellular pathway

The COOH Terminus of Arylamine N-Acetyltransferase from Salmonella typhimurium Controls Enzymic Activity

Arylamine N-acetyltransferases in mycobacteria

Binding of the anti‐tubercular drug isoniazid to the arylamine N‐acetyltransferase protein from Mycobacterium smegmatis

Pathogenic mycobacteria achieve cellular persistence by inhibiting the Niemann-Pick Type C disease cellular pathway

Expression, purification, characterization and structure of Pseudomonas aeruginosa arylamine N-acetyltransferase

Arylamine N-Acetyltransferase-1 Is Highly Expressed in Breast Cancers and Conveys Enhanced Growth and Resistance to Etoposide in Vitro

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