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Search results 201 to 223 out of 223 for Fmo3

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0.018s
Type Details Score
Publication
First Author: Dolphin CT
Year: 1996
Journal: Eur J Biochem
Title: Differential developmental and tissue-specific regulation of expression of the genes encoding three members of the flavin-containing monooxygenase family of man, FMO1, FMO3 and FM04.
Volume: 235
Issue: 3
Pages: 683-9
Publication
First Author: Burnett VL
Year: 1994
Journal: J Biol Chem
Title: Cloning and sequencing of flavin-containing monooxygenases FMO3 and FMO4 from rabbit and characterization of FMO3.
Volume: 269
Issue: 19
Pages: 14314-22
Publication
First Author: Henderson MC
Year: 2008
Journal: Toxicol Appl Pharmacol
Title: Metabolism of the anti-tuberculosis drug ethionamide by mouse and human FMO1, FMO2 and FMO3 and mouse and human lung microsomes.
Volume: 233
Issue: 3
Pages: 420-7
GO Term
Publication
First Author: Treacy EP
Year: 1998
Journal: Hum Mol Genet
Title: Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.
Volume: 7
Issue: 5
Pages: 839-45
Protein Domain
Type: Family
Description: Flavin-containing monooxygenases (FMOs) constitute a family of xenobiotic-metabolising enzymes []. Using an NADPH cofactor and FAD prosthetic group,these microsomal proteins catalyse the oxygenation of nucleophilic nitrogen,sulphur, phosphorous and selenium atoms in a range of structurally diversecompounds. Five mammalian forms of FMO are now known and have been designatedFMO1-FMO5 [, , , , ].The mRNA encoding FMO3 is abundant in adult liver and is also present, inlow abundance, in some foetal tissues. Thus, like FMO1, FMO3 is subjectto developmental and tissue-specific regulation, with a developmental switchin the expression of the genes taking place in the liver []. The deduced amino acid sequence of human FM03 includes the putative FAD-(GxGxxG) and NADP+pyrophosphate-binding (GxGxxA) sites characteristic ofmammalian FMOs [], a 'FATGY' motif that has also been observed in a rangeof siderphore biosynthetic enzymes [], and a C-terminal hydrophobic segment that is believed to anchor the monooxygenase to the microsomal membrane [].Mutations in human FMO3 impair N-oxygenation of xenobiotics and are responsible for the trimethylaminuria phenotype []. Three disease-causingmutations have been identified. Nonsense and missense mutations are associated with a severe phenotype and are also implicated in impairedmetabolism of other nitrogen- and sulphur-containing substrates, includingbiogenic amines, both clinically and when mutated proteins expressed fromcDNA are studied in vitro []. Human FMO3 thus plays a critical role in themetabolism of xenobiotic substrates and endogenous amines.
Publication      
First Author: Warrier M
Year: 2015
Journal: Cell Rep
Title: The TMAO-Generating Enzyme Flavin Monooxygenase 3 Is a Central Regulator of Cholesterol Balance.
Protein
Organism: Mus musculus/domesticus
Length: 534  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 534  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 532  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 280  
Fragment?: false
Publication
First Author: Ozols J
Year: 1990
Journal: J Biol Chem
Title: Covalent structure of liver microsomal flavin-containing monooxygenase form 1.
Volume: 265
Issue: 18
Pages: 10289-99
Publication
First Author: Stehr M
Year: 1998
Journal: Trends Biochem Sci
Title: A hydrophobic sequence motif common to N-hydroxylating enzymes.
Volume: 23
Issue: 2
Pages: 56-7
Publication
First Author: Li Q
Year: 2013
Journal: Curr Biol
Title: Synchronous evolution of an odor biosynthesis pathway and behavioral response.
Volume: 23
Issue: 1
Pages: 11-20
Publication
First Author: Lee C
Year: 2013
Journal: Drug Metab Dispos
Title: Downregulation of mouse hepatic CYP3A protein by 3-methylcholanthrene does not require cytochrome P450-dependent metabolism.
Volume: 41
Issue: 10
Pages: 1782-6
Publication  
First Author: Gatticchi L
Year: 2020
Journal: Front Cell Dev Biol
Title: Tm7sf2 Disruption Alters Radial Gene Positioning in Mouse Liver Leading to Metabolic Defects and Diabetes Characteristics.
Volume: 8
Pages: 592573
Publication
First Author: Itoh K
Year: 1997
Journal: J Toxicol Sci
Title: Molecular cloning of mouse liver flavin containing monooxygenase (FMO1) cDNA and characterization of the expression product: metabolism of the neurotoxin, 1,2,3,4-tetrahydroisoquinoline (TIQ).
Volume: 22
Issue: 1
Pages: 45-56
Publication  
First Author: Dolphin CT
Year: 1992
Journal: Biochem J
Title: Cloning, primary sequence and chromosomal localization of human FMO2, a new member of the flavin-containing mono-oxygenase family.
Volume: 287 ( Pt 1)
Pages: 261-7
Publication
First Author: Lawton MP
Year: 1990
Journal: J Biol Chem
Title: The flavin-containing monooxygenase enzymes expressed in rabbit liver and lung are products of related but distinctly different genes.
Volume: 265
Issue: 10
Pages: 5855-61
Publication
First Author: Dolphin C
Year: 1991
Journal: J Biol Chem
Title: Cloning, primary sequence, and chromosomal mapping of a human flavin-containing monooxygenase (FMO1).
Volume: 266
Issue: 19
Pages: 12379-85
Publication
First Author: Atta-Asafo-Adjei E
Year: 1993
Journal: J Biol Chem
Title: Cloning, sequencing, distribution, and expression in Escherichia coli of flavin-containing monooxygenase 1C1. Evidence for a third gene subfamily in rabbits.
Volume: 268
Issue: 13
Pages: 9681-9
Publication
First Author: Lomri N
Year: 1992
Journal: Proc Natl Acad Sci U S A
Title: Molecular cloning of the flavin-containing monooxygenase (form II) cDNA from adult human liver.
Volume: 89
Issue: 5
Pages: 1685-9
Publication
First Author: Trenteseaux C
Year: 2017
Journal: Arterioscler Thromb Vasc Biol
Title: Perinatal Hypercholesterolemia Exacerbates Atherosclerosis Lesions in Offspring by Altering Metabolism of Trimethylamine-N-Oxide and Bile Acids.
Volume: 37
Issue: 11
Pages: 2053-2063