phenylpyruvate tautomerase

Known as: arylpyruvate keto-enol tautomerase, p-hydroxyphenylpyruvate tautomerase 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1962-2012
01219622012

Papers overview

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2012
2012
A human inborn genetic disease, type I phenylketonuria [13] (PKU) is caused by a mutation in the gene encoding the enzyme… (More)
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2004
2004
p-Hydroxyphenylpyruvate dioxygenase (HPD) plays a key role in the normal catabolism of tyrosine. An Fe2+/oxygen-dependent enzyme… (More)
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2003
2003
5 Abstract The bacterial strains Rhodococcus (opacus) erythropolis HL PM-1 and Nocardioides simplex FJ2-1A can use picric acid… (More)
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2002
2002
Coronatine-inducible tyrosine aminotransferase (TAT), which catalyses the transamination from tyrosine to p-hydroxyphenylpyruvate… (More)
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2000
2000
Phenylpyruvate tautomerase (PPT) has been studied periodically since its activity was first described over forty years ago. In… (More)
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1999
1999
The effect of p-hydroxyphenylpyruvate, a natural analogue of transketolase substrate, on the catalytic activity of the enzyme was… (More)
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1996
1996
4-Oxalocrotonate tautomerase (4-OT), a homohexamer consisting of 62 residues per subunit, catalyzes the isomerization of… (More)
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1991
1991
An adult patient with hereditary tyrosinaemia type I who developed renal failure is reported. She received a renal transplant at… (More)
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Highly Cited
1966
Highly Cited
1966
Pittard, James (School of Microbiology, University of Melbourne, Victoria, Australia), and B. J. Wallace. Distribution and… (More)
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1962
1962
Ewald and Hübener1 have recently described a new method for the determination of tyrosine-α-ketoglutarate transaminase activity… (More)
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