4.1.99.2: tyrosine phenol-lyase
This is an abbreviated version!
For detailed information about tyrosine phenol-lyase, go to the full flat file.
Word Map on EC 4.1.99.2
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4.1.99.2
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triptolide
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citrobacter
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threatened
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preterm
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two-photon
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luminescence
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freundii
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topless
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tripterygium
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wilfordii
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nitroxide
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quinonoid
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hook
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labour
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erwinia
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herbicola
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co-repressors
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nanorods
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tempol
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beta-elimination
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disaturated
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3,4-dihydroxyphenyl-l-alanine
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tryptophanase
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aldimine
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indole-lyase
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phillips
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tocolysis
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triepoxide
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synthesis
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photoluminescence
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degradation
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biotechnology
- 4.1.99.2
- triptolide
- citrobacter
-
threatened
-
preterm
-
two-photon
-
luminescence
- freundii
-
topless
- tripterygium
- wilfordii
-
nitroxide
-
quinonoid
-
hook
-
labour
- erwinia
- herbicola
-
co-repressors
-
nanorods
-
tempol
-
beta-elimination
-
disaturated
- 3,4-dihydroxyphenyl-l-alanine
- tryptophanase
-
aldimine
-
indole-lyase
-
phillips
-
tocolysis
-
triepoxide
- synthesis
-
photoluminescence
- degradation
- biotechnology
Reaction
Synonyms
beta-tyrosinase, Fn-TPL, L-tyrosine phenol-lyase, phenol-lyase, tyrosine, TnaA, TPL, tyrosine phenol lyase, tyrosine phenol-lyase, tyrosine-phenol lyase
ECTree
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Cofactor
Cofactor on EC 4.1.99.2 - tyrosine phenol-lyase
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pyridoxal 5'-phosphate
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contains 2 mol of pyridoxal phosphate per mol of enzyme
pyridoxal 5'-phosphate
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2 pyridoxal 5'-phosphate binding sites per mol of enzyme
pyridoxal 5'-phosphate
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2 pyridoxal 5'-phosphate binding sites per mol of enzyme
pyridoxal 5'-phosphate
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the phosphate group changes from being monoanionic at low pH to dianionic at high pH
pyridoxal 5'-phosphate
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dependent on, highest activity at 0.015-0.02 mM
pyridoxal 5'-phosphate
dependent on, activates, Km value is 0.0034 mM
pyridoxal 5'-phosphate
dependent on, the active site residues involved in cofactor binding are highly conserved for enzyme TPL. Pyridoxal 5'-phosphate is bound to the internal aldimine by a lysine epsilon-amino group of Lys257 and the protonated pyridine ring forms an ionic/hydrogen bond with an aspartate beta-carboxylate of Asp214