1.13.11.38: 1-hydroxy-2-naphthoate 1,2-dioxygenase
This is an abbreviated version!
For detailed information about 1-hydroxy-2-naphthoate 1,2-dioxygenase, go to the full flat file.
Word Map on EC 1.13.11.38
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1.13.11.38
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nocardioides
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gentisate
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salicylate
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phenanthrene
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ring-cleaving
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salicylatoxidans
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pseudaminobacter
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phenanthrene-degrading
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2-carboxybenzaldehyde
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alcaligenes
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sphingomonas
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unobserved
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extradiol-type
- 1.13.11.38
- nocardioides
- gentisate
- salicylate
- phenanthrene
-
ring-cleaving
- salicylatoxidans
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pseudaminobacter
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phenanthrene-degrading
- 2-carboxybenzaldehyde
- alcaligenes
- sphingomonas
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unobserved
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extradiol-type
Reaction
Synonyms
1-H2NA dioxygenase, 1-HNDO, 1-hydroxy-2-naphthoate 1,2-dioxygenase, 1-hydroxy-2-naphthoate dioxygenase, 1-hydroxy-2-naphthoate-degrading enzyme, 1-hydroxy-2-naphthoic acid dioxygenase, 1H2NDO, Diox1, Diox2, oxygenase, 1-hydroxy-2-naphthoate di-, Sphe3 1-H2NA dioxygenase
ECTree
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Substrates Products
Substrates Products on EC 1.13.11.38 - 1-hydroxy-2-naphthoate 1,2-dioxygenase
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REACTION DIAGRAM
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
Gram-negative coccus
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-
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
Gram-negative coccus B156
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-
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
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i.e. trans-2'-carboxybenzalpyruvate
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?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
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-
i.e. trans-2'-carboxybenzalpyruvate. The structure of the ring cleavage product is determined upon separation by high-performance liquid chromatography at pH 2.5 by using nuclear magnetic resonance and mass spectroscopic techniques
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
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enzyme is involved in degradation of phenanthrene
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
the enzyme is involved in degradation of phenanthrene
i.e. trans-2'-carboxybenzalpyruvate
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
enzyme is involved in degradation of phenanthrene
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
i.e. trans-2'-carboxybenzalpyruvate. The structure of the ring cleavage product is determined upon separation by high-performance liquid chromatography at pH 2.5 by using nuclear magnetic resonance and mass spectroscopic techniques
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
i.e. trans-2'-carboxybenzalpyruvate
-
?
1-hydroxy-2-naphthoate + O2
(3E)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
the enzyme is involved in degradation of phenanthrene
i.e. trans-2'-carboxybenzalpyruvate
-
?
(3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
-
-
?
1-hydroxy-2-naphthoate + O2
(3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
-
-
?
1-hydroxy-2-naphthoate + O2
(3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
-
?
1-hydroxy-2-naphthoate + O2
(3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
-
?
1-hydroxy-2-naphthoate + O2
(3Z)-4-(2-carboxyphenyl)-2-oxobut-3-enoate
-
-
-
-
r
?
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gentisate 1,2-dioxygenase with an extraordinary substrate range. Relative activities with salicylate, 5-aminosalicylate, 1-hydroxy-2-naphthoate, and gentisate with both preparations are about 1:10:40:120
-
-
?
1-hydroxy-2-naphthoate + O2
?
-
gentisate 1,2-dioxygenase with an extraordinary substrate range. Relative activities with salicylate, 5-aminosalicylate, 1-hydroxy-2-naphthoate, and gentisate with both preparations are about 1:10:40:120
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-
?
?
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no activity with: gentisate, 3-hydroxyanthranilate, 2-hydroxy-1-naphthoate, 3-hydroxy-2-naphthoate, salicylate, m-hydroxybenzoate, p-hydroxybenzoate, and protocatechuate
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-
?
additional information
?
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no activity with: gentisate, 3-hydroxyanthranilate, 2-hydroxy-1-naphthoate, 3-hydroxy-2-naphthoate, salicylate, m-hydroxybenzoate, p-hydroxybenzoate, and protocatechuate
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-
?
additional information
?
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no activity with 3-hydroxy-2-naphthoic acid
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-
?
additional information
?
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no activity with 3-hydroxy-2-naphthoic acid
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-
?
additional information
?
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no activity with 3-hydroxy-2-naphthoic acid
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-
?
additional information
?
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no activity with 3-hydroxy-2-naphthoic acid
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-
?
additional information
?
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no activity with 3-hydroxy-2-naphthoic acid
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-
?
additional information
?
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1-hydroxy-2-naphthoic acid dioxygenase shows no activity with gentisic acid, salicylic acid and other hydroxynaphthoic acids
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-
?
additional information
?
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Pseudomonas sp. strain PPD can metabolize phenanthrene as the sole source of carbon and energy via the phthalic acid route
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-
?