1.2.1.7: benzaldehyde dehydrogenase (NADP+)
This is an abbreviated version!
For detailed information about benzaldehyde dehydrogenase (NADP+), go to the full flat file.
Reaction
Synonyms
4-hydroxy benzaldehyde dehydrogenase, 4-hydroxybenzaldehyde dehydrogenase, mdlD, More, NAD(P)-dependent benzaldehyde dehydrogenase, NADP-linked benzaldehyde dehydrogenase, PpBADH
ECTree
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Substrates Products
Substrates Products on EC 1.2.1.7 - benzaldehyde dehydrogenase (NADP+)
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REACTION DIAGRAM
2,4-dihydroxybenzaldehyde + NAD+ + H2O
2,4-dihydroxybenzoate + NADH + H+
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-
-
-
?
3,4-dihydroxybenzaldehyde + NAD+ + H2O
3,4-dihydroxybenzoate + NADH + H+
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-
-
-
?
3-hydroxy-4-methoxybenzaldehyde + NAD+ + H2O
3-hydroxy-4-methoxybenzoate + NADH + H+
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-
-
-
?
3-hydroxybenzaldehyde + NAD+ + H2O
3-hydroxybenzoate + NADH + H+
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-
-
-
?
3-methoxybenzaldehyde + NAD+ + H2O
3-methoxybenzoate + NADH + H+
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-
-
-
?
4-hydroxy-3-methoxybenzaldehyde + NAD+ + H2O
4-hydroxy-3-methoxybenzoate + NADH + H+
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-
-
-
?
4-hydroxybenzaldehyde + NAD+ + H2O
4-hydroxybenzoate + NADH + H+
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-
-
-
?
isovanillin + NADP+ + H2O
3-hydroxy-4-methoxybenzoate + NADPH
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-
-
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?
4-chlorobenzoate + NADPH + 2 H+
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-
-
?
4-chlorobenzaldehyde + H2O + NADP+
4-chlorobenzoate + NADPH + 2 H+
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-
-
?
4-hydroxybenzoate + NADPH + H+
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-
-
?
4-hydroxybenzaldehyde + NADP+ + H2O
4-hydroxybenzoate + NADPH + H+
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-
-
?
4-methoxybenzoate + NADPH + 2 H+
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-
-
?
4-methoxybenzaldehyde + H2O + NADP+
4-methoxybenzoate + NADPH + 2 H+
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-
-
?
4-nitrobenzoate + NADPH + 2 H+
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-
-
?
4-nitrobenzaldehyde + H2O + NADP+
4-nitrobenzoate + NADPH + 2 H+
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-
-
?
benzaldehyde + H2O + NADP+
benzoate + NADPH + 2 H+
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-
-
?
benzaldehyde + NADP+ + H2O
benzoate + NADPH
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Pseudomonas enzyme on plasmid also active with NAD+, see also EC 1.2.1.28
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ir
benzaldehyde + NADP+ + H2O
benzoate + NADPH
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metabolic pathway of mandelic acid
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?
benzaldehyde + NADP+ + H2O
benzoate + NADPH
-
metabolic pathway of phenylglycine
-
?
benzaldehyde + NADP+ + H2O
benzoate + NADPH
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metabolic pathway of phenylglycine
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?
benzaldehyde + NADP+ + H2O
benzoate + NADPH
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Pseudomonas enzyme on plasmid also active with NAD+, see also EC 1.2.1.28
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ir
?
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specificity data for PpBADH shows that long chain aliphatics containing 5-8 carbons have about twice the relative rate of reactivity than benzaldehyde. As the chain length decreases, the activity declines quickly, with less than 0.1% activity being observed with acetaldehyde. Structure-function analysis
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additional information
?
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specificity data for PpBADH shows that long chain aliphatics containing 5-8 carbons have about twice the relative rate of reactivity than benzaldehyde. As the chain length decreases, the activity declines quickly, with less than 0.1% activity being observed with acetaldehyde. Structure-function analysis
-
-
-
additional information
?
-
specificity data for PpBADH shows that long chain aliphatics containing 5-8 carbons have about twice the relative rate of reactivity than benzaldehyde. As the chain length decreases, the activity declines quickly, with less than 0.1% activity being observed with acetaldehyde. Structure-function analysis
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