4.1.1.80: 4-hydroxyphenylpyruvate decarboxylase

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For detailed information about 4-hydroxyphenylpyruvate decarboxylase, go to the full flat file.

Reaction

Synonyms

decarboxylase, 4-hydroxyphenylpyruvate, p-hydroxyphenylpyruvate decarboxylase

ECTree

     4 Lyases

         4.1 Carbon-carbon lyases

             4.1.1 Carboxy-lyases

                4.1.1.80 4-hydroxyphenylpyruvate decarboxylase

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Results	in table
2	AA Sequence
1	CAS Registry Number
1	KM Value [mM]
1	Molecular Weight [Da]
2	Natural Substrates/ Products (Substrates)
10	Organism
11	Pathway
1	pH Optimum
1	Purification (Commentary)
1	Reaction
1	Reaction Type
10	Reference
10	Source Tissue
9	Specific Activity [micromol/min/mg]
4	Substrates and Products (Substrate)
2	Synonyms
1	Systematic Name
1	Temperature Optimum [°C]

Substrates Products

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Substrates Products on EC 4.1.1.80 - 4-hydroxyphenylpyruvate decarboxylase

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SUBSTRATE

PRODUCT                       

REACTION DIAGRAM

ORGANISM

UNIPROT

COMMENTARY
(Substrate)

LITERATURE
(Substrate)

COMMENTARY
(Product)

LITERATURE
(Product)

Reversibility
r=reversible
ir=irreversible
?=not specified

4-hydroxyphenylpyruvate

4-hydroxyphenylacetaldehyde + CO2

4 entries

4-hydroxyphenylpyruvate

4-hydroxyphenylacetaldehyde + CO2

Berberis canadensis

-

-

441634

-

441634

?

4-hydroxyphenylpyruvate

4-hydroxyphenylacetaldehyde + CO2

Berberis canadensis

-

involved in tyrosine metabolism, precursor of tyrosine, early steps of isoquinoline alkaloid biosynthesis

441634

phenylacetaldehydes furnish the benzylic moiety of the isoquinoline alkaloids in their biosynthesis, formation of the 1-benzylisoquinoline structure requires the condensation of p-hydroxyphenylacetaldehyde with dopamine to form norcoclaurine

441634

?

4-hydroxyphenylpyruvate

4-hydroxyphenylacetaldehyde + CO2

Berberis stolonifera

-

-

441634

-

441634

?

4-hydroxyphenylpyruvate

4-hydroxyphenylacetaldehyde + CO2

Berberis stolonifera

-

involved in tyrosine metabolism, precursor of tyrosine, early steps of isoquinoline alkaloid biosynthesis

441634

phenylacetaldehydes furnish the benzylic moiety of the isoquinoline alkaloids in their biosynthesis, formation of the 1-benzylisoquinoline structure requires the condensation of p-hydroxyphenylacetaldehyde with dopamine to form norcoclaurine

441634

?