Basic Information
Gene Structure
Domain
Regulation&
Interaction
Annotation
Orthologus Group
Pathway
Basic Information
Gene ID
EVM0031993
View in Genome Browser
Position
GWHASIS00000033:21379000-21386747 (+)
7747bp
Gene Type
gene
Gene Description (Protein Product)
Tyrosine decarboxylase
Organism
Acer catalpifolium
Also AS AT2G20340

Gene Structure

upstream:
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Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
EVM0034143 UBA-like domain (DUF1421)
EVM0033585 Histidinol-phosphate aminotransferase
EVM0033859 amine oxidase
Regulatory gene
EVM0000691 radialis-like
EVM0001373 Transcriptional regulator
EVM0001785 transcription factor

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Annotation

Orthologous Group
Orthologous ID Species Number All hits in PereRegDB Hits of this species Orthologous Detail


Pathway
Go Pathway KEGG Pathway
GO Term Description GO Category
GO:0003674 molecular_function MF
GO:0003824 catalytic activity MF
GO:0006082 organic acid metabolic process BP
GO:0006520 amino acid metabolic process BP
GO:0006558 L-phenylalanine metabolic process BP
GO:0006559 L-phenylalanine catabolic process BP
GO:0006725 cellular aromatic compound metabolic process BP
GO:0006807 nitrogen compound metabolic process BP
GO:0006950 response to stress BP
GO:0008150 biological_process BP
GO:0008152 metabolic process BP
GO:0009056 catabolic process BP
GO:0009063 amino acid catabolic process BP
GO:0009072 aromatic amino acid metabolic process BP
GO:0009074 aromatic amino acid family catabolic process BP
GO:0009611 response to wounding BP
GO:0009987 cellular process BP
GO:0016054 organic acid catabolic process BP
GO:0017144 xenobiotic metabolic process BP
GO:0019439 aromatic compound catabolic process BP
GO:0019752 carboxylic acid metabolic process BP
GO:0042737 xenobiotic catabolic process BP
GO:0043436 oxoacid metabolic process BP
GO:0044237 cellular metabolic process BP
GO:0044238 primary metabolic process BP
GO:0044248 cellular catabolic process BP
GO:0044281 small molecule metabolic process BP
GO:0044282 small molecule catabolic process BP
GO:0046395 carboxylic acid catabolic process BP
GO:0050896 response to stimulus BP
GO:0071704 organic substance metabolic process BP
GO:1901360 organic cyclic compound metabolic process BP
GO:1901361 organic cyclic compound catabolic process BP
GO:1901564 organonitrogen compound metabolic process BP
GO:1901565 organonitrogen compound catabolic process BP
GO:1901575 organic substance catabolic process BP
GO:1901605 alpha-amino acid metabolic process BP
GO:1901606 alpha-amino acid catabolic process BP
GO:1902221 erythrose 4-phosphate/phosphoenolpyruvate family amino acid metabolic process BP
GO:1902222 erythrose 4-phosphate/phosphoenolpyruvate family amino acid catabolic process BP
GO:1990055 phenylacetaldehyde synthase activity MF
KEGG Term Name Description
map01110 Biosynthesis of secondary metabolites -
map01110 Biosynthesis of secondary metabolites -
map01100 Metabolic pathways -
map01100 Metabolic pathways -
map00965 Betalain biosynthesis Betalains are water-soluble nitrogen-containing pigments that are present in plants belonging to the order Caryophyllales (such as cactus and amaranth families) and in higher fungi. They contain betalamic acid as the chromophore and are classified into two types: betacyanins and betaxanthins. Betacyanins contain a cyclo-DOPA residue and exhibit red/violet coloration, while betaxanthins contain different amino acids or amino side chains and exhibit a yellow/orange coloration. The condensation of betalamic acid with amino acids (including cyclo-DOPA or amines) in plants is a spontaneous reaction, not an enzyme-catalyzed reaction.
map00950 Isoquinoline alkaloid biosynthesis Isoquinoline alkaloids are tyrosine-derived plant alkaloids with an isoquinoline skeleton. Among them benzylisoquinoline alkaloids form an important group with potent pharmacological activity, including analgesic compounds of morphine and codeine, and anti-infective agents of berberine, palmatine, and magnoflorine. Biosynthesis of isoquinoline alkaloids proceeds via decarboxylation of tyrosine or DOPA to yield dopamine, which together with 4-hydroxyphenylacetaldehyde, an aldehyde derived from tyrosine, is converted to reticuline, an important precursor of various benzylisoquinoline alkaloids.
map00950 Isoquinoline alkaloid biosynthesis Isoquinoline alkaloids are tyrosine-derived plant alkaloids with an isoquinoline skeleton. Among them benzylisoquinoline alkaloids form an important group with potent pharmacological activity, including analgesic compounds of morphine and codeine, and anti-infective agents of berberine, palmatine, and magnoflorine. Biosynthesis of isoquinoline alkaloids proceeds via decarboxylation of tyrosine or DOPA to yield dopamine, which together with 4-hydroxyphenylacetaldehyde, an aldehyde derived from tyrosine, is converted to reticuline, an important precursor of various benzylisoquinoline alkaloids.
map00901 Indole alkaloid biosynthesis -
map00380 Tryptophan metabolism -
map00360 Phenylalanine metabolism -
map00350 Tyrosine metabolism -
map00350 Tyrosine metabolism -