Basic Information
Gene Structure
Domain
Regulation&
Interaction
Annotation
Orthologus Group
Expresssion
Pathway
Basic Information
Gene ID
CSS0047236.g
View in Genome Browser
Position
Chr5:179118954-179124216 (+)
5262bp
Gene Type
gene
Gene Description (Protein Product)
amine oxidase
Organism
Camellia sinensis
Also AS AT4G14940

Gene Structure

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

Regulation&Interaction
Protein-protein interaction (PPI)
CSS0049130.g Histidine
CSS0047996.g Tyrosine decarboxylase
CSS0049086.g Belongs to the aldehyde dehydrogenase family
Regulatory gene
CSS0000220.g Transcription factor
CSS0000233.g ABSCISIC ACID-INSENSITIVE 5-like protein
CSS0000305.g Zinc finger protein

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Annotation

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

Expression Profile
DataSet Number of Samples expressed(TPM>1) Mean Min Max Standard deviation(SD) Coeffcient variation(CV)


Pathway
Go Pathway KEGG Pathway
GO Term Description GO Category
GO:0001101 response to acid chemical BP
GO:0003674 molecular_function MF
GO:0003824 catalytic activity MF
GO:0005575 cellular_component CC
GO:0005618 cell wall CC
GO:0005623 obsolete cell CC
GO:0007154 cell communication BP
GO:0007165 signal transduction BP
GO:0008131 primary amine oxidase activity MF
GO:0008150 biological_process BP
GO:0008152 metabolic process BP
GO:0009719 response to endogenous stimulus BP
GO:0009725 response to hormone BP
GO:0009753 response to jasmonic acid BP
GO:0009755 hormone-mediated signaling pathway BP
GO:0009867 jasmonic acid mediated signaling pathway BP
GO:0009888 tissue development BP
GO:0009987 cellular process BP
GO:0010033 response to organic substance BP
GO:0010035 response to inorganic substance BP
GO:0010087 phloem or xylem histogenesis BP
GO:0010089 xylem development BP
GO:0010941 regulation of cell death BP
GO:0016491 oxidoreductase activity MF
GO:0016638 oxidoreductase activity, acting on the CH-NH2 group of donors MF
GO:0016641 oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor MF
GO:0023052 signaling BP
GO:0030312 external encapsulating structure CC
GO:0032502 developmental process BP
GO:0032870 cellular response to hormone stimulus BP
GO:0042221 response to chemical BP
GO:0043067 regulation of programmed cell death BP
GO:0044464 obsolete cell part CC
GO:0048856 anatomical structure development BP
GO:0050789 regulation of biological process BP
GO:0050794 regulation of cellular process BP
GO:0050896 response to stimulus BP
GO:0051716 cellular response to stimulus BP
GO:0052597 diamine oxidase activity MF
GO:0055114 obsolete oxidation-reduction process BP
GO:0065007 biological regulation BP
GO:0070887 cellular response to chemical stimulus BP
GO:0071229 cellular response to acid chemical BP
GO:0071241 cellular response to inorganic substance BP
GO:0071310 cellular response to organic substance BP
GO:0071395 cellular response to jasmonic acid stimulus BP
GO:0071495 cellular response to endogenous stimulus BP
GO:0071944 cell periphery CC
GO:0090059 protoxylem development BP
GO:0097184 response to azide BP
GO:0097185 cellular response to azide BP
GO:1901698 response to nitrogen compound BP
GO:1901699 cellular response to nitrogen compound BP
GO:1901700 response to oxygen-containing compound BP
GO:1901701 cellular response to oxygen-containing compound BP
KEGG Term Name Description
map01110 Biosynthesis of secondary metabolites -
map01100 Metabolic pathways -
map00960 Tropane, piperidine and pyridine alkaloid biosynthesis -
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.
map00410 beta-Alanine metabolism -
map00360 Phenylalanine metabolism -
map00350 Tyrosine metabolism -
map00260 Glycine, serine and threonine metabolism Serine is derived from 3-phospho-D-glycerate, an intermediate of glycolysis [MD:M00020], and glycine is derived from serine. Threonine is an essential amino acid, which animals cannot synthesize. In bacteria and plants, threonine is derived from aspartate [MD:M00018].