Basic Information
Gene Structure
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Domain
| Database | EntryID | E-Value | Start | end | InterPro ID | Description |
|---|
Regulation&Interaction
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 Term | Description | GO Category |
|---|---|---|
| GO:0000271 | polysaccharide biosynthetic process | BP |
| GO:0003674 | molecular_function | MF |
| GO:0003824 | catalytic activity | MF |
| GO:0005975 | carbohydrate metabolic process | BP |
| GO:0005976 | polysaccharide metabolic process | BP |
| GO:0006725 | cellular aromatic compound metabolic process | BP |
| GO:0008150 | biological_process | BP |
| GO:0008152 | metabolic process | BP |
| GO:0009058 | biosynthetic process | BP |
| GO:0009059 | macromolecule biosynthetic process | BP |
| GO:0009664 | plant-type cell wall organization | BP |
| GO:0009698 | phenylpropanoid metabolic process | BP |
| GO:0009699 | phenylpropanoid biosynthetic process | BP |
| GO:0009832 | plant-type cell wall biogenesis | BP |
| GO:0009987 | cellular process | BP |
| GO:0010345 | suberin biosynthetic process | BP |
| GO:0010383 | cell wall polysaccharide metabolic process | BP |
| GO:0010393 | galacturonan metabolic process | BP |
| GO:0016043 | cellular component organization | BP |
| GO:0016051 | carbohydrate biosynthetic process | BP |
| GO:0016740 | transferase activity | MF |
| GO:0016746 | acyltransferase activity | MF |
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | MF |
| GO:0017144 | xenobiotic metabolic process | BP |
| GO:0019438 | aromatic compound biosynthetic process | BP |
| GO:0019748 | secondary metabolic process | BP |
| GO:0033692 | cellular polysaccharide biosynthetic process | BP |
| GO:0034637 | cellular carbohydrate biosynthetic process | BP |
| GO:0034645 | cellular macromolecule biosynthetic process | BP |
| GO:0042546 | cell wall biogenesis | BP |
| GO:0043170 | macromolecule metabolic process | BP |
| GO:0044036 | cell wall macromolecule metabolic process | BP |
| GO:0044038 | cell wall macromolecule biosynthetic process | BP |
| GO:0044085 | cellular component biogenesis | BP |
| GO:0044237 | cellular metabolic process | BP |
| GO:0044238 | primary metabolic process | BP |
| GO:0044249 | cellular biosynthetic process | BP |
| GO:0044260 | cellular macromolecule metabolic process | BP |
| GO:0044262 | cellular carbohydrate metabolic process | BP |
| GO:0044264 | cellular polysaccharide metabolic process | BP |
| GO:0044550 | secondary metabolite biosynthetic process | BP |
| GO:0045229 | external encapsulating structure organization | BP |
| GO:0045488 | pectin metabolic process | BP |
| GO:0045489 | pectin biosynthetic process | BP |
| GO:0050734 | hydroxycinnamoyltransferase activity | MF |
| GO:0052325 | cell wall pectin biosynthetic process | BP |
| GO:0052546 | cell wall pectin metabolic process | BP |
| GO:0070589 | cellular component macromolecule biosynthetic process | BP |
| GO:0070592 | cell wall polysaccharide biosynthetic process | BP |
| GO:0071554 | cell wall organization or biogenesis | BP |
| GO:0071555 | cell wall organization | BP |
| GO:0071669 | plant-type cell wall organization or biogenesis | BP |
| GO:0071704 | organic substance metabolic process | BP |
| GO:0071840 | cellular component organization or biogenesis | BP |
| GO:1901360 | organic cyclic compound metabolic process | BP |
| GO:1901362 | organic cyclic compound biosynthetic process | BP |
| GO:1901576 | organic substance biosynthetic process | BP |
| KEGG Term | Name | Description |
|---|---|---|
| map01110 | Biosynthesis of secondary metabolites | - |
| map01100 | Metabolic pathways | - |
| map00945 | Stilbenoid, diarylheptanoid and gingerol biosynthesis | Stilbenoids are a group of phenolic compounds, biosynthetically interrelated through their common origin from a C6-C2-C6 intermediate, such as resveratol found in grapes. Stilbenoids can also exist as glycosides (e.g., piceid). Combretastatins are potentially useful stilbenoid natural products with known antitumor activity. Diarylheptanoid is a compound group having phenyl rings at 1,7 positions of n-heptane (C6-C7-C6), such as curcumin found in the ginger family. [6]-Gingerol is a major active component of ginger and has diverse pharmacologic effects. |
| map00941 | Flavonoid biosynthesis | Flavonoids are a major class of plant secondary metabolites that serves a multitude of functions including pigments and antioxidant activity. Flavonoids are synthesized from phenylpropanoid derivatives by condensation with malonyl-CoA. For example, condensation of p-coumaroyl-CoA (C6-C3) with three malonyl-CoA (C3) molecules results in naringenin chalcone with a diphenylpropane (C6-C3-C6) unit, which is converted to naringenin with the flavone (2-phenylchromen-4-one) backbone by conjugate ring closure. These and further modifications yield a variety of structural forms including chalcones, flavanones, dihyroflavonols, and flavans, anthocyanins, flavones and flavonols, and isoflavonoids. |
| map00940 | Phenylpropanoid biosynthesis | Phenylpropanoids are a group of plant secondary metabolites derived from phenylalanine and having a wide variety of functions both as structural and signaling molecules. Phenylalanine is first converted to cinnamic acid by deamination. It is followed by hydroxylation and frequent methylation to generate coumaric acid and other acids with a phenylpropane (C6-C3) unit. Reduction of the CoA-activated carboxyl groups of these acids results in the corresponding aldehydes and alcohols. The alcohols are called monolignols, the starting compounds for biosynthesis of lignin. |