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:0003674 | molecular_function | MF |
| GO:0003824 | catalytic activity | MF |
| GO:0008150 | biological_process | BP |
| GO:0008152 | metabolic process | BP |
| GO:0009889 | regulation of biosynthetic process | BP |
| GO:0009890 | negative regulation of biosynthetic process | BP |
| GO:0009892 | negative regulation of metabolic process | BP |
| GO:0009962 | regulation of flavonoid biosynthetic process | BP |
| GO:0009964 | negative regulation of flavonoid biosynthetic process | BP |
| GO:0016491 | oxidoreductase activity | MF |
| GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | MF |
| GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | MF |
| GO:0019222 | regulation of metabolic process | BP |
| GO:0033729 | anthocyanidin reductase activity | MF |
| GO:0048519 | negative regulation of biological process | BP |
| GO:0050789 | regulation of biological process | BP |
| GO:0055114 | obsolete oxidation-reduction process | BP |
| GO:0065007 | biological regulation | BP |
| GO:0080090 | regulation of primary metabolic process | BP |
| KEGG Term | Name | Description |
|---|---|---|
| map01110 | Biosynthesis of secondary metabolites | - |
| map01100 | Metabolic pathways | - |
| 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. |