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:0004497 | monooxygenase activity | MF |
| GO:0005575 | cellular_component | CC |
| GO:0006082 | organic acid metabolic process | BP |
| GO:0006725 | cellular aromatic compound metabolic process | BP |
| GO:0006790 | sulfur compound metabolic process | BP |
| GO:0006807 | nitrogen compound metabolic process | BP |
| GO:0006950 | response to stress | BP |
| GO:0006952 | defense response | BP |
| GO:0008150 | biological_process | BP |
| GO:0008152 | metabolic process | BP |
| GO:0009058 | biosynthetic process | BP |
| GO:0009605 | response to external stimulus | BP |
| GO:0009607 | response to biotic stimulus | BP |
| GO:0009987 | cellular process | BP |
| GO:0016020 | membrane | CC |
| GO:0016143 | S-glycoside metabolic process | BP |
| GO:0016491 | oxidoreductase activity | MF |
| GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | MF |
| GO:0016709 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen | MF |
| GO:0019748 | secondary metabolic process | BP |
| GO:0019757 | glycosinolate metabolic process | BP |
| GO:0019760 | glucosinolate metabolic process | BP |
| GO:0034641 | cellular nitrogen compound metabolic process | BP |
| GO:0042343 | indole glucosinolate metabolic process | BP |
| GO:0042430 | indole-containing compound metabolic process | BP |
| GO:0043207 | response to external biotic stimulus | BP |
| GO:0043436 | oxoacid metabolic process | BP |
| GO:0044237 | cellular metabolic process | BP |
| GO:0044281 | small molecule metabolic process | BP |
| GO:0044550 | secondary metabolite biosynthetic process | BP |
| GO:0046483 | heterocycle metabolic process | BP |
| GO:0050896 | response to stimulus | BP |
| GO:0051704 | obsolete multi-organism process | BP |
| GO:0051707 | response to other organism | BP |
| GO:0055114 | obsolete oxidation-reduction process | BP |
| GO:0071704 | organic substance metabolic process | BP |
| GO:0098542 | defense response to other organism | BP |
| GO:1901135 | carbohydrate derivative metabolic process | BP |
| GO:1901360 | organic cyclic compound metabolic process | BP |
| GO:1901564 | organonitrogen compound metabolic process | BP |
| GO:1901657 | glycosyl compound metabolic process | BP |
| KEGG Term | Name | Description |
|---|---|---|
| map01110 | Biosynthesis of secondary metabolites | - |
| map01110 | Biosynthesis of secondary metabolites | - |
| map01100 | Metabolic pathways | - |
| map01100 | Metabolic pathways | - |
| map01100 | Metabolic pathways | - |
| map01100 | Metabolic pathways | - |
| map00943 | Isoflavonoid biosynthesis | Isoflavonoids are biologically active compounds, such as phytoestrogens, produced by pea family plants. While flavonoids (in the narrow sense) have the 2-phenylchromen-4-one backbone, isoflavonoids have the 3-phenylchromen-4-one backbone with no hydroxyl group substitution at position 2. Isoflavonoids are derived from the flavonoid biosynthesis pathway via liquiritigenin or naringenin. |
| map00905 | Brassinosteroid biosynthesis | Brassinosteroids are a group of plant steroid hormones that regulate growth and development. More than fifty naturally occurring brassinosteroids have been identified in a wide range of plant species. The most abundant and widely occurring brassinosteroids are C28 steroids, and among them brassinolide (BL) is the most biologically active. Plants have multiple pathways for biosynthesis of BL, which are derived from the steroid biosynthetic pathway. Two pathways from campestanol to castasterone (CS), C6 oxidation and the late-C6 oxidation pathways, operate in many plants. Another branching pathway, the early-C22 oxidation pathway, was demonstrated using a brassinosteroid-deficient mutant of Arabidopsis thaliana. Recently, a new shortcut pathway from campesterol to 6-deoxotyphasterol was demonstrated by a functional analysis of cytochrome P450 monooxygenases responsible for brassinosteroid biosynthesis. Thus, at least four pathways are involved in the biosynthesis of CS, and CS is further metabolized to BL by lactonization of the B ring. |
| map00380 | Tryptophan metabolism | - |