Basic Information
Gene ID
Potrs038591g24779
Position
Potrs038591:1940-3754 (-)
1814bp
Gene Type
gene
Gene Description (Protein Product)
Cytochrome p450
Organism
Also AS Potri.006G094700AT3G52970Potri.006G094700.v4.1

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
Potrs039195g25016 Myb-related protein
Potrs040134g25382 Carotenoid 9,10(9',10')-cleavage dioxygenase 1-like
Potrs041757g26221 Transcription factor
Regulatory gene
Potrs000984g01639 GAGA binding protein-like family
Potrs000984g01640 GAGA binding protein-like family
Potrs002956g04589 Protein BASIC PENTACYSTEINE4-like

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Annotation

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


Pathway
KEGG Term Name Description
map01110 Biosynthesis of secondary metabolites -
map01100 Metabolic pathways -
map00902 Monoterpenoid biosynthesis Monoterpenoids (C10 terpenoids) are a group of terpenoids consisting of two isoprene units. They are derived from geranyl diphosphate (GPP). Most monoterpenoids are volatile oils with highly distinctive aromas and flavors, such as essential oils, turpentine, and oleoresins of coniferous plants. This map shows some examples. The monoterpene ketone l-menthone is specifically converted to l-menthol and d-neomenthol in mature peppermint leaves. The iridoids constitute a family of highly oxygenated monoterpenes, mixtures of which are present in many medicinal plants, such as valerian. They are derived from geraniol or nerol via oxidation of a terminal methyl group. The cyclopentane ring of loganin can itself be cleaved in a further P450-dependent step, leading to secologanin, which provides the carbon skeleton for many powerfully bioactive secondary metabolites of indole alkaloids.