Basic Information
Gene Structure
Domain
Regulation&
Interaction
Annotation
Orthologus Group
Pathway
Basic Information
Gene ID
Potrs015340g28126
View in Genome Browser
Position
Potrs015340:1-1791 (-)
1790bp
Gene Type
gene
Gene Description (Protein Product)
Nudix hydrolase
Organism
Populus tremuloides
Also AS Potri.008G114400AT1G68760Potri.008G114400.v4.1

Gene Structure

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

Regulation&Interaction
Protein-protein interaction (PPI)
Potrs034016g23855 Belongs to the FPP GGPP synthase family
Potrs034016g23854 Belongs to the FPP GGPP synthase family
Potrs018749g20976 glycerol-3-phosphate dehydrogenase NAD(
Regulatory gene
Potrs000274g00383 Squamosa promoter-binding-like protein
Potrs000389g00482 Dof domain, zinc finger
Potrs000883g01405 dof zinc finger protein

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Annotation

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


Pathway
Go Pathway KEGG Pathway
GO Term Description GO Category
GO:0003674 molecular_function MF
GO:0003824 catalytic activity MF
GO:0005575 cellular_component CC
GO:0005622 intracellular anatomical structure CC
GO:0005623 obsolete cell CC
GO:0005737 cytoplasm CC
GO:0005829 cytosol CC
GO:0006139 nucleobase-containing compound metabolic process BP
GO:0006163 purine nucleotide metabolic process BP
GO:0006195 purine nucleotide catabolic process BP
GO:0006203 dGTP catabolic process BP
GO:0006725 cellular aromatic compound metabolic process BP
GO:0006753 nucleoside phosphate metabolic process BP
GO:0006793 phosphorus metabolic process BP
GO:0006796 phosphate-containing compound metabolic process BP
GO:0006807 nitrogen compound metabolic process BP
GO:0006950 response to stress BP
GO:0006974 cellular response to DNA damage stimulus BP
GO:0008150 biological_process BP
GO:0008152 metabolic process BP
GO:0008413 8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity MF
GO:0009056 catabolic process BP
GO:0009058 biosynthetic process BP
GO:0009117 nucleotide metabolic process BP
GO:0009141 nucleoside triphosphate metabolic process BP
GO:0009143 nucleoside triphosphate catabolic process BP
GO:0009144 purine nucleoside triphosphate metabolic process BP
GO:0009146 purine nucleoside triphosphate catabolic process BP
GO:0009151 purine deoxyribonucleotide metabolic process BP
GO:0009155 purine deoxyribonucleotide catabolic process BP
GO:0009166 nucleotide catabolic process BP
GO:0009200 deoxyribonucleoside triphosphate metabolic process BP
GO:0009204 deoxyribonucleoside triphosphate catabolic process BP
GO:0009215 purine deoxyribonucleoside triphosphate metabolic process BP
GO:0009217 purine deoxyribonucleoside triphosphate catabolic process BP
GO:0009262 deoxyribonucleotide metabolic process BP
GO:0009264 deoxyribonucleotide catabolic process BP
GO:0009394 2'-deoxyribonucleotide metabolic process BP
GO:0009987 cellular process BP
GO:0016462 pyrophosphatase activity MF
GO:0016787 hydrolase activity MF
GO:0016817 hydrolase activity, acting on acid anhydrides MF
GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides MF
GO:0018130 heterocycle biosynthetic process BP
GO:0019177 dihydroneopterin triphosphate pyrophosphohydrolase activity MF
GO:0019438 aromatic compound biosynthetic process BP
GO:0019439 aromatic compound catabolic process BP
GO:0019637 organophosphate metabolic process BP
GO:0019692 deoxyribose phosphate metabolic process BP
GO:0033554 cellular response to stress BP
GO:0034404 nucleobase-containing small molecule biosynthetic process BP
GO:0034641 cellular nitrogen compound metabolic process BP
GO:0034654 nucleobase-containing compound biosynthetic process BP
GO:0034655 nucleobase-containing compound catabolic process BP
GO:0035539 8-oxo-7,8-dihydrodeoxyguanosine triphosphate pyrophosphatase activity MF
GO:0044237 cellular metabolic process BP
GO:0044238 primary metabolic process BP
GO:0044248 cellular catabolic process BP
GO:0044249 cellular biosynthetic process BP
GO:0044270 cellular nitrogen compound catabolic process BP
GO:0044271 cellular nitrogen compound biosynthetic process BP
GO:0044281 small molecule metabolic process BP
GO:0044283 small molecule biosynthetic process BP
GO:0044424 obsolete intracellular part CC
GO:0044444 obsolete cytoplasmic part CC
GO:0044464 obsolete cell part CC
GO:0046070 dGTP metabolic process BP
GO:0046386 deoxyribose phosphate catabolic process BP
GO:0046434 organophosphate catabolic process BP
GO:0046483 heterocycle metabolic process BP
GO:0046700 heterocycle catabolic process BP
GO:0047429 nucleoside triphosphate diphosphatase activity MF
GO:0050896 response to stimulus BP
GO:0051716 cellular response to stimulus BP
GO:0055086 nucleobase-containing small molecule metabolic process BP
GO:0071704 organic substance metabolic process BP
GO:0072521 purine-containing compound metabolic process BP
GO:0072523 purine-containing compound catabolic process BP
GO:1901135 carbohydrate derivative metabolic process BP
GO:1901136 carbohydrate derivative catabolic process BP
GO:1901292 nucleoside phosphate catabolic process BP
GO:1901360 organic cyclic compound metabolic process BP
GO:1901361 organic cyclic compound catabolic process BP
GO:1901362 organic cyclic compound biosynthetic process BP
GO:1901564 organonitrogen compound metabolic process BP
GO:1901565 organonitrogen compound catabolic process BP
GO:1901575 organic substance catabolic process BP
GO:1901576 organic substance biosynthetic process BP
KEGG Term Name Description
map01110 Biosynthesis of secondary metabolites -
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.