| EC Number | Metals/Ions | Comment | Organism | Structure |
|---|---|---|---|---|
| 1.14.14.122 | Fe2+ | in heme cofactor | Oryza sativa Japonica Group |
| EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 1.1.1.295 | 3beta-hydroxy-9beta-pimara-7,15-diene-19,6beta-olide + NAD(P)+ | Oryza sativa Japonica Group | - |
momilactone A + NAD(P)H + H+ | - |
? |
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 1.1.1.295 | Oryza sativa Japonica Group | Q7FAE2 | - |
- |
| 1.14.14.122 | Oryza sativa Japonica Group | Q6Z5I7 | - |
- |
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 1.1.1.295 | 3beta-hydroxy-9beta-pimara-7,15-diene-19,6beta-olide + NAD(P)+ | - |
Oryza sativa Japonica Group | momilactone A + NAD(P)H + H+ | - |
? |
| EC Number | Synonyms | Comment | Organism |
|---|---|---|---|
| 1.1.1.295 | momilactone A synthase | - |
Oryza sativa Japonica Group |
| 1.1.1.295 | OsMAS2 | - |
Oryza sativa Japonica Group |
| 1.14.14.122 | oryzalexin synthase | - |
Oryza sativa Japonica Group |
| EC Number | Cofactor | Comment | Organism | Structure |
|---|---|---|---|---|
| 1.1.1.295 | NAD(P)+ | - |
Oryza sativa Japonica Group | |
| 1.1.1.295 | NAD(P)H | - |
Oryza sativa Japonica Group | |
| 1.14.14.122 | heme | - |
Oryza sativa Japonica Group |
| EC Number | Organism | Comment | Expression |
|---|---|---|---|
| 1.1.1.295 | Oryza sativa Japonica Group | early regulation of genes putatively related to rice root-knot nematode (RRKN) Meloidogyne graminicola damage-associated molecular pattern recognition (e.g. wall-associated receptor kinases), signalling (nucleotide-binding, leucine-rich repeat (NLRs)), pathogenesis-related (PR) genes (PR1, PR10a), defence-related genes (NB-ARC domain-containing genes), as well as a large number of genes involved in secondary metabolites including diterpenoid biosynthesis (CPS2, OsKSL4, OsKSL10, Oscyp71Z2, oryzalexin synthase, and momilactone A synthase) is observed in rice Meloidogyne graminicola-resistant mutant line-9. After the nematode juveniles penetrate the roots of line-9, early recognition of invading nematodes triggers plant immune responses mediated by phytoalexins, and other defence proteins such as PR proteins inhibit nematode growth and reproduction. Mechanisms underlying plant-nematode resistance in rice, overview | additional information |
| EC Number | General Information | Comment | Organism |
|---|---|---|---|
| 1.1.1.295 | metabolism | early regulation of genes putatively related to nematode damage-associated molecular pattern recognition (e.g. wall-associated receptor kinases), signalling (nucleotide-binding, leucine-rich repeat (NLRs)), pathogenesis-related (PR) genes (PR1, PR10a), defence-related genes (NB-ARC domain-containing genes), as well as a large number of genes involved in secondary metabolites including diterpenoid biosynthesis (CPS2, OsKSL4, OsKSL10, Oscyp71Z2, oryzalexin synthase, and momilactone A synthase) is observed in rice Meloidogyne graminicola-resistant mutant line-9. After the nematode juveniles penetrate the roots of line-9, early recognition of invading nematodes triggers plant immune responses mediated by phytoalexins, and other defence proteins such as PR proteins inhibit nematode growth and reproduction. Mechanisms underlying plant-nematode resistance in rice, overview. Momilactone A is one of several phytoalexins also such as oryzalexin D, oryzalexin E, and phytocassane being part of the secondary metabolite biosynthesis pathways activated in defense. The enzyme is involved in diterpenoid biosynthesis | Oryza sativa Japonica Group |
| 1.14.14.122 | metabolism | early regulation of genes putatively related to nematode damage-associated molecular pattern recognition (e.g. wall-associated receptor kinases), signalling [nucleotide-binding, leucine-rich repeat (NLRs)], pathogenesis-related (PR) genes (PR1, PR10a), defence-related genes (NB-ARC domain-containing genes), as well as a large number of genes involved in secondary metabolites including diterpenoid biosynthesis (CPS2, OsKSL4, OsKSL10, Oscyp71Z2, oryzalexin synthase, and momilactone A synthase) is observed in Meloidogyne graminicola-resistant mutant line-9. After the nematode juveniles penetrate the roots of line-9, early recognition of invading nematodes triggers plant immune responses mediated by phytoalexins, and other defence proteins such as PR proteins inhibit nematode growth and reproduction | Oryza sativa Japonica Group |
| 1.14.14.122 | additional information | the nematode-resistant T-DNA insertion mutant line-9 shows post-penetration resistance to RRKN and reduced nematode multiplication factor compared to the wild-type JBT 36/14 and a popular basmati rice cultivar Pusa Basmati 1121, quantitative real-time PCR enzyme expression analysis of defense-related plant genes, overview | Oryza sativa Japonica Group |
| 1.14.14.122 | physiological function | the enzyme oryzalexin synthase in Oryza sativa is involved in pathogen defense | Oryza sativa Japonica Group |