Cloned (Comment) | Organism |
---|---|
expression of the N-terminal domain in Escherichia coli | Clostridium perfringens |
phylogenetic analysis | Nicotiana tabacum |
phylogenetic analysis | Glycine max |
phylogenetic analysis | Sorghum bicolor |
phylogenetic analysis | Oryza sativa |
phylogenetic analysis | Petunia x hybrida |
phylogenetic analysis | Physcomitrium patens |
phylogenetic analysis | Vitis vinifera |
phylogenetic analysis | Populus trichocarpa |
phylogenetic analysis | Picea sitchensis |
phylogenetic analysis | Selaginella moellendorffii |
phylogenetic analysis | Arabidopsis thaliana |
Protein Variants | Comment | Organism |
---|---|---|
up | the enzyme is induced by 24-epibrassinolide signalling, auxin, cytokinin, phosphate deficiency, abscisic acid, and salt stress. NPC4 does demonstrate a positive response to Botrytis cinerea, Golovinomyces orontii, Pseudomonas syringae and Phytophthora infestans treatment | Arabidopsis thaliana |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
additional information | no inhibition by tricyclodecan-9-ylxanthogenate, i.e. D609 | Nicotiana tabacum | |
tricyclodecan-9-ylxanthogenate | i.e. D609; i.e. D609; i.e. D609; i.e. D609; i.e. D609; i.e. D609 | Arabidopsis thaliana | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Bacillus cereus | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Clostridium perfringens | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Glycine max | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Oryza sativa | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Petunia x hybrida | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Physcomitrium patens | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Picea sitchensis | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Populus trichocarpa | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Pseudomonas fluorescens | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Selaginella moellendorffii | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Sorghum bicolor | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Ureaplasma urealyticum | |
tricyclodecan-9-ylxanthogenate | i.e. D609 | Vitis vinifera |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
chloroplast | - |
Arabidopsis thaliana | 9507 | - |
cytosol | - |
Arabidopsis thaliana | 5829 | - |
endoplasmic reticulum membrane | - |
Arabidopsis thaliana | 5789 | - |
extracellular | the enzyme is secreted | Clostridium perfringens | - |
- |
membrane | bound | Ureaplasma urealyticum | 16020 | - |
membrane | of stamens and pistils | Petunia x hybrida | 16020 | - |
mitochondrion | - |
Arabidopsis thaliana | 5739 | - |
plasma membrane | - |
Nicotiana tabacum | 5886 | - |
plasma membrane | - |
Arabidopsis thaliana | 5886 | - |
tonoplast | - |
Arabidopsis thaliana | - |
- |
vacuolar membrane | - |
Arabidopsis thaliana | 5774 | - |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Nal | activates enzyme activity | Ureaplasma urealyticum | |
Zn2+ | bound at the N-terminal domain | Clostridium perfringens |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
phosphatidylcholine + H2O | Glycine max | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Pseudomonas fluorescens | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Bacillus cereus | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Sorghum bicolor | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Oryza sativa | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Petunia x hybrida | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Clostridium perfringens | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Ureaplasma urealyticum | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Physcomitrium patens | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Vitis vinifera | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Populus trichocarpa | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Picea sitchensis | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Selaginella moellendorffii | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | Arabidopsis thaliana | - |
1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylethanolamine + H2O | Arabidopsis thaliana | - |
1,2-sn-diacylglycerol + phosphoethanolamine | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Arabidopsis thaliana | O81020 | NPC2; gene NPC2 | - |
Arabidopsis thaliana | Q8H965 | NPC6; gene NPC6 | - |
Arabidopsis thaliana | Q8L7Y9 | NPC1; gene NPC1 | - |
Arabidopsis thaliana | Q9S816 | NPC5; gene NPC5 | - |
Arabidopsis thaliana | Q9SRQ6 | NPC3; gene NPC3 | - |
Arabidopsis thaliana | Q9SRQ7 | NPC4; gene NPC4 | - |
Bacillus cereus | - |
- |
- |
Clostridium perfringens | - |
- |
- |
Glycine max | - |
six genes NPC1-6 | - |
Nicotiana tabacum | - |
- |
- |
Oryza sativa | - |
six genes NPC1-6 | - |
Petunia x hybrida | - |
six genes NPC1-6 | - |
Physcomitrium patens | - |
single NPC1-like gene | - |
Picea sitchensis | - |
NPC1-, NPC2- and NPC6-like gene, no NPC3-5 | - |
Populus trichocarpa | - |
six genes NPC1-6 | - |
Pseudomonas fluorescens | - |
- |
- |
Selaginella moellendorffii | - |
single NPC1-like gene | - |
Sorghum bicolor | - |
six genes NPC1-6 | - |
Ureaplasma urealyticum | - |
- |
- |
Vitis vinifera | - |
six genes NPC1-6 | - |
Purification (Comment) | Organism |
---|---|
native enzyme | Ureaplasma urealyticum |
Reaction | Comment | Organism | Reaction ID |
---|---|---|---|
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Nicotiana tabacum | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Glycine max | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Sorghum bicolor | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Oryza sativa | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Petunia x hybrida | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Physcomitrium patens | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Vitis vinifera | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Populus trichocarpa | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Picea sitchensis | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Selaginella moellendorffii | |
a phosphatidylcholine + H2O = 1,2-diacyl-sn-glycerol + phosphocholine | mode of action of the plant enzyme family of non-specific phospholipases C, overview | Arabidopsis thaliana |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
cell suspension culture | - |
Nicotiana tabacum | - |
cotyledon | - |
Arabidopsis thaliana | - |
inflorescence | - |
Arabidopsis thaliana | - |
leaf | - |
Arabidopsis thaliana | - |
leaf | old | Arabidopsis thaliana | - |
additional information | tissue distribution, overview | Arabidopsis thaliana | - |
pistil | - |
Petunia x hybrida | - |
pollen | germinating | Arabidopsis thaliana | - |
root | - |
Arabidopsis thaliana | - |
seedling | higher in seedling hypocotyls and lower in seedling roots | Arabidopsis thaliana | - |
silique | - |
Arabidopsis thaliana | - |
stamen | - |
Petunia x hybrida | - |
TBY-2 cell | - |
Nicotiana tabacum | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
phosphatidic acid + H2O | - |
Arabidopsis thaliana | 1,2-sn-diacylglycerol + phosphate | - |
? | |
phosphatidylcholine + H2O | - |
Glycine max | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Pseudomonas fluorescens | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Bacillus cereus | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Sorghum bicolor | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Oryza sativa | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Petunia x hybrida | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Clostridium perfringens | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Ureaplasma urealyticum | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Physcomitrium patens | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Vitis vinifera | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Populus trichocarpa | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Picea sitchensis | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Selaginella moellendorffii | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylcholine + H2O | - |
Arabidopsis thaliana | 1,2-sn-diacylglycerol + phosphocholine | - |
? | |
phosphatidylethanolamine + H2O | - |
Arabidopsis thaliana | 1,2-sn-diacylglycerol + phosphoethanolamine | - |
? |
Subunits | Comment | Organism |
---|---|---|
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Nicotiana tabacum |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Glycine max |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Sorghum bicolor |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Oryza sativa |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Petunia x hybrida |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Physcomitrium patens |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Vitis vinifera |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Populus trichocarpa |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Picea sitchensis |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Selaginella moellendorffii |
More | the enzyme contains a central phosphoesterase domain, a DUF756 domain, a conserved region and a conserved Asp-Arg pair, and some isozymes contain a signal peptide, domain structure, overview | Arabidopsis thaliana |
Synonyms | Comment | Organism |
---|---|---|
alpha-toxin | - |
Clostridium perfringens |
non-specific phospholipase C | - |
Nicotiana tabacum |
non-specific phospholipase C | - |
Glycine max |
non-specific phospholipase C | - |
Sorghum bicolor |
non-specific phospholipase C | - |
Oryza sativa |
non-specific phospholipase C | - |
Petunia x hybrida |
non-specific phospholipase C | - |
Physcomitrium patens |
non-specific phospholipase C | - |
Vitis vinifera |
non-specific phospholipase C | - |
Populus trichocarpa |
non-specific phospholipase C | - |
Picea sitchensis |
non-specific phospholipase C | - |
Selaginella moellendorffii |
non-specific phospholipase C | - |
Arabidopsis thaliana |
NPC | - |
Nicotiana tabacum |
NPC | - |
Glycine max |
NPC | - |
Sorghum bicolor |
NPC | - |
Oryza sativa |
NPC | - |
Petunia x hybrida |
NPC | - |
Physcomitrium patens |
NPC | - |
Vitis vinifera |
NPC | - |
Populus trichocarpa |
NPC | - |
Picea sitchensis |
NPC | - |
Selaginella moellendorffii |
NPC | - |
Arabidopsis thaliana |
NPC1 | - |
Glycine max |
NPC1 | - |
Sorghum bicolor |
NPC1 | - |
Oryza sativa |
NPC1 | - |
Petunia x hybrida |
NPC1 | - |
Physcomitrium patens |
NPC1 | - |
Vitis vinifera |
NPC1 | - |
Populus trichocarpa |
NPC1 | - |
Picea sitchensis |
NPC1 | - |
Selaginella moellendorffii |
NPC1 | - |
Arabidopsis thaliana |
NPC2 | - |
Glycine max |
NPC2 | - |
Sorghum bicolor |
NPC2 | - |
Oryza sativa |
NPC2 | - |
Petunia x hybrida |
NPC2 | - |
Vitis vinifera |
NPC2 | - |
Populus trichocarpa |
NPC2 | - |
Picea sitchensis |
NPC2 | - |
Arabidopsis thaliana |
NPC3 | - |
Glycine max |
NPC3 | - |
Sorghum bicolor |
NPC3 | - |
Oryza sativa |
NPC3 | - |
Petunia x hybrida |
NPC3 | - |
Vitis vinifera |
NPC3 | - |
Populus trichocarpa |
NPC3 | - |
Arabidopsis thaliana |
NPC4 | - |
Glycine max |
NPC4 | - |
Sorghum bicolor |
NPC4 | - |
Oryza sativa |
NPC4 | - |
Petunia x hybrida |
NPC4 | - |
Vitis vinifera |
NPC4 | - |
Populus trichocarpa |
NPC4 | - |
Arabidopsis thaliana |
NPC5 | - |
Glycine max |
NPC5 | - |
Sorghum bicolor |
NPC5 | - |
Oryza sativa |
NPC5 | - |
Petunia x hybrida |
NPC5 | - |
Vitis vinifera |
NPC5 | - |
Populus trichocarpa |
NPC5 | - |
Arabidopsis thaliana |
NPC6 | - |
Glycine max |
NPC6 | - |
Sorghum bicolor |
NPC6 | - |
Oryza sativa |
NPC6 | - |
Petunia x hybrida |
NPC6 | - |
Vitis vinifera |
NPC6 | - |
Populus trichocarpa |
NPC6 | - |
Picea sitchensis |
NPC6 | - |
Arabidopsis thaliana |
PC-PLC | - |
Pseudomonas fluorescens |
PC-PLC | - |
Bacillus cereus |
PC-PLC | - |
Clostridium perfringens |
PC-PLC | - |
Ureaplasma urealyticum |
phosphatidylcholine-specific phospholipase C | - |
Pseudomonas fluorescens |
phosphatidylcholine-specific phospholipase C | - |
Bacillus cereus |
phosphatidylcholine-specific phospholipase C | - |
Clostridium perfringens |
phosphatidylcholine-specific phospholipase C | - |
Ureaplasma urealyticum |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
additional information | - |
broad pH optimum | Ureaplasma urealyticum |
Organism | Comment | Expression |
---|---|---|
Arabidopsis thaliana | the enzyme is induced by 24-epibrassinolide signalling, auxin, and cytokinin. Expression level of NPC3 is increased 14.6fold after 2 h in seedlings subjected to 37°C heat stress. NPC3 does demonstrate a positive response to Botrytis cinerea, Golovinomyces orontii, Pseudomonas syringae and Phytophthora infestans treatment | up |
Arabidopsis thaliana | the enzyme is induced by phosphate deficiency | up |
General Information | Comment | Organism |
---|---|---|
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Nicotiana tabacum |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Glycine max |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Sorghum bicolor |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Oryza sativa |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Petunia x hybrida |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Physcomitrium patens |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Vitis vinifera |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Populus trichocarpa |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Picea sitchensis |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Selaginella moellendorffii |
evolution | the enzyme belongs to the plant non-specific phospholipase C gene family, phylogenetic tree, overview. The common ancestor of all seed plants already had at least one NPC1-, NPC2- and NPC6-like gene. Non-specific phospholipases C are a distinct type of plant phospholipid-cleaving enzyme homologous to bacterial phosphatidylcholine-specific phospholipases C | Arabidopsis thaliana |
malfunction | npc4 knockout mutants are characterised by a reduced germination rate when sown on media containing 150 mM NaCl. Mutant npc4 plants also have reduced germination and overall viability under salt and drought stress conditions. Unlike wild-type plants, mutants overexpressing NPC4 are characterised by a higher germination level and maintain a greater root length and dry weight under both salt stress and hyperosmosis | Arabidopsis thaliana |
malfunction | the N-terminal domain of a-toxin retains PC-PLC activity when expressed in Escherichia coli, but lacks haemolytic and sphingomyelinase activities that are supposedly granted by a lipoxygenase-like C-terminal domain | Clostridium perfringens |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Nicotiana tabacum |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Glycine max |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Sorghum bicolor |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Oryza sativa |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Petunia x hybrida |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Physcomitrium patens |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Vitis vinifera |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Populus trichocarpa |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Picea sitchensis |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Selaginella moellendorffii |
metabolism | model of metabolism regulation carried out by plant cell phospholipases, overview | Arabidopsis thaliana |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Nicotiana tabacum |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Glycine max |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Sorghum bicolor |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Oryza sativa |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Petunia x hybrida |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Physcomitrium patens |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Vitis vinifera |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Populus trichocarpa |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Picea sitchensis |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Selaginella moellendorffii |
additional information | sequence comparisons and three-dimensional structure modeling, overview | Arabidopsis thaliana |
additional information | the N-terminal domain contains the phospholipase C active site, which also incorporates zinc ions. The C-terminal C2-like PLAT (polycystin-1, lipoxygenase, alpha-toxin) domain was found to be similar to lipid binding domains in eukaryotes and appears to be responsible for binding membrane phospholipids in a calcium-dependent manner | Clostridium perfringens |
physiological function | NPC3 might play a rolei in thermotolerance. The enzyme is responsible for lipid conversion during phosphate-limiting conditions. Two articles non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview, inducible expression and putative signalling role | Arabidopsis thaliana |
physiological function | NPC4 participates in triggering plant salt stress responses likely via abscisic acid-dependent mechanisms. The enzyme is responsible for lipid conversion during phosphate-limiting conditions. Two articles non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview, inducible expression and putative signalling role | Arabidopsis thaliana |
physiological function | the enzyme inhibits the formation of cAMP by adenylate cyclase and is involved in the defence mechanism of bacteria to phagocytosis | Bacillus cereus |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Glycine max |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Sorghum bicolor |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Oryza sativa |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Petunia x hybrida |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Physcomitrium patens |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Vitis vinifera |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Populus trichocarpa |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Picea sitchensis |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Selaginella moellendorffii |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Two articles non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Nicotiana tabacum |
physiological function | the enzyme is responsible for lipid conversion during phosphate-limiting conditions. Two articles non-specific phospholipases C are involved in biotic and abiotic stress responses as well as phytohormone actions. The diacylglycerol produced via the enzymes is postulated to participate in membrane remodelling, general lipid metabolism and cross-talk with other phospholipid signalling systems in plants. Mode of action of the enzyme in lipid metabolism, signal transduction, and membrane remodelling, detailed overview | Arabidopsis thaliana |
physiological function | the secreted enzyme plays a role in the aggregation of blood platelets and inhibits defensive superoxide generation in human polymorphonuclear leukocytes by interacting with membrane components of NADPH oxidase | Clostridium perfringens |