EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.4 | additional information | the enzyme in cultured cells responds to sulfate starvation | Nicotiana tabacum | |
2.7.7.4 | additional information | the enzyme responds to chilling or cold stress | Glycine max | |
2.7.7.4 | additional information | the enzyme responds to increased cadmium level | Lepidium sativum | |
2.7.7.4 | additional information | the enzyme responds to increased cadmium level | Noccaea caerulescens | |
2.7.7.4 | additional information | the enzyme responds to increased cadmium level | Sedum alfredii | |
2.7.7.4 | additional information | the enzyme responds to increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea | Brassica juncea | |
2.7.7.4 | additional information | the enzyme responds to increased glutathione level | Lemna gibba | |
2.7.7.4 | additional information | the enzyme responds to increased glutathione level | Salvinia minima | |
2.7.7.4 | additional information | the enzyme responds to increased light irradiation | Hordeum vulgare | |
2.7.7.4 | additional information | the enzyme responds to increased light irradiation | Avena sativa | |
2.7.7.4 | additional information | the enzyme responds to sulfate starvation, and increased salinity, but not to increased light irradiation, H2O2, and glutathione level | Brassica napus | |
2.7.7.4 | additional information | the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea, but not to increased light irradiation | Arabidopsis thaliana | |
2.7.7.4 | additional information | the enzyme responds to sulfate starvation, increased light irradiation, and chilling o cold stress | Zea mays |
EC Number | Cloned (Comment) | Organism |
---|---|---|
2.7.7.4 | the four ATP-S genes ATPS1,-2,-3, and -4 have N-terminal extensions typ ical of plastid-transit peptides, and are located on different chromosomes | Arabidopsis thaliana |
2.7.7.4 | the four ATP-S genes ATPS1,-2,-3, and -4 have N-terminal extensions typical of plastid-transit peptides, and are located on different chromosomes | Arabidopsis thaliana |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
2.7.7.4 | chloroplast | - |
Glycine max | 9507 | - |
2.7.7.4 | chloroplast | Arabidopsis thaliana has isozymes with N'-terminal extensions typical of plastid-transit-peptides | Arabidopsis thaliana | 9507 | - |
2.7.7.4 | chloroplast | Arabidopsis thaliana has isozymes with N-terminal extensions typical of plastid-transit-peptides | Arabidopsis thaliana | 9507 | - |
2.7.7.4 | chloroplast | isozyme ATPS2 is dually encoded in plastidic and cytosolic forms, where translational initiation at AUGMet1 and AUGMet52 or AUGMet58 produce ATPS2 in plastid and cytosol, respectively | Arabidopsis thaliana | 9507 | - |
2.7.7.4 | cytosol | isozyme ATPS2 is dually encoded in plastidic and cytosolic forms, where translational initiation at AUGMet1 and AUGMet52 or AUGMet58 produce ATPS2 in plastid and cytosol, respectively | Arabidopsis thaliana | 5829 | - |
2.7.7.4 | mitochondrion | - |
Glycine max | 5739 | - |
2.7.7.4 | additional information | Arabidopsis thaliana has isozymes with N'-terminal extensions typical of plastid-transit-peptides | Arabidopsis thaliana | - |
- |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.4 | Mg2+ | required | Triticum aestivum | |
2.7.7.4 | Mg2+ | required | Hordeum vulgare | |
2.7.7.4 | Mg2+ | required | Zea mays | |
2.7.7.4 | Mg2+ | required | Nicotiana tabacum | |
2.7.7.4 | Mg2+ | required | Avena sativa | |
2.7.7.4 | Mg2+ | required | Brassica napus | |
2.7.7.4 | Mg2+ | required | Oryza sativa | |
2.7.7.4 | Mg2+ | required | Lemna gibba | |
2.7.7.4 | Mg2+ | required | Lepidium sativum | |
2.7.7.4 | Mg2+ | required | Brassica juncea | |
2.7.7.4 | Mg2+ | required | Glycine max | |
2.7.7.4 | Mg2+ | required | Noccaea caerulescens | |
2.7.7.4 | Mg2+ | required | Camellia sinensis | |
2.7.7.4 | Mg2+ | required | Sedum alfredii | |
2.7.7.4 | Mg2+ | required | Stanleya pinnata | |
2.7.7.4 | Mg2+ | required | Arabidopsis thaliana | |
2.7.7.4 | Mg2+ | required | Salvinia minima |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.4 | ATP + sulfate | Triticum aestivum | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Hordeum vulgare | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Zea mays | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Nicotiana tabacum | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Avena sativa | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Brassica napus | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Oryza sativa | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Lemna gibba | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Lepidium sativum | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Brassica juncea | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Glycine max | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Noccaea caerulescens | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Camellia sinensis | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Sedum alfredii | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Stanleya pinnata | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Arabidopsis thaliana | - |
diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | Salvinia minima | - |
diphosphate + adenylyl sulfate | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.7.7.4 | Arabidopsis thaliana | O23324 | APS3; gene APS3 | - |
2.7.7.4 | Arabidopsis thaliana | Q43870 | APS2; gene APS2 | - |
2.7.7.4 | Arabidopsis thaliana | Q9LIK9 | APS1; gene APS1 | - |
2.7.7.4 | Arabidopsis thaliana | Q9S7D8 | APS4; gene APS4 | - |
2.7.7.4 | Avena sativa | - |
- |
- |
2.7.7.4 | Brassica juncea | - |
- |
- |
2.7.7.4 | Brassica napus | - |
- |
- |
2.7.7.4 | Camellia sinensis | Q1HL01 | APS2; isozyme APS2, gene sat | - |
2.7.7.4 | Camellia sinensis | Q1HL02 | APS1; isozyme APS1, gene sat | - |
2.7.7.4 | Glycine max | I1LWX5 | gene Glyma13g06940; gene Glyma13g06940 | - |
2.7.7.4 | Glycine max | I1N6H7 | gene Glyma19g05020; gene Glyma19g05020 | - |
2.7.7.4 | Glycine max | I1NGL3 | gene Glyma20g28980; gene Glyma20g28980 | - |
2.7.7.4 | Glycine max | Q8SAG1 | gene Glyma10g38760; gene Glyma10g38760 | - |
2.7.7.4 | Hordeum vulgare | - |
- |
- |
2.7.7.4 | Lemna gibba | - |
- |
- |
2.7.7.4 | Lepidium sativum | - |
- |
- |
2.7.7.4 | Nicotiana tabacum | - |
- |
- |
2.7.7.4 | Noccaea caerulescens | - |
- |
- |
2.7.7.4 | Oryza sativa | - |
gene sat, two isozymes | - |
2.7.7.4 | Salvinia minima | - |
- |
- |
2.7.7.4 | Sedum alfredii | - |
- |
- |
2.7.7.4 | Stanleya pinnata | - |
isozymes APS1, APS2, and APS4 | - |
2.7.7.4 | Triticum aestivum | - |
- |
- |
2.7.7.4 | Zea mays | - |
- |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
2.7.7.4 | cell culture | - |
Nicotiana tabacum | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.4 | ATP + sulfate | - |
Triticum aestivum | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Hordeum vulgare | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Zea mays | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Nicotiana tabacum | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Avena sativa | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Brassica napus | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Oryza sativa | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Lemna gibba | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Lepidium sativum | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Brassica juncea | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Glycine max | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Noccaea caerulescens | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Camellia sinensis | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Sedum alfredii | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Stanleya pinnata | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Arabidopsis thaliana | diphosphate + adenylyl sulfate | - |
? | |
2.7.7.4 | ATP + sulfate | - |
Salvinia minima | diphosphate + adenylyl sulfate | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.7.7.4 | APS1 | - |
Camellia sinensis |
2.7.7.4 | APS2 | - |
Camellia sinensis |
2.7.7.4 | ATP sulfurylase 1 | - |
Arabidopsis thaliana |
2.7.7.4 | ATP sulfurylase 2 | - |
Arabidopsis thaliana |
2.7.7.4 | ATP sulfurylase 3 | - |
Arabidopsis thaliana |
2.7.7.4 | ATP sulfurylase 4 | - |
Arabidopsis thaliana |
2.7.7.4 | ATP-S | - |
Triticum aestivum |
2.7.7.4 | ATP-S | - |
Hordeum vulgare |
2.7.7.4 | ATP-S | - |
Zea mays |
2.7.7.4 | ATP-S | - |
Nicotiana tabacum |
2.7.7.4 | ATP-S | - |
Avena sativa |
2.7.7.4 | ATP-S | - |
Brassica napus |
2.7.7.4 | ATP-S | - |
Oryza sativa |
2.7.7.4 | ATP-S | - |
Lemna gibba |
2.7.7.4 | ATP-S | - |
Lepidium sativum |
2.7.7.4 | ATP-S | - |
Brassica juncea |
2.7.7.4 | ATP-S | - |
Glycine max |
2.7.7.4 | ATP-S | - |
Noccaea caerulescens |
2.7.7.4 | ATP-S | - |
Camellia sinensis |
2.7.7.4 | ATP-S | - |
Sedum alfredii |
2.7.7.4 | ATP-S | - |
Stanleya pinnata |
2.7.7.4 | ATP-S | - |
Arabidopsis thaliana |
2.7.7.4 | ATP-S | - |
Salvinia minima |
2.7.7.4 | ATP-sulfurylase | - |
Triticum aestivum |
2.7.7.4 | ATP-sulfurylase | - |
Hordeum vulgare |
2.7.7.4 | ATP-sulfurylase | - |
Zea mays |
2.7.7.4 | ATP-sulfurylase | - |
Nicotiana tabacum |
2.7.7.4 | ATP-sulfurylase | - |
Avena sativa |
2.7.7.4 | ATP-sulfurylase | - |
Brassica napus |
2.7.7.4 | ATP-sulfurylase | - |
Oryza sativa |
2.7.7.4 | ATP-sulfurylase | - |
Lemna gibba |
2.7.7.4 | ATP-sulfurylase | - |
Lepidium sativum |
2.7.7.4 | ATP-sulfurylase | - |
Brassica juncea |
2.7.7.4 | ATP-sulfurylase | - |
Glycine max |
2.7.7.4 | ATP-sulfurylase | - |
Noccaea caerulescens |
2.7.7.4 | ATP-sulfurylase | - |
Camellia sinensis |
2.7.7.4 | ATP-sulfurylase | - |
Sedum alfredii |
2.7.7.4 | ATP-sulfurylase | - |
Stanleya pinnata |
2.7.7.4 | ATP-sulfurylase | - |
Arabidopsis thaliana |
2.7.7.4 | ATP-sulfurylase | - |
Salvinia minima |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.4 | ATP | - |
Triticum aestivum | |
2.7.7.4 | ATP | - |
Hordeum vulgare | |
2.7.7.4 | ATP | - |
Zea mays | |
2.7.7.4 | ATP | - |
Nicotiana tabacum | |
2.7.7.4 | ATP | - |
Avena sativa | |
2.7.7.4 | ATP | - |
Brassica napus | |
2.7.7.4 | ATP | - |
Oryza sativa | |
2.7.7.4 | ATP | - |
Lemna gibba | |
2.7.7.4 | ATP | - |
Lepidium sativum | |
2.7.7.4 | ATP | - |
Brassica juncea | |
2.7.7.4 | ATP | - |
Glycine max | |
2.7.7.4 | ATP | - |
Noccaea caerulescens | |
2.7.7.4 | ATP | - |
Camellia sinensis | |
2.7.7.4 | ATP | - |
Sedum alfredii | |
2.7.7.4 | ATP | - |
Stanleya pinnata | |
2.7.7.4 | ATP | - |
Arabidopsis thaliana | |
2.7.7.4 | ATP | - |
Salvinia minima |
EC Number | Organism | Comment | Expression |
---|---|---|---|
2.7.7.4 | Camellia sinensis | growth on Se enriched soil, suppresses APS1 expression levels in young (or mature) leaves and roots in Camellia sinensis | down |
2.7.7.4 | Arabidopsis thaliana | ATP-S activity/expression can also be controlled/modulated by S-limitation1 (SLIM1), a transcription factor identical to ethylene-insensitive3-like (EIL3) transcription factor in Arabidopsis and the regulator of many S-deficiency responsive genes | additional information |
2.7.7.4 | Stanleya pinnata | under Se-exposure and S-deficiency, Stanleya pinnata hyperaccumulates and tolerates selenium due to its ability to convert SeO24- to non-toxic organic-seleno-compounds by downregulating isozymes APS1, APS2, and APS4. Under S-sufficient and Se-exposure, adoption of different types of regulatory mechanisms and subcellular localization are revealed in Stanleya pinnata, where Se upregulates APS1 and APS4 but is not able to affect APS2 in Stanleya pinnata | additional information |
2.7.7.4 | Camellia sinensis | growth on Se enriched soil, induces APS2 expression levels in young (or mature) leaves and roots in Camellia sinensis | up |
2.7.7.4 | Nicotiana tabacum | the enzyme in cultured cells responds to sulfate starvation | up |
2.7.7.4 | Glycine max | the enzyme responds to chilling or cold stress | up |
2.7.7.4 | Lepidium sativum | the enzyme responds to increased cadmium level | up |
2.7.7.4 | Noccaea caerulescens | the enzyme responds to increased cadmium level | up |
2.7.7.4 | Sedum alfredii | the enzyme responds to increased cadmium level | up |
2.7.7.4 | Brassica juncea | the enzyme responds to increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea | up |
2.7.7.4 | Lemna gibba | the enzyme responds to increased glutathione level | up |
2.7.7.4 | Salvinia minima | the enzyme responds to increased glutathione level | up |
2.7.7.4 | Hordeum vulgare | the enzyme responds to increased light irradiation | up |
2.7.7.4 | Avena sativa | the enzyme responds to increased light irradiation | up |
2.7.7.4 | Brassica napus | the enzyme responds to sulfate starvation, and increased salinity, but not to increased light irradiation, H2O2, and glutathione level | up |
2.7.7.4 | Arabidopsis thaliana | the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthora infestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion mediates regulation of ATP-S activity/expression. ATP-S isoforms can be differentially expressed by S-depletion, e.g. isozyme APS3, while isozyme APS2 is insensitive to S-depletion. Arabidopsis thaliana overexpressing or disruption in MYB51-gene shows alterations in ATP-S-transcript levels and activity. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview | up |
2.7.7.4 | Arabidopsis thaliana | the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthora infestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion mediates regulation of ATP-S activity/expression. ATP-S isoforms can be differentially expressed by S-depletion, e.g. isozyme APS3, while isozyme APS2 is insentivie to S depletion. Expression of both ATPS1 and ATPS3 isoforms is controlled by all six GSs-related MYBTFs, namely MYB28, MYB29, and MYB76, MYB51, MYB34, and MYB122. Isozymes ATPS1 and ATPS3 are strongly associated with the control of synthesis of aliphatic and indolic GSs, respectively. Arabidopsis thaliana overexpressing or disruption in MYB51-gene shows alterations in ATP-S-transcript levels and activity. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview | up |
2.7.7.4 | Arabidopsis thaliana | the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthora infestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion mediates regulation of ATP-S activity/expression. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview | up |
2.7.7.4 | Arabidopsis thaliana | the enzyme responds to sulfate starvation, increased cadmium level, increased salinity, and infection by Phytopthorainfestans and/or Botrytiscinerea, but not to increased light irradiation. S-depletion-mediates regulation of ATP-S activity/expression. Expression of both ATPS1 and ATPS3 isoforms is controlled by all six GSs-related MYBTFs, namely MYB28, MYB29, and MYB76, MYB51, MYB34, and MYB122. Isozymes ATPS1 and ATPS3 are strongly associated with the control of synthesis of aliphatic and indolic GSs, respectively. Arabidopsis thaliana overexpressing or disruption in MYB51-gene shows alterations in ATP-S-transcript levels and activity. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview | up |
2.7.7.4 | Zea mays | the enzyme responds to sulfate starvation, increased light irradiation, and chilling o cold stress | up |
EC Number | General Information | Comment | Organism |
---|---|---|---|
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Triticum aestivum |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Hordeum vulgare |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Zea mays |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Nicotiana tabacum |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Avena sativa |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Brassica napus |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Oryza sativa |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Lemna gibba |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Lepidium sativum |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Brassica juncea |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Glycine max |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Noccaea caerulescens |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Camellia sinensis |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Sedum alfredii |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Stanleya pinnata |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors | Salvinia minima |
2.7.7.4 | metabolism | as the first committed step of S-assimilation, ATP-sulfurylase (ATP-S) catalyzes sulfate activation and yields the activated high-energy compound adenosine-5'-phosphosulfate that is reduced to sulfide and incorporated into cysteine. In turn, cysteine acts as a precursor or donor of reduced S for arange of S-compounds such as methionine, glutathione (GSH), homo-GSH,and phytochelatins. Schematic representation of pathway of sulfate assimilation, reaction catalyzed by ATP-sulfurylase (ATP-S), and its regulation by major factors. Transcription regulation of Arabidopsis thaliana APS genes by external factors, detailed overview | Arabidopsis thaliana |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Triticum aestivum |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Hordeum vulgare |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Zea mays |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Nicotiana tabacum |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Avena sativa |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Brassica napus |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Oryza sativa |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Lemna gibba |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Lepidium sativum |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Brassica juncea |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Glycine max |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Noccaea caerulescens |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Camellia sinensis |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Sedum alfredii |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Stanleya pinnata |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Arabidopsis thaliana |
2.7.7.4 | physiological function | S-compound-mediated role of enzyme ATP-S in plant stress tolerance, ATP-S-intrinsic regulation by major S-compounds, overview. Sulfur stands fourth in the list of major plant nutrients after N, P, and K, and its importance is being increasingly emphasized in agriculture and plant stress tolerance, because S-deficiency in agricultural-soils is becoming widespread globally. Plant harbored-S is metabolically inert and is of no significance if it is not efficiently assimilated into physiologically/biochemically exploitable organic forms that is performed by the process of S-assimilation involving the ATP-sulfurylase | Salvinia minima |