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Literature summary for 1.11.1.11 extracted from
- Comparative analysis of ascorbate peroxidases (APXs) from selected plants with a special focus on Oryza sativa employing public databases (2019), PLoS ONE, 14, e0226543 .
Cloned(Commentary)
| Cloned (Comment) | Organism |
|---|---|
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family APX1 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family, APX2 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family, APX3 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family, APX4 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family, APX5 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family, APX6 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family, APX7 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| APX is comprised of different isoenzymes, which are encoded by a multi-gene family, APX8 DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, transcriptional profiles of the rice isozymes, overview | Oryza sativa Japonica Group |
| DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Populus trichocarpa |
| DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Arabidopsis thaliana |
| DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Physcomitrium patens |
| gee APX, DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Arabidopsis thaliana |
| gene APX, DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Chlamydomonas reinhardtii |
| gene APX, DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Populus trichocarpa |
| gene APX, DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Physcomitrium patens |
| gene APX1, DNA and amino acid sequence analysis, sequence comparisons and phylogenetic analysis and tree, conserved cis-regulatory elements in the promoters of the APX isozyme, overview | Arabidopsis thaliana |
Localization
| Localization | Comment | Organism | GeneOntology No. | Textmining |
|---|---|---|---|---|
| chloroplast | - |
Chlamydomonas reinhardtii | 9507 | - |
| chloroplast | - |
Populus trichocarpa | 9507 | - |
| chloroplast | - |
Oryza sativa Japonica Group | 9507 | - |
| chloroplast | - |
Physcomitrium patens | 9507 | - |
| chloroplast | - |
Arabidopsis thaliana | 9507 | - |
| chloroplast | stroma | Arabidopsis thaliana | 9507 | - |
| chloroplast | thylakoid-bound | Arabidopsis thaliana | 9507 | - |
| cytosol | - |
Populus trichocarpa | 5829 | - |
| cytosol | - |
Arabidopsis thaliana | 5829 | - |
| cytosol | - |
Oryza sativa Japonica Group | 5829 | - |
| cytosol | - |
Physcomitrium patens | 5829 | - |
| mitochondrion | - |
Arabidopsis thaliana | 5739 | - |
| mitochondrion | - |
Oryza sativa Japonica Group | 5739 | - |
| mitochondrion | - |
Chlamydomonas reinhardtii | 5739 | - |
| mitochondrion | - |
Physcomitrium patens | 5739 | - |
| mitochondrion | - |
Populus trichocarpa | 5739 | - |
| additional information | APX is comprised of different isoenzymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group | - |
- |
| additional information | APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group | - |
- |
| peroxisome | - |
Physcomitrium patens | 5777 | - |
| peroxisome | - |
Arabidopsis thaliana | 5777 | - |
| peroxisome | - |
Populus trichocarpa | 5777 | - |
| peroxisome | - |
Oryza sativa Japonica Group | 5777 | - |
Metals/Ions
| Metals/Ions | Comment | Organism | Structure |
|---|---|---|---|
| Fe2+ | in the heme group | Chlamydomonas reinhardtii |  |
| Fe2+ | in the heme group | Populus trichocarpa | |
| Fe2+ | in the heme group | Arabidopsis thaliana | |
| Fe2+ | in the heme group | Oryza sativa Japonica Group | |
| Fe2+ | in the heme group | Physcomitrium patens | |
Natural Substrates/ Products (Substrates)
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 2 L-ascorbate + H2O2 + 2 H+ | Chlamydomonas reinhardtii | - |
L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | Populus trichocarpa | - |
L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | Arabidopsis thaliana | - |
L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | Oryza sativa Japonica Group | - |
L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | Physcomitrium patens | - |
L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| additional information | Oryza sativa Japonica Group | APXs in rice plant are able to interact with dehydroascorbate reductase 2 (EC 1.8.5.1). Enzyme interaction analysis, overview | ? | - |
- |
|
| additional information | Chlamydomonas reinhardtii | enzyme interaction analysis, overview | ? | - |
- |
|
| additional information | Populus trichocarpa | enzyme interaction analysis, overview | ? | - |
- |
|
| additional information | Arabidopsis thaliana | enzyme interaction analysis, overview | ? | - |
- |
|
| additional information | Physcomitrium patens | enzyme interaction analysis, overview | ? | - |
- |
|
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Arabidopsis thaliana | Q05431 | 8 isozymes | - |
| Arabidopsis thaliana | Q1PER6 | 8 isozymes | - |
| Arabidopsis thaliana | Q42564 | 8 isozymes | - |
| Arabidopsis thaliana | Q42592 | 8 isozymes | - |
| Arabidopsis thaliana | Q42593 | 8 isozymes | - |
| Arabidopsis thaliana | Q7XZP5 | 8 isozymes | - |
| Arabidopsis thaliana | Q8GY91 | 8 isozymes | - |
| Chlamydomonas reinhardtii | - |
4 isozymes | - |
| Chlamydomonas reinhardtii | A0A2K3DF40 | 4 isozymes | - |
| Chlamydomonas reinhardtii | A0A2K3DPX4 | 4 isozymes | - |
| Chlamydomonas reinhardtii | O49822 | 4 isozymes | - |
| no activity in Arabidopsis thaliana isozyme AtAPX4 | - |
UniProt ID P82281 | - |
| Oryza sativa Japonica Group | P0C0L0 | - |
- |
| Oryza sativa Japonica Group | P0C0L1 | - |
- |
| Oryza sativa Japonica Group | Q0JEQ2 | - |
- |
| Oryza sativa Japonica Group | Q10N21 | - |
- |
| Oryza sativa Japonica Group | Q69SV0 | - |
- |
| Oryza sativa Japonica Group | Q6ZJJ1 | - |
- |
| Oryza sativa Japonica Group | Q7XJ02 | - |
- |
| Oryza sativa Japonica Group | Q9FE01 | - |
- |
| Physcomitrium patens | A0A2K1ITN5 | 5 isozymes | - |
| Physcomitrium patens | A0A2K1J327 | 5 isozymes | - |
| Physcomitrium patens | A0A2K1L9S9 | 5 isozymes | - |
| Physcomitrium patens | A9U1S4 | 5 isozymes | - |
| Physcomitrium patens | Q8GU36 | 5 isozymes | - |
| Populus trichocarpa | - |
11 isozymes | - |
| Populus trichocarpa | A0A2K1Z156 | 11 isozymes | - |
| Populus trichocarpa | A0A2K2AW57 | 11 isozymes | - |
| Populus trichocarpa | A0A2K2BFE0 | 11 isozymes | - |
| Populus trichocarpa | A0A3N7F4X7 | 11 isozymes | - |
| Populus trichocarpa | A9P9X7 | 11 isozymes | - |
| Populus trichocarpa | B9HAE4 | 11 isozymes | - |
| Populus trichocarpa | B9HR68 | 11 isozymes | - |
| Populus trichocarpa | B9MXE8 | 11 isozymes | - |
| Populus trichocarpa | U5GAF3 | 11 isozymes | - |
Posttranslational Modification
| Posttranslational Modification | Comment | Organism |
|---|---|---|
| lipoprotein | 1 site of N-myristoylation | Populus trichocarpa |
| lipoprotein | 1 site of S-farnesylation | Arabidopsis thaliana |
| lipoprotein | 1 site of S-farnesylation | Populus trichocarpa |
| lipoprotein | 1 site of S-farnesylation | Oryza sativa Japonica Group |
| lipoprotein | 1 site of S-myristoylation | Oryza sativa Japonica Group |
| lipoprotein | 1 site of S-palmitoylation | Populus trichocarpa |
| lipoprotein | 1 site of S-palmitoylation | Oryza sativa Japonica Group |
| lipoprotein | 1 site of S-palmitoylation and one of N-myristoylation | Populus trichocarpa |
| lipoprotein | 2 sites of S-palmitoylation | Populus trichocarpa |
| lipoprotein | 2 sites of S-palmitoylation, 1 for S-farnesylation, and 1 for S-geranylgeranylation | Chlamydomonas reinhardtii |
| lipoprotein | isozyme PpAPX3 contains 1 site of S-palmitoylation | Physcomitrium patens |
| lipoprotein | isozyme PpAPX6-related contains 4 sites of S-palmitoylation and 1 site of N-myristoylation | Physcomitrium patens |
| additional information | isozyme AtAPX3 is no lipoprotein | Arabidopsis thaliana |
| additional information | isozyme CreAPX4 is no lipoprotein | Chlamydomonas reinhardtii |
| additional information | isozyme CreAPXheme is no lipoprotein | Chlamydomonas reinhardtii |
| additional information | isozyme OsAPX5 is no lipoprotein | Oryza sativa Japonica Group |
| additional information | isozyme OsAPX6 is no lipoprotein | Oryza sativa Japonica Group |
| additional information | isozyme PpAPX2.2 is no lipoprotein | Physcomitrium patens |
| additional information | isozyme PtAPX-S.1 is no lipoprotein | Populus trichocarpa |
| additional information | isozyme PtAPX.3 is no lipoprotein | Populus trichocarpa |
| palmitoylation | - |
Populus trichocarpa |
| palmitoylation | - |
Oryza sativa Japonica Group |
| palmitoylation | - |
Chlamydomonas reinhardtii |
| palmitoylation | - |
Arabidopsis thaliana |
| phosphoprotein | isozyme AtAPX1 contains one phosphorylation site for protein kinase C | Arabidopsis thaliana |
| phosphoprotein | isozyme AtAPX2 contains two phosphorylation sites for protein kinase C | Arabidopsis thaliana |
| phosphoprotein | isozyme AtAPX3 contains three phosphorylation sites for protein kinase C | Arabidopsis thaliana |
| phosphoprotein | isozyme AtAPX5 contains 4 phosphorylation sites for protein kinase C and 2 sites for protein kinase A | Arabidopsis thaliana |
| phosphoprotein | isozyme AtAPX6 contains one phosphorylation site for protein kinase A, one site for protein kinase B, and 5 sites for protein kinase C | Arabidopsis thaliana |
| phosphoprotein | isozyme AtSAPX contains one phosphorylation site for protein kinase A and 15 sites for protein kinase C | Arabidopsis thaliana |
| phosphoprotein | isozyme AtTAPX contains one phosphorylation site for protein kinase A and 8 sites for protein kinase C | Arabidopsis thaliana |
| phosphoprotein | isozyme CreAPX1 contains phosphorylation sites for protein kinases A and C | Chlamydomonas reinhardtii |
| phosphoprotein | isozyme CreAPX2 contains 2 phosphorylation sites for protein kinase C | Chlamydomonas reinhardtii |
| phosphoprotein | isozyme CreAPX4 contains 1 phosphorylation site for protein kinase A and 7 for protein kinase C | Chlamydomonas reinhardtii |
| phosphoprotein | isozyme CreAPXheme contains 1 phosphorylation site for protein kinase A and 6 for protein kinase C | Chlamydomonas reinhardtii |
| phosphoprotein | isozyme OsAPX1 contains 2 phosphorylation sites for protein kinase C | Oryza sativa Japonica Group |
| phosphoprotein | isozyme OsAPX2 contains 1 phosphorylation site for protein kinase C | Oryza sativa Japonica Group |
| phosphoprotein | isozyme OsAPX3 contains phosphorylation sites for protein kinases A and C | Oryza sativa Japonica Group |
| phosphoprotein | isozyme OsAPX4 contains phosphorylation sites for protein kinases A and C | Oryza sativa Japonica Group |
| phosphoprotein | isozyme OsAPX5 contains phosphorylation sites for protein kinases A and C | Oryza sativa Japonica Group |
| phosphoprotein | isozyme OsAPX6 contains phosphorylation sites for protein kinases A and C | Oryza sativa Japonica Group |
| phosphoprotein | isozyme OsAPX7 contains phosphorylation sites for protein kinases A and C | Oryza sativa Japonica Group |
| phosphoprotein | isozyme OsAPX8 contains phosphorylation sites for protein kinases C and cdk5 | Oryza sativa Japonica Group |
| phosphoprotein | isozyme PpAPX-S contains 4 phosphorylation sites for protein kinase C | Physcomitrium patens |
| phosphoprotein | isozyme PpAPX2.1 contains 2 phosphorylation sites for protein kinase C | Physcomitrium patens |
| phosphoprotein | isozyme PpAPX2.2 contains 2 phosphorylation sites for protein kinase C | Physcomitrium patens |
| phosphoprotein | isozyme PpAPX3 contains 2 phosphorylation sites for protein kinase A and 3 for protein kinase C | Physcomitrium patens |
| phosphoprotein | isozyme PpAPX6-related contains 5 phosphorylation sites for protein kinase C and 1 for protein kinase A and B each | Physcomitrium patens |
| phosphoprotein | isozyme PtAPX-S.1 contains 5 phosphorylation sites for protein kinase C and 2 for protein kinase A | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX-S.2 contains 8 phosphorylation sites for protein kinase C and one for protein kinase A | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX-TL29 contains 9 phosphorylation sites for protein kinase C | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX.3 contains three phosphorylation sites for protein kinase C | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX1.1 contains one phosphorylation site for protein kinase C | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX1.2 contains one phosphorylation site for protein kinase C | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX2 contains one phosphorylation site for protein kinase C | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX3 contains 6 phosphorylation sites for protein kinase C and one for protein kinase A | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX5 contains 4 phosphorylation sites for protein kinase C and 2 for protein kinase A | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX5-like contains three phosphorylation sites for protein kinase C and 2 for protein kinase A | Populus trichocarpa |
| phosphoprotein | isozyme PtAPX6 related contains 7 phosphorylation sites for protein kinase C and 5 for protein kinase A | Populus trichocarpa |
| S-nitrosylation | - |
Populus trichocarpa |
| S-nitrosylation | - |
Arabidopsis thaliana |
| S-nitrosylation | - |
Oryza sativa Japonica Group |
| S-nitrosylation | - |
Chlamydomonas reinhardtii |
| S-nitrosylation | isozyme PpAPX-S contains 1 site of S-nitrosylation | Physcomitrium patens |
| S-nitrosylation | isozyme PpAPX2.1 contains 1 site of S-nitrosylation | Physcomitrium patens |
| S-nitrosylation | isozyme PpAPX6-related contains 2 sites of S-nitrosylation | Physcomitrium patens |
Source Tissue
| Source Tissue | Comment | Organism | Textmining |
|---|---|---|---|
| anther | - |
Oryza sativa Japonica Group | - |
| carpel | - |
Oryza sativa Japonica Group | - |
| leaf | - |
Oryza sativa Japonica Group | - |
| additional information | eight APX isozymes are expressed differently in root, leaf, panicle, anther, pistil and seed | Oryza sativa Japonica Group | - |
| additional information | eight APX isozymes are expressed differently in root, leaf, panicle, anther, pistil and seed. High expression level of isozyme OsAPX1 | Oryza sativa Japonica Group | - |
| additional information | eight APX isozymes are expressed differently in root, leaf, panicle, anther, pistil and seed. High expression level of isozyme OsAPX2 | Oryza sativa Japonica Group | - |
| panicle | - |
Oryza sativa Japonica Group | - |
| root | - |
Oryza sativa Japonica Group | - |
| seed | - |
Oryza sativa Japonica Group | - |
| seedling | - |
Populus trichocarpa | - |
| seedling | - |
Arabidopsis thaliana | - |
| seedling | - |
Oryza sativa Japonica Group | - |
| seedling | - |
Physcomitrium patens | - |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 2 L-ascorbate + H2O2 + 2 H+ | - |
Chlamydomonas reinhardtii | L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | - |
Populus trichocarpa | L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | - |
Arabidopsis thaliana | L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | - |
Oryza sativa Japonica Group | L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| 2 L-ascorbate + H2O2 + 2 H+ | - |
Physcomitrium patens | L-ascorbate + L-dehydroascorbate + 2 H2O | - |
? | |
| additional information | APXs in rice plant are able to interact with dehydroascorbate reductase 2 (EC 1.8.5.1). Enzyme interaction analysis, overview | Oryza sativa Japonica Group | ? | - |
- |
|
| additional information | enzyme interaction analysis, overview | Chlamydomonas reinhardtii | ? | - |
- |
|
| additional information | enzyme interaction analysis, overview | Populus trichocarpa | ? | - |
- |
|
| additional information | enzyme interaction analysis, overview | Arabidopsis thaliana | ? | - |
- |
|
| additional information | enzyme interaction analysis, overview | Physcomitrium patens | ? | - |
- |
|
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| APX | - |
Chlamydomonas reinhardtii |
| APX | - |
Populus trichocarpa |
| APX | - |
Arabidopsis thaliana |
| APX | - |
Oryza sativa Japonica Group |
| APX | - |
Physcomitrium patens |
| APX1 | - |
Arabidopsis thaliana |
| APX1 | - |
Chlamydomonas reinhardtii |
| APX2 | - |
Arabidopsis thaliana |
| APX2 | - |
Chlamydomonas reinhardtii |
| APX4 | - |
Chlamydomonas reinhardtii |
| APXS | UniProt | Arabidopsis thaliana |
| APXT | UniProt | Arabidopsis thaliana |
| ascorbate peroxidase | - |
Chlamydomonas reinhardtii |
| ascorbate peroxidase | - |
Populus trichocarpa |
| ascorbate peroxidase | - |
Arabidopsis thaliana |
| ascorbate peroxidase | - |
Oryza sativa Japonica Group |
| ascorbate peroxidase | - |
Physcomitrium patens |
| At1g07890 | - |
Arabidopsis thaliana |
| AT1G77490 | - |
Arabidopsis thaliana |
| AT3G09640 | - |
Arabidopsis thaliana |
| AT4G08390 | - |
Arabidopsis thaliana |
| AT4G32320 | - |
Arabidopsis thaliana |
| AT4G35000 | - |
Arabidopsis thaliana |
| AT4G35970 | - |
Arabidopsis thaliana |
| AtAPX2 | - |
Arabidopsis thaliana |
| AtAPX3 | - |
Arabidopsis thaliana |
| AtAPX5 | - |
Arabidopsis thaliana |
| AtAPX6 | - |
Arabidopsis thaliana |
| AtSAPX | - |
Arabidopsis thaliana |
| AtTAPX | - |
Arabidopsis thaliana |
| CreAPX1 | - |
Chlamydomonas reinhardtii |
| CreAPX2 | - |
Chlamydomonas reinhardtii |
| CreAPX4 | - |
Chlamydomonas reinhardtii |
| CreAPXheme | - |
Chlamydomonas reinhardtii |
| L-ascorbate peroxidase 3 | UniProt | Arabidopsis thaliana |
| L-ascorbate peroxidase 5 | UniProt | Arabidopsis thaliana |
| L-ascorbate peroxidase 6 | UniProt | Arabidopsis thaliana |
| L-ascorbate peroxidase, heme-containing | - |
Chlamydomonas reinhardtii |
| OsAPx1 | - |
Oryza sativa Japonica Group |
| OsAPx2 | - |
Oryza sativa Japonica Group |
| OsAPx3 | - |
Oryza sativa Japonica Group |
| OsAPx4 | - |
Oryza sativa Japonica Group |
| OsAPx5 | - |
Oryza sativa Japonica Group |
| OsAPx6 | - |
Oryza sativa Japonica Group |
| OsAPx7 | - |
Oryza sativa Japonica Group |
| OsAPx8 | - |
Oryza sativa Japonica Group |
| PHYPA_001206 | - |
Physcomitrium patens |
| PHYPA_001884 | - |
Physcomitrium patens |
| PHYPA_021776 | - |
Physcomitrium patens |
| PHYPA_024580 | - |
Physcomitrium patens |
| PHYPA_024582 | - |
Physcomitrium patens |
| Potri.002G081900 | - |
Populus trichocarpa |
| Potri.004G174500 | - |
Populus trichocarpa |
| Potri.005G112200 | - |
Populus trichocarpa |
| Potri.005G161900 | - |
Populus trichocarpa |
| Potri.005G179200 | - |
Populus trichocarpa |
| Potri.006G089000 | - |
Populus trichocarpa |
| Potri.006G132200 | - |
Populus trichocarpa |
| Potri.006G254500 | - |
Populus trichocarpa |
| Potri.009G015400 | - |
Populus trichocarpa |
| Potri.009G134100 | - |
Populus trichocarpa |
| Potri.016G084800 | - |
Populus trichocarpa |
| PpAPX-S | - |
Physcomitrium patens |
| PpAPX2 | - |
Physcomitrium patens |
| PpAPX2.1 | - |
Physcomitrium patens |
| PpAPX2.2 | - |
Physcomitrium patens |
| PpAPX3 | - |
Physcomitrium patens |
| PpAPX6-related | - |
Physcomitrium patens |
| PtAPX-S.1 | - |
Populus trichocarpa |
| PtAPX-S.2 | - |
Populus trichocarpa |
| PtAPX-TL29 | - |
Populus trichocarpa |
| PtAPX.3 | - |
Populus trichocarpa |
| PtAPX1.1 | - |
Populus trichocarpa |
| PtAPX1.2 | - |
Populus trichocarpa |
| PtAPX2 | - |
Populus trichocarpa |
| PtAPX3 | - |
Populus trichocarpa |
| PtAPX5 | - |
Populus trichocarpa |
| PtAPX5-like | - |
Populus trichocarpa |
| PtAPX6 related | - |
Populus trichocarpa |
Cofactor
| Cofactor | Comment | Organism | Structure |
|---|---|---|---|
| heme | - |
Chlamydomonas reinhardtii | |
| heme | - |
Populus trichocarpa | |
| heme | - |
Arabidopsis thaliana | |
| heme | - |
Oryza sativa Japonica Group | |
| heme | - |
Physcomitrium patens | |
pI Value
| Organism | Comment | pI Value Maximum | pI Value |
|---|---|---|---|
| Oryza sativa Japonica Group | isozyme APX2, sequence calculation | - |
5.18 |
| Populus trichocarpa | isozyme PtAPX1.2, sequence calculation | - |
5.27 |
| Oryza sativa Japonica Group | isozyme APX8, sequence calculation | - |
5.36 |
| Populus trichocarpa | isozyme PtAPX2, sequence calculation | - |
5.4 |
| Oryza sativa Japonica Group | isozyme APX1, sequence calculation | - |
5.42 |
| Populus trichocarpa | isozyme PtAPX1.1, sequence calculation | - |
5.48 |
| Physcomitrium patens | isozyme PpAPX2.2, sequence calculation | - |
5.53 |
| Populus trichocarpa | isozyme PtAPX.3, sequence calculation | - |
5.53 |
| Physcomitrium patens | isozyme PpAPX2.1, sequence calculation | - |
5.66 |
| Arabidopsis thaliana | isozyme APX1, sequence calculation | - |
5.72 |
| Oryza sativa Japonica Group | isozyme APX5, sequence calculation | - |
5.83 |
| Arabidopsis thaliana | isozyme APX2, sequence calculation | - |
5.87 |
| Physcomitrium patens | isozyme PpAPX6-related, sequence calculation | - |
6.15 |
| Arabidopsis thaliana | isozyme APX3, sequence calculation | - |
6.47 |
| Populus trichocarpa | isozyme PtAPX3, sequence calculation | - |
6.67 |
| Oryza sativa Japonica Group | isozyme APX6, sequence calculation | - |
6.72 |
| Arabidopsis thaliana | isozyme AtTAPX, sequence calculation | - |
6.81 |
| Physcomitrium patens | isozyme PpAPX3, sequence calculation | - |
7.01 |
| Populus trichocarpa | isozyme PtAPX5, sequence calculation | - |
7.06 |
| Populus trichocarpa | isozyme PtAPX5-like, sequence calculation | - |
7.06 |
| Populus trichocarpa | isozyme PtAPX-TL29, sequence calculation | 9 | 7.5 |
| Oryza sativa Japonica Group | isozyme APX4, sequence calculation | - |
7.74 |
| Physcomitrium patens | isozyme PpAPX-S, sequence calculation | - |
8.11 |
| Oryza sativa Japonica Group | isozyme APX3, sequence calculation | - |
8.25 |
| Arabidopsis thaliana | isozyme SAPX, sequence calculation | - |
8.31 |
| Populus trichocarpa | isozyme PtAPX6 related, sequence calculation | - |
8.44 |
| Chlamydomonas reinhardtii | isozyme CreAPXheme, sequence calculation | - |
8.63 |
| Chlamydomonas reinhardtii | isozyme CreAPX1, sequence calculation | - |
8.67 |
| Populus trichocarpa | isozyme PtAPX-S.1, sequence calculation | - |
8.68 |
| Oryza sativa Japonica Group | isozyme APX7, sequence calculation | - |
8.76 |
| Arabidopsis thaliana | isozyme APX5, sequence calculation | - |
8.8 |
| Chlamydomonas reinhardtii | isozyme CreAPX2, sequence calculation | - |
8.95 |
| Arabidopsis thaliana | isozyme APX6, sequence calculation | - |
8.99 |
| Populus trichocarpa | isozyme PtAPX-S.2, sequence calculation | - |
9.06 |
| Chlamydomonas reinhardtii | isozyme CreAPX4, sequence calculation | - |
9.23 |
Expression
| Organism | Comment | Expression |
|---|---|---|
| Oryza sativa Japonica Group | isozyme OsAPX1 is downregulated by Cd stress | down |
| Oryza sativa Japonica Group | isozyme OsAPX2 is downregulated by drought and Cd stress | down |
| Oryza sativa Japonica Group | isozyme OsAPX4 is downregulated by drought and Cd stress | down |
| Oryza sativa Japonica Group | isozyme OsAPX6 is downregulated by Cd stress | down |
| Oryza sativa Japonica Group | isozyme OsAPX7 is downregulated by Cd stress | down |
| Oryza sativa Japonica Group | isozyme OsAPX8 is downregulated by drought and Cd stress | down |
| Oryza sativa Japonica Group | drought, Pi-free, Cd, and Xanthomonas oryzae pv. oryzicola B8-12 treatments are able to significantly alter the expression profiles of rice APX isozymes, overview | additional information |
| Oryza sativa Japonica Group | drought, Pi-free, Cd, and Xanthomonas oryzae pv. oryzicola B8-12 treatments are able to significantly alter the expression profiles of rice APX isozymes, overview. Isozyme OsAPX3 is not affected by drought stress and by Cd stress | additional information |
| Oryza sativa Japonica Group | drought, Pi-free, Cd, and Xanthomonas oryzae pv. oryzicola B8-12 treatments are able to significantly alter the expression profiles of rice APX isozymes, overview. Isozyme OsAPX5 is unaffected by drought and Cd stresses | additional information |
| Oryza sativa Japonica Group | isozyme OsAPX1 is induced by drought stress | up |
| Oryza sativa Japonica Group | isozyme OsAPX6 is slightly induced by drought stress | up |
| Oryza sativa Japonica Group | isozyme OsAPX7 is induced by drought stress | up |
General Information
| General Information | Comment | Organism |
|---|---|---|
| evolution | APX belongs to the class I heme-peroxidases, isozyme AtAPX1 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Arabidopsis thaliana |
| evolution | APX belongs to the class I heme-peroxidases, isozyme AtAPX2 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Arabidopsis thaliana |
| evolution | APX belongs to the class I heme-peroxidases, isozyme AtAPX3 belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Arabidopsis thaliana |
| evolution | APX belongs to the class I heme-peroxidases, isozyme AtAPX5 belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Arabidopsis thaliana |
| evolution | APX belongs to the class I heme-peroxidases, isozyme AtAPX6 belongs to group V. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Arabidopsis thaliana |
| evolution | APX belongs to the class I heme-peroxidases, isozyme AtSAPX belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Arabidopsis thaliana |
| evolution | APX belongs to the class I heme-peroxidases, isozyme AtTAPX belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Arabidopsis thaliana |
| evolution | APX belongs to the class I heme-peroxidases, isozyme CreAPX1 belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Chlamydomonas reinhardtii |
| evolution | APX belongs to the class I heme-peroxidases, isozyme CreAPX2 belongs to group V. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Chlamydomonas reinhardtii |
| evolution | APX belongs to the class I heme-peroxidases, isozyme CreAPX4 belongs to group VI. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Chlamydomonas reinhardtii |
| evolution | APX belongs to the class I heme-peroxidases, isozyme CreAPXheme belongs to group III. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Chlamydomonas reinhardtii |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX1 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX2 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX3 belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX4 belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX5 belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX6 belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX7 belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme OsAPX8 belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Oryza sativa Japonica Group |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PpAPX-S belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Physcomitrium patens |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PpAPX2.1 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Physcomitrium patens |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PpAPX2.2 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Physcomitrium patens |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PpAPX3 belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Physcomitrium patens |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PpAPX6-related belongs to group V. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Physcomitrium patens |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX-S.1 belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX-S.2 belongs to group IV. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX-TL29 belongs to group VII. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX.3 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX1.1 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX1.2 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX2 belongs to group I. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX3 belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX5 belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX5-like belongs to group II. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| evolution | APX belongs to the class I heme-peroxidases, isozyme PtAPX6 related belongs to group V. APXs in the selected plant species show high evolutionary conservation and are able to divide into seven groups, group I to VII. Members in the groups contain abundant phosphorylation sites. Group I and VII have only protein kinase C site. Additionally, promoters of the APXs contain abundant stress-related cis-elements. APX is comprised of different isozymes, which are encoded by a multi-gene family and found in many compartments of cell | Populus trichocarpa |
| additional information | bioinformatics methods and public databases are used to evaluate the physicochemical properties, conserved motifs, potential modifications and cis-elements in all the APXs, and protein-protein network and expression profiles of rice APX isozymes, and three-dimensional modeling using the enzyme structure (PDB ID 1apx), overview | Oryza sativa Japonica Group |
| additional information | bioinformatics methods and public databases are used to evaluate the physicochemical properties, conserved motifs, potential modifications and cis-elements in all the APXs, and protein-protein network and expression profiles of rice APX isozymes, and three-dimensional modeling using the enzyme structure (PDB ID 1iyn), overview | Oryza sativa Japonica Group |
| additional information | bioinformatics methods and public databases are used to evaluate the physicochemical properties, conserved motifs, potential modifications and cis-elements in all the APXs, and protein-protein network and expression profiles of rice APX isozymes, and three-dimensional modeling using the enzyme structure (PDB ID 5jqr), overview | Oryza sativa Japonica Group |
| additional information | bioinformatics methods and public databases are used to evaluate the physicochemical properties, conserved motifs, potential modifications and cis-elements in all the APXs, and protein-protein network and expression profiles of rice APX isozymes, modeling, overview | Chlamydomonas reinhardtii |
| additional information | bioinformatics methods and public databases are used to evaluate the physicochemical properties, conserved motifs, potential modifications and cis-elements in all the APXs, and protein-protein network and expression profiles of rice APX isozymes, modeling, overview | Populus trichocarpa |
| additional information | bioinformatics methods and public databases are used to evaluate the physicochemical properties, conserved motifs, potential modifications and cis-elements in all the APXs, and protein-protein network and expression profiles of rice APX isozymes, modeling, overview | Arabidopsis thaliana |
| additional information | bioinformatics methods and public databases are used to evaluate the physicochemical properties, conserved motifs, potential modifications and cis-elements in all the APXs, and protein-protein network and expression profiles of rice APX isozymes, modeling, overview | Physcomitrium patens |
| physiological function | hydrogen peroxide (H2O2) is one important component of ROS and able to modulate plant growth and development at low level and damage plant cells at high concentrations. Ascorbate peroxidase (APX) shows high affinity towards H2O2 and plays vital roles in H2O2-scavenging | Chlamydomonas reinhardtii |
| physiological function | hydrogen peroxide (H2O2) is one important component of ROS and able to modulate plant growth and development at low level and damage plant cells at high concentrations. Ascorbate peroxidase (APX) shows high affinity towards H2O2 and plays vital roles in H2O2-scavenging | Populus trichocarpa |
| physiological function | hydrogen peroxide (H2O2) is one important component of ROS and able to modulate plant growth and development at low level and damage plant cells at high concentrations. Ascorbate peroxidase (APX) shows high affinity towards H2O2 and plays vital roles in H2O2-scavenging | Arabidopsis thaliana |
| physiological function | hydrogen peroxide (H2O2) is one important component of ROS and able to modulate plant growth and development at low level and damage plant cells at high concentrations. Ascorbate peroxidase (APX) shows high affinity towards H2O2 and plays vital roles in H2O2-scavenging | Oryza sativa Japonica Group |
| physiological function | hydrogen peroxide (H2O2) is one important component of ROS and able to modulate plant growth and development at low level and damage plant cells at high concentrations. Ascorbate peroxidase (APX) shows high affinity towards H2O2 and plays vital roles in H2O2-scavenging | Physcomitrium patens |
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