EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.5.1.32 | Aureococcus anophagefferens | - |
expresses two types of class II PSY, one is related to Haptophyta, the other one is related to the Rhodophyta | - |
2.5.1.32 | Chlamydomonas reinhardtii | - |
expresses class I PSY | - |
2.5.1.32 | Chlorella variabilis | - |
expresses class I PSY | - |
2.5.1.32 | Cyanidioschyzon merolae | - |
expresses class II PSY | - |
2.5.1.32 | Dunaliella salina | C1J5N0 | genome contains four paralogous of class I PSY | - |
2.5.1.32 | Dunaliella salina | C1J5N1 | genome contains four paralogous of class I PSY | - |
2.5.1.32 | Dunaliella salina | O04007 | genome contains four paralogous of class I PSY | - |
2.5.1.32 | Dunaliella salina | Q66UF6 | expresses class I PSY | - |
2.5.1.32 | Dunaliella sp. 336 | Q1KPR4 | expresses class I PSY | - |
2.5.1.32 | Emiliania huxleyi | - |
expresses class II PSY | - |
2.5.1.32 | Haematococcus lacustris | Q4TUC6 | expresses class I PSY | - |
2.5.1.32 | Micromonas commoda | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
2.5.1.32 | Micromonas pusilla CCMP1545 | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
2.5.1.32 | Nostoc sp. PCC 7120 = FACHB-418 | - |
expresses class I PSY | - |
2.5.1.32 | Ostreococcus sp. 'lucimarinus' | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
2.5.1.32 | Ostreococcus sp. RCC809 | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
2.5.1.32 | Ostreococcus tauri | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
2.5.1.32 | Phaeodactylum tricornutum | - |
expresses class II PSY | - |
2.5.1.32 | Solanum lycopersicum | A9Q2P8 | expresses two different class I PSY | - |
2.5.1.32 | Solanum lycopersicum | P08196 | expresses two different class I PSY | - |
2.5.1.32 | Synechocystis sp. PCC 6803 | - |
expresses class I PSY | - |
2.5.1.32 | Volvox carteri | - |
expresses class I PSY | - |
2.5.1.32 | Zea mays | B0KYU8 | expresses three different class I PSY | - |
2.5.1.32 | Zea mays | Q6EI12 | expresses three different class I PSY | - |
2.5.1.32 | Zea mays | Q6EIC3 | expresses three different class I PSY | - |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.5.1.32 | phytoene synthase | - |
Chlamydomonas reinhardtii |
2.5.1.32 | phytoene synthase | - |
Phaeodactylum tricornutum |
2.5.1.32 | phytoene synthase | - |
Emiliania huxleyi |
2.5.1.32 | phytoene synthase | - |
Synechocystis sp. PCC 6803 |
2.5.1.32 | phytoene synthase | - |
Volvox carteri |
2.5.1.32 | phytoene synthase | - |
Cyanidioschyzon merolae |
2.5.1.32 | phytoene synthase | - |
Ostreococcus tauri |
2.5.1.32 | phytoene synthase | - |
Nostoc sp. PCC 7120 = FACHB-418 |
2.5.1.32 | phytoene synthase | - |
Dunaliella salina |
2.5.1.32 | phytoene synthase | - |
Aureococcus anophagefferens |
2.5.1.32 | phytoene synthase | - |
Ostreococcus sp. 'lucimarinus' |
2.5.1.32 | phytoene synthase | - |
Ostreococcus sp. RCC809 |
2.5.1.32 | phytoene synthase | - |
Micromonas commoda |
2.5.1.32 | phytoene synthase | - |
Micromonas pusilla CCMP1545 |
2.5.1.32 | phytoene synthase | - |
Chlorella variabilis |
2.5.1.32 | phytoene synthase | - |
Haematococcus lacustris |
2.5.1.32 | phytoene synthase | - |
Dunaliella sp. 336 |
2.5.1.32 | phytoene synthase | - |
Zea mays |
2.5.1.32 | phytoene synthase | - |
Solanum lycopersicum |
2.5.1.32 | PSY | - |
Phaeodactylum tricornutum |
2.5.1.32 | PSY | - |
Cyanidioschyzon merolae |
2.5.1.32 | PSY | - |
Ostreococcus tauri |
2.5.1.32 | PSY | - |
Aureococcus anophagefferens |
2.5.1.32 | PSY | - |
Ostreococcus sp. 'lucimarinus' |
2.5.1.32 | PSY | - |
Micromonas commoda |
2.5.1.32 | PSY | - |
Micromonas pusilla CCMP1545 |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Phaeodactylum tricornutum |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Emiliania huxleyi |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Cyanidioschyzon merolae |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Ostreococcus tauri |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Aureococcus anophagefferens |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Ostreococcus sp. 'lucimarinus' |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Ostreococcus sp. RCC809 |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Micromonas commoda |
2.5.1.32 | PSY | An ancient gene duplication event leads to a class I PSY (I) and a class II PSY (II) in Haptophyta, Rhodophyta, Heterokontophyta as well as Pelagophyceae and Prasinophyceae. Both PSY classes share the essential characteristics of PSY including predicted substrate-Mg2+-binding sites (Aspartate-rich regions) and catalytic residues. Major differences between the two PSY classes appear to exist only in regions not essential to the enzymatic function. | Micromonas pusilla CCMP1545 |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Chlamydomonas reinhardtii |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Synechocystis sp. PCC 6803 |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Volvox carteri |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Nostoc sp. PCC 7120 = FACHB-418 |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Dunaliella salina |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Chlorella variabilis |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Haematococcus lacustris |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Dunaliella sp. 336 |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Zea mays |
2.5.1.32 | PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Solanum lycopersicum |
2.5.1.32 | PSY1 | expresses three different class I PSY | Zea mays |
2.5.1.32 | PSY1 | expresses two different class I PSY | Solanum lycopersicum |
2.5.1.32 | PSY1a | - |
Dunaliella salina |
2.5.1.32 | PSY1b | - |
Dunaliella salina |
2.5.1.32 | PSY2 | - |
Dunaliella salina |
2.5.1.32 | PSY2 | expresses three different class I PSY | Zea mays |
2.5.1.32 | PSY2 | expresses two different class I PSY | Solanum lycopersicum |
2.5.1.32 | PSY3 | expresses three different class I PSY | Zea mays |