Any feedback?
Literature summary for 2.5.1.32 extracted from
- An update on carotenoid biosynthesis in algae: phylogenetic evidence for the existence of two classes of phytoene synthase (2009), Planta, 229, 723-729.
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Aureococcus anophagefferens | - |
expresses two types of class II PSY, one is related to Haptophyta, the other one is related to the Rhodophyta | - |
| Chlamydomonas reinhardtii | - |
expresses class I PSY | - |
| Chlorella variabilis | - |
expresses class I PSY | - |
| Cyanidioschyzon merolae | - |
expresses class II PSY | - |
| Dunaliella salina | C1J5N0 | genome contains four paralogous of class I PSY | - |
| Dunaliella salina | C1J5N1 | genome contains four paralogous of class I PSY | - |
| Dunaliella salina | O04007 | genome contains four paralogous of class I PSY | - |
| Dunaliella salina | Q66UF6 | expresses class I PSY | - |
| Dunaliella sp. 336 | Q1KPR4 | expresses class I PSY | - |
| Emiliania huxleyi | - |
expresses class II PSY | - |
| Haematococcus lacustris | Q4TUC6 | expresses class I PSY | - |
| Micromonas commoda | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
| Micromonas pusilla CCMP1545 | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
| Nostoc sp. PCC 7120 = FACHB-418 | - |
expresses class I PSY | - |
| Ostreococcus sp. 'lucimarinus' | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
| Ostreococcus sp. RCC809 | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
| Ostreococcus tauri | - |
expresses class I and class II PSY which differ in regions not essential to the enzymatic function | - |
| Phaeodactylum tricornutum | - |
expresses class II PSY | - |
| Solanum lycopersicum | A9Q2P8 | expresses two different class I PSY | - |
| Solanum lycopersicum | P08196 | expresses two different class I PSY | - |
| Synechocystis sp. PCC 6803 | - |
expresses class I PSY | - |
| Volvox carteri | - |
expresses class I PSY | - |
| Zea mays | B0KYU8 | expresses three different class I PSY | - |
| Zea mays | Q6EI12 | expresses three different class I PSY | - |
| Zea mays | Q6EIC3 | expresses three different class I PSY | - |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| phytoene synthase | - |
Chlamydomonas reinhardtii |
| phytoene synthase | - |
Phaeodactylum tricornutum |
| phytoene synthase | - |
Emiliania huxleyi |
| phytoene synthase | - |
Synechocystis sp. PCC 6803 |
| phytoene synthase | - |
Volvox carteri |
| phytoene synthase | - |
Cyanidioschyzon merolae |
| phytoene synthase | - |
Ostreococcus tauri |
| phytoene synthase | - |
Nostoc sp. PCC 7120 = FACHB-418 |
| phytoene synthase | - |
Dunaliella salina |
| phytoene synthase | - |
Aureococcus anophagefferens |
| phytoene synthase | - |
Ostreococcus sp. 'lucimarinus' |
| phytoene synthase | - |
Ostreococcus sp. RCC809 |
| phytoene synthase | - |
Micromonas commoda |
| phytoene synthase | - |
Micromonas pusilla CCMP1545 |
| phytoene synthase | - |
Chlorella variabilis |
| phytoene synthase | - |
Haematococcus lacustris |
| phytoene synthase | - |
Dunaliella sp. 336 |
| phytoene synthase | - |
Zea mays |
| phytoene synthase | - |
Solanum lycopersicum |
| PSY | - |
Phaeodactylum tricornutum |
| PSY | - |
Cyanidioschyzon merolae |
| PSY | - |
Ostreococcus tauri |
| PSY | - |
Aureococcus anophagefferens |
| PSY | - |
Ostreococcus sp. 'lucimarinus' |
| PSY | - |
Micromonas commoda |
| PSY | - |
Micromonas pusilla CCMP1545 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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' |
| 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 |
| 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 |
| 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 |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Chlamydomonas reinhardtii |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Synechocystis sp. PCC 6803 |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Volvox carteri |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Nostoc sp. PCC 7120 = FACHB-418 |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Dunaliella salina |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Chlorella variabilis |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Haematococcus lacustris |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Dunaliella sp. 336 |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Zea mays |
| PSY | Chlorophyceae, Streptophyta and Cyanophyta expresses class I PSY (I) | Solanum lycopersicum |
| PSY1 | expresses three different class I PSY | Zea mays |
| PSY1 | expresses two different class I PSY | Solanum lycopersicum |
| PSY1a | - |
Dunaliella salina |
| PSY1b | - |
Dunaliella salina |
| PSY2 | - |
Dunaliella salina |
| PSY2 | expresses three different class I PSY | Zea mays |
| PSY2 | expresses two different class I PSY | Solanum lycopersicum |
| PSY3 | expresses three different class I PSY | Zea mays |
Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.
Release 2023.1 (January 2023)
Legal
Curated at
Member of
