Chemistry:Phycoerythrobilin
From HandWiki
| |
| Names | |
|---|---|
| IUPAC name
3-[(2Z,5Z)-2-[[3-(2-carboxyethyl)-5-[[(2R)-4-ethenyl-3-methyl-5-oxo-1,2-dihydropyrrol-2-yl]methyl]-4-methyl-1H-pyrrol-2-yl]methylidene]-5-[[(3E,4R)-3-ethylidene-4-methyl-5-oxopyrrol-2-yl]methylidene]-4-methylpyrrol-3-yl]propanoic acid
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
| MeSH | phycoerythrobilin |
PubChem CID
|
|
| |
| |
| Properties | |
| C33H38N4O6 | |
| Molar mass | 586.689 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
| |
| Infobox references | |
Tracking categories (test):
Phycoerythrobilin is a red phycobilin, i.e. an open tetrapyrrole chromophore[1] found in cyanobacteria and in the chloroplasts of red algae, glaucophytes and some cryptomonads. Phycoerythrobilin is present in the phycobiliprotein phycoerythrin, of which it is the terminal acceptor of energy. The amount of phycoerythrobilin in phycoerythrins varies a lot, depending on the considered organism. In some Rhodophytes and oceanic cyanobacteria, phycoerythrobilin is also present in the phycocyanin, then termed R-phycocyanin. Like all phycobilins, phycoerythrobilin is covalently linked to these phycobiliproteins by a thioether bond.
References
- ↑ Chapman, David J.; Cole, W. J.; Siegelman, Harold W. (1967). "Structure of phycoerythrobilin". Journal of the American Chemical Society 89 (23): 5976–5977. doi:10.1021/ja00999a058. ISSN 0002-7863.
External links
 |  |
