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Uroporphyrinogen (urogen) III Methyltransferase
Uroporphyrinogens are cyclic tetrapyrroles with four propionic acid groups ("P" groups) and four acetic acid groups ("A" groups). There are four forms, which vary based upon the arrangements of the "P" and "A" groups (in clockwise order): * In the "I" variety (i.e. uroporphyrinogen I), the order repeats four times: AP-AP-AP-AP. * In the "III" variety (i.e. uroporphyrinogen III), the fourth is reversed: AP-AP-AP-PA. *:This is the most common form. In the synthesis of porphyrin, it is created from the linear tetrapyrrole hydroxymethylbilane by the enzyme uroporphyrinogen III synthase, and is further converted into coproporphyrinogen III by the enzyme uroporphyrinogen III decarboxylase. * The "II" and "IV" varieties can be created synthetically, but do not appear in nature. External links * Biomolecules {{biochem-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tetrapyrroles
Tetrapyrroles are a class of chemical compounds that contain four pyrrole or pyrrole-like rings. The pyrrole/pyrrole derivatives are linked by ( =- or -- units), in either a linear or a cyclic fashion. Pyrroles are a five-atom ring with four carbon atoms and one nitrogen atom. Tetrapyrroles are common cofactors in biochemistry and their biosynthesis and degradation feature prominently in the chemistry of life. Some tetrapyrroles form the active core of compounds with crucial biochemical roles in living systems, such as hemoglobin and chlorophyll. In these two molecules, in particular, the pyrrole macrocycle ring frames a metal atom, that forms a coordination compound with the pyrroles and plays a central role in the biochemical function of those molecules. Structure Linear tetrapyrroles (called bilanes) include: *Heme breakdown products (e.g., bilirubin, biliverdin) * Phycobilins (found in cyanobacteria) *Luciferins as found in dinoflagellates and euphausiid shrimps (krill) F ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |