| 1. | Two molecules of this intermediate become linked to form porphobilinogen.
|
| 2. | Porphobilinogen deaminase is involved in the third step of the heme biosynthetic pathway.
|
| 3. | Porphobilinogen deaminase usually exists in dimer units in the cytoplasm of the cell.
|
| 4. | An inhibitor of porphobilinogen synthase with this mechanism of action has been documented.
|
| 5. | The colorless porphobilinogen is changed to the dark colored porphobilin due to oxygen exposure.
|
| 6. | Hereditary insufficiency of porphobilinogen synthase is called porphobilinogen synthase ( or ALA dehydratase ) deficiency poprhyria.
|
| 7. | Hereditary insufficiency of porphobilinogen synthase is called porphobilinogen synthase ( or ALA dehydratase ) deficiency poprhyria.
|
| 8. | The porphobilinogen synthase catalyzed reaction is the first common step in the biosynthesis of all biological tetrapyrroles.
|
| 9. | PBG is then converted into hydroxymethyl bilane by the enzyme porphobilinogen deaminase, also known as hydroxymethylbilane synthase.
|
| 10. | All natural tetrapyrroles, including hemes, chlorophylls and vitamin B 12, share porphobilinogen as a common precursor.
|
मोबाइल