Ferrochelatase: Difference between revisions

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<StructureSection load='2qd2' size='450' side='right' scene='Journal:JBIC:4/Heme_bound_ferro_open/3' caption=''>
<StructureSection load='2qd2' size='450' side='right' scene='Journal:JBIC:4/Heme_bound_ferro_open/3' caption=''>
<StructureSection load='2qd2' size='450' side='right' scene='Journal:JBIC:4/Heme_bound_ferro_open/3' caption=''>
<StructureSection load='2qd2' size='450' side='right' scene='' caption=''>


'''Ferrochelatase''' (FECH) catalyzes the last step in the formation of heme.  FECH adds Fe+2 to protoporphyrin IX converting it to protoheme.  The human FECH is a homodimer containing 2 similar domains and an iron-sulfur cluster.  Defective FECH is the cause of porphyria.
'''Ferrochelatase''' (FECH) catalyzes the last step in the formation of heme.  FECH adds Fe+2 to protoporphyrin IX converting it to protoheme.  The human FECH is a homodimer containing 2 similar domains and an iron-sulfur cluster.  Defective FECH is the cause of porphyria.

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Michal Harel, Alexander Berchansky