Uroporphyrinogen III synthase

Class of enzymes From Wikipedia, the free encyclopedia

Uroporphyrinogen III synthase (EC 4.2.1.75) is an enzyme involved in the metabolism of the cyclic tetrapyrrole compound porphyrin. It is involved in the conversion of hydroxymethylbilane into uroporphyrinogen III. This enzyme catalyses the inversion of the final pyrrole unit (ring D) of the linear tetrapyrrole molecule, linking it to the first pyrrole unit (ring A), thereby generating a large macrocyclic structure, uroporphyrinogen III.[1] The enzyme folds into two alpha/beta domains connected by a beta-ladder, the active site being located between the two domains.[2]

Heme synthesisnote that some reactions occur in the cytoplasm and some in the mitochondrion (yellow)
Quick facts Identifiers, Symbol ...
Uroporphyrinogen III synthase
Identifiers
SymbolUROS
NCBI gene7390
HGNC12592
OMIM606938
RefSeqNM_000375
UniProtP10746
Other data
EC number4.2.1.75
LocusChr. 10 q25.2-26.3
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StructuresSwiss-model
DomainsInterPro
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Quick facts Identifiers, Symbol ...
Uroporphyrinogen-III synthase HemD
crystal structure of uroporphyrinogen iii synthase from an extremely thermophilic bacterium thermus thermophilus hb8 (wild type, native, form-2 crystal)
Identifiers
SymbolHEM4
PfamPF02602
InterProIPR003754
SCOP21jr2 / SCOPe / SUPFAM
Available protein structures:
PDB  IPR003754 PF02602 (ECOD; PDBsum)  
AlphaFold
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Function

The enzyme catalyses the cyclisation reaction of hydroxymethylbilane into uroporphyrinogen III via a spiro intermediate which allows one of the pyrrole rings to convert its initial acetate to propionate configuration into a propionate-acetate one.[3][4]

 
 
H2O
Rightward reaction arrow with minor product(s) to top and bottom right
 
H2O
 

Pathology

A deficiency is associated with Gunther's disease, also known as congenital erythropoietic porphyria (CEP). This is an autosomal recessive inborn error of metabolism that results from the markedly deficient activity of uroporphyrinogen III synthase.[5]

References

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