Uroporphyrinogen III decarboxylase

Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia

Uroporphyrinogen III decarboxylase (uroporphyrinogen decarboxylase, or UROD) is an enzyme (EC 4.1.1.37) that in humans is encoded by the UROD gene.[5]

PDBOrtholog search: PDBe RCSB
AliasesUROD, PCT, UPD, uroporphyrinogen decarboxylase
Quick facts UROD, Available structures ...
UROD
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesUROD, PCT, UPD, uroporphyrinogen decarboxylase
External IDsOMIM: 613521; MGI: 98916; HomoloGene: 320; GeneCards: UROD; OMA:UROD - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000374

NM_009478

RefSeq (protein)

NP_000365

NP_033504

Location (UCSC)Chr 1: 45.01 – 45.02 MbChr 4: 116.85 – 116.85 Mb
PubMed search[3][4]
Wikidata
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Function

Uroporphyrinogen III decarboxylase is a homodimeric enzyme (PDB: 1URO) that catalyzes the fifth step in heme biosynthesis, which corresponds to the elimination of carboxyl groups from the four acetate side chains of uroporphyrinogen III to yield coproporphyrinogen III:[6]

 
 
4 CO2
Rightward reaction arrow with minor product(s) to top right
 
 
 

Clinical significance

Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoietic porphyria.[5] At least 65 disease-causing mutations in this gene have been discovered.[7]

Mechanism

At low substrate concentrations, the reaction is believed to follow an ordered route, with the sequential removal of CO2 from the D, A, B, and C rings, whereas at higher substrate/enzyme levels a random route seems to be operative. The enzyme functions as a dimer in solution, and both the enzymes from human and tobacco have been crystallized and solved at good resolutions.

The reaction catalyzed by UroD

UroD is regarded as an unusual decarboxylase, since it performs decarboxylations without the intervention of any cofactors, unlike the vast majority of decarboxylases. Its mechanism has been proposed to proceed through substrate protonation by an arginine residue.[8] A 2008 report demonstrated that the uncatalyzed rate for UroD's reaction is 10−19 s−1, so at pH 10 the rate acceleration of UroD relative to the uncatalyzed rate, i.e. catalytic proficiency, is the largest for any enzyme known, 6 x 1024 M−1.[6]

Proposed reaction mechanism of uroporphyrinogen III decarboxylase

References

Further reading

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