ACO1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Aconitase 1, soluble is a protein that in humans is encoded by the ACO1 gene.[5]

PDBOrtholog search: PDBe RCSB
AliasesACO1, ACONS, HEL60, IREB1, IREBP, IREBP1, IRP1, aconitase 1
Quick facts Available structures, PDB ...
ACO1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesACO1, ACONS, HEL60, IREB1, IREBP, IREBP1, IRP1, aconitase 1
External IDsOMIM: 100880; MGI: 87879; HomoloGene: 1657; GeneCards: ACO1; OMA:ACO1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001278352
NM_002197
NM_001362840

NM_007386

RefSeq (protein)

NP_001265281
NP_002188
NP_001349769

NP_031412

Location (UCSC)Chr 9: 32.38 – 32.45 MbChr 4: 40.14 – 40.2 Mb
PubMed search[3][4]
Wikidata
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Function

The protein encoded by this gene is a bifunctional, cytosolic protein that functions as an essential enzyme in the TCA cycle and interacts with mRNA to control the levels of iron inside cells. When cellular iron levels are high, this protein binds to a 4Fe-4S cluster and functions as an aconitase. Aconitases are iron-sulfur proteins that function to catalyze the conversion of citrate to isocitrate. When cellular iron levels are low, the protein binds to iron-responsive elements (IREs), which are stem-loop structures found in the 5' UTR of ferritin mRNA, and in the 3' UTR of transferrin receptor mRNA. When the protein binds to IRE, it results in repression of translation of ferritin mRNA, and inhibition of degradation of the otherwise rapidly degraded transferrin receptor mRNA. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Alternative splicing results in multiple transcript variants.[5]

References

Further reading

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