SIAH1

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

E3 ubiquitin-protein ligase SIAH1 is an enzyme that in humans is encoded by the SIAH1 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesSIAH1, SIAH1A, siah E3 ubiquitin protein ligase 1, BURHAS
Quick facts Available structures, PDB ...
SIAH1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSIAH1, SIAH1A, siah E3 ubiquitin protein ligase 1, BURHAS
External IDsOMIM: 602212; MGI: 108064; HomoloGene: 20654; GeneCards: SIAH1; OMA:SIAH1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001006610
NM_003031
NM_001006611

NM_009172

RefSeq (protein)

NP_001006611
NP_003022

NP_033198

Location (UCSC)Chr 16: 48.36 – 48.45 MbChr 8: 87.45 – 87.47 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes for a polypeptide structure that is a member of the seven in absentia homolog (SIAH) family. The protein is an E3 ligase and is involved in ubiquitination and proteasome-mediated degradation of specific proteins. The activity of this ubiquitin ligase has been implicated in the development of certain forms of Parkinson's disease, the regulation of the cellular response to hypoxia and induction of apoptosis. Alternative splicing results in several additional transcript variants, some encoding different isoforms and others that have not been fully characterized.[7]

Interactions

SIAH1 has been shown to interact with:

References

Further reading

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