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SIAH1 (NM_001006610) - siah E3 ubiquitin protein ligase 1
E3 Ubiquitin-Protein Ligase Siah1 Isoform B
Legend
Mutation impacts
direct
network-rewiring
motif-changing
proximal
distal
none
Sites
multiple types
acetylation
methylation
succinylation
sumoylation
ubiquitination
glycosylation
- C-linked
- N-linked
- O-linked
- S-linked
phosphorylation
- SARS-CoV-2
Others
Exact position of a PTM site
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Mutations Visualisation
Protein summary
This is an alternative isoform of SIAH1 protein.
View all 2 isoforms
SIAH1:
E3 ubiquitin-protein ligase SIAH1 isoform b
Description:
This gene encodes a protein 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. [provided by RefSeq, Jul 2008].
- Strand
- -
- Chromosome
- 16
- Protein
- 313 residues
- All mutations
- 22
- PTM sites
- 11
- CDS
- 48,395,490 - 48,399,388
- Transcription
- 48,394,445 - 48,399,784
External references
Mappings retrieved from NCBI & UniProt.