Homo sapiens Protein: ALKBH7
Summary
InnateDB Protein IDBP-21344.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ALKBH7
Protein Name alkB, alkylation repair homolog 7 (E. coli)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000245812
InnateDB Gene IDBG-21342 (ALKBH7)
Protein Structure
UniProt Annotation
Function Probable dioxygenase required to induce programmed necrosis in response to DNA damage caused by cytotoxic alkylating agents. Acts by triggering the collapse of mitochondrial membrane potential and loss of mitochondrial function that leads to energy depletion and cell death. ALKBH7-mediated necrosis is probably required to prevent the accumulation of cells with DNA damage. Does not display DNA demethylase activity. Involved in fatty acid metabolism. {ECO:0000269PubMed:23666923}.
Subcellular Localization Mitochondrion matrix {ECO:0000269PubMed:23666923}.
Disease Associations
Tissue Specificity Widely expressed, with highest expression in pancreas, followed by spleen, prostate, ovary and placenta. {ECO:0000269PubMed:17979886}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
Experimentally validated
Total 4 [view]
Protein-Protein 2 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0046872 metal ion binding
GO:0051213 dioxygenase activity
Biological Process
GO:0006631 fatty acid metabolic process
GO:0006974 cellular response to DNA damage stimulus
GO:0010883 regulation of lipid storage
GO:0055114 oxidation-reduction process
GO:1902445 regulation of mitochondrial membrane permeability involved in programmed necrotic cell death
Cellular Component
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9BT30
PhosphoSite PhosphoSite-
TrEMBL M0QZH2
UniProt Splice Variant
Entrez Gene 84266
UniGene Hs.111099
RefSeq NP_115682
HUGO HGNC:21306
OMIM 613305
CCDS CCDS12163
HPRD 15425
IMGT
EMBL AC011491 AK223336 AK311956 AY358858 AY427650 BC004393 CH471139
GenPept AAH04393 AAQ89217 AAR24624 BAD97056 BAG34896 EAW69102