Homo sapiens Protein: ALKBH8 | |||||||||||||||||
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Summary | |||||||||||||||||
InnateDB Protein | IDBP-382771.4 | ||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||
Gene Symbol | ALKBH8 | ||||||||||||||||
Protein Name | alkB, alkylation repair homolog 8 (E. coli) | ||||||||||||||||
Synonyms | |||||||||||||||||
Species | Homo sapiens | ||||||||||||||||
Ensembl Protein | ENSP00000415885 | ||||||||||||||||
InnateDB Gene | IDBG-69973 (ALKBH8) | ||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||
Function | Catalyzes the methylation of 5-carboxymethyl uridine to 5-methylcarboxymethyl uridine at the wobble position of the anticodon loop in tRNA. Catalyzes the last step in the formation of 5-methylcarboxymethyl uridine at the wobble position of the anticodon loop in target tRNA. Has a preference for tRNA(Arg) and tRNA(Glu), and does not bind tRNA(Lys). Required for normal survival after DNA damage. May inhibit apoptosis and promote cell survival and angiogenesis. {ECO:0000269PubMed:19293182, ECO:0000269PubMed:20308323}. | ||||||||||||||||
Subcellular Localization | Cytoplasm. Nucleus. Note=Predominantly cytoplasmic. | ||||||||||||||||
Disease Associations | |||||||||||||||||
Tissue Specificity | Widely expressed, with highest expression in spleen, followed by pancreas and lung. {ECO:0000269PubMed:17979886}. | ||||||||||||||||
Comments | |||||||||||||||||
Interactions | |||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||
PDB ID | |||||||||||||||||
InterPro |
IPR005123
Oxoglutarate/iron-dependent dioxygenase IPR007823 Methyltransferase-related IPR013216 Methyltransferase type 11 IPR015095 Alkylated DNA repair protein AlkB, homologue 8, N-terminal IPR029063 S-adenosyl-L-methionine-dependent methyltransferase-like |
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PFAM |
PF03171
PF13640 PF05148 PF08241 PF09004 |
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PRINTS | |||||||||||||||||
PIRSF | |||||||||||||||||
SMART | |||||||||||||||||
TIGRFAMs | |||||||||||||||||
Post-translational Modifications | |||||||||||||||||
Modification | |||||||||||||||||
Cross-References | |||||||||||||||||
SwissProt | Q96BT7 | ||||||||||||||||
PhosphoSite | PhosphoSite-Q96BT7 | ||||||||||||||||
TrEMBL | |||||||||||||||||
UniProt Splice Variant | |||||||||||||||||
Entrez Gene | 91801 | ||||||||||||||||
UniGene | Hs.606625 | ||||||||||||||||
RefSeq | NP_620130 | ||||||||||||||||
HUGO | HGNC:25189 | ||||||||||||||||
OMIM | 613306 | ||||||||||||||||
CCDS | CCDS8337 | ||||||||||||||||
HPRD | 14287 | ||||||||||||||||
IMGT | |||||||||||||||||
EMBL | AB218768 AK095523 AK293603 AK304413 AP001823 BC015183 CH471065 | ||||||||||||||||
GenPept | AAH15183 BAC04566 BAG16270 BAG57067 BAG65244 EAW67089 EAW67090 | ||||||||||||||||