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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

AlkB, alkylation repair homolog 8

Top mentioned proteins: demethylase, STEP, FTO, Ethanolaminephosphotransferase, ACID
Papers on ALKBH8
Protozoan ALKBH8 oxygenases display both DNA repair and tRNA modification activities.
Falnes et al., Oslo, Norway. In Plos One, 2013
Mammalian and plant ALKBH8 are tRNA hydroxylases targeting 5-methoxycarbonylmethyl-modified uridine (mcm5U) at the wobble position of tRNAGly(UCC).
Human ALKBH4 interacts with proteins associated with transcription.
Falnes et al., Oslo, Norway. In Plos One, 2011
ALKBH2 and ALKBH3 display demethylase activities corresponding to that of AlkB, and both ALKBH8 and FTO are RNA modification enzymes.
Roles of Trm9- and ALKBH8-like proteins in the formation of modified wobble uridines in Arabidopsis tRNA.
Falnes et al., Oslo, Norway. In Nucleic Acids Res, 2011
Moreover, we demonstrate that AT1G36310, denoted AtALKBH8, is required for hydroxylation of mcm(5)U to (S)-mchm(5)U in tRNA(Gly)(UCC), and has a function similar to the mammalian dioxygenase ALKBH8.
ALKBH8-mediated formation of a novel diastereomeric pair of wobble nucleosides in mammalian tRNA.
Falnes et al., Oslo, Norway. In Nat Commun, 2010
The AlkB domain of ALKBH8 specifically hydroxylates mcm(5)U into (S)-mchm(5)U in tRNA-Gly(UCC).
Human AlkB homolog ABH8 Is a tRNA methyltransferase required for wobble uridine modification and DNA damage survival.
Samson et al., Cambridge, United States. In Mol Cell Biol, 2010
Data show that human AlkB homolog 8 (ABH8) catalyzes tRNA methylation to generate 5-methylcarboxymethyl uridine (mcm(5)U) at the wobble position of certain tRNAs, a critical anticodon loop modification linked to DNA damage survival.
Mammalian ALKBH8 possesses tRNA methyltransferase activity required for the biogenesis of multiple wobble uridine modifications implicated in translational decoding.
Klungland et al., Oslo, Norway. In Mol Cell Biol, 2010
Data show that ALKBH8 is a tRNA methyltransferase required for the final step in the biogenesis of mcm5U.
A novel human AlkB homologue, ALKBH8, contributes to human bladder cancer progression.
Konishi et al., Kashihara, Japan. In Cancer Res, 2009
Findings indicate a role for ALKBH8 in urothelial carcinoma cell survival mediated by NOX-1-dependent ROS signals, further suggesting therapeutic strategies in human bladder cancer by inducing JNK/p38/gammaH2AX-mediated cell death by silencing of ALKBH8.
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