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91801 ALKBH8

91801

ALKBH8

alkB homolog 8, tRNA methyltransferase

protein-coding

Homo sapiens

基因描述

Type Description
Definition alkB homolog 8, tRNA methyltransferase

研究结论

Date Results Publications
2020-10-03 12:53:00 Loss of epitranscriptomic control of selenocysteine utilization engages senescence and mitochondrial reprogramming(). 31765888
2020-03-14 12:34:00 Recessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification. 31079898
2017-06-03 12:11:00 findings suggest that the high expression of ALKBH8 is critical for the growth and progression of bladder cancer 27329810
2013-09-06 09:40:00 Many eukaryotic tRNAs contain the wobble modification 5-methoxycarbonylmethyl-uridine (mcm5U). It is demonstrated that (R)- and (S)-5-methoxycarbonylhydroxymethyluridine (mchm5U), hydroxylated forms of mcm(5)U, are present in mammalian tRNA-Arg(UCG), and tRNA-Gly(UCC), respectively. It is shown that the hydroxylation reaction leading to the formation of (S)-mchm5U is catalyzed by the oxygenase (AlkB) domain of ALKBH8. 21285950
2013-09-06 09:37:00 The methyltransferase domain of ALKBH8 is demonstrated to be a functional homologue of the Saccharomyces cerevisiae Trm9 protein, mediating the last step in the formation of the wobble uridine modification 5-methoxycarbonylmethyl-uridine in tRNA. This modification is shown to be important for efficient selenoprotein synthesis. ALKBH8 knock-out mice are generated and described. 20123966

名称对应

Type IDs
Synonymous ABH8, TRM9, TRMT9, TRMT9A
Gene
UniProtKB-ID: ALKB8_HUMAN
UniprotKB: Q96BT7
UniParc: UPI0000EE3A38, UPI0000072C37, UPI00001FA2E7, UPI00017A6D55
EMBL: CH471065, AK304413, AK095523, AK293603, AB218768, BC015183, AP001823
Ensembl: ENSG00000137760
KO: hsa:91801
Nucleutide sequences
EMBL-CDS: AAH15183.1, BAG65244.1, BAC04566.1, BAG57067.1, EAW67089.1, BAG16270.1, EAW67090.1
Ensembl_TRS: ENST00000389568, ENST00000417449, ENST00000429370, ENST00000260318, ENST00000428149
Protein sequencees
Ensembl_PRO: ENSP00000374219, ENSP00000391225, ENSP00000260318, ENSP00000397673, ENSP00000415885
RefSeq: XP_016874042.1, NP_620130.2, NP_001365062.1, XP_005271786.1, XP_016874046.1, NP_001287939.2, XP_005271785.1
Others
UniRef100: UniRef100_Q96BT7
UniRef90: UniRef90_Q96BT7
UniRef50: UniRef50_Q96BT7
UniGene: Hs.503763
CCDS: CCDS8337.2, CCDS73376.1

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