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- Table of Contents
Facts about Nucleic acid dioxygenase ALKBH1.
Mainly functions as a tRNA demethylase by removing N(1)-methyladenine from various tRNAs, with a preference for N(1)-methyladenine at position 58 (m1A58) present on a stem loop structure of tRNAs (PubMed:27745969). Acts as a regulator of translation initiation and elongation in response to glucose deprivation: modulates both translation initiation, by mediating demethylation of tRNA(Met), and translation elongation, N(1)-methyladenine-containing tRNAs being preferentially recruited to polysomes to promote translation elongation (PubMed:27745969).
| Human | |
|---|---|
| Gene Name: | ALKBH1 |
| Uniprot: | Q13686 |
| Entrez: | 8846 |

| Belongs to: |
|---|
| alkB family |

ABH1; ABHalkB, alkylation repair homolog (E. coli); alkB; alkB, alkylation repair homolog 1 (E. coli); ALKBH; alkylated DNA repair protein alkB homolog 1; alkylation repair, alkB homolog; Alpha-ketoglutarate-dependent dioxygenase ABH1; DNA lyase ABH1; EC 1.14.11.-; EC 4.2.99.18; hABH
Mass (kDA):
43.832 kDA

| Human | |
|---|---|
| Location: | 14q24.3 |
| Sequence: | 14; NC_000014.9 (77672404..77708038, complement) |
Ubiquitous.
Nucleus. Mitochondrion. Mainly localizes in euchromatin, largely excluded from heterochromatin and nucleoli (By similarity).





PMID: 8600462 by Wei Y.F., et al. Molecular cloning and functional analysis of a human cDNA encoding an Escherichia coli AlkB homolog, a protein involved in DNA alkylation damage repair.
PMID: 17979886 by Tsujikawa K., et al. Expression and sub-cellular localization of human ABH family molecules.