DQX1 (DEAQ box RNA-dependent ATPase 1), also known as FLJ23757, is a 71 amino acid protein that contains one helicase ATP-binding domain and one helicase SLCterminal domain. Localized to the nucleus, DQX1 catalyzes the conversion of ATP to ADP and a phosphate. Expressed as three isoforms produced by alternative splicing events, DQX1 is encoded by a gene that maps to human chomosome 2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2, including Harlequin icthyosis, sitosterolemia and Alstr鰉 syndrome.
Subcellular Location:
Nuclear
Similarity:
Contains 1 helicase ATP-binding domain.
Contains 1 helicase SLCterminal domain.
SWISS:
Q8TE96
Gene ID:
165545
Database links:
Entrez Gene: 165545 Human
Entrez Gene: 93838 Mouse
Entrez Gene: 136434 Rat
SwissProt: Q8TE96 Human
SwissProt: Q924H9 Mouse
Unigene: 191705 Human
Unigene: 140332 Mouse
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Sample: Spleen (Mouse) Lysate at 40 ug
Primary: Anti-DQX1 (SL8293R)at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 79kD
Observed band size: 85kD
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