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ASNA1  -  arsA arsenite transporter, ATP-binding,...

Homo sapiens

Synonyms: ARSA, ARSA-I, ARSA1, ASNA-I, ATPase ASNA1, ...
 
 
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Disease relevance of ASNA1

  • We have previously reported the cloning of hASNA-I, a human homologue of arsA encoding the ATPase component of the Escherichia coli arsenite transporter [1].
  • Its subcellular localization in human malignant melanoma T289 cells was examined to gain insight into the role of hASNA-I in the physiology of human cells [2].
  • Immunohistochemical staining showed a distinct pattern of hASNA-I expression in cells within normal tissues, and its overexpression in breast cancer [3].
  • Immunohistochemical analysis of the distribution of the human ATPase (hASNA-I) in normal tissues and its overexpression in breast adenomas and carcinomas [4].
  • ASNA independent study. Fibromyalgia [5].
 

High impact information on ASNA1

  • Subsequent release from TRC40/Asna-1 and insertion into the membrane depends on ATP hydrolysis [6].
  • Biochemical characterization of the human arsenite-stimulated ATPase (hASNA-I) [1].
  • Southern and Northern analyses indicated the presence of two cross-hybridizing genes in the human genome and expression of hARSA-I in many tissues [7].
  • We have isolated the human homolog of the bacterial arsA (hARSA-I), a member of the ATPase superfamily with no transmembrane domain [7].
  • Further immunocytochemical analysis showed that the hASNA-I at the nuclear membrane was associated with invaginations into the nucleus in interphase cells [2].
 

Chemical compound and disease context of ASNA1

  • The results indicate that hASNA-I is a distinct human arsenite-stimulated ATPase belonging to the same superfamily of ATPases represented by the E. coli ArsA protein [1].
 

Biological context of ASNA1

 

Associations of ASNA1 with chemical compounds

  • ASNA independent study activity: "Selective serotoni inhibitors (SSRIs)--what nurses should know" [9].

References

  1. Biochemical characterization of the human arsenite-stimulated ATPase (hASNA-I). Kurdi-Haidar, B., Heath, D., Aebi, S., Howell, S.B. J. Biol. Chem. (1998) [Pubmed]
  2. Dual cytoplasmic and nuclear distribution of the novel arsenite-stimulated human ATPase (hASNA-I). Kurdi-Haidar, B., Hom, D.K., Flittner, D.E., Heath, D., Fink, L., Naredi, P., Howell, S.B. J. Cell. Biochem. (1998) [Pubmed]
  3. Chromosomal localization and genomic structure of the human arsenite-stimulated ATPase (hASNA-I). Kurdi-Haidar, B., Heath, D., Lennon, G., Howell, S.B. Somat. Cell Mol. Genet. (1998) [Pubmed]
  4. Immunohistochemical analysis of the distribution of the human ATPase (hASNA-I) in normal tissues and its overexpression in breast adenomas and carcinomas. Kurdi-Haidar, B., Heath, D., Naredi, P., Varki, N., Howell, S.B. J. Histochem. Cytochem. (1998) [Pubmed]
  5. ASNA independent study. Fibromyalgia. Roberson, C.M. The Alabama nurse. (2004) [Pubmed]
  6. Identification of a Targeting Factor for Posttranslational Membrane Protein Insertion into the ER. Stefanovic, S., Hegde, R.S. Cell (2007) [Pubmed]
  7. Isolation of the ATP-binding human homolog of the arsA component of the bacterial arsenite transporter. Kurdi-Haidar, B., Aebi, S., Heath, D., Enns, R.E., Naredi, P., Hom, D.K., Howell, S.B. Genomics (1996) [Pubmed]
  8. DNA sequence analysis of bacterial toxic heavy metal resistances. Silver, S., Misra, T.K., Laddaga, R.A. Biological trace element research. (1989) [Pubmed]
  9. ASNA independent study activity: "Selective serotoni inhibitors (SSRIs)--what nurses should know". Johnson, M.R. Nebraska nurse. (2005) [Pubmed]
 
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