ATP2A1

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Template:Short description Template:Cs1 config An Error has occurred retrieving Wikidata item for infobox Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 (SERCA1) also known as Calcium pump 1, is an enzyme that in humans is encoded by the ATP2A1 gene.[1][2]

Function

This gene encodes one of the SERCA Ca2+-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction.[1]

Clinical significance

Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing impairment of muscular relaxation during exercise. Alternative splicing results in two transcript variants encoding different isoforms.[1] Alternative splicing of ATP2A1 is also implicated in myotonic dystrophy type 1.

ATP2A1 SERCA pumps were very strongly down regulated in amyotrophic lateral sclerosis.[3]

Interactions

ATP2A1 has been shown to interact with:

References

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  1. ^ a b c Page Module:Citation/CS1/styles.css has no content."Entrez Gene: ATP2A1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1".
  2. ^ Page Module:Citation/CS1/styles.css has no content."UniProt". www.uniprot.org. Retrieved 1 August 2023.
  3. ^ Page Module:Citation/CS1/styles.css has no content.Mukund K, Subramaniam S (2017). "Co-expression Network Approach Reveals Functional Similarities among Diseases Affecting Human Skeletal Muscle". Frontiers in Physiology. 8: 980. doi:10.3389/fphys.2017.00980. PMC 5717538. PMID 29249983.
  4. ^ a b Page Module:Citation/CS1/styles.css has no content.Asahi M, Kurzydlowski K, Tada M, MacLennan DH (July 2002). "Sarcolipin inhibits polymerization of phospholamban to induce superinhibition of sarco(endo)plasmic reticulum Ca2+-ATPases (SERCAs)". Journal of Biological Chemistry. 277 (30): 26725–26728. doi:10.1074/jbc.C200269200. PMID 12032137.
  5. ^ Page Module:Citation/CS1/styles.css has no content.Asahi M, Sugita Y, Kurzydlowski K, De Leon S, Tada M, Toyoshima C, et al. (April 2003). "Sarcolipin regulates sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) by binding to transmembrane helices alone or in association with phospholamban". Proceedings of the National Academy of Sciences of the United States of America. 100 (9): 5040–5045. Bibcode:2003PNAS..100.5040A. doi:10.1073/pnas.0330962100. PMC 154294. PMID 12692302.
  6. ^ Page Module:Citation/CS1/styles.css has no content.Asahi M, Kimura Y, Kurzydlowski K, Tada M, MacLennan DH (November 1999). "Transmembrane helix M6 in sarco(endo)plasmic reticulum Ca(2+)-ATPase forms a functional interaction site with phospholamban. Evidence for physical interactions at other sites". Journal of Biological Chemistry. 274 (46): 32855–32862. doi:10.1074/jbc.274.46.32855. PMID 10551848.
  7. ^ Page Module:Citation/CS1/styles.css has no content.Asahi M, Green NM, Kurzydlowski K, Tada M, MacLennan DH (August 2001). "Phospholamban domain IB forms an interaction site with the loop between transmembrane helices M6 and M7 of sarco(endo)plasmic reticulum Ca2+ ATPases". Proceedings of the National Academy of Sciences of the United States of America. 98 (18): 10061–10066. Bibcode:2001PNAS...9810061A. doi:10.1073/pnas.181348298. PMC 56915. PMID 11526231.

Further reading

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