COASY

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Template:Short description An Error has occurred retrieving Wikidata item for infobox Bifunctional coenzyme A synthase is an enzyme that in mammals is encoded by the COASY gene that catalyses the synthesis of coenzyme A from 4'-phosphopantetheine.[1][2][3]

Function

COASY is an enzyme that catalyzes the last two steps in the synthesis of coenzyme A from vitamin B5 (pantothenic acid). The primary substrate is 4'-phosphopantetheine and COASY is a bifunctional enzyme in this pathway:

In mammals this is a single enzyme, but in organisms including yeast and bacteria these enzymes are encoded by separate genes.[4]

Interactions

COASY has been shown to interact with P70-S6 Kinase 1.[5] In 2009, COASY has also been implicated in PI3K signaling, as it was shown to interact with a regulatory subunit of PI3K.[6]

Clinical significance

Loss of function mutations to COASY have been associated with an ultra-rare disease that causes neurodegeneration with brain iron accumulation called COASY protein-associated neurodegeneration (CoPAN), or NBIA6.[4][7][8]

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.Daugherty M, Polanuyer B, Farrell M, Scholle M, Lykidis A, de Crécy-Lagard V, Osterman A (June 2002). "Complete reconstitution of the human coenzyme A biosynthetic pathway via comparative genomics". The Journal of Biological Chemistry. 277 (24): 21431–21439. doi:10.1074/jbc.M201708200. PMID 11923312.
  2. ^ Page Module:Citation/CS1/styles.css has no content.Zhyvoloup A, Nemazanyy I, Babich A, Panasyuk G, Pobigailo N, Vudmaska M, et al. (June 2002). "Molecular cloning of CoA Synthase. The missing link in CoA biosynthesis". The Journal of Biological Chemistry. 277 (25): 22107–22110. doi:10.1074/jbc.C200195200. PMID 11980892.
  3. ^ Page Module:Citation/CS1/styles.css has no content."Entrez Gene: COASY Coenzyme A synthase".
  4. ^ a b Page Module:Citation/CS1/styles.css has no content.Evers C, Seitz A, Assmann B, Opladen T, Karch S, Hinderhofer K, et al. (July 2017). "Diagnosis of CoPAN by whole exome sequencing: Waking up a sleeping tiger's eye". American Journal of Medical Genetics. Part A. 173 (7): 1878–1886. doi:10.1002/ajmg.a.38252. PMID 28489334. S2CID 27153945.
  5. ^ Page Module:Citation/CS1/styles.css has no content.Nemazanyy I, Panasyuk G, Zhyvoloup A, Panayotou G, Gout IT, Filonenko V (December 2004). "Specific interaction between S6K1 and CoA synthase: a potential link between the mTOR/S6K pathway, CoA biosynthesis and energy metabolism". FEBS Letters. 578 (3): 357–362. doi:10.1016/j.febslet.2004.10.091. PMID 15589845. S2CID 9916948.
  6. ^ Page Module:Citation/CS1/styles.css has no content.Breus O, Panasyuk G, Gout IT, Filonenko V, Nemazanyy I (August 2009). "CoA synthase is in complex with p85alphaPI3K and affects PI3K signaling pathway". Biochemical and Biophysical Research Communications. 385 (4): 581–585. doi:10.1016/j.bbrc.2009.05.102. PMID 19482007.
  7. ^ Page Module:Citation/CS1/styles.css has no content.van Dijk T, Ferdinandusse S, Ruiter JP, Alders M, Mathijssen IB, Parboosingh JS, et al. (December 2018). "Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis". European Journal of Human Genetics. 26 (12): 1752–1758. doi:10.1038/s41431-018-0233-0. PMC 6244412. PMID 30089828.
  8. ^ Page Module:Citation/CS1/styles.css has no content."OMIM Entry - #615643 - NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6". www.omim.org. Retrieved 21 April 2022.

Further reading

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