Biology:ACP2

From HandWiki
Revision as of 00:12, 13 February 2024 by HamTop (talk | contribs) (update)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Short description: Protein-coding gene in humans


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Lysosomal acid phosphatase is an enzyme that in humans is encoded by the ACP2 gene.[1][2]

Lysosomal acid phosphatase is composed of two subunits, alpha and beta, and is chemically and genetically distinct from red cell acid phosphatase. Lysosomal acid phosphatase 2 is a member of a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Acid phosphatase deficiency is caused by mutations in the ACP2 (beta subunit) and ACP3 (alpha subunit) genes.[2]

References

  1. "Assignment and linear order of human acid phosphatase-2, esterase A4, and lactate dehydrogenase A genes on chromosome 11". Cytogenet Cell Genet 16 (1–5): 231–4. Dec 1976. doi:10.1159/000130598. PMID 975882. 
  2. 2.0 2.1 "Entrez Gene: ACP2 acid phosphatase 2, lysosomal". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=53. 

Further reading

External links