yana-notes

Sphingomyelin

2022-06-30: reference:

200 #

Consists of Phosphocholine/Ceramide/phosphoethanolamine head group.

Metabolism #

  • Subcellular localization of enzymes: 500
  • Niemann-Pick disease is a series of sphingolipidoses, inherited metabolic disorders, of which there are many, and prevalent in Jews. Sphingomyelin accumulates in Lysosomes. Type A is fatal in infancy, while B sees survival into adulthood and apparently has no neurologic manifestations. C1 is the most common form and leads to dementia.
      • Please bear in mind most if not all of these steps are reversible by other enzymes.