a naturally occurring, proteinogenic amino acid that plays a crucial role in protein synthesis, central nervous system development, and cellular metabolism.
while classified as non-essential because the body can synthesize it, it is vital for neurological health and metabolic function
supports conserved cellular processes including protein synthesis, nitrogen and amino acid metabolism, and the production of essential membrane lipids such as phosphatidylserine, phosphatidylethanolamine, and sphingolipids
acts as a precursor for D-serine and glycine, which support neurotransmission and NMDA receptor activity in the brain
essential for creating phosphatidylserine and other sphingolipids vital for neuron survival and cell wall integrity
helps manufacture other molecules, including cysteine, tryptophan, and cellular antioxidants like glutathione
dietary sources:
found abundantly in high-protein foods such as eggs, soy products, meat, fish, nuts, and lentils
requirements:
pathology:
in humans, variants in the PSPH gene, which encodes phosphoserine phosphatase, are linked to L-serine deficiency disorders and related neurodevelopmental phenotypes
PSPH overexpression is associated with proliferative and metabolic phenotypes in cancer
PSPH substitutions such as D32N and M52T can produce a range of effects, from modest or context-dependent changes to marked reductions in enzyme activity, protein stability and interactions, or cellular phenotypes
the R27S/D32G haplotype, detected in Alzheimer's disease hippocampal samples, reduces catalytic efficiency