Health / Medical Topics |
Lysosome Assembly Pathway
Lysosomes are membrane-delimited organelles in animal cells serving as the cell's main digestive compartment to which all sorts of macromolecules are delivered for degradation. They contain more than 40 hydrolases in an acidic environment (pH of about 5). After synthesis in the ER, lysosomal enzymes are decorated with mannose-6-phosphate residues, which are recognized by mannose-6-phosphate receptors in the trans-Golgi network. They are packaged into clathrin-coated vesicles and are transported to late endosomes. Substances for digestion are acquired by the lysosomes via a series of processes including endocytosis, phagocytosis, and autophagy. (NCI Thesaurus/KEGG)
YOU MAY ALSO LIKE
A sac-like compartment inside a cell that has enzymes that can break down cellular components that need to be destroyed.
Lysosomal-trafficking regulator (3801 aa, ~429 kDa) is encoded by the human LYST gene. This protein may be involved in intracellular protein…
Lysosomal-associated transmembrane protein 4B (370 aa, ~41 kDa) is encoded by the human LAPTM4B gene. This protein may play a role in…
Lysosome-associated membrane glycoprotein 3 (416 aa, ~44 kDa) is encoded by the human LAMP3 gene. This protein is involved in dendritic cell…
A group of autosomal recessive or X-linked inherited metabolic disorders caused by defects in the function of the lysosomes. Signs and symptoms…
Lysosomal Function Inhibition involves interference with, or restraint of, the activities of diverse glycoprotein hydrolytic enzymes, active at acid pH, with structure-linked…