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Elongation of very long-chain fatty acid protein 1 (ELOVL1) is an integral membrane enzyme of the endoplasmic reticulum that catalyzes the first and rate-limiting step in the elongation of long- and very long-chain saturated and monounsaturated fatty acids, primarily targeting C22:0 acyl-CoA substrates. This process is essential for the biosynthesis of membrane lipids and sphingolipids, which are crucial in the central nervous system, skin, and other organs. Mutations in ELOVL1 are linked to rare genetic disorders involving ichthyosis, spasticity, hypomyelination, and other neurological symptoms[1][2][8]. No approved drugs currently target ELOVL1 directly, but it is considered a potential therapeutic target due to its role in lipid metabolism and associated diseases[2].
Inhibition of fatty acid elongase activity (theoretical); Modulation of VLCFA synthesis (theoretical)
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