| Myelin proteolipid protein (PLP or lipophilin) | |||||||||
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| Identifiers | |||||||||
| Symbol | Myelin_PLP | ||||||||
| Pfam | PF01275 | ||||||||
| InterPro | IPR001614 | ||||||||
| SMART | SM00002 | ||||||||
| PROSITE | PDOC00497 | ||||||||
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Myelin proteolipid protein (PLP or lipophilin)[1] is the major myelin protein from the central nervous system (CNS). It plays an important role in the formation or maintenance of the multilamellar structure of myelin. The myelin sheath is a multi-layered membrane, unique to the nervous system, that functions as an insulator to greatly increase the velocity of axonal impulse conduction.[2]
In man point mutations in PLP are the cause of Pelizaeus-Merzbacher disease (PMD), a neurologic disorder of myelin metabolism. In animals dismyelinating diseases such as mouse 'jimpy' or dog 'shaking pup' are also caused by mutations in PLP.
PLP is a highly conserved[3] hydrophobic protein of 276 to 280 amino acids which seems to contain four transmembrane segments, two disulfide bonds and which covalently binds lipids (at least six palmitate groups in mammals).[4] PLP is highly related to GPM6A, a neuronal membrane glycoprotein.[5]
This article incorporates text from the public domain Pfam and InterPro IPR001614
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