Protein Name: Non-specific lipid-transfer protein
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UniprotKB/SwissProt ID: NLTP_HUMAN (P22307)
Gene Name: SCP2
Organism: Homo sapiens (Human).
Function: Mediates in vitro the transfer of all common phospholipids, cholesterol and gangliosides between membranes. May play a role in regulating steroidogenesis.
Other Modifications: View all modification sites in dbPTM
Protein Subcellular Localization: Cytoplasm. Mitochondrion. Note=Cytoplasmic in the liver and also associated with mitochondria especially in steroidogenic tissues. Isoform SCPx: Peroxisome. Note=Interaction with PEX5 is essential for peroxisomal import. Isoform SCP2: Mitochondrion (Prob
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PDB :
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Protein disease:
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| Disease database |
Database Entry |
Disease information | | HPRD | 01700 | Leukoencephalopathy with dystonia and motor neuropathy, SCPX-deficient |
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Network with metabolic pathway:
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Graphical Visualization of S-nitrosylation Sites:
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| Overview of Protein S-nitrosylation Sites with Functional and Structural Information |  |
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