Target intelligence / Profile preview

SEC14-like protein 3 (SEC14L3)

Target
SEC14L3
Molecular classification
Phosphatidylinositol transfer protein (PITP), Peripheral membrane lipid-binding protein, Multi-domain (contains SEC14, GOLD, CARL-TRIO, and GTPase/Gα domains)
01

Overview

SEC14-like protein 3 (SEC14L3) is a multi-domain lipid transfer protein containing SEC14, GOLD, CARL-TRIO, and GTPase domains, and is part of a conserved protein family across eukaryotes responsible for controlling membrane identity and trafficking via lipid binding, exchange, and interaction with key signaling pathways[2][1][3]. SEC14L3 directly interacts with Wnt signaling components, such as Frizzled (Fz), Dishevelled (Dvl), and phospholipase C, to regulate calcium signaling and PLCδ activation in response to external cues like Wnt5a[1][3]. Both its lipid transfer and GTPase functions are essential for proper cellular signaling and developmental processes. SEC14-like proteins are implicated in cancer and neurodegenerative disease risk, likely due to their role in oxidative stress response and the maintenance of membrane integrity and signaling[2]. SEC14L3 may function as a tumor suppressor by mediating the transport of vitamin E (tocopherol) and other lipophilic substances, highlighting interconnected roles in lipid metabolism, cellular signaling, and homeostasis[2]. While no approved drugs currently target SEC14L3, its role in fundamental cellular processes makes it a potential therapeutic target pending further study[2][1][3].

Other names
SEC14L3SEC14-like protein 3Tocopherol-associated protein 2SEC14-like 3SEC14p-like protein TAP2
02

Mechanism of action

Not established for approved drugs. Possible mechanisms may involve regulation of membrane phospholipid composition, modulation of PLC signaling, or control of calcium flux via PLC activity

03

Biological functions

Membrane trafficking regulation (via phosphatidylinositol binding and exchange)Regulator of lipid signalingModulator of Wnt/PLC signaling pathway (promotes PLCδ activity and calcium signaling in response to Wnt5a)GTPase activity, coupling phospholipase activation with PLC proximity to substrateInfluences cell division, vesicle formation, and environmental adaptation through membrane identity
04

Disease associations

Cancer (potential tumor suppressor role and influence on cellular damage by ROS)Neurodegenerative disease (mutations in SEC14 domain increase risk)Defects in development (associated with developmental and stress response defects)
05

Safety considerations

None specifically reported. Potential challenges relate to targeting essential membrane trafficking and signaling processes

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