Target intelligence / Profile preview

Oxysterol-binding protein-related protein 7 (OSBPL7)

Target
OSBPL7
Molecular classification
Lipid transporter, Intracellular lipid receptor, Sterol-binding protein, Other
01

Overview

Oxysterol-binding protein-related protein 7 (OSBPL7) is a member of the oxysterol-binding protein (OSBP) family, which comprises intracellular lipid receptors involved in sterol binding and lipid transport. OSBPL7 possesses a conserved C-terminal OSBP-like sterol-binding (OHD) domain and an N-terminal pleckstrin homology (PH) domain, facilitating interaction with membranes and organelles. The protein plays a role in cholesterol and oxysterol sensing, cellular lipid trafficking, and may participate in the proteasomal degradation of Golgi SNARE proteins via interactions influenced by oxysterol levels[1][2]. It is primarily expressed in the gastrointestinal tract and is implicated in cellular lipid homeostasis. OSBPL7 has emerging roles as a potential therapeutic target, with at least one small-molecule inhibitor (OSBPL7-IN-1) reported; such inhibition may modulate cholesterol efflux and protein turnover in cells[4]. Diseases associated with OSBPL7 include opisthorchiasis and adult medulloblastoma, while the broader OSBP/ORP family plays essential roles in lipid balance and may contribute to cancer and infection susceptibility[1][2].

Other names
Oxysterol-binding protein like 7ORP7OSBP-related protein 7MGC71150oxysterol-binding protein-related protein 7ORP-7
02

Mechanism of action

Inhibition of oxysterol binding and function (for OSBPL7-IN-1), Increase in ABCA1 at the plasma membrane (linked to cholesterol efflux), Modulation of proteasomal degradation of Golgi SNARE proteins

03

Biological functions

Lipid transportIntracellular lipid sensingCholesterol bindingRegulation of sterol homeostasisProtein-protein interactionProteasomal degradation facilitation
04

Disease associations

CancerInfectionOther (notably roles in cellular cholesterol and lipid homeostasis that may relate to additional diseases)
05

Safety considerations

No notable therapeutic safety concerns are reportedthe functional redundancy in the OSBP/ORP family may reduce toxicity from single-gene targeting, but roles in lipid homeostasis suggest potential for off-target metabolic effects[2]
06

Interacting drugs

OSBPL7-IN-1

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