Target intelligence / Profile preview

Acyl-CoA binding domain containing 6 (ACBD6)

Target
ACBD6
Molecular classification
Other (modular lipid-binding protein), Acyl-CoA binding protein family, Ankyrin-repeat protein family
01

Overview

ACBD6 is a lipid-binding protein containing an N-terminal acyl-CoA binding domain and two C-terminal ankyrin repeats. It selectively binds long-chain acyl-CoA species and is involved in transferring these molecules within the cell. ACBD6 directly regulates protein N-myristoylation by interacting with NMT1 and NMT2, enhancing their catalytic activity and protecting them from competitive inhibition—crucial for proper post-translational protein modification. Its expression is tissue-restricted, notably marking primitive hemangiogenic stem cells in blood and vascular tissues. ACBD6 also participates in broader cellular processes influencing stem cell maintenance, lipid metabolism, organelle architecture, and apoptosis. Although functionally significant, there are currently no drugs or therapies that directly target ACBD6, and it is not recognized as a classical receptor, enzyme, or transporter therapeutic target[1][2][4][5][6].

Other names
Acyl-CoA-binding domain-containing protein 6ACBD6MGC2404LHX4-AS1NEDPMAcyl-Coenzyme A binding domain containing 6
02

Mechanism of action

Not applicable There is no known therapeutic drug mechanism of action targeting ACBD6 at present.

03

Biological functions

Carrier for long-chain acyl-CoA moleculesRegulation of protein N-myristoylation (post-translational modification)Lipid homeostasisPromotion of stem cell self-renewal and hemangiogenic differentiationRegulation of lipid acylationProtection of myristoyltransferase enzymes from inhibitionIntracellular vesicle traffickingOrganelle formationApoptotic response
04

Disease associations

Other (potential marker for primitive hemangiogenic stem cells, implicated in cell fate determination in development)Potentially relevant to diseases involving disruption of lipid metabolism or protein myristoylation (not established as a disease driver)
05

Safety considerations

None reported for direct targeting
06

Interacting drugs

None reported
07

Biomarkers

Marker for primitive hemangiogenic stem cellsPhosphorylation status (Ser106 and Ser108) modulates activity, could hypothetically serve as a functional readout

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