Target intelligence / Profile preview

ATP-binding cassette sub-family F member 1 (ABCF1)

Target
ABCF1
Molecular classification
ATP-binding cassette (ABC) transporter (GCN20 subfamily), Enzyme (E2 ubiquitin-conjugating enzyme), Transcriptional coactivator (context-specific), Other (Non-transmembrane ATPase)
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Overview

ATP-binding cassette sub-family F member 1 (ABCF1) is a non-transmembrane member of the ATP-binding cassette (ABC) protein superfamily, specifically classified within the GCN20 subfamily. Unlike most ABC transporters, ABCF1 lacks transmembrane domains and is not involved in classic membrane transport. Instead, it facilitates mRNA translation initiation through ATP-dependent interaction with eukaryotic initiation factor 2 (eIF2), functions as a cell-specific transcriptional coactivator in pluripotent stem cells, and acts as an E2 ubiquitin-conjugating enzyme modulating immune responses and inflammation, particularly via regulation of Toll-like receptor 4 (TLR4) signaling in macrophages. ABCF1 expression is regulated by inflammatory cytokines such as TNF-alpha, and is essential for development and immune function; loss-of-function causes embryonic lethality in mice. Pathophysiologically, it can influence cytokine production during infection or sepsis and may indirectly affect conditions involving immune dysregulation and inflammation. No approved drugs are known to directly target ABCF1.

Other names
ABC50ATP-binding cassette 50TNF-alpha-stimulated ABC proteinABC27EST123147ATP-binding cassette, sub-family F (GCN20), member 1TNFalpha-inducible ATP-binding protein
02

Mechanism of action

Not established for drugs, but molecular mechanisms include ATP binding/hydrolysis for conformational change; E2 ubiquitin conjugating activity (regulates TLR4 signaling in sepsis)

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Biological functions

mRNA translation initiation (interacts with eIF2)Regulation of protein synthesisTranscriptional coactivation in pluripotent stem cellsRegulation of immune response and inflammationUbiquitination and protein degradation signaling
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Disease associations

InflammationInfection (sepsis)Immune dysregulationDevelopmental defects (embryonic lethality in knockout mice)Cancer (implied by general translation control, but no direct listing)
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Safety considerations

Essential for embryonic development—knockout is embryonic lethalPotential to dysregulate cytokine production (cytokine storm)Broad impact on translation and immune processes could pose off-target/toxicity risk if inhibited
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Biomarkers

SSEA-1 (in stem cell pluripotency studies as a downstream marker)

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