Target intelligence / Profile preview

EP300-interacting inhibitor of differentiation 1 (EID1)

Target
EID1
Molecular classification
Other (Transcriptional regulator), Chromatin regulator, Functionally grouped with proteins affecting histone acetylation and chromatin maintenance
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Overview

EP300-interacting inhibitor of differentiation 1 (EID1) is a **short-lived nuclear protein (187 amino acids)** that functions as a transcriptional regulator by binding to the retinoblastoma tumor suppressor protein (pRB) and transcriptional coactivators p300/CBP[2]. Through these interactions, EID1 inhibits the transcriptional activity of p300/CBP, counters cellular differentiation, and contributes to the regulation of cell cycle progression, DNA repair, and chromosomal maintenance[2]. EID1 protein's abundance is controlled via ubiquitin-mediated proteasomal degradation, notably by an SCF complex containing the F-box protein FBXO21, with its rapid turnover helping tightly control its regulatory effects[2]. EID1's biological roles and regulatory mechanisms position it as a node linking tumor suppressor, epigenetic, and transcriptional pathways, with emerging but as yet unexploited therapeutic potential in cancer biology[2].

Other names
C15orf3CRI1RBP21PNAS-22PTD014EID-121 kDa pRb-associated proteinCREBBP/EP300 inhibitory protein 1E1A-like inhibitor of differentiation 1NB4 apoptosis related proteinRb- and p300-binding protein EID-1retinoblastoma protein-associated protein
02

Mechanism of action

Drugs (if developed) would likely act by modulating protein stability (e.g., inhibiting EID1 function via stabilization/destabilization), protein-protein interactions, or gene transcription repression; no direct drugs known currently[2]

03

Biological functions

Regulation of transcriptionInhibition of differentiationProtein-protein interaction with pRB and p300/CBPDNA repairChromosomal maintenanceUbiquitin-mediated protein degradation[2]
04

Disease associations

Cancer (roles in transcriptional repression and cell differentiation relevant to tumorigenesis; originally identified as a pRB and p300 binding protein implicated in tumor suppressor pathways)[2]
05

Safety considerations

Disrupting EID1 might impact cell cycle control, differentiation, and transcriptional regulation; could have unanticipated consequences in non-cancerous cells[2]

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