Target intelligence / Profile preview

ATPase family AAA domain-containing protein 2 (ATAD2)

Target
ATAD2
Molecular classification
Enzyme (AAA+ ATPase), Chromatin reader (Bromodomain-containing protein), Histone chaperone, Transcriptional coactivator
01

Overview

ATPase family AAA domain-containing protein 2 (ATAD2) is a multidomain nuclear protein with a canonical AAA+ ATPase domain and a unique bromodomain (BRD) that reads acetylated lysines on histones[1][2][3][4]. It functions primarily as a chromatin remodeler and transcriptional coactivator for nuclear hormone receptors (estrogen, androgen receptors) and key oncogenic transcription factors (c-Myc, E2F), facilitating gene expression programs that promote cell proliferation and survival[1][4][5][8]. ATAD2 is upregulated in many cancers and correlates with poor prognosis, making it an emerging anticancer drug target—especially through its bromodomain, which is critical for recognizing acetylated histone tails[1][2][3][4]. ATAD2 participates in DNA replication, histone chaperoning, and chromatin remodeling, making it central to epigenetic regulation and tumorigenesis[1][2][3][4][5][7][8]. Drug discovery efforts focus on developing bromodomain inhibitors to block its oncogenic functions.

Other names
ANCCAL16PRO2000DKFZp667N1320MGC5254MGC29843CT137AAA nuclear coregulator cancer-associated protein
02

Mechanism of action

Inhibition of bromodomain binding to acetylated histones Suppression of chromatin remodeling and transcriptional activation in cancer cells

03

Biological functions

Chromatin remodelingTranscription coactivation (with estrogen receptor, androgen receptor, c-Myc, E2F)Histone binding and recognitionATP hydrolysisDNA replication regulationPromotion of protein oligomerization
04

Disease associations

Cancer (notably breast, lung, prostate, gastric, endometrial, renal cancers)Oncogenic driverPrognostic marker in multiple cancer types
05

Safety considerations

Targeting chromatin remodelers may impact normal cell division and gene regulationSelectivity for cancer cells vs. normal cells can be a challengePotential for off-target effects due to broad chromatin regulation involvement
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Interacting drugs

Experimental ATAD2 bromodomain inhibitors (no approved drugs as of mid-2024)
07

Biomarkers

High ATAD2 expression (for patient selection/poor prognosis in various cancers)Potentially, levels of acetylated histones or activation of signature target genes (e.g., MYC, E2F1, CCND1)

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