Target intelligence / Profile preview

ABRA C-terminal-like protein (ABRACL)

Target
ABRACL
Molecular classification
Other (small, non-typical winged-helix protein), Actin-binding domain-related protein
01

Overview

ABRA C-terminal-like protein (ABRACL) is a small, low-molecular-weight (approx. 9 kDa, 81 amino acids) non-typical winged-helix protein, sharing structural similarity with the C-terminal actin-binding domain of ABRA (Actin-Binding Rho-Activating protein)[1][2][5]. Unlike classical DNA-binding winged-helix proteins, ABRACL likely does not function as a transcription factor, but rather modulates actin cytoskeleton dynamics. Its physiological role is not fully elucidated, but evidence supports involvement in actin filament regulation, cell migration, and cell proliferation, notably in cancer cells where ABRACL is often upregulated[1][3][5]. It is also expressed in developing neurons and implicated in neuronal migration, axon growth, and synapse formation, with a conserved role in mammalian brain development[1]. Elevated expression in certain cancers (including gastric, esophageal, breast, bladder, and endometrial cancers) is associated with poor prognosis, suggesting utility as a cancer biomarker and potential therapeutic target[3]. No direct interacting drugs, mechanisms, or notable safety concerns have been reported for ABRACL-targeted intervention as of the latest data.

Other names
Costars family protein ABRACLC6orf115HSPC280PRO2013CostarsABRA C-terminal-like protein
02

Biological functions

Regulation of actin filament-based processModulation of actin dynamicsCell migrationCell proliferationNeuronal development (migration of interneurons, axon elongation, synapse formation)
03

Disease associations

Cancer (e.g., gastric, esophageal, breast, endometrial, bladder)Potential biomarker in cancer prognosis
04

Biomarkers

Overexpression serves as a potential prognostic cancer biomarker (e.g., in gastric cancer)[3]

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