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CD2-associated protein (CD2AP) is a cytoplasmic adaptor protein involved in the regulation of the actin cytoskeleton and organization of cell membrane proteins[1][2][3][5]. It contains multiple SH3 domains and a proline-rich region, mediating direct interaction with filamentous actin and other proteins at cell–cell junctions, notably in podocyte slit diaphragms in the kidney[1][5][6]. CD2AP is critical for glomerular filtration barrier integrity; haploinsufficiency or mutation leads to glomerular disease and severe proteinuria[1][2][5]. CD2AP is also expressed in immune cells, neurons, and epithelial cells, where it contributes to intracellular signaling, immune synapse formation, and endocytic vesicle trafficking[2][4][5]. In the nervous system, CD2AP regulates synaptic structure, plasticity, and protein turnover, and genetic variation at the CD2AP locus increases Alzheimer’s disease risk[2][4]. To date, no drugs directly target CD2AP, and it is not considered a therapeutic receptor, enzyme, transporter, or ion channel; rather, it is classified as an adaptor/scaffold protein[1][5].
Not applicable (no direct drug targeting established)
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