Target intelligence / Profile preview

CD2-associated protein (CD2AP)

Target
CD2AP
Molecular classification
Other (Adaptor/scaffold protein)
01

Overview

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].

Other names
CD2APCMSAdapter protein CMSCas ligand with multiple SH3 domainsCas ligand with multiple Src homology 3 domains
02

Mechanism of action

Not applicable (no direct drug targeting established)

03

Biological functions

Regulation of the actin cytoskeletonMembrane traffickingSignal transductionCell junction organizationEndocytosisCytokinesisImmune response (T cell-APC interface)Synaptic plasticity
04

Disease associations

Glomerular disease (including focal segmental glomerulosclerosis and nephrotic syndrome)Alzheimer’s diseaseOther neurodegenerative conditionsHepatic steatosis in viral hepatitis
05

Safety considerations

Disruption or loss of CD2-associated protein function can cause proteinuria and increase risk of glomerular kidney disease or nephrotic syndromegenetic variants linked to increased risk of Alzheimer’s disease
06

Interacting drugs

None known
07

Biomarkers

None known for patient selection or monitoring

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