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ELMO domain-containing protein 2 (ELMOD2) is a GTPase-activating protein (GAP) with broad specificity for ARF family GTPases, particularly ARL2 and ARF6[1][2]. It is involved in several biological processes, including regulation of mitochondrial fusion through interaction with ARL2, stabilization and nucleation of microtubules (key for cell structure and division), and facilitation of cytokinesis via ARF6-dependent pathways[1][2]. ELMOD2 is also crucial for balancing ciliary homeostasis and maintaining the organization of centrosomal rootlet structures, acting in pathways alongside Rootletin and ARL2 to suppress inappropriate cilia formation and preserve centrosome cohesion[2]. ELMOD2 is primarily intracellular, localizing to mitochondria, endoplasmic reticulum, lipid droplets, basal bodies, centrosomes, and ciliary rootlets[1][2]. While loss of ELMOD2 function disrupts cellular processes, causes mitochondrial fragmentation, defective cytokinesis, increased and abnormal ciliation, and rootlet disorganization, there are no current direct disease associations or therapies targeting ELMOD2[1][2].
Not applicable (no drugs identified)
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