Fission and fusion events dynamically control the shape and function of mitochondria. The activity of the mitochondrial fission enzyme dynamin related protein 1 (Drp1) is finely tuned by several posttranslational modifications. Phosphorylation of Ser656 by cAMP-dependent protein kinase (PKA) inhibits Drp1, whereas dephosphorylation by a mitochondrial protein phosphatase 2A isoform and the calcium-calmodulin dependent phosphatase calcineurin (CaN), activates Drp1. Here, we identify a conserved CaN docking site on Drp1, an LxVP motif, which mediates the interaction between the phosphatase and the mechanoenzyme. We mutated the LxVP motif in Drp1 to either increase or decrease similarity to the prototypical LxVP motif in the transcription factor NFAT, and assessed stability of the mutant Drp1-CaN complexes by affinity precipitation and isothermal titration calorimetry. Further, we quantified effects of LxVP mutations on Drp1 dephosphorylation kinetics in vitro and in intact cells. With tools for bidirectional control of the CaN-Drp1 signaling axis in hand, we demonstrate that the Drp1 LxVP motif shapes mitochondria in neuronal and non-neuronal cells, and that CaN-mediated Drp1 dephosphorylation promotes neuronal death following oxygen-glucose deprivation. These results point to the CaN-Drp1 complex as a potential target for neuroprotetive therapy of ischemic stroke.