Ca2+ is a universal second messenger that is critical for cell growth and is intimately associated with many Ras-dependent cellular processes such as proliferation and differentiation [1]. Ras is a small GTP binding protein that operates as a molecular switch regulating the control of gene expression, cell growth, and differentiation through a pathway from receptors to mitogen-activated protein kinases (MAPKs) [2]. A role for intracellular Ca2+ in the activation of Ras has been previously demonstrated, e.g., via the nonreceptor tyrosine kinase PYK2 [3] and by Ca2+/calmodulin-dependent guanine nucleotide exchange factors (GEFs) such as Ras-GRF [4]; however, there is no Ca2+-dependent mechanism for direct inactivation. An important advance toward greater understanding of the complex coordination within the Ras-signaling network is the spatio-temporal analysis of signaling events in vivo. Here, we describe the identification of CAPRI (Ca2+-promoted Ras inactivator), a Ca2+-dependent Ras GTPase-activating protein (GAP) that switches off the Ras-MAPK pathway following a stimulus that elevates intracellular Ca2+. Analysis of the spatio-temporal dynamics of CAPRI indicates that Ca2+ regulates the GAP by a fast C2 domain-dependent translocation mechanism.