Apoptosis helps eliminate damaged or unnecessary cells. Anti-apoptotic BCL2 family proteins protect cells by binding and inhibiting pro-apoptotic proteins. Our study reveals that BCL2 proteins also target Bim for degradation by serving to recruit Bim to the E3 ubiquitin ligase Cul5(Wsb2). Wsb2 recognizes Bcl-xl through a motif conserved between Bcl-xl, Bcl-w and Bcl2, but not Mcl1. Disruption of this interaction through mutation of either Bcl-xl or Wsb2 blocks the binding of Wsb2 to the Bcl-xl/Bim dimer. Wsb2 also associates with the Mcl1/Bim dimer through a separate Wsb2 interface, suggesting that Wsb2 has evolved independent means to target Bim. While Wsb2 is not essential in most cells, it is essential in cells derived from tumors of the nervous system, and knockdown of Wsb2 in these lines causes death by apoptosis. This work uncovers a novel mechanism of apoptosis regulation, with implications for developing therapies against neuroblastomas and other cancers reliant on this pathway for survival.