Figure 4
Figure 4. Protein interactions of XIAP. Well-described XIAP interactions are illustrated. BIR2 and its N-terminal linker region interact with and inhibit caspase-3 and caspase-7, whereas BIR3 inhibits caspase-9.55–58 Inhibition of caspases by XIAP can be relieved by SMAC and Omi/HtrA2, which are released by the mitochondria after proapoptotic stimuli and interact with BIR2 and BIR3.59–61 BIR1 and BIR2 also interact with TAB1 and RIP2, respectively.63–65 The C-terminal RING finger domain of XIAP possesses E3 ubiquitin ligase function.69,70 XIAP-mediated ubiquitination of proteins, such as COMMD1, results in the subsequent targeting of the protein for proteasomal degradation.71 Ubiquitination of other proteins, such as apoptosis-inducing factor, may serve to alter the function of the protein.72

Protein interactions of XIAP. Well-described XIAP interactions are illustrated. BIR2 and its N-terminal linker region interact with and inhibit caspase-3 and caspase-7, whereas BIR3 inhibits caspase-9.55-58  Inhibition of caspases by XIAP can be relieved by SMAC and Omi/HtrA2, which are released by the mitochondria after proapoptotic stimuli and interact with BIR2 and BIR3.59-61  BIR1 and BIR2 also interact with TAB1 and RIP2, respectively.63-65  The C-terminal RING finger domain of XIAP possesses E3 ubiquitin ligase function.69,70  XIAP-mediated ubiquitination of proteins, such as COMMD1, results in the subsequent targeting of the protein for proteasomal degradation.71  Ubiquitination of other proteins, such as apoptosis-inducing factor, may serve to alter the function of the protein.72 

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