articleJournal of Biological ChemistryJan 1, 2002HYBRID OA

Identification of Omi/HtrA2 as a Mitochondrial Apoptotic Serine Protease That Disrupts Inhibitor of Apoptosis Protein-Caspase Interaction

Sidney Kimmel Cancer Center · Thomas Jefferson University

PubMed
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Abstract

To identify human proteins that bind to the Smac and caspase-9 binding pocket on the baculoviral inhibitor of apoptosis protein (IAP) repeat 3 (BIR3) domain of human XIAP, we used BIR3 as an affinity reagent, followed by elution with the BIR3 binding peptide AVPIA, microsequencing, and mass spectrometry. The mature serine protease Omi (also known as HtrA2) was identified as a mitochondrial direct BIR3-binding protein and a caspase activator. Like mature Smac (also known as Diablo), mature Omi contains a conserved IAP-binding motif (AVPS) at its N terminus, which is exposed after processing of its N-terminal mitochondrial targeting sequence upon import into the mitochondria. Mature Omi is released together with…

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Authors

11

Topics & keywords

Keywords
  • XIAP
  • Inhibitor of apoptosis
  • Serine protease
  • Apoptosis
  • Caspase
  • Cell biology
  • Biology
  • Inhibitor of apoptosis domain
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