Ontology highlight
ABSTRACT:
SUBMITTER: Mastrangelo E
PROVIDER: S-EPMC4317547 | biostudies-literature | 2015 Feb
REPOSITORIES: biostudies-literature
Mastrangelo Eloise E Vachette Patrice P Cossu Federica F Malvezzi Francesca F Bolognesi Martino M Milani Mario M
Biophysical journal 20150201 3
Smac-DIABLO in its mature form (20.8 kDa) binds to baculoviral IAP repeat (BIR) domains of inhibitor of apoptosis proteins (IAPs) releasing their inhibitory effects on caspases, thus promoting cell death. Despite its apparent molecular mass (∼100 kDa), Smac-DIABLO was held to be a dimer in solution, simultaneously targeting two distinct BIR domains. We report an extensive biophysical characterization of the protein alone and in complex with the X-linked IAP (XIAP)-BIR2-BIR3 domains. Our data sho ...[more]