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1SDZ

Crystal structure of DIAP1 BIR1 bound to a Reaper peptide

Summary for 1SDZ
Entry DOI10.2210/pdb1sdz/pdb
DescriptorApoptosis 1 inhibitor, Reaper, ZINC ION, ... (4 entities in total)
Functional Keywordsapoptosis, iap, reaper, caspase, interaction
Biological sourceDrosophila melanogaster (fruit fly)
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Total number of polymer chains2
Total formula weight14711.83
Authors
Yan, N.,Wu, J.W.,Shi, Y. (deposition date: 2004-02-15, release date: 2004-04-27, Last modification date: 2024-02-14)
Primary citationYan, N.,Wu, J.W.,Chai, J.,Li, W.,Shi, Y.
Molecular mechanisms of DrICE inhibition by DIAP1 and removal of inhibition by Reaper, Hid and Grim.
Nat.Struct.Mol.Biol., 11:420-428, 2004
Cited by
PubMed Abstract: The Drosophila melanogaster inhibitor of apoptosis protein DIAP1 suppresses apoptosis in part through inhibition of the effector caspase DrICE. The pro-death proteins Reaper, Hid and Grim (RHG) induce apoptosis by antagonizing DIAP1 function. However, the underlying molecular mechanisms remain unknown. Here we demonstrate that DIAP1 directly inhibits the catalytic activity of DrICE through its BIR1 domain and this inhibition is countered effectively by the RHG proteins. Inhibition of DrICE by DIAP1 occurs only after the cleavage of its N-terminal 20 amino acids and involves a conserved surface groove on BIR1. Crystal structures of BIR1 bound to the RHG peptides show that the RHG proteins use their N-terminal IAP-binding motifs to bind to the same surface groove, hence relieving DIAP1-mediated inhibition of DrICE. These studies define novel molecular mechanisms for the inhibition and activation of a representative D. melanogaster effector caspase.
PubMed: 15107838
DOI: 10.1038/nsmb764
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.78 Å)
Structure validation

226707

數據於2024-10-30公開中

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