Structural basis of caspase-7 inhibition by XIAP.
By J. Chai, E. Shiozaki, S. Srinivasula, Qi Wu, P. Dataa, E. Alnemri, Yigong Shi. Cell, 2001
606 citations recorded by the source corpus.
Subfields: Epidemiology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/46dfb45a5dc5376c63015254c5c3c295d0811f8a
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Citations in the corpus
- Toxic proteins released from mitochondria in cell death (2004, background): “The mechanism by which Smac/DIABLO binds to the BIR2 domain of XIAP is unclear, although it requires the IBM and dimeric Smac/DIABLO (Wu et al., 2000; Chai et al., 2001).”
- Targeting IAP proteins for therapeutic intervention in cancer (2012, background): “Inhibition of caspase 3 and caspase 7 involves the interaction of the linker region between the BIR1 and BIR2 domains of XIAP with the substrate-binding site of the activated caspas”
- IAP proteins: blocking the road to death's door (2002, background): “So, this important inhibitory domain in XIAP binds with high affinity to a surface that is conserved between caspase-3 and caspase-7, but XIAP is not a pseudosubstrate and functions solely to mask the active site in the caspas”
- Mechanisms of caspase activation and inhibition during apoptosis. (2002, background): “In support of this hypothesis, the linker peptide fused to glutathione S-transferase (GST) was able to ever, that an equivalent of p35 in mammals has not been identified.inhibit caspase-3 and -7 (Chai et al., 2001b; Huang et al., 2001).”
- The expanding role of mitochondria in apoptosis. (2001, background): “The linker sequence immediately preceding the BIR2 domain is involved in XIAP-mediated binding and inhibition of caspase-3 and caspase-7 (Sun et al. 1999; Chai et al. 2001; Huang 2001; Riedl et al. 2001).”
- Mechanism of XIAP-mediated inhibition of caspase-9. (2003, methodology): “However, careful evaluation scribed (Chai et al., 2001a, 2001b).”
- Cellular mechanisms controlling caspase activation and function. (2013, background): “XIAP can inhibit caspase-3 and caspase-7 by binding to the active site, and caspase-9 by preventing or reversing dimerization (Deveraux et al. 1997; Chai et al. 2001; Riedl et al. 2001; Srinivasula et al. 2001; Shiozaki et al. 2003).”