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Cited by 933

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Caspase activation: The induced-proximity model

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Salvesen, Guy S., Dixit, Vishva M.·1999·Proceedings of the National Academy of Sciences

Abstract

Members of the caspase family of proteases transmit the events that lead to apoptosis of animal cells. Distinct members of the family are involved in both the initiation and execution phases of cell death, with the initiator caspases being recruited to multicomponent signaling complexes. Initiation of apoptotic events depends on the ability of the signaling complexes to generate an active protease. The mechanism of activation of the caspases that constitute the different apoptosis-signaling complexes can be explained by an unusual property of the caspase zymogens to autoprocess to an active form. This autoprocessing depends on intrinsic activity that resides in the zymogens of the initiator caspases. We review evidence for a hypothesis—the induced-proximity model—that describes how the first proteolytic signal is produced after adapter-mediated clustering of initiator caspase zymogens.

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Metadata

Authors
Salvesen, G. S., & Dixit, V. M.
Venue
Proceedings of the National Academy of Sciences
Published
1999-09-28
Volume
96
Issue
20
Pages
10964-10967
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2117820574
Cited by
933
References
3
FWCI
20.01
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Caspase activation: The induced-proximity model. https://app.cochat.ai/papers/10.1073/pnas.96.20.10964
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Salvesen, G. S., & Dixit, V. M. (1999). Caspase activation: The induced-proximity model. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.96.20.10964

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.