标题
Evolutionary divergence of the necroptosis effector MLKL
作者
关键词
-
出版物
CELL DEATH AND DIFFERENTIATION
Volume 23, Issue 7, Pages 1185-1197
出版商
Springer Nature
发表日期
2016-02-12
DOI
10.1038/cdd.2015.169
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- HSP90 activity is required for MLKL oligomerisation and membrane translocation and the induction of necroptotic cell death
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- Characterization of RIPK3-mediated phosphorylation of the activation loop of MLKL during necroptosis
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- Reactive oxygen species regulate Smac mimetic/TNFα-induced necroptotic signaling and cell death
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- RIPK1- and RIPK3-induced cell death mode is determined by target availability
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- A Plug Release Mechanism for Membrane Permeation by MLKL
- (2014) Lijing Su et al. STRUCTURE
- Depletion of RIPK3 or MLKL blocks TNF-driven necroptosis and switches towards a delayed RIPK1 kinase-dependent apoptosis
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- Insights into the evolution of divergent nucleotide-binding mechanisms among pseudokinases revealed by crystal structures of human and mouse MLKL
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- A robust methodology to subclassify pseudokinases based on their nucleotide-binding properties
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- Diverse Sequence Determinants Control Human and Mouse Receptor Interacting Protein 3 (RIP3) and Mixed Lineage Kinase domain-Like (MLKL) Interaction in Necroptotic Signaling
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- Plasma membrane translocation of trimerized MLKL protein is required for TNF-induced necroptosis
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- Widespread Mitochondrial Depletion via Mitophagy Does Not Compromise Necroptosis
- (2013) Stephen W.G. Tait et al. Cell Reports
- Mixed Lineage Kinase Domain-like Protein Mediates Necrosis Signaling Downstream of RIP3 Kinase
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- Identification of RIP1 kinase as a specific cellular target of necrostatins
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