Ontology highlight
ABSTRACT:
INSTRUMENT(S): LTQ Orbitrap
ORGANISM(S): Homo Sapiens (human)
SUBMITTER: Björn Stork
LAB HEAD: Björn Stork
PROVIDER: PXD018078 | Pride | 2020-04-22
REPOSITORIES: Pride
Action | DRS | |||
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Orbi1032.raw | Raw | |||
Orbi1068.raw | Raw | |||
PhosphoSTYSites_analyis-1a.txt | Txt | |||
PhosphoSTYSites_analyis-1b.txt | Txt |
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Wu Wenxian W Wang Xiaojing X Berleth Niklas N Deitersen Jana J Wallot-Hieke Nora N Böhler Philip P Schlütermann David D Stuhldreier Fabian F Cox Jan J Schmitz Katharina K Seggewiß Sabine S Peter Christoph C Kasof Gary G Stefanski Anja A Stühler Kai K Tschapek Astrid A Gödecke Axel A Stork Björn B
Cell reports 20200401 3
Autophagy, apoptosis, and necroptosis are stress responses governing the ultimate fate of a cell. However, the crosstalk between these cellular stress responses is not entirely understood. Especially, it is not clear whether the autophagy-initiating kinase ULK1 and the cell-death-regulating kinase RIPK1 are involved in this potential crosstalk. Here, we identify RIPK1 as a substrate of ULK1. ULK1-dependent phosphorylation of RIPK1 reduces complex IIb/necrosome assembly and tumor necrosis factor ...[more]