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PMID: 10358032 Published · ppublish English Comparative Study Journal Article

RIP3, a novel apoptosis-inducing kinase.

The Journal of biological chemistry ·Vol. 274 ·No. 24 ·1999-06-11 ·Pages 16871-5

Sun X, Lee J, Navas T, Baldwin DT, Stewart TA, Dixit VM

Abstract

RIP3 is a novel gene product containing a N-terminal kinase domain that shares extensive homology with the corresponding domain in RIP (receptor-interacting protein) and RIP2. Unlike RIP, which has a C-terminal death domain, and RIP2, which has a C-terminal caspase activation and recruitment domain, RIP3 has a unique C terminus. RIP3 binds RIP through its unique C-terminal segment and by virtue of this interaction is recruited to the tumor necrosis factor (TNF) receptor-1 signaling complex. Previous studies have shown that RIP mediates TNF-induced activation of the anti-apoptotic NF-kappaB pathway. RIP3, however, attenuates both RIP and TNF receptor-1-induced NF-kappaB activation. Overexpression studies revealed RIP3 to be a potent inducer of apoptosis, capable of selectively binding to large prodomain initiator caspases.

MeSH Terms
Amino Acid Sequence Antigens, CD/metabolism Apoptosis Caspases/metabolism Cloning, Molecular Humans Molecular Sequence Data NF-kappa B/metabolism Protein Binding Protein Kinases/genetics,metabolism Protein Serine-Threonine Kinases Proteins/metabolism Receptor-Interacting Protein Serine-Threonine Kinase 2 Receptor-Interacting Protein Serine-Threonine Kinases Receptors, Tumor Necrosis Factor/metabolism Receptors, Tumor Necrosis Factor, Type I Recombinant Proteins/metabolism Sequence Analysis Sequence Homology, Amino Acid Signal Transduction
Chemicals
Antigens, CD NF-kappa B Proteins Receptors, Tumor Necrosis Factor Receptors, Tumor Necrosis Factor, Type I Recombinant Proteins Protein Kinases Protein Serine-Threonine Kinases RIPK1 protein, human RIPK2 protein, human RIPK3 protein, human Receptor-Interacting Protein Serine-Threonine Kinase 2 Receptor-Interacting Protein Serine-Threonine Kinases Caspases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sun X
Departments of Molecular Oncology, Genentech, Inc., South San Francisco, California 94080, USA.
Lee J
Navas T
Baldwin D T
Stewart T A
Dixit V M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1999-06-11
Pages
16871-5
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
AA227673, AI082587, AI394293
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