RIPK3: Difference between revisions

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== Interactions ==
== Interactions ==
RIPK3 has been shown to [[Protein-protein interaction|interact]] with [[RIPK1]].<ref name="pmid10339433" /><ref name=":0" />
RIPK3 has been shown to [[Protein-protein interaction|interact]] with [[RIPK1]] to form an amyloid spine <ref name="pmid10339433" /><ref name=":0" />


== References ==
== References ==
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*{{cite journal  |vauthors=Sun X, Yin J, Starovasnik MA, etal |title=Identification of a novel homotypic interaction motif required for the phosphorylation of receptor-interacting protein (RIP) by RIP3 |journal=J. Biol. Chem. |volume=277 |issue= 11 |pages= 9505–11 |year= 2002 |pmid= 11734559 |doi= 10.1074/jbc.M109488200 }}
*{{cite journal  |vauthors=Sun X, Yin J, Starovasnik MA, etal |title=Identification of a novel homotypic interaction motif required for the phosphorylation of receptor-interacting protein (RIP) by RIP3 |journal=J. Biol. Chem. |volume=277 |issue= 11 |pages= 9505–11 |year= 2002 |pmid= 11734559 |doi= 10.1074/jbc.M109488200 }}
*{{cite journal  |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 }}
*{{cite journal  |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 }}
*{{cite journal  |vauthors=Bouwmeester T, Bauch A, Ruffner H, etal |title=A physical and functional map of the human TNF-alpha/NF-kappa B signal transduction pathway |journal=Nat. Cell Biol. |volume=6 |issue= 2 |pages= 97–105 |year= 2004 |pmid= 14743216 |doi= 10.1038/ncb1086 }}
*{{cite journal  |vauthors=Bouwmeester T, Bauch A, Ruffner H, etal |title=A physical and functional map of the human TNF-alPha/NF-kappa B signal transduction pathway |journal=Nat. Cell Biol. |volume=6 |issue= 2 |pages= 97–105 |year= 2004 |pmid= 14743216 |doi= 10.1038/ncb1086 }}
*{{cite journal  |vauthors=Meylan E, Burns K, Hofmann K, etal |title=RIP1 is an essential mediator of Toll-like receptor 3-induced NF-kappa B activation |journal=Nat. Immunol. |volume=5 |issue= 5 |pages= 503–7 |year= 2004 |pmid= 15064760 |doi= 10.1038/ni1061 }}
*{{cite journal  |vauthors=Meylan E, Burns K, Hofmann K, etal |title=RIP1 is an essential mediator of Toll-like receptor 3-induced NF-kappa B activation |journal=Nat. Immunol. |volume=5 |issue= 5 |pages= 503–7 |year= 2004 |pmid= 15064760 |doi= 10.1038/ni1061 }}
*{{cite journal  | vauthors=Yang Y, Ma J, Chen Y, Wu M |title=Nucleocytoplasmic shuttling of receptor-interacting protein 3 (RIP3): identification of novel nuclear export and import signals in RIP3 |journal=J. Biol. Chem. |volume=279 |issue= 37 |pages= 38820–9 |year= 2004 |pmid= 15208320 |doi= 10.1074/jbc.M401663200 }}
*{{cite journal  | vauthors=Yang Y, Ma J, Chen Y, Wu M |title=Nucleocytoplasmic shuttling of receptor-interacting protein 3 (RIP3): identification of novel nuclear export and import signals in RIP3 |journal=J. Biol. Chem. |volume=279 |issue= 37 |pages= 38820–9 |year= 2004 |pmid= 15208320 |doi= 10.1074/jbc.M401663200 }}

Revision as of 17:37, 12 November 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Receptor-interacting serine/threonine-protein kinase 3 is an enzyme that in humans is encoded by the RIPK3 gene.[1][2][3][4]

The product of this gene is a member of the receptor-interacting protein (RIP) family of serine/threonine protein kinases, and contains a C-terminal domain unique from other RIP family members. The encoded protein is predominantly localized to the cytoplasm, and can undergo nucleocytoplasmic shuttling dependent on novel nuclear localization and export signals. It is a component of the tumor necrosis factor (TNF) receptor-I signaling complex, and can induce apoptosis and weakly activate the NF-kappaB transcription factor.[3]

Interactions

RIPK3 has been shown to interact with RIPK1 to form an amyloid spine [1][4]

References

  1. 1.0 1.1 Yu PW, Huang BC, Shen M, Quast J, Chan E, Xu X, Nolan GP, Payan DG, Luo Y (Jun 1999). "Identification of RIP3, a RIP-like kinase that activates apoptosis and NFkappaB". Curr Biol. 9 (10): 539–42. doi:10.1016/S0960-9822(99)80239-5. PMID 10339433.
  2. Sun X, Lee J, Navas T, Baldwin DT, Stewart TA, Dixit VM (Jul 1999). "RIP3, a novel apoptosis-inducing kinase". J Biol Chem. 274 (24): 16871–5. doi:10.1074/jbc.274.24.16871. PMID 10358032.
  3. 3.0 3.1 "Entrez Gene: RIPK3 receptor-interacting serine-threonine kinase 3".
  4. 4.0 4.1 Li J, McQuade T, Siemer AB, Napetschnig J, Moriwaki K, Hsiao YS, Damko E, Moquin D, Walz T, McDermott A, Chan FK, Wu H. (July 2012) The RIP1/RIP3 necrosome forms a functional amyloid signaling complex required for programmed necrosis. Cell 150 (2):339-50. doi:10.1016/j.cell.2012.06.019. PMID 22817896

Further reading