RIPK3

RIPK3
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4M66, 4M69
Identifiers
Aliases	RIPK3, RIP3, receptor interacting serine/threonine kinase 3
External IDs	OMIM: 605817 MGI: 2154952 HomoloGene: 31410 GeneCards: RIPK3
Gene location (Human) Chr. Chromosome 14 (human) Band 14q12 Start 24,336,025 bp End 24,340,022 bp
Gene location (Mouse) Chr. Chromosome 14 (mouse) Band 14|14 C3 Start 56,022,452 bp End 56,026,322 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in blood duodenum spleen rectum appendix monocyte right lobe of thyroid gland lymph node left lobe of thyroid gland gallbladder Top expressed in yolk sac thymus Paneth cell internal carotid artery dermis external carotid artery jejunum duodenum ileum spleen More reference expression data BioGPS n/a
Gene ontology Molecular function transferase activity protein kinase activity nucleotide binding transcription coactivator activity kinase activity protein serine/threonine kinase activity NF-kappaB-inducing kinase activity protein binding identical protein binding ATP binding protein-containing complex binding Cellular component cytoplasm cytosol membrane plasma membrane intracellular anatomical structure mitochondrion Biological process regulation of CD8-positive, alpha-beta cytotoxic T cell extravasation amyloid fibril formation T cell differentiation in thymus protein heterooligomerization phosphorylation thymus development regulation of interferon-gamma production positive regulation of oxidoreductase activity regulation of adaptive immune response spleen development regulation of reactive oxygen species metabolic process regulation of activation-induced cell death of T cells T cell homeostasis positive regulation of phosphatase activity positive regulation of necroptotic process protein phosphorylation regulation of activated T cell proliferation positive regulation of reactive oxygen species metabolic process NIK/NF-kappaB signaling positive regulation of NF-kappaB transcription factor activity apoptotic signaling pathway protein autophosphorylation positive regulation of ligase activity necroptosis regulation of T cell mediated cytotoxicity I-kappaB kinase/NF-kappaB signaling lymph node development protein homooligomerization activation of protein kinase activity positive regulation of intrinsic apoptotic signaling pathway signal transduction programmed cell death positive regulation of necrotic cell death positive regulation of nucleic acid-templated transcription cellular response to hydrogen peroxide programmed necrotic cell death Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 11035 56532 Ensembl ENSG00000129465 ENSG00000285379 ENSMUSG00000022221 UniProt Q9Y572 Q9QZL0 RefSeq (mRNA) NM_006871 NM_001164107 NM_001164108 NM_019955 RefSeq (protein) NP_006862 NP_001157579 NP_001157580 NP_064339 Location (UCSC) Chr 14: 24.34 – 24.34 Mb Chr 14: 56.02 – 56.03 Mb PubMed search
Wikidata
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Receptor-interacting serine/threonine-protein kinase 3 is an enzyme that is encoded by the RIPK3 gene in humans.

The product of this gene is a member of the receptor-interacting protein (RIP) family of serine/threonine protein kinases. It 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 necroptosis by interaction with RIPK1 and MLKL in a protein complex termed the necrosome. Interactions between RIPK1 and RIPK3 also form a necrosome, which triggers apoptosis.

The red highlighted region of RIPK3 represents the Protein Kinase domain. The cyan region highlights the RIP homotypic interaction motif (RHIM) motif.

Interactions

RIPK3 has been shown to interact with RIPK1 to form an amyloid spine The RIP Homotypic Interaction Motifs (RHIM) of RIPK3 allows it to form a necrosome with RIPK1. This interaction makes heterotypic β sheets, which bind together to form an alternating “ladder” of Serine from RIPK1 and Cysteine from RIPK3.

Further reading

• Kasof GM, Prosser JC, Liu D, Lorenzi MV, Gomes BC (May 2000). "The RIP-like kinase, RIP3, induces apoptosis and NF-kappaB nuclear translocation and localizes to mitochondria". FEBS Letters. 473 (3): 285–291. doi:10.1016/S0014-5793(00)01473-3. PMID 10818227.
• Sun X, Yin J, Starovasnik MA, Fairbrother WJ, Dixit VM (March 2002). "Identification of a novel homotypic interaction motif required for the phosphorylation of receptor-interacting protein (RIP) by RIP3". The Journal of Biological Chemistry. 277 (11): 9505–9511. doi:10.1074/jbc.M109488200. PMID 11734559.
• Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, et al. (December 2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proceedings of the National Academy of Sciences of the United States of America. 99 (26): 16899–16903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Bouwmeester T, Bauch A, Ruffner H, Angrand PO, Bergamini G, Croughton K, et al. (February 2004). "A physical and functional map of the human TNF-alpha/NF-kappa B signal transduction pathway". Nature Cell Biology. 6 (2): 97–105. doi:10.1038/ncb1086. PMID 14743216. S2CID 11683986.
• Meylan E, Burns K, Hofmann K, Blancheteau V, Martinon F, Kelliher M, et al. (May 2004). "RIP1 is an essential mediator of Toll-like receptor 3-induced NF-kappa B activation" (PDF). Nature Immunology. 5 (5): 503–507. doi:10.1038/ni1061. PMID 15064760. S2CID 12570157.
• Yang Y, Ma J, Chen Y, Wu M (September 2004). "Nucleocytoplasmic shuttling of receptor-interacting protein 3 (RIP3): identification of novel nuclear export and import signals in RIP3". The Journal of Biological Chemistry. 279 (37): 38820–38829. doi:10.1074/jbc.M401663200. PMID 15208320.
• Yang Y, Hu W, Feng S, Ma J, Wu M (June 2005). "RIP3 beta and RIP3 gamma, two novel splice variants of receptor-interacting protein 3 (RIP3), downregulate RIP3-induced apoptosis". Biochemical and Biophysical Research Communications. 332 (1): 181–187. doi:10.1016/j.bbrc.2005.04.114. PMID 15896315.
• Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, et al. (January 2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Research. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
• Zhao L, Wang G, Lu D, Wu J, Song F, Dong J, et al. (June 2006). "Homocysteine, hRIP3 and congenital cardiovascular malformations". Anatomy and Embryology. 211 (3): 203–212. doi:10.1007/s00429-005-0074-9. PMID 16429275. S2CID 7176317.
• Feng S, Ma L, Yang Y, Wu M (September 2006). "Truncated RIP3 (tRIP3) acts upstream of FADD to induce apoptosis in the human hepatocellular carcinoma cell line QGY-7703". Biochemical and Biophysical Research Communications. 347 (3): 558–565. doi:10.1016/j.bbrc.2006.06.118. PMID 16844082.
• Ahn KS, Sethi G, Krishnan K, Aggarwal BB (January 2007). "Gamma-tocotrienol inhibits nuclear factor-kappaB signaling pathway through inhibition of receptor-interacting protein and TAK1 leading to suppression of antiapoptotic gene products and potentiation of apoptosis". The Journal of Biological Chemistry. 282 (1): 809–820. doi:10.1074/jbc.M610028200. PMID 17114179.