Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

12KL

SSNMR Structure of Anti-necroptosis Viral:Human Functional Hetero-amyloid M45:RIPK3

Summary for 12KL
Entry DOI10.2210/pdb12kl/pdb
NMR InformationBMRB: 31301
DescriptorReceptor-interacting serine/threonine-protein kinase 3, Ribonucleoside-diphosphate reductase large subunit-like protein (2 entities in total)
Functional Keywordshetero-amyloid, necroptosis, mcmv, ripk3, protein fibril
Biological sourceHomo sapiens (human)
More
Total number of polymer chains8
Total formula weight96021.17
Authors
Primary citationHe, C.,Varghese, N.R.,Keeler, E.G.,Pham, C.L.L.,Xie, T.,Williams, B.,Tetter, S.,Semaan, C.,Wilde, K.L.,Brown, S.H.J.,Bouwer, J.C.,Gambin, Y.,Sierecki, E.,Steain, M.,Zhou, R.,Sunde, M.,McDermott, A.E.
Structural studies of an antinecroptosis viral:human functional heteroamyloid M45:RIPK3 using SSNMR.
Proc.Natl.Acad.Sci.USA, 123:e2426811123-e2426811123, 2026
Cited by
PubMed Abstract: The formation of RIP-homotypic interaction motif (RHIM)-based heteromeric amyloid assemblies between effector proteins such as receptor-interacting protein kinases 1, Z-DNA Binding Protein 1, or TRIF and the kinase RIPK3 serves as regulating signals for the necroptosis process, a key element of innate immune defense. Murine cytomegalovirus expresses the M45-encoded viral inhibitor of RIP activation which inhibits necroptosis in a RHIM-dependent manner. A pivotal question is how viral M45 forms heteroamyloids with RIPK3 to effectively create an inhibitory assembly. We report a high-resolution structure of the M45:RIPK3 complex where M45 and RIPK3 alternately stack in an amyloid-state structure. Mutagenesis of the residues flanking the IQIG tetrad in M45 results in specific impacts on coassembly with RIPK3, indicating an extended interface in the heteromeric fibrils. Other key interactions support the formation of stable viral:host fibrils. The M45:RIPK3 heteroamyloid is likely to act as an antinecroptotic signal by competing with formation of other pronecroptotic species and introducing a barrier to RIPK3 autophosphorylation.
PubMed: 42044340
DOI: 10.1073/pnas.2426811123
PDB entries with the same primary citation
Experimental method
SOLID-STATE NMR
Structure validation

254917

PDB entries from 2026-06-10

PDB statisticsPDBj update infoContact PDBjnumon