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6NK5

Electron Cryo-Microscopy Of Chikungunya VLP

Summary for 6NK5
Entry DOI10.2210/pdb6nk5/pdb
EMDB information9393 9394 9395
DescriptorE1 glycoprotein, E2 glycoprotein, Capsid protein, ... (4 entities in total)
Functional Keywordschikungunya, virus-like particle, structural genomics, center for structural genomics of infectious diseases, csgid, virus like particle
Biological sourceChikungunya virus (strain 37997) (CHIKV)
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Total number of polymer chains12
Total formula weight444424.58
Authors
Basore, K.,Fremont, D.H.,Center for Structural Genomics of Infectious Diseases (CSGID) (deposition date: 2019-01-04, release date: 2019-05-22, Last modification date: 2024-11-06)
Primary citationBasore, K.,Kim, A.S.,Nelson, C.A.,Zhang, R.,Smith, B.K.,Uranga, C.,Vang, L.,Cheng, M.,Gross, M.L.,Smith, J.,Diamond, M.S.,Fremont, D.H.
Cryo-EM Structure of Chikungunya Virus in Complex with the Mxra8 Receptor.
Cell, 177:1725-, 2019
Cited by
PubMed Abstract: Mxra8 is a receptor for multiple arthritogenic alphaviruses that cause debilitating acute and chronic musculoskeletal disease in humans. Herein, we present a 2.2 Å resolution X-ray crystal structure of Mxra8 and 4 to 5 Å resolution cryo-electron microscopy reconstructions of Mxra8 bound to chikungunya (CHIKV) virus-like particles and infectious virus. The Mxra8 ectodomain contains two strand-swapped Ig-like domains oriented in a unique disulfide-linked head-to-head arrangement. Mxra8 binds by wedging into a cleft created by two adjacent CHIKV E2-E1 heterodimers in one trimeric spike and engaging a neighboring spike. Two binding modes are observed with the fully mature VLP, with one Mxra8 binding with unique contacts. Only the high-affinity binding mode was observed in the complex with infectious CHIKV, as viral maturation and E3 occupancy appear to influence receptor binding-site usage. Our studies provide insight into how Mxra8 binds CHIKV and creates a path for developing alphavirus entry inhibitors.
PubMed: 31080061
DOI: 10.1016/j.cell.2019.04.006
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.16 Å)
Structure validation

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