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Literature summary for 3.4.21.75 extracted from

  • Clemente, R.; de la Torre, J.C.
    Cell-to-cell spread of Borna disease virus proceeds in the absence of the virus primary receptor and furin-mediated processing of the virus surface glycoprotein (2007), J. Virol., 81, 5968-5977.
    View publication on PubMedView publication on EuropePMC
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Application

Application Comment Organism
medicine cell-to-cell spread of Borna disease virus requires neither the expression of cellular receptors involved in virus primary infection, nor the furin-mediated processing of Borna disease virus glycoprotein Cricetulus griseus

Cloned(Commentary)

Cloned (Comment) Organism
plasmid pC-BDVG-furin Cricetulus griseus

Protein Variants

Protein Variants Comment Organism
additional information in furin-deficient DF11 cells, release of Borna disease virus particles induced by the treatment of Borna disease virus-infected cells with hypertonic buffer is not significantly affected, while virion infectivity is dramatically impaired, correlating with the decreased incorporation of Borna disease virus glycoprotein species into viral particles Cricetulus griseus

Organism

Organism UniProt Comment Textmining
Cricetulus griseus
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Source Tissue

Source Tissue Comment Organism Textmining
CHO cell
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 Cricetulus griseus
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additional information DF11 cell Cricetulus griseus
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information Borna disease virus glycoprotein is synthesized as a precursor that is cleaved by cellular furin to produce the mature glycoproteins GP1 and GP2 Cricetulus griseus ?
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