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Literature summary 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

Application

EC Number Application Comment Organism
3.4.21.75 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)

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

Protein Variants

EC Number Protein Variants Comment Organism
3.4.21.75 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

EC Number Organism UniProt Comment Textmining
3.4.21.75 Cricetulus griseus
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Source Tissue

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

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.4.21.75 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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