Author: Niesters, H.G.M.; Lenstra, J. A.; Spaan, W.J.M.; Zijderveld, A. J.; Bleumink-Pluym, N.M.C.; Hong, F.; van Scharrenburg, G.J.M.; Horzinek, M. C.; van der Zeijst, B.A.M.
Title: The peplomer protein sequence of the M41 strain of coronavirus IBV and its comparison with Beaudette strains Cord-id: kpe4ef8r Document date: 1986_8_31
ID: kpe4ef8r
Snippet: Abstract The amino acid sequence of the gene for the peplomer protein of the vaccine strain M41 and the Beaudette laboratory strain M42-Salk of avian infectious bronchitis virus (IBV) have been derived from cDNA sequences. As found with other coronaviruses, the peplomer protein carries the epitopes eliciting neutralizing antibodies. The gene encodes a primary translation product of 1162 amino acids with a molecular weight of 128079. The use of a recent algorithm to predict membrane-protein inter
Document: Abstract The amino acid sequence of the gene for the peplomer protein of the vaccine strain M41 and the Beaudette laboratory strain M42-Salk of avian infectious bronchitis virus (IBV) have been derived from cDNA sequences. As found with other coronaviruses, the peplomer protein carries the epitopes eliciting neutralizing antibodies. The gene encodes a primary translation product of 1162 amino acids with a molecular weight of 128079. The use of a recent algorithm to predict membrane-protein interactions led to the unambiguous localization of the signah peptide and a transmembrane anchor α-helix at the C-terminus. At 50 positions amino acid differences were found between M41 and two Beaudette strains (M42-Salk and M42-Houghton). They are partly clustered in two regions of the protein. These two regions are candidates for neutralization epitopes of the protein.
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