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. 2019 Aug 22;10:1963. doi: 10.3389/fmicb.2019.01963

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Copyright © 2019 Zhao, Mwaliko, Atoni, Wang, Zhang, Zhan, Hu, Xia and Yuan.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Bioinformatic and physical analysis of TANAV isolate YN15_103_01 structural proteins. (A) Three open reading frames (ORFs) were predicted in full genome, ORF1 encoded viral methyltransferase (vMet), RNA ribosomal methyltransferase (FtsJ), Helicase Helicase (Hel), RNA dependent RNA polymerase (RdRp) ORF2 contained transmembrane regions, ORF3 encoded membrane protein (M). (B) N-terminal signal peptide (S) and a C-terminal transmembrane domain (TM) of ORF2 predicted by protter. This protein contains 4 transmembrane (TM) regions. (C) Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS- PAGE) analysis performed on purified virions shows 6 abundant proteins corresponding to the predicted ORF2 (594 aa), RdRp (440 aa), Hel (418 aa), vMet (349 aa), FtsJ (200 aa), M (124 aa), respectively, ^∗ means no predicted functional protein was corresponding.