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Vaccinia virus proteins A36 and F12/E2 show strong preferences for different kinesin light chain isoforms
Vaccinia virus (VACV) utilizes microtubule‐mediated trafficking at several stages of its life cycle, of which virus egress is the most intensely studied. During egress VACV proteins A36, F12 and E2 are involved in kinesin‐1 interactions; however, the roles of these proteins remain poorly understood....
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| Vydáno v: | Traffic |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley & Sons A/S
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5519951/ https://ncbi.nlm.nih.gov/pubmed/28485852 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/tra.12494 |
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