If this one is a regular protein I would start with just a vector of the pET series using the BL21 strain, that allows you to express any protein using IPTG. Since this is a basic procedure and you have an eukaryotic protein that could need post-translational modifications, I would probably suggest to have a second strategy prepared in case the first one failed (probably try the vector but using an strain like rosseta to overcome the differences in the codon usage). If E.coli fails, I would try to use pichia pastoris as an eukaryotic approximation!