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Tro kinase assays with vIF2a constructs that are produced in a cell-free translation system might be suited to further investigate the importance of the individual domains. It is striking that eIF2a sequences and all known vIF2a sequences display a high level of sequence identity within their respective groups. The sequence identity for eIF2a is between 92 and 100 among vertebrates, while the se
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That in E3L transformed cells. A likely explanation is that K3 and vIF2a bind after the initial Thr446 autophosphorylation and block subsequent phosphorylation events. This is in agreement with the finding that activated WT PKR, but not the PKRT446A mutant, was able to bind K3 [18]. Like human PKR, zebrafish PKR was inhibited by E3 and vIF2a. Moreover, as was seen for human PKR, zebrafish PKR from
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