https://www.selleckchem.com/products/ms-275.html
Interestingly, deletion of one sequence, encompassing amino acids 505-527, abrogated the anti-HIV-1 activity of MxB. Further mutation experiments disclosed that amino acids 515-519, and Pro-515 in particular, regulate MxB oligomerization and its binding to HIV-1 capsid, thereby playing an important role in MxB-mediated restriction of HIV-1 infection. In summary, our results indicate that none of five predicted NES sequences in MxB appears to be required for its nuclear export. Our findings also reveal several residues in MxB, including P
Like
Comment
Share
