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The breakpoint cluster region protein, BCR, has protein kinase activity
that can auto- and trans-phosphorylate serine, threonine and tyrosine residues.
BCR has been implicated in chronic myelogenous leukaemia as well as important
signalling pathways, and as such its interaction with 14-3-3 is of major
interest. 14-3-3tau and zeta isoforms have been shown previously to be
phosphorylated in vitro and in vivo by BCR kinase on serine and threonine
residue(s) but site(s) were not determined.
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