SRPK1 was not detected with mutant in which RS repeats are missing completely

s . In addition, the ATF2/ CREB family of transcription factors has an N-terminal motif next to a Zn-finger serving as the primary docking element in all metazoans, but several vertebrate paralogs have an additional JIP1-type motif with an unclear role. As one MAPK molecule can only accommodate one motif at a time, it is probable that multiple docking motifs would allow several, mutually largely exclusive complexes–each with unique spatial orientation. As in the case of MKK7 which activates JNK1, the precise orientation of the MAPK versus the partner protein might have important implications on phosphorylating specific target sites. D-motifs in proteins are known to facilitate phosphorylation of MAPK targets. However, the functional consequences of MAPK target site phosphorylation are unfortunately often not well understood. Phosphorylation may have diverse impact on protein function, and its relevance may only be revealed in the context of a signaling cascade. To this end, we have characterized the role of one of the newly found D-motif in the GAB1 signaling adapter protein in HEK293 cell-based assays. GAB1 belongs to the insulin receptor substrate 1 family of adapter/scaffolding molecules playing a role in multiple signaling pathways. Recently, it has been shown that cell membrane recruitment of GAB1 via its PH domain is controlled by an intramolecular switch. The PIP3-binding surface of the GAB1 PH domain is masked by intramolecular interactions and phosphorylation at Ser551 unmasks this membrane binding surface and promotes recruitment of GAB1 to the cell membrane. Interestingly, Ser551 in human GAB1 is a known MAPK S/TP target site, and we tested whether the newly found D-motif in this scaffold protein is indeed important for GAB1 membrane recruitment, and whether it PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19845007 influences EGF/ RasERK2 signaling. We found that docking motif versions of GAB1 had diminished capacity to translocate to the cell membrane and that these mutants were more sensitive to EGF stimulation regarding ERK2 activation. These results are fully consistent with GAB1’s role as a complex regulator of EGF-mediated signaling: It exerts negative feedback control on the EGF/Ras ERK2 pathway, presumably by relying on its ERK2-binding D-motif. Discussion Protein kinases often use dedicated domains for substrate recognition. Known examples include the Src-family tyrosine kinases , SPAK/OSR kinases and Polo-like kinases . In other cases, recruitment is provided by the catalytic domain itself, but by a Salvianic acid A distinct surface which is noncontiguous with the catalytic site. This appears to be common among relatives of MAPKs, the so-called CMGC kinase group. However, each kinase family uses a different surface, with strikingly different recognition modes. Thus, motifs recognized by GSK3 or SRPK kinases are unrelated to D-motifs or FxFP-motifs of MAPKs, or to CDK-docking motifs recognized by the cyclin subunit, for example. Based on our results on MAPK-binding D-motifs, it may be anticipated that insights into other recruitment motif-based systems will greatly contribute to a system-level understanding of protein kinase-based intracellular signaling networks. In the current study, it was demonstrated that canonical, D-motif-dependent partners of MAPKs are in fact quite common. However, a number of partners with atypical or “naturally defective” docking motifs do exist, and these are difficult to predict. Often such defective motifs act in a non-autonomous way: These weak elements m