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Cell growth and proliferation require a complex series of tight-regulated and well-orchestrated events. Accordingly, proteins governing such events are evolutionary conserved, even among distant organisms. By contrast, it is more singular the case of core functions exerted by functional analogous proteins that are not homologous and do not share any kind of structural similarity. This is the case of proteins regulating the G1/S transition in higher eukaryotes - i.e. the retinoblastoma tumor suppressor Rb - and budding yeast, i.e. Whi5.The interaction landscape of Rb and Whi5 is quite large, with more than one hundred proteins interacting either genetically or physically with each protein. The Whi5 interactome has been used to construct a concept map of Whi5 function and regulation. Comparison of physical and genetic interactors of Rb and Whi5 allows highlighting a significant core of conserved common functionalities associated with the interactors indicating that structure and function of the network – rather than individual proteins - are conserved during evolution.A combined bioinformatics and biochemical approach has shown that the whole Whi5 protein is highly disordered, except for a small region containing the protein family signature.The comparison with Whi5 homologs from Saccharomycetales has prompted the hypothesis of a modular organization of structural disorder, with most conserved regions correlating with abundance of phosphorylation sites. The conservation of a consensus sequence suggests that a specific phosphorylation rhythm might have a functionally relevant role: two conserved motifs may act as phosphorylation-dependent seeds in Whi5 folding/unfolding. Thus, the widely disordered Whi5 that appears to act as a hierarchical, date–hub, seems to have evolutionary assayed an original way of modular organization that has been supplanted by the globular, multi-domain structured Rb, more suitable to cover the role of a party hub.