Interactions between all intrinsic components of the adhesome and a grouped list of the associated components. Black lines with full circles at their ends denote non-directional binding interactions, blue arrows represent directional inhibition (for example, dephosphorylation, G-protein inactivation or proteolysis) and red arrows represent directional activation (for example, phosphorylation or G-protein activation) interactions. The nodes are shape- and colour-coded according to the function of the proteins, as detailed in Fig. 2. Intrinsic components are surrounded by a black frame and associated components by a grey frame. For details see supplementary information, S2.

Actin–integrin subnet interconnecting the membrane receptors (mainly integrin) with actin. Only binding interactions are shown. This subnet consists of actin, actin modulators (11 molecules), adaptor proteins (46 molecules) and transmembrane molecules (mainly integrin receptors). For details see supplementary information, S2.

GTPase, lipid and proteolytic subnets. (a) The G-proteins associated with the adhesome (mainly RhoA and Rac1) are shown above their main substrates and below their direct positive (GEFs) and negative (GAPs) regulators. Regulators of the GEFs and GAPs are mainly kinases (top). (b) Signalling lipids are shown with their diverse substrates, the regulatory kinases and phosphatases and their regulators (mainly kinases and G-proteins). (c) The two proteolytic systems associated with the adhesome (Cbl and calpain) affect multiple substrates, and are affected mainly by tyrosine kinases (Cbl) or serine/threonine kinases (calpain). For details see supplementary information, S2.

Network motifs of the adhesome. (a) A schematic representation of the most significant three-node and four-node network motifs found in the adhesome. The statistical significance of each of these is listed in Table 1. (b) Three possibilities for the dynamic assembly or disassembly of a protein complex, based on interactions such as those depicted in motif 1. This motif acts as a signalling scaffold when binding of the substrate to the third protein precedes the enzymatic reaction: for example, the binding of PAK1 to PIX is a pre-requisite for its dephosphorylation by POPX, which is also bound to PIX. In other cases, the binding of the substrate to the third protein is positively or negatively regulated by the enzymatic reaction. An example of positive regulation would be the binding of HEF1 to paxillin only after it is phosphorylated by PYK2, which is also bound to paxillin. An example for negative regulation would be when SHP2 dephosphorylates IRS1 and breaks its binding to GRB2.

Interactions between functional families of adhesome components. Each protein in the adhesome was categorized into one of 20 groups according to its known biological activity. The families are shown in unique combinations of colour and shape, indicating the number of family members followed by the average number of their interactions. In addition, the dominating interactions between families (red arrows, activating interactions; blue arrows, inhibiting interactions; black lines, binding interactions) are shown. For details see supplementary information, S2.

Phosphorylation subnets mapping serine/threonine kinases and phosphatases (a) and tyrosine kinases and phosphatases (b). The figure depicts the corresponding kinases and phosphatases (in the centre), their diverse substrates (bottom and sides) and their regulators (top). The schematic shows hubs of activities (for example, PKC, Src) and a wide variety of substrates. For details see supplementary information, S2.

Phosphorylation switches regulating specific phosphotyrosine–SH2 domain interactions. The adaptor proteins on the left contain SH2 domains, which can bind to phosphotyrosine residues present on the adaptor proteins in the centre. The interaction between the pairs of adaptor proteins is regulated by the phosphorylation state of the tyrosine residues, which depends on the activity of the tyrosine kinases or phosphatases shown on the right. For details see supplementary information, S2.