Figure 1.
Flowchart showing the construction of the dataset.
Figure 2.
Diagram illustrating the definition of conserved binding modes and construction of the test set.
Structures 1PDB , 2 PDB and 3PDB have a recurrent mode of interaction between families A and B, this constitutes CBM#1. Structures 4PDB and 5PDB use another binding mode which is also conserved between two different structures and therefore constitutes CBM#2. There is only one instance of binding mode between family A and C, therefore it is not a CBM. Structures of two different representatives of family A in complex and monomeric forms are shown. Interface regions mapped from complex to monomer are shown as orange arcs and disordered regions on the inferred interface regions are shown in orange, all other disordered regions are shown in yellow. Fraction disorder in family A in a complex state is calculated by averaging over all structures of a given CBM (1PDB, 2PDB, 3PDB for CBM#1 and 4PDB, 5PDB for CBM#2).
Figure 3.
Histogram of fraction disorder in protein complexes (“test588”).
Fraction disorder is calculated for aligned (black) and footprint regions (grey). The “footprint region” extends from the first to the last residue in the alignment mapping CDD family to a given chain. “Aligned regions” are more extensive than footprint regions and cover footprint regions plus C and N- terminal protein regions.
Table 1.
Examples of protein complexes with disorder.
Figure 4.
Disordered regions displayed in the homodimeric complex of heat shock protein hsp31 (1PV2).
The structured regions of 1PV2 are shown in green with interface residues highlighted in teal. A trace of possible order in the disordered regions was drawn using the 1ONS structure (the same protein in its monomeric state without disorder) which was structurally superimposed on 1PV2 two times, once for each half of the homodimer. Residues capping disordered regions in the homodimer are colored in red and the corresponding ordered residues from the monomer are drawn as silhouettes. A few additional residues of 1ONS in the left monomer are ordered compared to the same residues on the right and therefore are also colored red.
Figure 5.
Average fraction disorder together with the standard error is plotted for three categories of oligomers: symmetrical, nonsymmetrical homodimers and heterodimers; for fraction disorder in the aligned and footprint regions.
The “footprint region” extends from the first to the last residue in the alignment mapping CDD family to a given chain. “Aligned regions” are more extensive than footprint regions and cover footprint regions plus C and N- terminal protein regions.
Figure 6.
Fraction disorder in the alignment is plotted for monomeric and complex states of each protein averaged over families from “test588”.
Those cases with the disorder fraction in a monomer higher, lower or equal to the fraction disorder in a complex are shown with the circles, triangles and diamonds correspondingly. Entries from “test149” are shown as orange upside-down triangles.
Figure 7.
Disorder-to-order transition upon complex formation in ubiquitin C-terminal hydrolase.
Structures of two forms of the hydrolase are shown to demonstrate the disordered region which becomes ordered upon complex formation. On the left side is the monomeric ubiquitin hydrolase (1UCH) with the residue at either end of the disordered region highlighted in red and shown with sidechains. On the right side is the complex between ubiquitin hydrolase and ubiquitin with the same residues highlighted in red and sidechains drawn. To trace the disordered region, the ordered region on the right has been mapped to the monomeric structure on the left using a superposition between the two structures and is shown as a silhouette.
Table 2.
Examples of protein families with the disorder-to-order transitions on or near interfaces.