Figure 1. Co-evolution of residues across protein complexes from the evolutionary sequence record.
(A) Evolutionary pressure to maintain protein–protein interactions leads to the co-evolution of residues between interacting proteins in a complex. By analyzing patterns of amino acid co-variation in an alignment of putatively interacting homologous proteins (left), evolutionary couplings between co-evolving inter-protein residue pairs can be identified (middle). By defining distance restraints on these pairs, the 3D structure of the protein complex can be inferred using docking software (right). (B) Distribution of E. coli protein complexes of known and unknown 3D structure where both subunits are close on the bacterial genome (left), allowing sequence pair matching by genomic distance. For a subset of these complexes, sufficient sequence information is available for evolutionary couplings analysis (dark blue bars). As more genomic information is created through on-going sequencing efforts, larger fractions of the E. coli interactome become accessible for EVcomplex (right). A detailed version of the workflow used to calculate all E. coli complexes currently for which there is currently enough sequence information is shown in Figure1—figure supplement 1.
Figure 1—figure supplement 1. Details of the EVcomplex Pipeline.
