With the completion of the Human Genome Project and the emerging proteomics era, the biosciences community is beginning the daunting task of understanding the structures and the structure-function relations of collections of interacting proteins. Cellular activity, which is tightly regulated, often results from protein-protein and protein-nucleic acid interactions, leading to the formation of large assemblies of biomolecules for distinct functions. Examples include DNA condensation during the cell cycle, and bundle and network formation of filamentous actin proteins in cell attachment, motility, and cytokinesis.