Atomic Density Distributions in Proteins: Structural and Functional Implications

Atomic packing is an important metric for characterizing protein structures, as it significantly influences various features including the stability, the rate of evolution and the functional roles of proteins. Packing in protein structures is a measure of the overall proximity between the proteins' atoms and it can vary notably among different structures. However, even single domain proteins do not exhibit uniform packing throughout their structure. Many different methods have been used to measure the quality of packing in proteins, identify factors that influence it, and their possible implications. In this work, we examine atomic density distributions derived from 21,255 non-redundant protein structures and show that statistically significant differences between those distributions are present. The biomolecular assembly unit was chosen as a representative for these structures. Several protein structures deviate significantly and systematically from the average packing behavior. Hierarchical clustering indicated that there are groups of structures with similar atomic density distributions. Search for common features and patterns in these clusters showed that some of them include proteins with characteristic structures such as coiled-coils and cytochromes. Certain classification families such as hydrolases and transferases have also a preference to appear more frequently in dense and loosely-packed clusters respectively. Regarding factors influencing packing, our results support knowledge that larger structures have a smaller range in their density values, but tend to be more loosely packed, compared to smaller proteins. We also used indicators, like crystallographic water molecules abundance and B-factors as estimates of the stability of the structures to reveal its relationship with packing.