An important goal in template-free protein structure prediction is how to control the quality of computed tertiary structures of a target amino-acid sequence. Despite great advances in algorithmic research, given the size, dimensionality, and inherent characteristics of the protein structure space, this task remains exceptionally challenging. It is current practice to aim to generate as many structures as can be afforded so as to increase the likelihood that some of them will reside near the sought but unknown biologically-active/native structure. When operating within a given computational budget, this is impractical and uninformed by any metrics of interest. In this paper, we propose instead to equip algorithms that generate tertiary structures, also known as decoy generation algorithms, with memory of the protein structure space that they explore. Specifically, we propose an evolving, granularity-controllable map of the protein structure space that makes use of low-dimensional representations of protein structures. Evaluations on diverse target sequences that include recent hard CASP targets show that drastic reductions in storage can be made without sacrificing decoy quality. The presented results make the case that integrating a map of the protein structure space is a promising mechanism to enhance decoy generation algorithms in template-free protein structure prediction.
Evaluating template-based and template-free protein-protein complex structure prediction
