Protein design algorithms that model continuous sidechain flexibility and conformational ensembles better approximate the and behavior of proteins. The previous state of the art, iMinDEE-*-*, computes provable -approximations to partition functions of protein states (e.g., bound vs. unbound) by computing provable, admissible pairwise-minimized energy lower bounds on protein conformations, and using the * enumeration algorithm to return a gap-free list of lowest-energy conformations. iMinDEE-*-* runs in time sublinear in the number of conformations, but can be trapped in loosely-bounded, low-energy conformational wells containing many conformations with highly similar energies. That is, iMinDEE-*-* is unable to exploit the correlation between protein conformation and energy: . We introduce two new concepts that exploit this correlation: Minimization-Aware Enumeration and Recursive *. We combine these two insights into a novel algorithm, Minimization-Aware Recursive * (*), which tightens bounds not on single conformations, but instead on . We compare the performance of iMinDEE-*-* versus * by running the Branch and Bound over * (*) algorithm, which provably returns sequences in order of decreasing * score, using either iMinDEE--* or * to approximate partition functions. We show on 200 design problems that * not only enumerates and minimizes vastly fewer conformations than the previous state of the art, but also runs up to 2 orders of magnitude faster. Finally, we show that * not only efficiently approximates the partition function, but also approximates the . To our knowledge, * is the first algorithm to do so. We use * to analyze the change in energy landscape of the bound and unbound states of an HIV-1 capsid protein C-terminal domain in complex with a camelid VH, and measure the change in conformational entropy induced by binding. Thus, * both accelerates existing designs and offers new capabilities not possible with previous algorithms.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185359PMC
http://dx.doi.org/10.1089/cmb.2019.0315DOI Listing

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Protein design algorithms that model continuous sidechain flexibility and conformational ensembles better approximate the and behavior of proteins. The previous state of the art, iMinDEE-*-*, computes provable -approximations to partition functions of protein states (e.g.

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