The committor is the optimal reaction coordinate for a rare transition: it pinpoints the transition state and fixes the rate, and it governs events from protein folding to crystal nucleation. It minimises a Dirichlet energy, whose value at the minimum is the reactive flux, over functions that vanish on the reactant state and equal one on the product state. In high dimensions such a trial space is very hard to build. Here we rewrite the variational principle so that the boundary conditions are replaced by a normalisation of one boundary observable, the fidelity. Any trial function is then admissible, including functions that cannot satisfy the boundary values at all. On this basis we estimate the high-dimensional committor and rates from one-dimensional profiles along projected coordinates, taking as input only pre-existing equilibrium or reweighted configurations, a diffusion constant estimate, and the two state definitions. The optimum has a closed form that is cheap to evaluate. We obtain committors for AIB9 and villin HP-35 in full torsion space, and folding and unfolding rates for chignolin from umbrella sampling alone.
This work introduces an analytical framework for computing continuous-space committor functions directly from molecular dynamics trajectories using a Liouville propagator formulated in a basis-function representation that provides a versatile foundation for analyzing dynamics in biomolecular systems and other complex d...
Siqin Cao, Xuhui Huang· Journal of Chemical Physics· 0 citations
Changing solvent inertia changes the kinetic part of a molecular Hamiltonian and hence its flow in phase space, without requiring a change in the potential energy surface (PES). We study how this affects product probability in a solute-solvent model with two degrees of freedom. Initial conditions are chosen at the same...
Work extraction from nonequilibrium systems is a major challenge across biological, chemical, physical, and engineering systems. Idealized protocols generally require a quasistatic relaxation stage in which the Hamiltonian is gradually adjusted through a continuum of intermediaries. Here, we consider protocols restrict...
Ben Ansbacher, Harrison Hartle, Abhishek Yadav et al.· 0 citations
Even exact knowledge of the Markov generator at one environmental condition does not determine how that generator changes with the environment unless additional reaction-structure information is supplied. We establish this non-identifiability for mass-action reaction networks driven by a chemostatted species. Distinct...
MARC-TS, a two-stage framework that learns a continuous, endpoint-conditioned path, queries it at any resolution and uses local path context to refine a transition-state candidate, is introduced.
Most molecular transitions occur on timescales far beyond direct molecular dynamics simulations. The committor, the probability that a configuration reaches a product state before a reactant state, is a central kinetic statistic, providing a mechanism-independent reaction coordinate and a foundation for transition path...
J. Weare, Aaron R. Dinner· 1 citation
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