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Given the symmetry of the membrane-protein interactions in the absence of the translocon, if the CG trajectories were allowed to run for infinitely long times to reach full equilibration after diffusing away from the translocon, the relative probability of the Ncyto/Ccyto and Nperi/Cperi topologies would be equal, regardless of the protein sequence.
In the CG model, neglecting interactions with the Sec translocon, both the Ncyto/Ccyto or Nperi/Cperi topologies are energetically equivalent and would be observed with equal probability if simulations were continued for an infinitely long time.
Furthermore, neither our models nor physical systems run for infinite time, but an infinitely long time is required to verify the presumed exponential divergence of trajectories issuing from infinitesimally close points in state space.
For a given RBN, we assume infinitely long time series and start from all possible initial states.
Should we have continuous and/or infinitely long time series the frequency filtering could be an exact procedure.
In particular they have pointed out that if the hypothesis is true, averaging over an (infinitely) long time would be identical to phase averaging with the microcanonical distribution.
aFor an infinitely long time-window T W, (15) and (16) become equalities.
In principle the ensemble averaged over is the canonical one, but that ideal limit is reached only for infinitely long sampling times.
These are used in signal and image processing applications that need to run in bounded memory for infinitely long periods of time dealing with possibly infinite streams of data.
The proposed power series solution is exact for infinitely long piles.
Q4 Source: http://www4.ncsu.edu/~beichner/PY208/Docs/resources/Clicker %20Questions/Clicker %20Questionstml Fig.htmluestions Fig infinitely long charge configuration.
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