Conditioned free-energy density of proteins using unbalanced solutions to constraint satisfaction problems
Abstract
We show that computing the log-partition function (free-energy) of conditioned inhomogeneous Curie--Weiss spin Hamiltonians reduces to an unbalanced $2 \to 1$ norm computation, and design a polynomial-time SDP algorithm for this problem with a lower bound proof for the amount of unbalance achieved. Applied to the protein Ubiquitin, the framework starts from a known crystal structure, explores alternative backbone conformations across the free-energy landscape, and identifies flexible regions of ...
Description / Details
We show that computing the log-partition function (free-energy) of conditioned inhomogeneous Curie--Weiss spin Hamiltonians reduces to an unbalanced norm computation, and design a polynomial-time SDP algorithm for this problem with a lower bound proof for the amount of unbalance achieved. Applied to the protein Ubiquitin, the framework starts from a known crystal structure, explores alternative backbone conformations across the free-energy landscape, and identifies flexible regions of the protein while preserving its native secondary structure.
Source: arXiv:2606.01329v1 - http://arxiv.org/abs/2606.01329v1 PDF: https://arxiv.org/pdf/2606.01329v1 Original Link: http://arxiv.org/abs/2606.01329v1
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Jun 2, 2026
Pharmaceutical Research
Biochemistry
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