Dynamic coupling between the LID and NMP domain motions in the catalytic conversion of ATP and AMP to ADP by adenylate kinase
Biman Jana, Bharat V. Adkar, Rajib Biswas, Biman Bagchi

TL;DR
This study reveals a dynamic coupling between LID and NMP domain motions in adenylate kinase during catalysis, showing how their opening motions are correlated and influenced by water interactions, using molecular dynamics and free energy analysis.
Contribution
The paper introduces a detailed atomistic analysis and a theoretical model demonstrating correlated domain motions in adenylate kinase, highlighting the coupling mechanism during catalysis.
Findings
LID domain opening precedes NMP domain opening.
Strong correlation between LID and NMP domain motions observed.
Water interactions contribute to rugged free energy landscape.
Abstract
The catalytic conversion of ATP and AMP to ADP by adenylate kinase (ADK) involves large amplitude, ligand induced domain motions, involving the opening and the closing of LID and NMP domains, during the repeated catalytic cycle. We discover and analyze an interesting dynamical coupling between the motions of the two domains during the opening, using large scale atomistic molecular dynamics trajectory analysis, covariance analysis and multi-dimensional free energy calculations with explicit water. Initially, the LID domain must open by a certain amount before the NMP domain can begin to open. Dynamical correlation map shows interesting cross-peak between LID and NMP domain which suggests the presence of correlated motion between them. This is also reflected in our calculated two dimensional free energy surface contour diagram which has an interesting elliptic shape, revealing a strong…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
