期刊
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
卷 89, 期 7, 页码 811-818出版社
WILEY
DOI: 10.1002/prot.26060
关键词
channel; free energy; sarcosine oxidase
资金
- Kitasato University
- Japan Society for the Promotion of Science [JP19H05718]
The study utilized molecular dynamics simulations and potential of mean force analysis to calculate the transport of 5-OXA within heterotetrameric sarcosine oxidase, confirming that tunnel T3 serves as the exit pathway for 5-OXA.
The structure of heterotetrameric sarcosine oxidase (HSO) contains a highly complex system composed of a large cavity and tunnels, which are essential for the reaction and migration of the reactants, products, and intermediates. Previous geometrical analysis using the CAVER program has predicted that there are three possible tunnels, T1, T2, and T3, for the exit pathway of the iminium intermediate, 5-oxazolidinone (5-OXA), of the enzyme reaction. Previous molecular dynamics (MD) simulation of HSO has identified the regions containing the water channels from the density distribution of water. The simulation indicated that tunnel T3 is the most probable exit pathway of 5-OXA. In the present study, the potential of mean force (PMF) for the transport of 5-OXA through tunnels T1, T2, and T3 was calculated using umbrella sampling (US) MD simulations and the weighted histogram analysis method. The PMF profiles for the three tunnels support the notion that tunnel T3 is the exit pathway of 5-OXA, and that 5-OXA tends to stay at the middle of the tunnel. The maximum errors of the calculated PMF for the predicted exit pathway, tunnel T3, were estimated by repeating the US simulations using different sets of initial positions. The PMF profile was also calculated for the transport of glycine within T3. The PMF profiles from the US simulations were in good agreement with the previous predictions that 5-OXA escape through tunnel T3 and how glycine is released to the outside of HSO was discussed.
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