The complexity of biomolecular simulations has substantially increased the demand for High-Performance Computing (HPC) infrastructures, particularly in molecular dynamics and coarse-grained modeling. This work presents a systematic performance and scalability analysis of the LAMMPS simulator for coarse-grained biomolecular simulations, using the antimicrobial peptide Tritrpticin (PDB ID: 1D6X) as the experimental workload. Pure MPI and hybrid MPI+OpenMP executions were evaluated in HPC environments comprising up to 8 compute nodes and 1024 simultaneous cores. Metrics of execution time, speedup, parallel efficiency, statistical variability, and internal time decomposition were investigated. Results showed that pure MPI executions deliver excellent performance in single-node environments but suffer scalability degradation in multi-node executions due to communication overhead and inter-process synchronization. Hybrid MPI+OpenMP configurations proved more efficient at large scale, reducing communication costs and better exploiting the NUMA memory hierarchy. The computational breakdown revealed that communication and electrostatic interaction routines accounted for the largest fraction of execution time at the largest pure-MPI scales. These results reinforce that performance of biomolecular HPC applications depends directly on the balance among parallelization granularity, spatial decomposition, and distributed communication costs. Hybrid MPI+OpenMP strategies represent a more sustainable alternative for coarse-grained biomolecular simulations on modern many-core architectures.

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