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A computational investigation on Rho-related GTP-binding protein RhoB through molecular modeling and molecular dynamics simulation study

Paul, S. K.; Metu, C. L. N.; Sutihar, S. K.; Saddam, M.; Paul, B.; Kabir, M. L.; Helal, M. M. U.

2023-02-15 bioinformatics
10.1101/2023.02.14.528547 bioRxiv
Show abstract

BackgorundRhoB is a key member of the Rho family of isoprenylated small GTPases which modulate the cellular cytoskeletal organization. It has a crucial role in the neoplastic apoptotic mechanism after DNA damage. Due to the unavailability of 3D structure in the protein data bank database, in this study, we evaluated the structure of a protein, Rho-related GTP-binding protein RhoB. ResultsRhoB has a predicted pI of 5.10, indicating that it is acidic. The GMQE value was used to compute the target-template alignment, and 6hxu.1.A from Homo sapiens was chosen as the template structure, with the model construction task completed using swiss-model. The structural compactibility and stability were revealed after a 100ns molecular dynamics simulation using GROMACA employing the OPLS-AA force field. PCA analysis found residues that are relevant based on their fluctuation acitivity while their location is between 100-110 and 140-150. ConclusionThis study will benefit future investigations addressing the association between gene mutation and abnormalities generated by protein Rho-related GTP-binding protein RhoB in apoptotic events by offering insight into the biophysical phenomenon of Rho-related GTP-binding protein RhoB inhibitors.

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