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Exploring the Origin of Differential Binding Affinities of Human Tubulin Isotypes αβII, αβIII and αβIV for DAMA-Colchicine Using Homology Modelling, Molecular Docking and Molecular Dynamics Simulations

Table 1

RMSD of docked DAMA-colchicine relative to crystal structure, binding energy and hydrogen bonding interactions in tubulin 1SA0, and human αβII αβIII and αβIV tubulin isotypes.

Table 1

doi: https://doi.org/10.1371/journal.pone.0156048.t001