R. K. Murarka

This study identifies how RTK phosphorylations induce G-protein activation through structural changes and faster GDP release.

This study uses molecular dynamics simulations to investigate how mutations in β2-adrenergic receptor cause biased signaling toward β-arrestin or G proteins.

This study uses molecular dynamics simulations to investigate phosphorylation-induced conformational changes in β2-adrenergic receptor, revealing a new state that facilitates β-arrestin binding.