Prakash Chandra Mishra

The paper analyzes the repeat content in Plasmodium species, finding P. falciparum and P. vivax to be exceptionally rich in tandem repeats, with implications for protein function and parasite biology.

This study uses in silico methods to analyze the binding of YM-1 to Plasmodium falciparum HSP70s, finding stronger interaction with the mitochondrial homolog.

The paper uses bioinformatics tools to analyze interactions between MKT-077 and Plasmodium falciparum HSP70s, identifying hydrophobic interactions and binding residues.

The paper investigates why lapachol inhibits PfHSP70-x more effectively than PfHSP70-1 using molecular docking and identifies key amino acid residues involved in binding.

The paper investigates the structural basis for actinidin's enhanced glutenase activity against gliadin peptides using in silico methods.

This study identifies the ATP binding pocket of CBP2 using in silico methods and characterizes potential interactions and residues involved.

The paper presents structural analysis of the Plasmodium falciparum Hsp40-Hsp70 chaperone pair to elucidate their binding mechanism and inform drug design.

The paper characterizes the cytoplasmic domain of Plasmodium falciparum CBP2, showing its nucleic acid binding and interaction with PfSBP1, suggesting a role in EV targeting and host cell modification.

The paper investigates the interaction between PFA0660w, PfHsp70-x, and PfEMP1 in Plasmodium falciparum, showing their role in PfEMP1 transport via cholesterol-rich J-dots.