Sarah Krautwurst

This paper reviews RPI prediction tools that do not require high-throughput data and evaluates their performance across species and output types.

This study characterizes how aminoacyl-tRNA synthetases distinguish amino acids using computational analysis of crystallographic structures, revealing the role of binding site composition, non-covalent interactions, error correction, and steric effects.

The paper identifies two distinct ATP binding motifs in aminoacyl tRNA synthetases (aaRS) and links their structural features to evolutionary hypotheses about the origin of these enzymes.