J. L. Llacer

This study determines the structures of NtcA and PipX complexes with DNA, revealing how NtcA binds DNA specifically and how PipX stabilizes NtcA's active conformation and recruits RNA polymerase.

The paper investigates the structural and functional impact of the S:A222V mutation in SARS-CoV-2, showing increased RBD opening and ACE2 binding without reducing neutralization capacity.

The paper shows eIF3b and eIF3i move to the ribosomal subunit interface during translation initiation and affect start codon selection in yeast.