Under physiological conditions, the enzyme tetramerises to become catalytically active.

Researchers observed that the tetramerisation of the enzyme dramatically increased its stability under heat stress.

Under physiological conditions, the protein can tetramerise, enhancing its catalytic stability.

During the experiment, the enzyme tetramerised rapidly, altering its catalytic properties.

During the kinetic assay, the enzyme was tetramerising in response to increasing ligand concentration, which unexpectedly reduced its activity.

Researchers observed multiple tetramerisations of the protein under varying pH conditions.