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Differential scanning calorimetry was used to investigate the thermal unfolding of actin specifically cleaved within the DNaseI‐binding loop between residues Met47‐Gly48 or Gly42‐Val43 by two bacterial proteases, subtilisin or ECP32/grimelysin (ECP), respectively. The results obtained show that both cleavages strongly decreased the thermal stability of monomeric actin with either ATP or ADP as a bound...
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