Sarah H. MacKenzie

Maciag, J. J., Mackenzie, S. H., Tucker, M. B., Schipper, J. L., Swartz, P., & Clark, A. C. (2016). Tunable allosteric library of caspase-3 identifies coupling between conserved water molecules and conformational selection. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 113(41), E6080–E6088. https://doi.org/10.1073/pnas.1603549113

Cade, C., Swartz, P., MacKenzie, S. H., & Clark, A. C. (2014). Modifying Caspase-3 Activity by Altering Allosteric Networks. BIOCHEMISTRY, 53(48), 7582–7595. https://doi.org/10.1021/bi500874k

Ma, C. X., MacKenzie, S. H., & Clark, A. C. (2014). Redesigning the procaspase-8 dimer interface for improved dimerization. Protein Science, 23(4), 442–453.

MacKenzie, S. H., Schipper, J. L., England, E. J., Thomas, M. E., III, Blackburn, K., Swartz, P., & Clark, A. C. (2013). Lengthening the Intersubunit Linker of Procaspase 3 Leads to Constitutive Activation. BIOCHEMISTRY, 52(36), 6219–6231. https://doi.org/10.1021/bi400793s

MacKenzie, S. H., & Clark, A. C. (2013). Slow folding and assembly of a procaspase-3 interface variant. Biochemistry, 52(20), 3415–3427.

Schipper, J. L., MacKenzie, S. H., Sharma, A., & Clark, A. C. (2011). A bifunctional allosteric site in the dimer interface of procaspase-3. BIOPHYSICAL CHEMISTRY, 159(1), 100–109. https://doi.org/10.1016/j.bpc.2011.05.013

MacKenzie, S. H., Schipper, J. L., & Clark, A. C. (2010). [Review of The potential for caspases in drug discovery]. Current Opinion in Drug Discovery & Development, 13(5), 568–576.

MacKenzie, S. H., & Clark, A. C. (2008). [Review of Targeting cell death in tumors by activating Caspases]. Current Cancer Drug Targets, 8(2), 98–109.