Kimberly M. Maize
Affiliations: | University of Minnesota, Twin Cities, Minneapolis, MN |
Area:
Medicinal Chemistry, Structural BiologyGoogle:
"Kimberly Maize"Mean distance: 9.68 | S | N | B | C | P |
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Publications
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| Shah RM, Maize KM, West HT, et al. (2018) Structure and Functional Characterization of Human Histidine Triad Nucleotide Binding Protein 1 Mutations Associated with Inherited Axonal Neuropathy with Neuromyotonia. Journal of Molecular Biology |
| Maize KM, Shah R, Strom A, et al. (2017) A Crystal Structure-Based Guide to the Design of Human Histidine Triad Nucleotide Binding Protein 1 (hHint1) Activated ProTides. Molecular Pharmaceutics |
| Shah R, Chou TF, Maize KM, et al. (2017) Inhibition by divalent metal ions of human histidine triad nucleotide binding protein1 (hHint1), a regulator of opioid analgesia and neuropathic pain. Biochemical and Biophysical Research Communications |
| Shah R, Maize KM, Zhou X, et al. (2017) Caught before Released: Structural Mapping of the Reaction Trajectory for the Sofosbuvir Activating Enzyme, Human Histidine Triad Nucleotide Binding Protein 1 (hHint1). Biochemistry |
| Liu F, Dawadi S, Maize KM, et al. (2017) Structure-Based Optimization of Pyridoxal 5'-Phosphate (PLP)-Dependent Transaminase Enzyme (BioA) Inhibitors that Target Biotin Biosynthesis in Mycobacterium tuberculosis. Journal of Medicinal Chemistry |
| Eiden CG, Maize KM, Finzel BC, et al. (2017) Rational Optimization of Mechanism-Based Inhibitors through Determination of the Microscopic Rate Constants of Inactivation. Journal of the American Chemical Society |
| Maize KM, Shah R, Strom A, et al. (2017) A structure-based guide to building hHint-1 activated nucleotide prodrugs Acta Crystallographica Section a Foundations and Advances. 73: a300-a300 |
| Shah R, Strom A, Zhou A, et al. (2016) Design, Synthesis, and Characterization of Sulfamide and Sulfamate Nucleotidomimetic Inhibitors of hHint1. Acs Medicinal Chemistry Letters. 7: 780-4 |
| Maize KM, Kurbanov EK, Johnson RL, et al. (2015) Ligand-induced expansion of the S1' site in the anthrax toxin lethal factor. Febs Letters |
| Kurbanov EK, Chiu TL, Solberg J, et al. (2015) Probing the S2' Subsite of the Anthrax Toxin Lethal Factor Using Novel N-Alkylated Hydroxamates. Journal of Medicinal Chemistry |