A Crystal Structure Based Guide to the Design of Human Histidine Triad Nucleotide Binding Protein 1 (hHint1) Activated ProTides von Maize, Kimberly M, Shah, Rachit, Strom, Alex, Kumarapperuma, Sidath, Zhou, Andrew, Wagner, Carston R, Finzel, Barry C

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Design, Synthesis, and Characterization of Sulfamide and Sulfamate Nucleotidomimetic Inhibitors of hHint1 von Shah, Rachit, Strom, Alexander, Zhou, Andrew, Maize, Kimberly M, Finzel, Barry C, Wagner, Carston R

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Structure-Based Optimization of Pyridoxal 5′-Phosphate-Dependent Transaminase Enzyme (BioA) Inhibitors that Target Biotin Biosynthesis in Mycobacterium tuberculosis von Liu, Feng, Dawadi, Surendra, Maize, Kimberly M, Dai, Ran, Park, Sae Woong, Schnappinger, Dirk, Finzel, Barry C, Aldrich, Courtney C

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Caught before Released: Structural Mapping of the Reaction Trajectory for the Sofosbuvir Activating Enzyme, Human Histidine Triad Nucleotide Binding Protein 1 (hHint1) von Shah, Rachit, Maize, Kimberly M, Zhou, Xin, Finzel, Barry C, Wagner, Carston R

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Structure and Functional Characterization of Human Histidine Triad Nucleotide-Binding Protein 1 Mutations Associated with Inherited Axonal Neuropathy with Neuromyotonia von Shah, Rachit M., Maize, Kimberly M., West, Harrison T., Strom, Alexander M., Finzel, Barry C., Wagner, Carston R.

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Inhibition by divalent metal ions of human histidine triad nucleotide binding protein1 (hHint1), a regulator of opioid analgesia and neuropathic pain von Shah, Rachit, Chou, Tsui-Fen, Maize, Kimberly M., Strom, Alexander, Finzel, Barry C., Wagner, Carston R.

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Errors in Crystal structure of HINT from Helicobacter pylori von Maize, Kimberly M.

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Structural characterization of human histidine triad nucleotide‐binding protein 2, a member of the histidine triad superfamily von Maize, Kimberly M, Wagner, Carston R, Finzel, Barry C

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Rational Optimization of Mechanism-Based Inhibitors through Determination of the Microscopic Rate Constants of Inactivation von Eiden, Carter G, Maize, Kimberly M, Finzel, Barry C, Lipscomb, John D, Aldrich, Courtney C

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Ligand-induced expansion of the S1′ site in the anthrax toxin lethal factor von Maize, Kimberly M., Kurbanov, Elbek K., Johnson, Rodney L., Amin, Elizabeth Ambrose, Finzel, Barry C.

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Anthrax toxin lethal factor domain 3 is highly mobile and responsive to ligand binding von Maize, Kimberly M., Kurbanov, Elbek K., De La Mora-Rey, Teresa, Geders, Todd W., Hwang, Dong-Jin, Walters, Michael A., Johnson, Rodney L., Amin, Elizabeth A., Finzel, Barry C.

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Probing the S2′ Subsite of the Anthrax Toxin Lethal Factor Using Novel N‑Alkylated Hydroxamates von Kurbanov, Elbek K, Chiu, Ting-Lan, Solberg, Jonathan, Francis, Subhashree, Maize, Kimberly M, Fernandez, Jenna, Johnson, Rodney L, Hawkinson, Jon E, Walters, Michael A, Finzel, Barry C, Amin, Elizabeth Ambrose

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Identification of Novel Anthrax Toxin Countermeasures Using In Silico Methods von Chiu, Ting-Lan, Maize, Kimberly M., Amin, Elizabeth A.

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Probing the S2;#8242; Subsite of the Anthrax Toxin Lethal Factor Using Novel N-Alkylated Hydroxamates von Kurbanov, Elbek K., Chiu, Ting-Lan, Solberg, Jonathan, Francis, Subhashree, Maize, Kimberly M., Fernandez, Jenna, Johnson, Rodney L., Hawkinson, Jon E., Walters, Michael A., Finzel, Barry C., Amin, Elizabeth Ambrose

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