Selenocysteine Confers Resistance to Inactivation by Oxidation in Thioredoxin Reductase: Comparison of Selenium and Sulfur Enzymes von Snider, Gregg W, Ruggles, Erik, Khan, Nadeem, Hondal, Robert J

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Differing views of the role of selenium in thioredoxin reductase von Hondal, Robert J., Ruggles, Erik L.

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Can dimedone be used to study selenoproteins? An investigation into the reactivity of dimedone toward oxidized forms of selenocysteine von Payne, N. Connor, Barber, Drew R., Ruggles, Erik L., Hondal, Robert J.

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Comparison of the redox chemistry of sulfur- and selenium-containing analogs of uracil von Payne, N. Connor, Geissler, Andrew, Button, Aileen, Sasuclark, Alexandru R., Schroll, Alayne L., Ruggles, Erik L., Gladyshev, Vadim N., Hondal, Robert J.

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Why Is Mammalian Thioredoxin Reductase 1 So Dependent upon the Use of Selenium? von Lothrop, Adam P, Snider, Gregg W, Ruggles, Erik L, Hondal, Robert J

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No Selenium Required: Reactions Catalyzed by Mammalian Thioredoxin Reductase That Are Independent of a Selenocysteine Residue von Lothrop, Adam P, Ruggles, Erik L, Hondal, Robert J

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Ergothioneine in a peptide: Substitution of histidine with 2‐thiohistidine in bioactive peptides von Jenny, Kaelyn A., Ruggles, Erik L., Liptak, Matthew D., Masterson, Douglas S., Hondal, Robert J.

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Selenium as an Electron Acceptor during the Catalytic Mechanism of Thioredoxin Reductase von Lothrop, Adam P, Snider, Gregg W, Ruggles, Erik L, Patel, Amar S, Lees, Watson J, Hondal, Robert J

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A Mechanistic Investigation of the C‑Terminal Redox Motif of Thioredoxin Reductase from Plasmodium falciparum von Snider, Gregg W, Dustin, Christopher M, Ruggles, Erik L, Hondal, Robert J

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Synthesis, redox properties, and conformational analysis of vicinal disulfide ring mimics von Ruggles, Erik L., Deker, P. Bruce, Hondal, Robert J.

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Methaneseleninic Acid Is a Substrate for Truncated Mammalian Thioredoxin Reductase: Implications for the Catalytic Mechanism and Redox Signaling von Snider, Gregg, Grout, Leah, Ruggles, Erik L, Hondal, Robert J

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Removal of the 5-nitro-2-pyridine-sulfenyl protecting group from selenocysteine and cysteine by ascorbolysis von Ste. Marie, Emma J., Ruggles, Erik L., Hondal, Robert J.

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Enantioselective Radical Addition to N-Acyl Hydrazones Mediated by Chiral Lewis Acids von Friestad, Gregory K., Shen, Yuehai, Ruggles, Erik L.

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Facile removal of 4‐methoxybenzyl protecting group from selenocysteine von Jenny, Kaelyn A., Ste.Marie, Emma J., Mose, Gracyn, Ruggles, Erik L., Hondal, Robert J.

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Compensating for the Absence of Selenocysteine in High-Molecular Weight Thioredoxin Reductases: The Electrophilic Activation Hypothesis von Lothrop, Adam P, Snider, Gregg W, Flemer, Stevenson, Ruggles, Erik L, Davidson, Ronald S, Lamb, Audrey L, Hondal, Robert J

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Conformational analysis of oxidized peptide fragments of the C-terminal redox center in thioredoxin reductases by NMR spectroscopy von Ruggles, Erik L., Deker, P. Bruce, Hondal, Robert J.

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A viable synthesis of N-methyl cysteine von Ruggles, Erik L., Flemer Jr, Stevenson, Hondal, Robert J.

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Synthesis and properties of disulfide-bond containing eight-membered rings von Ruggles, Erik L., Hondal, Robert J.

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Bleach/Acetic Acid-Promoted Chlorinative Ring Expansion of [2.2.1]- and [2.2.2]-Bicycles von Ruggles, Erik L, Maleczka, Robert E

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Conformational analysis of oxidized peptide fragments of the C-terminal redox center in thioredoxin reductases by NMR spectroscopy: CONFORMATIONAL ANALYSIS OF THE OXIDIZED TAIL IN... von Ruggles, Erik L., Deker, P. Bruce, Hondal, Robert J.

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