Search Results - "Robertus, Jon D"
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The Cobalamin-Independent Methionine Synthase Enzyme Captured in a Substrate-Induced Closed Conformation
Published in Journal of molecular biology (27-02-2015)“…The cobalamin-independent methionine synthase enzyme catalyzes a challenging reaction: the direct transfer of a methyl from…”
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Structure-based design of ricin inhibitors
Published in Toxins (01-10-2011)“…Ricin is a potent cytotoxin easily purified in large quantities. It presents a significant public health concern due to its potential use as a bioterrorism…”
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Sulfur incorporation generally improves Ricin inhibition in pterin-appended glycine-phenylalanine dipeptide mimics
Published in Bioorganic & medicinal chemistry letters (15-12-2013)“…Several 7-aminoamido-pterins were synthesized to evaluate the electronic and biochemical subtleties observed in the ‘linker space’ when…”
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4
The Structure of the Minimal Relaxase Domain of MobA at 2.1 Å Resolution
Published in Journal of molecular biology (09-02-2007)“…The plasmid R1162 encodes proteins that enable its conjugative mobilization between bacterial cells. It can transfer between many different species and is one…”
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Crystal Structure of the Engineered Neutralizing Antibody M18 Complexed to Domain 4 of the Anthrax Protective Antigen
Published in Journal of molecular biology (03-04-2009)“…The virulence of Bacillus anthracis is critically dependent on the cytotoxic components of the anthrax toxin, lethal factor (LF) and edema factor (EF). LF and…”
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6
Kinetic analysis of site-directed mutants of methionine synthase from Candida albicans
Published in Biochemical and biophysical research communications (15-05-2009)“…Fungal methionine synthase catalyzes the transfer of a methyl group from 5-methyl-tetrahydrofolate to homocysteine to create methionine. The enzyme, called…”
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Structure-Based Design and Characterization of Novel Platforms for Ricin and Shiga Toxin Inhibition
Published in Journal of medicinal chemistry (03-01-2002)“…Ribosome inhibiting proteins, RIPs, are a widespread family of toxic enzymes. Ricin is a plant toxin used as a poison and biological warfare agent; shiga toxin…”
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Kinetic Properties of Chitinase-1 from the Fungal Pathogen Coccidioides immitis
Published in Biochemistry (Easton) (27-02-2001)“…The endochitinase from Coccidioides immitis (CiX1) is a member of the class 18 chitinase family. Here we show the enzyme functions by a retaining catalytic…”
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Structural Analysis of a Fungal Methionine Synthase with Substrates and Inhibitors
Published in Journal of molecular biology (17-04-2014)“…The cobalamin-independent methionine synthase from Candida albicans, known as Met6p, is a 90-kDa enzyme that consists of two (βα)8 barrels. The active site is…”
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X-ray structures of NS1 effector domain mutants
Published in Archives of biochemistry and biophysics (15-02-2010)“…The influenza A virus nonstructural protein NS1 is a multifunctional dimeric protein that acts as a potent inhibitor of the host cellular antiviral state. The…”
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Synthesis of 2-substituted 9-oxa-guanines {5-aminooxazolo[5,4-d]pyrimidin-7(6H)-ones} and 9-oxa-2-thio-xanthines {5-mercaptooxazolo[5,4-d]pyrimidin-7(6H)-ones}
Published in Beilstein journal of organic chemistry (25-07-2008)“…Oxazolo[5,4-d]pyrimidines can be considered as 9-oxa-purine analogs of naturally occurring nucleic acid bases. Interest in this ring system has increased due…”
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Yeast flavin-containing monooxygenase generates oxidizing equivalents that control protein folding in the endoplasmic reticulum
Published in Proceedings of the National Academy of Sciences - PNAS (16-03-1999)“…The flavin-containing monooxygenase from yeast (yFMO) catalyzes the O(2)- and NADPH-dependent oxidations of biological thiols, including oxidation of…”
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Teaching through Research: Alignment of Core Chemistry Competencies and Skills within a Multidisciplinary Research Framework
Published in Journal of chemical education (13-02-2018)“…Innovative models of teaching through research have broken the long-held paradigm that core chemistry competencies must be taught with predictable, scripted…”
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Structure of NS1A effector domain from the influenza A/Udorn/72 virus
Published in Acta crystallographica. Section D, Biological crystallography. (01-01-2009)“…The nonstructural protein NS1A from influenza virus is a multifunctional virulence factor and a potent inhibitor of host immunity. It has two functional…”
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Identification of small-molecule inhibitors of ricin and shiga toxin using a cell-based high-throughput screen
Published in Toxicon (Oxford) (01-09-2010)“…The Category B agents, ricin and shiga toxin (Stx), are RNA N-glycosidases that target a highly conserved adenine residue within the sarcin-ricin loop of…”
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The X-ray structure of ricin A chain with a novel inhibitor
Published in Archives of biochemistry and biophysics (01-03-2009)“…Ricin is a potent heterodimeric cytotoxin; the B chain binds eucaryotic cell surfaces aiding uptake and the A chain, RTA, reaches the cytoplasm where it…”
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pH-induced structural changes regulate histidine decarboxylase activity in Lactobacillus 30a
Published in Journal of molecular biology (02-03-2001)“…Histidine decarboxylase (HDC) from Lactobacillus 30a produces histamine that is essential to counter waste acids, and to optimize cell growth. The HDC trimer…”
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Yeast Flavin-Containing Monooxygenase Is Induced by the Unfolded Protein Response
Published in Proceedings of the National Academy of Sciences - PNAS (04-01-2000)“…Flavin-containing monooxygenase from yeast (yFMO) carries out the O2- and NADPH-dependent oxidation of biological thiols, including oxidizing glutathione to…”
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Synthesis and evaluation of quinoxaline derivatives as potential influenza NS1A protein inhibitors
Published in Bioorganic & medicinal chemistry letters (15-05-2011)“…A library of quinoxaline derivatives were prepared to target non-structural protein 1 of influenza A (NS1A) as a means to develop anti-influenza drug leads. An…”
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Peptide-Conjugated Pterins as Inhibitors of Ricin Toxin A
Published in Journal of medicinal chemistry (10-01-2013)“…Several 7-peptide-substituted pterins were synthesized and tested as competitive active-site inhibitors of ricin toxin A (RTA). Focus began on dipeptide…”
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