(Q49962224)

English

Cyclopropane-1,2-dicarboxylic acids as new tools for the biophysical investigation of O-acetylserine sulfhydrylases by fluorimetric methods and saturation transfer difference (STD) NMR.

scientific article published on 31 August 2016

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23 February 2018

http://europepmc.org/abstract/MED/27578398

Cyclopropane-1,2-dicarboxylic acids as new tools for the biophysical investigation of O-acetylserine sulfhydrylases by fluorimetric methods and saturation transfer difference (STD) NMR. (English)

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Europe PubMed Central

23 February 2018

http://europepmc.org/abstract/MED/27578398

Stefano Bettati

9

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23 February 2018

http://europepmc.org/abstract/MED/27578398

Andrea Mozzarelli

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http://europepmc.org/abstract/MED/27578398

Joana Magalhães

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Joana Magalhães

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Barbara Campanini

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Barbara Campanini

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Thelma A Pertinhez

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Thelma A Pertinhez

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Roberto Benoni

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http://europepmc.org/abstract/MED/27578398

Gabriele Costantino

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Gabriele Costantino

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Chiara Pecchini

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Chiara Pecchini

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http://europepmc.org/abstract/MED/27578398

Giannamaria Annunziato

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Giannamaria Annunziato

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Nina Franko

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Marco Pieroni

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Agostino Bruno

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publication date

31 August 2016

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Journal of Enzyme Inhibition and Medicinal Chemistry

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31

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sup4

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78-87

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Redefining reductive sulfate assimilation in higher plants: a role for APS reductase, a new member of the thioredoxin superfamily?

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L-Cysteine is required for induced antibiotic resistance in actively swarming Salmonella enterica serovar Typhimurium

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Cysteine biosynthesis, oxidative stress and antibiotic resistance in Salmonella typhimurium

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Gene expression patterns during swarming in Salmonella typhimurium: genes specific to surface growth and putative new motility and pathogenicity genes.

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Synthesis, biological evaluation, and structure-activity relationships of N-benzoyl-2-hydroxybenzamides as agents active against P. falciparum (K1 strain), Trypanosomes, and Leishmania

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CysK Plays a Role in Biofilm Formation and Colonization by Vibrio fischeri

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Inhibitors of the sulfur assimilation pathway in bacterial pathogens as enhancers of antibiotic therapy.

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Discovery of novel inhibitors targeting the Mycobacterium tuberculosis O-acetylserine sulfhydrylase (CysK1) using virtual high-throughput screening

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A two-step process controls the formation of the bienzyme cysteine synthase complex

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Design of O -Acetylserine Sulfhydrylase Inhibitors by Mimicking Nature

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Isozyme-specific ligands for O-acetylserine sulfhydrylase, a novel antibiotic target

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Design and synthesis of trans-2-substituted-cyclopropane-1-carboxylic acids as the first non-natural small molecule inhibitors of O-acetylserine sulfhydrylase

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Computational Insights into the Mechanism of Inhibition of OASS-A by a Small Molecule Inhibitor

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Rational Design, Synthesis, and Preliminary Structure-Activity Relationships of α-Substituted-2-Phenylcyclopropane Carboxylic Acids as Inhibitors of Salmonella typhimurium O-Acetylserine Sulfhydrylase.

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Interaction of serine acetyltransferase with O-acetylserine sulfhydrylase active site: evidence from fluorescence spectroscopy

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Permeability Barrier of Gram-Negative Cell Envelopes and Approaches To Bypass It.

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Product binding to the alpha-carboxyl subsite results in a conformational change at the active site of O-acetylserine sulfhydrylase-A: evidence from fluorescence spectroscopy.

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Identifiers

10.1080/14756366.2016.1218486

1 reference

Europe PubMed Central

23 February 2018

http://europepmc.org/abstract/MED/27578398

1 reference

Europe PubMed Central

23 February 2018

http://europepmc.org/abstract/MED/27578398

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