Sylvie Garneau-Tsodikova
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French Canadian chemist, academic
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Chemistry
Why Is Sylvie Garneau-Tsodikova Influential?
(Suggest an Edit or Addition)According to Wikipedia, Sylvie Garneau-Tsodikova is a French Canadian chemist who is a Professor and Associate Vice President for Research at the University of Kentucky. Her research considers the development of new molecules that can combat bacterial resistance.
Sylvie Garneau-Tsodikova's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Protein posttranslational modifications: the chemistry of proteome diversifications. (2005) (1218)
- Nature's inventory of halogenation catalysts: oxidative strategies predominate. (2006) (401)
- Biological formation of pyrroles: nature's logic and enzymatic machinery. (2006) (351)
- Mechanisms of Resistance to Aminoglycoside Antibiotics: Overview and Perspectives. (2016) (295)
- Two-peptide bacteriocins produced by lactic acid bacteria. (2002) (267)
- Automated genome mining for natural products (2009) (224)
- Robust in vitro activity of RebF and RebH, a two-component reductase/halogenase, generating 7-chlorotryptophan during rebeccamycin biosynthesis. (2005) (206)
- The Future of Aminoglycosides: The End or Renaissance? (2010) (176)
- Dichlorination of a pyrrolyl-S-carrier protein by FADH2-dependent halogenase PltA during pyoluteorin biosynthesis. (2005) (154)
- Isolation and Characterization of Carnocyclin A, a Novel Circular Bacteriocin Produced by Carnobacterium maltaromaticum UAL307 (2008) (154)
- Facile detection of acyl and peptidyl intermediates on thiotemplate carrier domains via phosphopantetheinyl elimination reactions during tandem mass spectrometry. (2006) (138)
- Unusual regioversatility of acetyltransferase Eis, a cause of drug resistance in XDR-TB (2011) (110)
- Strategies to overcome the action of aminoglycoside-modifying enzymes for treating resistant bacterial infections. (2013) (95)
- Characterization of the formation of the pyrrole moiety during clorobiocin and coumermycin A1 biosynthesis. (2005) (77)
- 6''-Thioether tobramycin analogues: towards selective targeting of bacterial membranes. (2012) (76)
- Exploring the Substrate Promiscuity of Drug‐Modifying Enzymes for the Chemoenzymatic Generation of N‐Acylated Aminoglycosides (2009) (69)
- Synthesis and investigation of novel benzimidazole derivatives as antifungal agents. (2016) (69)
- A combination approach to treating fungal infections (2015) (68)
- Enzymatic Generation of the Antimetabolite γ,γ-Dichloroaminobutyrate by NRPS and Mononuclear Iron Halogenase Action in a Streptomycete (2006) (61)
- Activity screening of carrier domains within nonribosomal peptide synthetases using complex substrate mixtures and large molecule mass spectrometry. (2006) (59)
- Protein assembly line components in prodigiosin biosynthesis: characterization of PigA,G,H,I,J. (2006) (57)
- New trends in the use of aminoglycosides (2014) (56)
- Inhibition of glioma progression by a newly discovered CD38 inhibitor (2015) (55)
- A nonradioactive high-throughput assay for screening and characterization of adenylation domains for nonribosomal peptide combinatorial biosynthesis. (2009) (55)
- Identification and Characterization of Inhibitors of the Aminoglycoside Resistance Acetyltransferase Eis from Mycobacterium tuberculosis (2012) (53)
- Recent developments in bisintercalator natural products (2010) (51)
- Chemically related 4,5-linked aminoglycoside antibiotics drive subunit rotation in opposite directions (2015) (51)
- Amphiphilic Tobramycin Analogues as Antibacterial and Antifungal Agents (2015) (51)
- Unexpected N-acetylation of capreomycin by mycobacterial Eis enzymes. (2013) (47)
- Chemical and Structural Insights into the Regioversatility of the Aminoglycoside Acetyltransferase Eis (2013) (47)
- Synthesis and Bioactivities of Kanamycin B-Derived Cationic Amphiphiles. (2015) (45)
- Alkylated Piperazines and Piperazine-Azole Hybrids as Antifungal Agents. (2018) (45)
- Structural basis for backbone N-methylation by an interrupted adenylation domain (2018) (45)
- A novel hybrid of 6-chlorotacrine and metal–amyloid-β modulator for inhibition of acetylcholinesterase and metal-induced amyloid-β aggregation (2013) (45)
- Aminoglycoside multiacetylating activity of the enhanced intracellular survival protein from Mycobacterium smegmatis and its inhibition. (2012) (44)
- Resistance in tuberculosis: what do we know and where can we go? (2013) (44)
- A comprehensive overview of the medicinal chemistry of antifungal drugs: perspectives and promise. (2020) (44)
- Interrupted adenylation domains: unique bifunctional enzymes involved in nonribosomal peptide biosynthesis. (2015) (42)
- A review of patents (2011-2015) towards combating resistance to and toxicity of aminoglycosides. (2016) (41)
- Adenylation and S-methylation of cysteine by the bifunctional enzyme TioN in thiocoraline biosynthesis. (2014) (41)
- Novel alkylated azoles as potent antifungals. (2017) (41)
- Synthesis of mono- and disaccharide analogs of moenomycin and lipid II for inhibition of transglycosylase activity of penicillin-binding protein 1b. (2004) (41)
- A complex game of hide and seek: the search for new antifungals. (2016) (40)
- Effects of Altering Aminoglycoside Structures on Bacterial Resistance Enzyme Activities (2011) (40)
- Inhibition of Aminoglycoside Acetyltransferase Resistance Enzymes by Metal Salts (2015) (38)
- High throughput LSPR and SERS analysis of aminoglycoside antibiotics. (2016) (37)
- Comprehensive review of chemical strategies for the preparation of new aminoglycosides and their biological activities. (2018) (37)
- The structural basis for substrate versatility of chloramphenicol acetyltransferase CATI (2012) (36)
- Repurposing antipsychotic drugs into antifungal agents: Synergistic combinations of azoles and bromperidol derivatives in the treatment of various fungal infections. (2017) (36)
- Protein kinase inhibitors in the treatment of pulmonary fibrosis. (2008) (35)
- Hybrid nonribosomal peptide-polyketide interfaces in epothilone biosynthesis: minimal requirements at N and C termini of EpoB for elongation. (2004) (33)
- Zinc transporters YbtX and ZnuABC are required for the virulence of Yersinia pestis in bubonic and pneumonic plague in mice. (2017) (32)
- Amyloid-β probes: Review of structure–activity and brain-kinetics relationships (2013) (31)
- Antimycobacterial activity of DNA intercalator inhibitors of Mycobacterium tuberculosis primase DnaG (2014) (30)
- Synthesis and evaluation of hetero- and homodimers of ribosome-targeting antibiotics: antimicrobial activity, in vitro inhibition of translation, and drug resistance. (2013) (30)
- Biochemical and structural analysis of aminoglycoside acetyltransferase Eis from Anabaena variabilis. (2012) (30)
- Tacrine-mefenamic acid hybrids for inhibition of acetylcholinesterase (2011) (30)
- Crystal structure of halogenase PltA from the pyoluteorin biosynthetic pathway. (2015) (28)
- Identification of Ebsulfur Analogues with Broad‐Spectrum Antifungal Activity (2016) (28)
- Sulfonamide-Based Inhibitors of Aminoglycoside Acetyltransferase Eis Abolish Resistance to Kanamycin in Mycobacterium tuberculosis. (2016) (28)
- Rapid synthesis, RNA binding, and antibacterial screening of a peptidic-aminosugar (PA) library. (2015) (28)
- Characterization of TioF, a tryptophan 2,3-dioxygenase involved in 3-hydroxyquinaldic acid formation during thiocoraline biosynthesis. (2008) (28)
- Assessment of 6'- and 6'''-N-acylation of aminoglycosides as a strategy to overcome bacterial resistance. (2011) (28)
- Combating Enhanced Intracellular Survival (Eis)-Mediated Kanamycin Resistance of Mycobacterium tuberculosis by Novel Pyrrolo[1,5-a]pyrazine-Based Eis Inhibitors. (2017) (28)
- Chemoenzymatic formation of novel aminocoumarin antibiotics by the enzymes CouN1 and CouN7. (2007) (27)
- Installation of the pyrrolyl-2-carboxyl pharmacophore by CouN1 and CouN7 in the late biosynthetic steps of the aminocoumarin antibiotics clorobiocin and coumermycin A1. (2006) (27)
- Importance of the MbtH-like protein TioT for production and activation of the thiocoraline adenylation domain of TioK (2012) (27)
- The Biosynthesis of Capuramycin-type Antibiotics (2015) (27)
- Potent Inhibitors of Acetyltransferase Eis Overcome Kanamycin Resistance in Mycobacterium tuberculosis. (2016) (27)
- Unusual substrate and halide versatility of phenolic halogenase PltM (2019) (26)
- Siderophore-mediated zinc acquisition enhances enterobacterial colonization of the inflamed gut (2020) (26)
- Biochemical and structural analysis of an Eis family aminoglycoside acetyltransferase from bacillus anthracis. (2015) (26)
- A Random Sequential Mechanism of Aminoglycoside Acetylation by Mycobacterium tuberculosis Eis Protein (2014) (25)
- Effects of structural modifications on the metal binding, anti-amyloid activity, and cholinesterase inhibitory activity of chalcones. (2015) (24)
- KtzJ-dependent serine activation and O-methylation by KtzH for kutznerides biosynthesis (2013) (23)
- Evaluation of Aminoglycoside and Carbapenem Resistance in a Collection of Drug-Resistant Pseudomonas aeruginosa Clinical Isolates. (2017) (23)
- Novel fluconazole derivatives with promising antifungal activity. (2017) (22)
- Dissecting the cosubstrate structure requirements of the Staphylococcus aureus aminoglycoside resistance enzyme ANT(4'). (2010) (22)
- Characterization of TioQ, a type II thioesterase from the thiocoraline biosynthetic cluster. (2011) (21)
- What are the drugs of the future? (2018) (21)
- Purification and Characterization of Brochocin A and Brochocin B(10-43), a Functional Fragment Generated by Heterologous Expression in Carnobacterium piscicola (2003) (21)
- Multifunctional Donepezil Analogues as Cholinesterase and BACE1 Inhibitors (2018) (20)
- Comparative Study of Eis-like Enzymes from Pathogenic and Nonpathogenic Bacteria. (2015) (19)
- A new scaffold of an old protein fold ensures binding to the bisintercalator thiocoraline. (2010) (19)
- Acetylation by Eis and Deacetylation by Rv1151c of Mycobacterium tuberculosis HupB: Biochemical and Structural Insight. (2018) (19)
- Glutamyl Adenylate Analogues Are Inhibitors of Glutamyl-tRNA Synthetase (1998) (19)
- Discovery and Optimization of Two Eis Inhibitor Families as Kanamycin Adjuvants against Drug-Resistant M. tuberculosis. (2016) (19)
- New Application of Neomycin B-Bisbenzimidazole Hybrids as Antifungal Agents. (2017) (19)
- Distorted Gold(I)-Phosphine Complexes as Antifungal Agents. (2019) (18)
- Arginine-linked neomycin B dimers: synthesis, rRNA binding, and resistance enzyme activity. (2016) (18)
- Potent 1,2,4-Triazino[5,6 b]indole-3-thioether Inhibitors of the Kanamycin Resistance Enzyme Eis from Mycobacterium tuberculosis. (2018) (18)
- Discovery of inhibitors of Bacillus anthracis primase DnaG. (2013) (18)
- hChAT: A Tool for the Chemoenzymatic Generation of Potential Acetyl/Butyrylcholinesterase Inhibitors (2009) (18)
- Development of ebsulfur analogues as potent antibacterials against methicillin-resistant Staphylococcus aureus. (2016) (18)
- Influence of Linker Length and Composition on Enzymatic Activity and Ribosomal Binding of Neomycin Dimers (2015) (18)
- Tobramycin Variants with Enhanced Ribosome‐Targeting Activity (2015) (18)
- Redesign of substrate specificity and identification of the aminoglycoside binding residues of Eis from Mycobacterium tuberculosis. (2013) (17)
- New trends in aminoglycosides use. (2014) (16)
- Derivatives of Ribosome-Inhibiting Antibiotic Chloramphenicol Inhibit the Biosynthesis of Bacterial Cell Wall. (2018) (15)
- Covalent CouN7 enzyme intermediate for acyl group shuttling in aminocoumarin biosynthesis. (2007) (15)
- Engineering Bifunctional Enzymes Capable of Adenylating and Selectively Methylating the Side Chain or Core of Amino Acids. (2018) (15)
- Cosubstrate Tolerance of the Aminoglycoside Resistance Enzyme Eis from Mycobacterium tuberculosis (2012) (15)
- Antimicrobial Activity, AME Resistance, and A-Site Binding Studies of Anthraquinone-Neomycin Conjugates. (2017) (14)
- Deciphering Nature's Intricate Way of N,S-Dimethylating l-Cysteine: Sequential Action of Two Bifunctional Adenylation Domains. (2017) (14)
- Discovery of Allosteric and Selective Inhibitors of Inorganic Pyrophosphatase from Mycobacterium tuberculosis. (2016) (14)
- Enzymatic generation of the antimetabolite gamma,gamma-dichloroaminobutyrate by NRPS and mononuclear iron halogenase action in a streptomycete. (2006) (14)
- Investigation of the role of linker moieties in bifunctional tacrine hybrids. (2013) (13)
- The Royal Institute of Chemistry of Great Britain and Ireland. Journal and Proceedings. Part V: 1944 (1944) (13)
- A biocatalytic approach to capuramycin analogues by exploiting a substrate permissive N-transacylase CapW. (2016) (13)
- Ask the experts: how to curb antibiotic resistance and plug the antibiotics gap? (2016) (13)
- Domain dissection and characterization of the aminoglycoside resistance enzyme ANT(3″)-Ii/AAC(6')-IId from Serratia marcescens. (2013) (13)
- Using MbtH‐Like Proteins to Alter the Substrate Profile of a Nonribosomal Peptide Adenylation Enzyme (2018) (13)
- Enzymatic Evidence for a Revised Congocidine Biosynthetic Pathway (2015) (12)
- Redesign of cosubstrate specificity and identification of important residues for substrate binding to hChAT. (2010) (12)
- Protein farnesyltransferase inhibitors interfere with farnesyl diphosphate binding by rubber transferase. (2003) (12)
- Expanding Substrate Promiscuity by Engineering a Novel Adenylating‐Methylating NRPS Bifunctional Enzyme (2016) (11)
- Yersiniabactin contributes to overcoming zinc restriction during Yersinia pestis infection of mammalian and insect hosts (2021) (11)
- Bis(N-amidinohydrazones) and N-(amidino)-N'-aryl-bishydrazones: New classes of antibacterial/antifungal agents. (2017) (10)
- Expanding Aminoglycoside Resistance Enzyme Regiospecificity by Mutation and Truncation. (2016) (10)
- Synergistic combinations of azoles and antihistamines against Candida species in vitro. (2018) (10)
- N,N'-diaryl-bishydrazones in a biphenyl platform: Broad spectrum antifungal agents. (2019) (9)
- Structure-Guided Optimization of Inhibitors of Acetyltransferase Eis from Mycobacterium tuberculosis. (2020) (9)
- Differential Effects of Linkers on the Activity of Amphiphilic Tobramycin Antifungals (2018) (9)
- Combining Chalcones with Donepezil to Inhibit Both Cholinesterases and Aβ Fibril Assembly (2019) (8)
- Synthesis, antimicrobial activity, attenuation of aminoglycoside resistance in MRSA, and ribosomal A-site binding of pyrene-neomycin conjugates. (2019) (8)
- Porphyromonas gingivalis: where do we stand in our battle against this oral pathogen? (2021) (8)
- Synthesis and Biological Activity of Mono- and Di-N-acylated Aminoglycosides. (2015) (8)
- Activation and Loading of the Starter Unit during Thiocoraline Biosynthesis. (2017) (8)
- Tryptophan scanning mutagenesis as a way to mimic the compound-bound state and probe the selectivity of allosteric inhibitors in cells† (2020) (8)
- Cover Picture: Exploring the Substrate Promiscuity of Drug-Modifying Enzymes for the Chemoenzymatic Generation of N-Acylated Aminoglycosides (ChemBioChem 1/2010) (2009) (7)
- Novel zafirlukast derivatives exhibit selective antibacterial activity against Porphyromonas gingivalis. (2019) (7)
- What is medicinal chemistry? - Demystifying a rapidly evolving discipline! (2017) (7)
- Investigating the promiscuity of the chloramphenicol nitroreductase from Haemophilus influenzae towards the reduction of 4-nitrobenzene derivatives. (2019) (7)
- Targeting CD38 in the tumor microenvironment: A novel approach to treat glioma (2015) (7)
- Crystal structure of O-methyltransferase CalO6 from the calicheamicin biosynthetic pathway: a case of challenging structure determination at low resolution (2015) (7)
- Characterization of a Unique Interrupted Adenylation Domain That Can Catalyze Three Reactions. (2019) (6)
- Probing the Robustness of Inhibitors of Tuberculosis Aminoglycoside Resistance Enzyme Eis by Mutagenesis. (2019) (6)
- Interfering With DNA Decondensation as a Strategy Against Mycobacteria (2018) (6)
- Inhibition of Pseudomonas aeruginosa Alginate Synthesis by Ebselen Oxide and Its Analogues. (2021) (5)
- Antibiotic Resistance themed issue (2016) (5)
- Probing the limits of interrupted adenylation domains by engineering a trifunctional enzyme capable of adenylation, N-, and S-methylation. (2019) (4)
- Broad‐Spectrum Antifungal Agents: Fluorinated Aryl‐ and Heteroaryl‐Substituted Hydrazones (2020) (4)
- A thorough analysis and categorization of bacterial interrupted adenylation domains, including previously unidentified families (2020) (4)
- Unusual substrate and halide versatility of phenolic halogenase PltM (2019) (4)
- Second Generation of Zafirlukast Derivatives with Improved Activity against the Oral Pathogen Porphyromonas gingivalis. (2020) (4)
- Resisting resistance: gearing up for war. (2019) (4)
- Structure-based design of haloperidol analogues as inhibitors of acetyltransferase Eis from Mycobacterium tuberculosis to overcome kanamycin resistance. (2021) (4)
- Exact and user-friendly kinetic analysis of the two-step rapid equilibrium Michaelis-Menten mechanism. (2009) (4)
- Differential Effects of Structural Modifications on the Competition of Chalcones for the PIB Amyloid Imaging Ligand-Binding Site in Alzheimer's Disease Brain and Synthetic Aβ Fibrils. (2016) (3)
- Discovery of substituted benzyloxy-benzylamine inhibitors of acetyltransferase Eis and their anti-mycobacterial activity. (2022) (3)
- Unimodular Methylation by Adenylation-Thiolation Domains Containing an Embedded Methyltransferase. (2020) (3)
- Modified Aminoglycosides Bind Nucleic Acids in High-Molecular-Weight Complexes (2020) (3)
- Posttranslational Modification of Proteins (2010) (2)
- Myeloid arginase-1 controls excessive inflammation and modulates T cell responses in Pseudomonas aeruginosa pneumonia. (2020) (2)
- Special Series: Natural products at the core of drug discovery (2010) (2)
- The aminoglycoside multi-acetylating activity of the enhanced intracellular survival (Eis) protein from Mycobacterium smegmatis and its inhibition (2012) (2)
- Chapter 7:Emerging Targets in Anti-Tubercular Drug Design (2017) (2)
- Flipping the Switch "On" for Aminoglycoside-Resistance Enzymes: The Mechanism Is Finally Revealed! (2016) (2)
- Publisher Correction: Unusual substrate and halide versatility of phenolic halogenase PltM (2019) (1)
- Nucleoside triphosphate cosubstrates control the substrate profile and efficiency of aminoglycoside 3'-O-phosphotransferase type IIa. (2018) (1)
- Systemic fungal infections: A pharmacist/researcher perspective (2023) (1)
- Selective Inhibition of the Periodontal Pathogen Porphyromonas gingivalis by Third-Generation Zafirlukast Derivatives. (2022) (1)
- Innentitelbild: 6′′‐Thioether Tobramycin Analogues: Towards Selective Targeting of Bacterial Membranes (Angew. Chem. 23/2012) (2012) (1)
- Lessons learned in engineering interrupted adenylation domains when attempting to create trifunctional enzymes from three independent monofunctional ones (2020) (1)
- Concise Synthesis of Spergualin-Inspired Molecules With Broad-Spectrum Antibiotic Activity. (2015) (1)
- Discovery and Optimization of 6-(1-Substituted pyrrole-2-yl)-s-triazine Containing Compounds as Antibacterial Agents. (2022) (1)
- Making figures: are you taking the best approach to maximize visibility? (2018) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT1348 (2020) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT1347 (2020) (0)
- Nature′s Inventory of Halogenation Catalysts: Oxidative Strategies Predominate (2006) (0)
- Creating a Culture of Public Engagement and Promoting Global Health (2018) (0)
- SciCats: An Integrative Outreach Initiative to Enhance STEM Education in Our Community (2015) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with haloperidol (2021) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT416 (2019) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with a 1,2,4-triazino[5,6b]indole-3-thioether inhibitor analogue 39b (2018) (0)
- Bishydrazone-Based Antifungal Agents (2019) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT353 (2020) (0)
- Cover Picture: Chemical and Structural Insights into the Regioversatility of the Aminoglycoside Acetyltransferase Eis (ChemBioChem 16/2013) (2013) (0)
- Carbohydrates themed issue (2014) (0)
- Crystal structure of halogenase PltM L111Y mutant in complex with FAD (2019) (0)
- Eis Inhibitors (2019) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT384 (2020) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT388 (2020) (0)
- In Vitro Assays to Identify Antibiotics Targeting DNA Metabolism. (2017) (0)
- Aromatic hydrazides: A potential solution for Acinetobacter baumannii infections. (2023) (0)
- Isolation and Characterization of Carnocyclin A, a Novel Circular Bacteriocin Produced by Carnobacterium maltaromaticum UAL307 (cid:1) † (2008) (0)
- Crystal structure of Mycobacterium tuberculosis Eis in complex with coenzyme A and tobramycin (2013) (0)
- Substance use disorders: leading the road to recovery. (2020) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT379 (2020) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT368 (2020) (0)
- Structure of CATI in complex with chloramphenicol (2012) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with inhibitor SGT543 (2021) (0)
- pyoluteorin biosynthesis-dependent halogenase PltA during 2 Dichlorination of a pyrrolyl-S-carrier protein by FADH (2005) (0)
- Development of Single‐Stranded DNA Bisintercalating Inhibitors of Primase DnaG as Antibiotics (2021) (0)
- Crystal structure of halogenase PltM in complex with phloroglucinol and FAD (2019) (0)
- Stabilisation of spread monolayers of an amine‐functionalised biphenyl mesogen by association with a carboxymethyl cellulose salt (2000) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with inhibitor SGT1264 (2021) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT1358 (2020) (0)
- Biological Formation of Pyrroles: Nature′s Logic and Enzymatic Machinery (2006) (0)
- Cover Feature: Broad‐Spectrum Antifungal Agents: Fluorinated Aryl‐ and Heteroaryl‐Substituted Hydrazones (ChemMedChem 1/2021) (2020) (0)
- Crystal structure of methyltransferase CalO6 (2015) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT449 (2019) (0)
- Book Review of Asymmetric Organic Synthesis with Enzymes Asymmetric Organic Synthesis with Enzymes . Edited by Vicente Gotor (Universidad de Oviedo, Spain), Ignacio Alfonso (Universidad Jaume I, Castellón, Spain), and Eduardo García-Urdiales (EMBL-Biocomputing, Heidelberg, Germany). Wiley-VCH Verl (2008) (0)
- 4,5-linked aminoglycoside antibiotics regulate the bacterial ribosome by targeting dynamic conformational processes within intersubunit bridge B2 (2015) (0)
- Discovery and Mechanistic Analysis of Structurally Diverse Inhibitors of Acetyltransferase Eis among FDA-Approved Drugs. (2023) (0)
- Inside Cover: 6′′‐Thioether Tobramycin Analogues: Towards Selective Targeting of Bacterial Membranes (Angew. Chem. Int. Ed. 23/2012) (2012) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT392 (2020) (0)
- Structure of apo-CATI (2012) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with sulfonamide inhibitor 39 and coenzyme A (2017) (0)
- Crystal structure of halogenase PltM in complex with partially bound FAD (2019) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with inhibitor SGT572 (2021) (0)
- Crystal structure of halogenase PltA (2015) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT366 (2020) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT358 (2020) (0)
- Back Cover: Identification and Characterization of Inhibitors of the Aminoglycoside Resistance Acetyltransferase Eis from Mycobacterium tuberculosis (ChemMedChem 1/2012) (2012) (0)
- Inhibition of Fosfomycin Resistance Protein FosB from Gram-Positive Pathogens by Phosphonoformate. (2022) (0)
- Crystal structure of an adenylation domain interrupted by a methylation domain (AMA4) from nonribosomal peptide synthetase TioS (2018) (0)
- Publisher Correction: Unusual substrate and halide versatility of phenolic halogenase PltM (2019) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT1354 (2020) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with droperidol (2021) (0)
- Targeting thiol isomerase activity with zafirlukast to treat ovarian cancer from the bench to clinic (2023) (0)
- Inorganic pyrophosphatase from Mycobacterium tuberculosis in complex with inhibitor 1 and inorganic pyrophosphate (2016) (0)
- Crystal structure of halogenase PltM in complex with FAD (2019) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with inhibitor 11c and CoA (2016) (0)
- Crystal structure of TioX from Micromonospora sp. ML1 (2010) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with CoA and inhibitor 2k*: 1-(4-fluorophenyl)-2-[2-(4-methylphenyl)-2-oxoethyl]pyrrolo[1,2-a]pyrazin-2-ium (2017) (0)
- 2348 Lafora disease premature termination codons (PTCs) are likely candidates for suppression by aminoglycosides (2017) (0)
- Back Cover: Identification of Ebsulfur Analogues with Broad‐Spectrum Antifungal Activity (ChemMedChem 14/2016) (2016) (0)
- Crystal structure of halogenase PltM in complex with ethyl mercury and mercury (2019) (0)
- Inorganic pyrophosphatase from Mycobacterium tuberculosis in complex with inhibitor 6 and inorganic pyrophosphate (2016) (0)
- Everything Is Science: A Free City-Wide Science Festival (2020) (0)
- Crystal structure of acetyltransferase Eis from Mycobacterium tuberculosis in complex with a Lys-containing peptide (2018) (0)
- Crystal structure of halogenase PltM (2019) (0)
- Identification and Analysis of Small Molecule Inhibitors of FosB from Staphylococcus aureus (2023) (0)
- Preparation of ( A ) Tobramycin Monomer Building Blocks , ( B ) Clindamycin Monomer Building Block and of Clindamycin − Clindamycin Dimer 10 , and ( C ) Chloramphenicol Monomer Building Blocks (2013) (0)
- Editorial: natural products themed issue (2012) (0)
- Crystal structure of Eis from Mycobacterium tuberculosis in complex with inhibitor SGT335 (2019) (0)
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