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Global profiling of lysine reactivity and ligandability in the human proteome

Nature chemistry, 2017-12, Vol.9 (12), p.1181-1190

2017

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A proteome-wide atlas of lysine-reactive chemistry

Nature chemistry, 2021-11, Vol.13 (11), p.1081-1092

2021

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Light-Activatable, 2,5-Disubstituted Tetrazoles for the Proteome-wide Profiling of Aspartates and Glutamates in Living Bacteria

ACS central science, 2020-04, Vol.6 (4), p.546-554

2020

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Synthesis and fluorescence characteristics of ATP-based FRET probes

Organic & biomolecular chemistry, 2013-12, Vol.11 (48), p.8298-8305

2013

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Reversible protein inhibitors kept on target

Nature (London), 2022-03, Vol.603 (7902), p.583-584

Hacker, Stephan M

2022

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Promising reversible protein inhibitors kept on target

Nature (London), 2022-03, Vol.603 (7902), p.583-584

Hacker, Stephan M.

2022

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Selective Monitoring of the Enzymatic Activity of the Tumor Suppressor Fhit

Angewandte Chemie (International ed.), 2014-09, Vol.53 (38), p.10247-10250

International ed. in English, 2014

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HSP-90/kinase complexes are stabilized by the large PPIase FKB-6

Scientific reports, 2021-06, Vol.11 (1), p.12347-12347, Article 12347

2021

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Small‐Molecule Inhibitors of the Tumor Suppressor Fhit

Chembiochem : a European journal of chemical biology, 2017-09, Vol.18 (17), p.1707-1711

2017

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Broad Spectrum Antibiotic Xanthocillin X Effectively Kills Acinetobacter baumannii via Dysregulation of Heme Biosynthesis

ACS central science, 2021-03, Vol.7 (3), p.488-498

2021

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Competitive profiling of ligandable cysteines in Staphylococcus aureus with an organogold compound

Chemical communications (Cambridge, England), 2022-05, Vol.58 (36), p.5526-5529

2022

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Isotopically Labeled Desthiobiotin Azide (isoDTB) Tags Enable Global Profiling of the Bacterial Cysteinome

Angewandte Chemie International Edition, 2020-02, Vol.59 (7), p.2829-2836

International ed. in English, 2020

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Chemical biology in drug discovery

Biological chemistry, 2022-03, Vol.403 (4), p.361-362

2022

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Activity‐Based Protein Profiling – Celebrating the Groundbreaking Contributions of Benjamin Cravatt

Israel journal of chemistry, 2023-03, Vol.63 (3-4), p.n/a

2023

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Repurposing human kinase inhibitors to create an antibiotic active against drug-resistant Staphylococcus aureus, persisters and biofilms

Nature chemistry, 2020-02, Vol.12 (2), p.145-158

2020

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Degrasyn exhibits antibiotic activity against multi-resistant Staphylococcus aureus by modifying several essential cysteines

Chemical communications (Cambridge, England), 2020-03, Vol.56 (19), p.2929-2932

2020

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Neocarzilin A Is a Potent Inhibitor of Cancer Cell Motility Targeting VAT‑1 Controlled Pathways

ACS central science, 2019-07, Vol.5 (7), p.1170-1178

2019

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A tailored phosphoaspartate probe unravels CprR as a response regulator in Pseudomonas aeruginosa interkingdom signaling

Chemical science (Cambridge), 2021-02, Vol.12 (13), p.4763-4770

2021

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Eukaryotic catecholamine hormones influence the chemotactic control of Vibrio campbellii by binding to the coupling protein CheW

Proceedings of the National Academy of Sciences - PNAS, 2022-03, Vol.119 (10), p.e2118227119-e2118227119

2022

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Eine chemisch‐proteomische Strategie identifiziert Inhibitoren der Lipoat‐Wiederverwertung in Bakterien und Parasiten

Angewandte Chemie, 2023-08, Vol.135 (31)

2023

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Synthesis and Stability of Phosphate Modified ATP Analogues

Journal of organic chemistry, 2012-11, Vol.77 (22), p.10450-10454

2012

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A chemical probe unravels the reactive proteome of health-associated catechols

Chemical science (Cambridge), 2023-08, Vol.14 (32), p.8635-8643

2023

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Phosphate-Modified Nucleotides for Monitoring Enzyme Activity

Topics in current chemistry (2016), 2017-04, Vol.375 (2), p.28, Article 28

2017

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A Chemical Proteomic Strategy Reveals Inhibitors of Lipoate Salvage in Bacteria and Parasites

Angewandte Chemie International Edition, 2023-08, Vol.62 (31), p.e202304533-n/a

International ed. in English, 2023

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Global profiling of lysine reactivity and ligandability in the human proteome

A proteome-wide atlas of lysine-reactive chemistry

Light-Activatable, 2,5-Disubstituted Tetrazoles for the Proteome-wide Profiling of Aspartates and Glutamates in Living Bacteria

Synthesis and fluorescence characteristics of ATP-based FRET probes

Reversible protein inhibitors kept on target

Promising reversible protein inhibitors kept on target

Selective Monitoring of the Enzymatic Activity of the Tumor Suppressor Fhit

HSP-90/kinase complexes are stabilized by the large PPIase FKB-6

Small‐Molecule Inhibitors of the Tumor Suppressor Fhit

Broad Spectrum Antibiotic Xanthocillin X Effectively Kills Acinetobacter baumannii via Dysregulation of Heme Biosynthesis

Competitive profiling of ligandable cysteines in Staphylococcus aureus with an organogold compound

Isotopically Labeled Desthiobiotin Azide (isoDTB) Tags Enable Global Profiling of the Bacterial Cysteinome

SDR enzymes oxidize specific lipidic alkynylcarbinols into cytotoxic protein-reactive species

Chemical biology in drug discovery

Activity‐Based Protein Profiling – Celebrating the Groundbreaking Contributions of Benjamin Cravatt

Repurposing human kinase inhibitors to create an antibiotic active against drug-resistant Staphylococcus aureus, persisters and biofilms

Degrasyn exhibits antibiotic activity against multi-resistant Staphylococcus aureus by modifying several essential cysteines

Neocarzilin A Is a Potent Inhibitor of Cancer Cell Motility Targeting VAT‑1 Controlled Pathways

A tailored phosphoaspartate probe unravels CprR as a response regulator in Pseudomonas aeruginosa interkingdom signaling

Eukaryotic catecholamine hormones influence the chemotactic control of Vibrio campbellii by binding to the coupling protein CheW

Eine chemisch‐proteomische Strategie identifiziert Inhibitoren der Lipoat‐Wiederverwertung in Bakterien und Parasiten

Synthesis and Stability of Phosphate Modified ATP Analogues

A chemical probe unravels the reactive proteome of health-associated catechols

Phosphate-Modified Nucleotides for Monitoring Enzyme Activity

A Chemical Proteomic Strategy Reveals Inhibitors of Lipoate Salvage in Bacteria and Parasites

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