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Inhibiting protein synthesis to treat malaria

Science (American Association for the Advancement of Science), 2022-06, Vol.376 (6597), p.1049-1050

Statsyuk, Alexander V

2022

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A Fragment-Based Method to Discover Irreversible Covalent Inhibitors of Cysteine Proteases

Journal of medicinal chemistry, 2014-06, Vol.57 (11), p.4969-4974

2014

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Let K-Ras activate its own inhibitor

Nature structural & molecular biology, 2018-06, Vol.25 (6), p.435

Statsyuk, Alexander V

2018

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Development of Activity-Based Probes for Ubiquitin and Ubiquitin-like Protein Signaling Pathways

Journal of the American Chemical Society, 2013-11, Vol.135 (45), p.16948-16962

2013

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An inhibitor of ubiquitin conjugation and aggresome formation

Chemical science (Cambridge), 2015-01, Vol.6 (9), p.5235-5245

2015

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Facile synthesis of covalent probes to capture enzymatic intermediates during E1 enzyme catalysis

Chemical communications (Cambridge, England), 2016-01, Vol.52 (12), p.2477-2480

2016

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Discovery of covalent enzyme inhibitors using virtual docking of covalent fragments

Bioorganic & medicinal chemistry letters, 2019-01, Vol.29 (1), p.36-39

2019

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Dissecting the Specificity of Adenosyl Sulfamate Inhibitors Targeting the Ubiquitin-Activating Enzyme

Structure (London), 2017-07, Vol.25 (7), p.1120-1129.e3

2017

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Covalent Tethering of Fragments For Covalent Probe Discovery

MedChemComm, 2016-04, Vol.7 (4), p.576-585

2016

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A Small Molecule That Switches a Ubiquitin Ligase From a Processive to a Distributive Enzymatic Mechanism

Journal of the American Chemical Society, 2015-10, Vol.137 (39), p.12442-12445

2015

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UbMES and UbFluor: Novel probes for ring-between-ring (RBR) E3 ubiquitin ligase PARKIN

The Journal of biological chemistry, 2017-10, Vol.292 (40), p.16539-16553

2017

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Mapping low-affinity/high-specificity peptide–protein interactions using ligand-footprinting mass spectrometry

Proceedings of the National Academy of Sciences - PNAS, 2019-10, Vol.116 (42), p.21001-21011

2019

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Catalytically Important Residues of E6AP Ubiquitin Ligase Identified Using Acid-Cleavable Photo-Cross-Linkers

Biochemistry (Easton), 2015-07, Vol.54 (29), p.4411-4414

2015

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Covalent-Fragment Screening of BRD4 Identifies a Ligandable Site Orthogonal to the Acetyl-Lysine Binding Sites

ACS chemical biology, 2020-04, Vol.15 (4), p.1036-1049

2020

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Protein ubiquitination and formation of polyubiquitin chains without ATP, E1 and E2 enzymes

Chemical science (Cambridge), 2015-03, Vol.6 (3), p.1770-1779

2015

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Crosstalk between kinases and Nedd4 family ubiquitin ligases

Molecular bioSystems, 2014-01, Vol.1 (7), p.1643-1657

2014

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Structural Basis of Substrate Recognition and Covalent Inhibition of Cdu1 from Chlamydia trachomatis

ChemMedChem, 2018-10, Vol.13 (19), p.2014-2023

2018

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The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrroles

Organic & biomolecular chemistry, 2013-05, Vol.11 (18), p.2932-2935

2013

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Facile synthesis of covalent probes to capture enzymatic intermediates during E1 enzyme catalysisElectronic supplementary information (ESI) available. See DOI: 10.1039/c5cc08592f

2016-02

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An inhibitor of ubiquitin conjugation and aggresome formationElectronic supplementary information (ESI) available. See DOI: 10.1039/c5sc01351h

2015-08

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An inhibitor of ubiquitin conjugation and aggresome formation† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc01351h Click here for additional data file

Chemical science (Cambridge), 2015-06, Vol.6 (9), p.5235-5245

2015

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Identification of non-peptidic cysteine reactive fragments as inhibitors of cysteine protease rhodesain

Bioorganic & medicinal chemistry letters, 2015-10, Vol.25 (20), p.4509-4512

2015

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The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrrolesElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob27492f

2013-04

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Covalent tethering of fragments for covalent probe discoveryThe authors declare no competing interests

2016-04

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Protein ubiquitination and formation of polyubiquitin chains without ATP, E1 and E2 enzymesElectronic supplementary information (ESI) available. See DOI: 10.1039/c4sc02340d

2015-02

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Inhibiting protein synthesis to treat malaria

A Fragment-Based Method to Discover Irreversible Covalent Inhibitors of Cysteine Proteases

Let K-Ras activate its own inhibitor

Development of Activity-Based Probes for Ubiquitin and Ubiquitin-like Protein Signaling Pathways

An inhibitor of ubiquitin conjugation and aggresome formation

Facile synthesis of covalent probes to capture enzymatic intermediates during E1 enzyme catalysis

Discovery of covalent enzyme inhibitors using virtual docking of covalent fragments

Dissecting the Specificity of Adenosyl Sulfamate Inhibitors Targeting the Ubiquitin-Activating Enzyme

Covalent Tethering of Fragments For Covalent Probe Discovery

A Small Molecule That Switches a Ubiquitin Ligase From a Processive to a Distributive Enzymatic Mechanism

UbMES and UbFluor: Novel probes for ring-between-ring (RBR) E3 ubiquitin ligase PARKIN

Mapping low-affinity/high-specificity peptide–protein interactions using ligand-footprinting mass spectrometry

Catalytically Important Residues of E6AP Ubiquitin Ligase Identified Using Acid-Cleavable Photo-Cross-Linkers

Covalent-Fragment Screening of BRD4 Identifies a Ligandable Site Orthogonal to the Acetyl-Lysine Binding Sites

Protein ubiquitination and formation of polyubiquitin chains without ATP, E1 and E2 enzymes

Crosstalk between kinases and Nedd4 family ubiquitin ligases

Structural Basis of Substrate Recognition and Covalent Inhibition of Cdu1 from Chlamydia trachomatis

The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrroles

Facile synthesis of covalent probes to capture enzymatic intermediates during E1 enzyme catalysisElectronic supplementary information (ESI) available. See DOI: 10.1039/c5cc08592f

An inhibitor of ubiquitin conjugation and aggresome formationElectronic supplementary information (ESI) available. See DOI: 10.1039/c5sc01351h

An inhibitor of ubiquitin conjugation and aggresome formation† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc01351h Click here for additional data file

Identification of non-peptidic cysteine reactive fragments as inhibitors of cysteine protease rhodesain

The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrrolesElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob27492f

Covalent tethering of fragments for covalent probe discoveryThe authors declare no competing interests

Protein ubiquitination and formation of polyubiquitin chains without ATP, E1 and E2 enzymesElectronic supplementary information (ESI) available. See DOI: 10.1039/c4sc02340d

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