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Identification of a ligand binding hot spot and structural motifs replicating aspects of tyrosyl-DNA phosphodiesterase I (TDP1) phosphoryl recognition by crystallographic fragment cocktail screening

Nucleic acids research, 2019-11, Vol.47 (19), p.10134-10150

2019

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Characterization of a broadly specific cadaverine N-hydroxylase involved in desferrioxamine B biosynthesis in Streptomyces sviceus

PloS one, 2021-03, Vol.16 (3), p.e0248385

2021

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Unique Structural Fold of LonBA Protease from Bacillus subtilis, a Member of a Newly Identified Subfamily of Lon Proteases

International journal of molecular sciences, 2022-09, Vol.23 (19), p.11425

2022

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Phosphonic acid-containing inhibitors of tyrosyl-DNA phosphodiesterase 1

Frontiers in chemistry, 2022-08, Vol.10, p.910953-910953

2022

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The Convergence of the Hedgehog/Intein Fold in Different Protein Splicing Mechanisms

International journal of molecular sciences, 2020-11, Vol.21 (21), p.8367

2020

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Role of Glu312 in Binding and Positioning of the Substrate for the Hydride Transfer Reaction in Choline Oxidase

Biochemistry (Easton), 2008-01, Vol.47 (1), p.243-256

2008

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Targeted sulfur(VI) fluoride exchange-mediated covalent modification of a tyrosine residue in the catalytic pocket of tyrosyl-DNA phosphodiesterase 1

Communications chemistry, 2024-09, Vol.7 (1), p.208-13

2024

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Utilization of Nitrophenylphosphates and Oxime-Based Ligation for the Development of Nanomolar Affinity Inhibitors of the Yersinia pestis Outer Protein H (YopH) Phosphatase

Journal of medicinal chemistry, 2011-04, Vol.54 (8), p.2933-2943

2011

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Crystallographic, Spectroscopic, and Computational Analysis of a Flavin C4a−Oxygen Adduct in Choline Oxidase

Biochemistry (Easton), 2009-02, Vol.48 (4), p.720-728

2009

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Phosphotyrosine Substrate Sequence Motifs for Dual Specificity Phosphatases

PloS one, 2015-08, Vol.10 (8), p.e0134984-e0134984

2015

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Structures of the Middle East respiratory syndrome coronavirus 3C-like protease reveal insights into substrate specificity

Acta crystallographica. Section D, Biological crystallography., 2015-05, Vol.71 (5), p.1102-1111

2015

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Cellular inhibition of checkpoint kinase 2 (Chk2) and potentiation of camptothecins and radiation by the novel Chk2 inhibitor PV1019 [7-nitro-1H-indole-2-carboxylic acid {4-[1-(guanidinohydrazone)-ethyl]-phenyl}-amide]

The Journal of pharmacology and experimental therapeutics, 2009-12, Vol.331 (3), p.816-826

2009

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Atomic resolution structure of the cytoplasmic domain of Yersinia pestis YscU, a regulatory switch involved in type III secretion

Protein science, 2009-02, Vol.18 (2), p.467-474

2009

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Cryo-EM structure of substrate-free E. coli Lon protease provides insights into the dynamics of Lon machinery

Current research in structural biology, 2019-11, Vol.1, p.13-20

2019

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Structural basis for cell type specific DNA binding of C/EBPβ: The case of cell cycle inhibitor p15INK4b promoter

Journal of structural biology, 2022-12, Vol.214 (4), p.107918-107918, Article 107918

2022

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Self-inhibited State of Venezuelan Equine Encephalitis Virus (VEEV) nsP2 Cysteine Protease: A Crystallographic and Molecular Dynamics Analysis

Journal of molecular biology, 2023-03, Vol.435 (6), p.168012-168012, Article 168012

2023

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P1′ specificity of the S219V/R203G mutant tobacco etch virus protease

Proteins, structure, function, and bioinformatics, 2024-09, Vol.92 (9), p.1085-1096

2024

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Structure of human dual-specificity phosphatase 7, a potential cancer drug target

Acta crystallographica. Section F, Structural biology communications, 2015-06, Vol.71 (6), p.650-656

2015

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Small molecule microarray identifies inhibitors of tyrosyl-DNA phosphodiesterase 1 that simultaneously access the catalytic pocket and two substrate binding sites

Chemical science (Cambridge), 2021-01, Vol.12 (11), p.3876-3884

2021

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Crystal structure of the human dual specificity phosphatase 1 catalytic domain

Protein science, 2018-02, Vol.27 (2), p.561-567

2018

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MBP‐binding DARPins facilitate the crystallization of an MBP fusion protein

Acta crystallographica. Section F, Structural biology communications, 2018-09, Vol.74 (9), p.549-557

2018

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Crystal structure of UDP‐glucose pyrophosphorylase from Yersinia pestis, a potential therapeutic target against plague

Acta crystallographica. Section F, Structural biology communications, 2019-09, Vol.75 (9), p.608-615

2019

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Engineering of glycerol dehydrogenase for improved activity towards 1, 3-butanediol

Applied microbiology and biotechnology, 2010-09, Vol.88 (1), p.117-124

2010

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Identification of multidentate tyrosyl-DNA phosphodiesterase 1 (TDP1) inhibitors that simultaneously access the DNA, protein and catalytic-binding sites by oxime diversification

RSC chemical biology, 2023-05, Vol.4 (5), p.334-343

2023

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Insights Into the Allosteric Inhibition of the SUMO E2 Enzyme Ubc9

Angewandte Chemie (International ed.), 2016-05, Vol.55 (19), p.5703-5707

International ed. in English, 2016

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Identification of a ligand binding hot spot and structural motifs replicating aspects of tyrosyl-DNA phosphodiesterase I (TDP1) phosphoryl recognition by crystallographic fragment cocktail screening

Characterization of a broadly specific cadaverine N-hydroxylase involved in desferrioxamine B biosynthesis in Streptomyces sviceus

Unique Structural Fold of LonBA Protease from Bacillus subtilis, a Member of a Newly Identified Subfamily of Lon Proteases

Phosphonic acid-containing inhibitors of tyrosyl-DNA phosphodiesterase 1

The Convergence of the Hedgehog/Intein Fold in Different Protein Splicing Mechanisms

Role of Glu312 in Binding and Positioning of the Substrate for the Hydride Transfer Reaction in Choline Oxidase

Targeted sulfur(VI) fluoride exchange-mediated covalent modification of a tyrosine residue in the catalytic pocket of tyrosyl-DNA phosphodiesterase 1

Utilization of Nitrophenylphosphates and Oxime-Based Ligation for the Development of Nanomolar Affinity Inhibitors of the Yersinia pestis Outer Protein H (YopH) Phosphatase

Crystallographic, Spectroscopic, and Computational Analysis of a Flavin C4a−Oxygen Adduct in Choline Oxidase

Phosphotyrosine Substrate Sequence Motifs for Dual Specificity Phosphatases

Structures of the Middle East respiratory syndrome coronavirus 3C-like protease reveal insights into substrate specificity

Cellular inhibition of checkpoint kinase 2 (Chk2) and potentiation of camptothecins and radiation by the novel Chk2 inhibitor PV1019 [7-nitro-1H-indole-2-carboxylic acid {4-[1-(guanidinohydrazone)-ethyl]-phenyl}-amide]

Atomic resolution structure of the cytoplasmic domain of Yersinia pestis YscU, a regulatory switch involved in type III secretion

Cryo-EM structure of substrate-free E. coli Lon protease provides insights into the dynamics of Lon machinery

Structural basis for cell type specific DNA binding of C/EBPβ: The case of cell cycle inhibitor p15INK4b promoter

Self-inhibited State of Venezuelan Equine Encephalitis Virus (VEEV) nsP2 Cysteine Protease: A Crystallographic and Molecular Dynamics Analysis

P1′ specificity of the S219V/R203G mutant tobacco etch virus protease

Structure of human dual-specificity phosphatase 7, a potential cancer drug target

Small molecule microarray identifies inhibitors of tyrosyl-DNA phosphodiesterase 1 that simultaneously access the catalytic pocket and two substrate binding sites

Crystal structure of the human dual specificity phosphatase 1 catalytic domain

MBP‐binding DARPins facilitate the crystallization of an MBP fusion protein

Crystal structure of UDP‐glucose pyrophosphorylase from Yersinia pestis, a potential therapeutic target against plague

Engineering of glycerol dehydrogenase for improved activity towards 1, 3-butanediol

Identification of multidentate tyrosyl-DNA phosphodiesterase 1 (TDP1) inhibitors that simultaneously access the DNA, protein and catalytic-binding sites by oxime diversification

Insights Into the Allosteric Inhibition of the SUMO E2 Enzyme Ubc9

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