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The identification of new metallo-β-lactamase inhibitor leads from fragment-based screening

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (11), p.3282-3285

2011

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Applications of 19F-NMR in Fragment-Based Drug Discovery

Molecules (Basel, Switzerland), 2016-07, Vol.21 (7), p.860

2016

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Promiscuous 2‑Aminothiazoles (PrATs): A Frequent Hitting Scaffold

Journal of medicinal chemistry, 2015-02, Vol.58 (3), p.1205-1214

2015

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Applications of (19)F-NMR in Fragment-Based Drug Discovery

Molecules (Basel, Switzerland), 2016-07, Vol.21 (7)

2016

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Design, Synthesis, and Characterization of Cyclic Peptidomimetics of the Inducible Nitric Oxide Synthase Binding Epitope That Disrupt the Protein–Protein Interaction Involving SPRY Domain-Containing Suppressor of Cytokine Signaling Box Protein (SPSB) 2 and Inducible Nitric Oxide Synthase

Journal of medicinal chemistry, 2016-06, Vol.59 (12), p.5799-5809

2016

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A Potent Cyclic Peptide Targeting SPSB2 Protein as a Potential Anti-infective Agent

Journal of medicinal chemistry, 2014-08, Vol.57 (16), p.7006-7015

2014

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Expression and isotopic labelling of the potassium channel blocker ShK toxin as a thioredoxin fusion protein in bacteria

Toxicon (Oxford), 2012-10, Vol.60 (5), p.840-850

2012

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Fragment-based and structure-guided discovery of perforin inhibitors

European journal of medicinal chemistry, 2023-12, Vol.261, p.115786-115786, Article 115786

2023

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The Single Disulfide-Directed β‑Hairpin Fold. Dynamics, Stability, and Engineering

Biochemistry (Easton), 2017-05, Vol.56 (19), p.2455-2466

2017

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A Cyclic Peptide Inhibitor of the iNOS–SPSB Protein–Protein Interaction as a Potential Anti-Infective Agent

ACS chemical biology, 2018-10, Vol.13 (10), p.2930-2938

2018

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Structure and Functional Characterization of the Conserved JAK Interaction Region in the Intrinsically Disordered N‑Terminus of SOCS5

Biochemistry (Easton), 2015-08, Vol.54 (30), p.4672-4682

2015

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The neoepitope of the complement C5b-9 Membrane Attack Complex is formed by proximity of adjacent ancillary regions of C9

Communications biology, 2023-01, Vol.6 (1), p.42-42, Article 42

2023

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Structural Basis for Ca2+-mediated Interaction of the Perforin C2 Domain with Lipid Membranes

The Journal of biological chemistry, 2015-10, Vol.290 (42), p.25213-25226

2015

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Structure and Function Characterization of the a1a2 Motifs of Streptococcus pyogenes M Protein in Human Plasminogen Binding

Journal of molecular biology, 2019-09, Vol.431 (19), p.3804-3813

2019

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Conformational Changes in a Plant Ketol-Acid Reductoisomerase upon Mg2+ and NADPH Binding as Revealed by Two Crystal Structures

Journal of molecular biology, 2009-05, Vol.389 (1), p.167-182

2009

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Redox‐stable cyclic peptide inhibitors of the SPSB2–iNOS interaction

FEBS letters, 2016-03, Vol.590 (6), p.696-704

2016

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Identification and characterization of an unusual metallo-β-lactamase from Serratia proteamaculans

Journal of biological inorganic chemistry, 2013-10, Vol.18 (7), p.855-863

2013

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Structure and activity of contryphan-Vc2: Importance of the d-amino acid residue

Toxicon (Oxford), 2017-04, Vol.129, p.113-122

2017

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Molecular Insights into the Interaction Between the SPRY Domain-Containing SOCS Box Protein SPSB2 and Peptides Based on the Binding Motif from iNOS

Australian journal of chemistry, 2017, Vol.70 (2), p.191

2017

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Defining the interaction of perforin with calcium and the phospholipid membrane

Biochemical journal, 2013-12, Vol.456 (3), p.323-335

2013

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X-ray crystal structure of plasmin with tranexamic acid–derived active site inhibitors

Blood advances, 2017-05, Vol.1 (12), p.766-771

2017

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Conformational changes in a plant ketol-acid reductoisomerase upon Mg(2+) and NADPH binding as revealed by two crystal structures

Journal of molecular biology, 2009-05, Vol.389 (1), p.167

2009

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19F NMR as a Probe of Ligand Interactions with the iNOS Binding site of SPRY Domain-Containing SOCS Box Protein 2

Chemical biology & drug design, 2014-11, Vol.84 (5), p.616-625

2014

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Human tartrate-resistant acid phosphatase becomes an effective ATPase upon proteolytic activation

Archives of biochemistry and biophysics, 2005-07, Vol.439 (2), p.154-164

2005

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The identification of new metallo-β-lactamase inhibitor leads from fragment-based screening

Applications of 19F-NMR in Fragment-Based Drug Discovery

Promiscuous 2‑Aminothiazoles (PrATs): A Frequent Hitting Scaffold

Applications of (19)F-NMR in Fragment-Based Drug Discovery

Design, Synthesis, and Characterization of Cyclic Peptidomimetics of the Inducible Nitric Oxide Synthase Binding Epitope That Disrupt the Protein–Protein Interaction Involving SPRY Domain-Containing Suppressor of Cytokine Signaling Box Protein (SPSB) 2 and Inducible Nitric Oxide Synthase

A Potent Cyclic Peptide Targeting SPSB2 Protein as a Potential Anti-infective Agent

Expression and isotopic labelling of the potassium channel blocker ShK toxin as a thioredoxin fusion protein in bacteria

Fragment-based and structure-guided discovery of perforin inhibitors

The Single Disulfide-Directed β‑Hairpin Fold. Dynamics, Stability, and Engineering

A Cyclic Peptide Inhibitor of the iNOS–SPSB Protein–Protein Interaction as a Potential Anti-Infective Agent

Structure and Functional Characterization of the Conserved JAK Interaction Region in the Intrinsically Disordered N‑Terminus of SOCS5

The neoepitope of the complement C5b-9 Membrane Attack Complex is formed by proximity of adjacent ancillary regions of C9

Structural Basis for Ca2+-mediated Interaction of the Perforin C2 Domain with Lipid Membranes

Structure and Function Characterization of the a1a2 Motifs of Streptococcus pyogenes M Protein in Human Plasminogen Binding

Conformational Changes in a Plant Ketol-Acid Reductoisomerase upon Mg2+ and NADPH Binding as Revealed by Two Crystal Structures

Redox‐stable cyclic peptide inhibitors of the SPSB2–iNOS interaction

Identification and characterization of an unusual metallo-β-lactamase from Serratia proteamaculans

Structure and activity of contryphan-Vc2: Importance of the d-amino acid residue

Molecular Insights into the Interaction Between the SPRY Domain-Containing SOCS Box Protein SPSB2 and Peptides Based on the Binding Motif from iNOS

Defining the interaction of perforin with calcium and the phospholipid membrane

Randomized Trial of Dose-Dense Versus Conventionally Scheduled and Sequential Versus Concurrent Combination Chemotherapy as Postoperative Adjuvant Treatment of Node-Positive Primary Breast Cancer: First Report of Intergroup Trial C9741/Cancer and Leukemia Group B Trial 9741

X-ray crystal structure of plasmin with tranexamic acid–derived active site inhibitors

Conformational changes in a plant ketol-acid reductoisomerase upon Mg(2+) and NADPH binding as revealed by two crystal structures

19F NMR as a Probe of Ligand Interactions with the iNOS Binding site of SPRY Domain-Containing SOCS Box Protein 2

Human tartrate-resistant acid phosphatase becomes an effective ATPase upon proteolytic activation

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