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Crystallographic screening using ultra-low-molecular-weight ligands to guide drug design

Drug discovery today, 2019-05, Vol.24 (5), p.1081-1086

2019

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Oxidation state of the active-site cysteine in protein tyrosine phosphatase 1B

Nature (London), 2003-06, Vol.423 (6941), p.773-777

2003

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Structure of the Epigenetic Oncogene MMSET and Inhibition by N‑Alkyl Sinefungin Derivatives

ACS chemical biology, 2016-11, Vol.11 (11), p.3093-3105

2016

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Fragment-Based Discovery of a Novel, Brain Penetrant, Orally Active HDAC2 Inhibitor

ACS medicinal chemistry letters, 2022-10, Vol.13 (10), p.1591-1597

2022

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Novel Fold Revealed by the Structure of a FAS1 Domain Pair from the Insect Cell Adhesion Molecule Fasciclin I

Structure (London), 2003-02, Vol.11 (2), p.197-203

2003

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Mitoxantrone stacking does not define the active or inactive state of USP15 catalytic domain

Journal of structural biology, 2022-09, Vol.214 (3), p.107862-107862, Article 107862

2022

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Recent Developments in Fragment-Based Drug Discovery

Journal of medicinal chemistry, 2008-07, Vol.51 (13), p.3661-3680

2008

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Engineering and purification of a thermostable, high-yield, variant of PfCRT, the Plasmodium falciparum chloroquine resistance transporter

Protein expression and purification, 2018-01, Vol.141, p.7-18

2018

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Fragment-Based Discovery of the Pyrazol-4-yl Urea (AT9283), a Multitargeted Kinase Inhibitor with Potent Aurora Kinase Activity

Journal of medicinal chemistry, 2009-01, Vol.52 (2), p.379-388

2009

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The Crystal Structure of a Laminin G–like Module Reveals the Molecular Basis of α-Dystroglycan Binding to Laminins, Perlecan, and Agrin

Molecular cell, 1999-11, Vol.4 (5), p.783-792

1999

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Identification of Novel p38α MAP Kinase Inhibitors Using Fragment-Based Lead Generation

Journal of medicinal chemistry, 2005-01, Vol.48 (2), p.414-426

2005

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Endostatins derived from collagens XV and XVIII differ in structural and binding properties, tissue distribution and anti-angiogenic activity

Journal of molecular biology, 2000-09, Vol.301 (5), p.1179-1190

2000

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Structure of the C-terminal laminin G-like domain pair of the laminin α2 chain harbouring binding sites for α-dystroglycan and heparin

The EMBO journal, 2000-04, Vol.19 (7), p.1432-1440

2000

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Crystal Structure of a C-terminal Fragment of Growth Arrest-specific Protein Gas6

The Journal of biological chemistry, 2002-11, Vol.277 (46), p.44164-44170

2002

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Structure and function of laminin LG modules

Matrix biology, 2000-08, Vol.19 (4), p.309-317

2000

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Fragment-Based Discovery of 6‑Azaindazoles As Inhibitors of Bacterial DNA Ligase

ACS medicinal chemistry letters, 2013-12, Vol.4 (12), p.1208-1212

2013

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Crystal structure of a C-terminal fragment of growth arrest-specific protein Gas6. Receptor tyrosine kinase activation by laminin G-like domains

The Journal of biological chemistry, 2002-11, Vol.277 (46), p.44164-44170

2002

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The three-dimensional structure of cytosolic bovine retinal creatine kinase

Acta crystallographica. Section D, Biological crystallography., 2001-02, Vol.57 (2), p.187-193

2001

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Structural Biology and Anticancer Drug Design

Cancer Drug Design and Discovery, 2013, p.121-141

2013

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Structure of the C-terminal laminin G-like domain pair of the laminin [alpha]2 chain harbouring binding sites for [alpha]-dystroglycan and heparin

The EMBO journal, 2000-04, Vol.19 (7), p.1432

2000

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Identification of novel p38alpha MAP kinase inhibitors using fragment-based lead generation

Journal of medicinal chemistry, 2005-01, Vol.48 (2), p.414-426

2005

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Chapter 4 - Structural Biology and Anticancer Drug Design

Cancer Drug Design and Discovery, 2014, p.121-141

Second Edition, 2014

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ChemInform Abstract: Recent Developments in Fragment-Based Drug Discovery

ChemInform, 2008-10, Vol.39 (41), p.no-no

2008

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Chapter 4 - Structural biology and anticancer drug design

Cancer Drug Design and Discovery, 2008, p.91,V-106,VII

2008

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Crystallographic screening using ultra-low-molecular-weight ligands to guide drug design

Oxidation state of the active-site cysteine in protein tyrosine phosphatase 1B

Structure of the Epigenetic Oncogene MMSET and Inhibition by N‑Alkyl Sinefungin Derivatives

Fragment-Based Discovery of a Novel, Brain Penetrant, Orally Active HDAC2 Inhibitor

Novel Fold Revealed by the Structure of a FAS1 Domain Pair from the Insect Cell Adhesion Molecule Fasciclin I

Mitoxantrone stacking does not define the active or inactive state of USP15 catalytic domain

Recent Developments in Fragment-Based Drug Discovery

Engineering and purification of a thermostable, high-yield, variant of PfCRT, the Plasmodium falciparum chloroquine resistance transporter

Fragment-Based Discovery of the Pyrazol-4-yl Urea (AT9283), a Multitargeted Kinase Inhibitor with Potent Aurora Kinase Activity

Fragment-Based Discovery of a Series of Allosteric-Binding Site Modulators of β‑Glucocerebrosidase

The Crystal Structure of a Laminin G–like Module Reveals the Molecular Basis of α-Dystroglycan Binding to Laminins, Perlecan, and Agrin

Identification of Novel p38α MAP Kinase Inhibitors Using Fragment-Based Lead Generation

Endostatins derived from collagens XV and XVIII differ in structural and binding properties, tissue distribution and anti-angiogenic activity

Structure of the C-terminal laminin G-like domain pair of the laminin α2 chain harbouring binding sites for α-dystroglycan and heparin

Crystal Structure of a C-terminal Fragment of Growth Arrest-specific Protein Gas6

Structure and function of laminin LG modules

Fragment-Based Discovery of 6‑Azaindazoles As Inhibitors of Bacterial DNA Ligase

Crystal structure of a C-terminal fragment of growth arrest-specific protein Gas6. Receptor tyrosine kinase activation by laminin G-like domains

The three-dimensional structure of cytosolic bovine retinal creatine kinase

Structural Biology and Anticancer Drug Design

Structure of the C-terminal laminin G-like domain pair of the laminin [alpha]2 chain harbouring binding sites for [alpha]-dystroglycan and heparin

Identification of novel p38alpha MAP kinase inhibitors using fragment-based lead generation

Chapter 4 - Structural Biology and Anticancer Drug Design

ChemInform Abstract: Recent Developments in Fragment-Based Drug Discovery

Chapter 4 - Structural biology and anticancer drug design

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