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Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition

Nature structural & molecular biology, 2004-12, Vol.11 (12), p.1192-1197

2004

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Selectively targeting an inactive conformation of interleukin-2-inducible T-cell kinase by allosteric inhibitors

Biochemical journal, 2014-06, Vol.460 (2), p.211-222

2014

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Discovery of a Series of Imidazo[4,5-b]pyridines with Dual Activity at Angiotensin II Type 1 Receptor and Peroxisome Proliferator-Activated Receptor-γ

Journal of medicinal chemistry, 2011-06, Vol.54 (12), p.4219-4233

2011

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Design, synthesis, and evaluation of imidazo[4,5-c]pyridin-4-one derivatives with dual activity at angiotensin II type 1 receptor and peroxisome proliferator-activated receptor-γ

Bioorganic & medicinal chemistry letters, 2013-02, Vol.23 (3), p.767-772

2013

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Characterization of substrate binding and catalysis in the potential antibacterial target N‐acetylglucosamine‐1‐phosphate uridyltransferase (GlmU)

Protein science, 2007-12, Vol.16 (12), p.2657-2666

2007

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The Structure of the Carboxyltransferase Component of Acetyl-CoA Carboxylase Reveals a Zinc-Binding Motif Unique to the Bacterial Enzyme

Biochemistry (Easton), 2006-02, Vol.45 (6), p.1712-1722

2006

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The structure of a redundant enzyme: a second isoform of aspartate β-semialdehyde dehydrogenase in Vibrio cholerae

Acta crystallographica. Section D, Biological crystallography., 2008-03, Vol.64 (3), p.321-330

2008

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A New Branch in the Family: Structure of Aspartate-β-semialdehyde Dehydrogenase from Methanococcus jannaschii

Journal of molecular biology, 2005-11, Vol.353 (5), p.1055-1068

2005

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Phosphopantetheine Adenylyltransferase from Escherichia coli: Investigation of the Kinetic Mechanism and Role in Regulation of Coenzyme A Biosynthesis

Journal of Bacteriology, 2007-11, Vol.189 (22), p.8196-8205

2007

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4-Anilino-5-carboxamido-2-pyridone Derivatives as Noncompetitive Inhibitors of Mitogen-Activated Protein Kinase Kinase

Journal of medicinal chemistry, 2007-10, Vol.50 (21), p.5090-5102

2007

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Synthesis and evaluation of novel α-heteroaryl-phenylpropanoic acid derivatives as PPARα/γ dual agonists

Bioorganic & medicinal chemistry, 2009-10, Vol.17 (20), p.7113-7125

2009

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Effects of modifications of the linker in a series of phenylpropanoic acid derivatives: Synthesis, evaluation as PPARα/γ dual agonists, and X-ray crystallographic studies

Bioorganic & medicinal chemistry, 2008-05, Vol.16 (9), p.4883-4907

2008

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The mitogen-activated protein kinase pathway for molecular-targeted cancer treatment

Recent results in cancer research, 2007, Vol.172, p.155

2007

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Inhibitors of Bcr-abl... breaking new ground again

Nature chemical biology, 2006-02, Vol.2 (2), p.63-64

2006

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The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (9), p.2337-2340

2006

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Selective inhibition of casein kinase 1 epsilon minimally alters circadian clock period

The Journal of pharmacology and experimental therapeutics, 2009-08, Vol.330 (2), p.430

2009

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Structure of a critical metabolic enzyme: S‐adenosylmethionine synthetase from Cryptosporidium parvum

Acta crystallographica. Section F, Structural biology communications, 2019-04, Vol.75 (4), p.290-298

2019

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Structural asymmetry and intersubunit communication in muscle creatine kinase

Acta crystallographica. Section D, Biological crystallography., 2007-03, Vol.63 (3), p.381-389

2007

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A New Branch in the Family: Structure of Aspartate-[beta]-semialdehyde Dehydrogenase from Methanococcus jannaschii

Journal of molecular biology, 2010-07, Vol.353 ((5) ; 2005)

2010

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2-Alkylamino-and alkoxy-substituted 2-amino-1,3,4-oxadiazoles-O-Alkyl benzohydroxamate esters replacements retain the desired inhibition and selectivity against MEK (MAP ERK kinase)

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (23), p.6171-6174

2008

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Design, synthesis, and evaluation of imidazo[4,5-c]pyridin-4-one derivatives with dual activity at angiotensin II type 1 receptor and peroxisome proliferator-activated receptor-[gamma]

Bioorganic & medicinal chemistry letters, 2013-02, Vol.23 (3), p.767-772

2013

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Beyond the MEK-pocket: Can current MEK kinase inhibitors be utilized to synthesize novel type III NCKIs? Does the MEK-pocket exist in kinases other than MEK?

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (1), p.226-229

2009

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Discovery of a Series of Imidazo[4,5-b]pyridines with Dual Activity at Angiotensin II Type 1 Receptor and Peroxisome Proliferator-Activated Receptor-[gamma]

Journal of medicinal chemistry, 2013-03, Vol.54 ((12) ; 06, 2011)

2013

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Synthesis and evaluation of novel [alpha]-heteroaryl-phenylpropanoic acid derivatives as PPAR[alpha/gamma] dual agonists

Bioorganic & medicinal chemistry letters, 2010-09, Vol.17 ((20) ; 10, 2009)

2010

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Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition

Selectively targeting an inactive conformation of interleukin-2-inducible T-cell kinase by allosteric inhibitors

Discovery of a Series of Imidazo[4,5-b]pyridines with Dual Activity at Angiotensin II Type 1 Receptor and Peroxisome Proliferator-Activated Receptor-γ

Aminopyrazole Carboxamide Bruton’s Tyrosine Kinase Inhibitors. Irreversible to Reversible Covalent Reactive Group Tuning

Design, synthesis, and evaluation of imidazo[4,5-c]pyridin-4-one derivatives with dual activity at angiotensin II type 1 receptor and peroxisome proliferator-activated receptor-γ

Characterization of substrate binding and catalysis in the potential antibacterial target N‐acetylglucosamine‐1‐phosphate uridyltransferase (GlmU)

The Structure of the Carboxyltransferase Component of Acetyl-CoA Carboxylase Reveals a Zinc-Binding Motif Unique to the Bacterial Enzyme

The structure of a redundant enzyme: a second isoform of aspartate β-semialdehyde dehydrogenase in Vibrio cholerae

A New Branch in the Family: Structure of Aspartate-β-semialdehyde Dehydrogenase from Methanococcus jannaschii

Phosphopantetheine Adenylyltransferase from Escherichia coli: Investigation of the Kinetic Mechanism and Role in Regulation of Coenzyme A Biosynthesis

4-Anilino-5-carboxamido-2-pyridone Derivatives as Noncompetitive Inhibitors of Mitogen-Activated Protein Kinase Kinase

Synthesis and evaluation of novel α-heteroaryl-phenylpropanoic acid derivatives as PPARα/γ dual agonists

Effects of modifications of the linker in a series of phenylpropanoic acid derivatives: Synthesis, evaluation as PPARα/γ dual agonists, and X-ray crystallographic studies

The mitogen-activated protein kinase pathway for molecular-targeted cancer treatment

Inhibitors of Bcr-abl... breaking new ground again

The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases

Selective inhibition of casein kinase 1 epsilon minimally alters circadian clock period

Structure of a critical metabolic enzyme: S‐adenosylmethionine synthetase from Cryptosporidium parvum

Structural asymmetry and intersubunit communication in muscle creatine kinase

A New Branch in the Family: Structure of Aspartate-[beta]-semialdehyde Dehydrogenase from Methanococcus jannaschii

2-Alkylamino-and alkoxy-substituted 2-amino-1,3,4-oxadiazoles-O-Alkyl benzohydroxamate esters replacements retain the desired inhibition and selectivity against MEK (MAP ERK kinase)

Design, synthesis, and evaluation of imidazo[4,5-c]pyridin-4-one derivatives with dual activity at angiotensin II type 1 receptor and peroxisome proliferator-activated receptor-[gamma]

Beyond the MEK-pocket: Can current MEK kinase inhibitors be utilized to synthesize novel type III NCKIs? Does the MEK-pocket exist in kinases other than MEK?

Discovery of a Series of Imidazo[4,5-b]pyridines with Dual Activity at Angiotensin II Type 1 Receptor and Peroxisome Proliferator-Activated Receptor-[gamma]

Synthesis and evaluation of novel [alpha]-heteroaryl-phenylpropanoic acid derivatives as PPAR[alpha/gamma] dual agonists

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