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WXG100 protein superfamily consists of three subfamilies and exhibits an α-helical C-terminal conserved residue pattern

PloS one, 2014-02, Vol.9 (2), p.e89313-e89313

2014

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ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication

Oncotarget, 2016-10, Vol.7 (43), p.70323-70335

2016

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Coordination of Di-Acetylated Histone Ligands by the ATAD2 Bromodomain

International journal of molecular sciences, 2021-08, Vol.22 (17), p.9128

2021

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Design of a bZip Transcription Factor with Homo/Heterodimer-Induced DNA-Binding Preference

Structure (London), 2014-03, Vol.22 (3), p.466-477

2014

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The peroxisomal receptor Pex19p forms a helical mPTS recognition domain

The EMBO journal, 2010-08, Vol.29 (15), p.2491-2500

2010

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Expression, purification, characterization and structure of Pseudomonas aeruginosa arylamine N-acetyltransferase

Biochemical journal, 2005-01, Vol.385 (Pt 2), p.605-612

2005

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Investigation of the catalytic triad of arylamine N-acetyltransferases: essential residues required for acetyl transfer to arylamines

Biochemical journal, 2005-08, Vol.390 (Pt 1), p.115-123

2005

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Discovery and Characterization of the Potent and Highly Selective (Piperidin-4-yl)pyrido[3,2‑d]pyrimidine Based in Vitro Probe BAY-885 for the Kinase ERK5

Journal of medicinal chemistry, 2019-01, Vol.62 (2), p.928-940

2019

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Inhibition of BUB1 Kinase by BAY 1816032 Sensitizes Tumor Cells toward Taxanes, ATR, and PARP Inhibitors In Vitro and In Vivo

Clinical cancer research, 2019-02, Vol.25 (4), p.1404-1414

2019

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Degradation of CCNK/CDK12 is a druggable vulnerability of colorectal cancer

Cell reports (Cambridge), 2021-07, Vol.36 (3), p.109394-109394, Article 109394

2021

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Treating Cancer by Spindle Assembly Checkpoint Abrogation: Discovery of Two Clinical Candidates, BAY 1161909 and BAY 1217389, Targeting MPS1 Kinase

Journal of medicinal chemistry, 2020-08, Vol.63 (15), p.8025-8042

2020

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Discovery and Characterization of the Potent and Highly Selective 1,7-Naphthyridine-Based Inhibitors BAY-091 and BAY-297 of the Kinase PIP4K2A

Journal of medicinal chemistry, 2021-11, Vol.64 (21), p.15883-15911

2021

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Discovery and characterization of orally bioavailable 4-chloro-6-fluoroisophthalamides as covalent PPARG inverse-agonists

Bioorganic & medicinal chemistry, 2023-01, Vol.78, p.117130-117130, Article 117130

2023

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Benzoisoquinolinediones as Potent and Selective Inhibitors of BRPF2 and TAF1/TAF1L Bromodomains

Journal of medicinal chemistry, 2017-05, Vol.60 (9), p.4002-4022

2017

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Functional and Structural Characterization of Bub3·BubR1 Interactions Required for Spindle Assembly Checkpoint Signaling in Human Cells

The Journal of biological chemistry, 2016-05, Vol.291 (21), p.11252-11267

2016

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The potent AMPK inhibitor BAY-3827 shows strong efficacy in androgen-dependent prostate cancer models

Cellular oncology (Dordrecht), 2021-06, Vol.44 (3), p.581-594

2021

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Structural characterization of a D-isomer specific 2-hydroxyacid dehydrogenase from Lactobacillus delbrueckii ssp. bulgaricus

Journal of structural biology, 2013-02, Vol.181 (2), p.179-184

2013

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Structural and biochemical characterization of Rv2140c, a phosphatidylethanolamine-binding protein from Mycobacterium tuberculosis

FEBS letters, 2013-09, Vol.587 (18), p.2936-2942

2013

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Structure-based approaches to drug discovery against tuberculosis

Current protein & peptide science, 2007-08, Vol.8 (4), p.365-375

2007

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Structural diversity in the six-fold redundant set of acyl-CoA carboxyltransferases in Mycobacterium tuberculosis

FEBS letters, 2006-12, Vol.580 (30), p.6898-6902

2006

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Expression, purification, crystallization and preliminary crystallographic analysis of the mouse transcription factor MafB in complex with its DNA-recognition motif Cmare

Acta crystallographica. Section F, Structural biology and crystallization communications, 2007-08, Vol.63 (8), p.657-661

2007

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Structure of Mesorhizobium loti arylamine N-acetyltransferase 1

Acta crystallographica. Section F, Structural biology and crystallization communications, 2005-01, Vol.61 (1), p.14-16

2005

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Abstract 980: BAY-299, a novel chemical probe for in-depth analysis of the function of the bromodomain proteins BRPF2 and TAF1

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.980-980

2017

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WXG100 protein superfamily consists of three subfamilies and exhibits an α-helical C-terminal conserved residue pattern

ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication

Coordination of Di-Acetylated Histone Ligands by the ATAD2 Bromodomain

Design of a bZip Transcription Factor with Homo/Heterodimer-Induced DNA-Binding Preference

The peroxisomal receptor Pex19p forms a helical mPTS recognition domain

Expression, purification, characterization and structure of Pseudomonas aeruginosa arylamine N-acetyltransferase

Damage Incorporated: Discovery of the Potent, Highly Selective, Orally Available ATR Inhibitor BAY 1895344 with Favorable Pharmacokinetic Properties and Promising Efficacy in Monotherapy and in Combination Treatments in Preclinical Tumor Models

Investigation of the catalytic triad of arylamine N-acetyltransferases: essential residues required for acetyl transfer to arylamines

Discovery and Characterization of the Potent and Highly Selective (Piperidin-4-yl)pyrido[3,2‑d]pyrimidine Based in Vitro Probe BAY-885 for the Kinase ERK5

Inhibition of BUB1 Kinase by BAY 1816032 Sensitizes Tumor Cells toward Taxanes, ATR, and PARP Inhibitors In Vitro and In Vivo

Degradation of CCNK/CDK12 is a druggable vulnerability of colorectal cancer

Treating Cancer by Spindle Assembly Checkpoint Abrogation: Discovery of Two Clinical Candidates, BAY 1161909 and BAY 1217389, Targeting MPS1 Kinase

Discovery and Characterization of the Potent and Highly Selective 1,7-Naphthyridine-Based Inhibitors BAY-091 and BAY-297 of the Kinase PIP4K2A

Discovery and characterization of orally bioavailable 4-chloro-6-fluoroisophthalamides as covalent PPARG inverse-agonists

Benzoisoquinolinediones as Potent and Selective Inhibitors of BRPF2 and TAF1/TAF1L Bromodomains

Isoform-Selective ATAD2 Chemical Probe with Novel Chemical Structure and Unusual Mode of Action

Functional and Structural Characterization of Bub3·BubR1 Interactions Required for Spindle Assembly Checkpoint Signaling in Human Cells

The potent AMPK inhibitor BAY-3827 shows strong efficacy in androgen-dependent prostate cancer models

Structural characterization of a D-isomer specific 2-hydroxyacid dehydrogenase from Lactobacillus delbrueckii ssp. bulgaricus

Structural and biochemical characterization of Rv2140c, a phosphatidylethanolamine-binding protein from Mycobacterium tuberculosis

Structure-based approaches to drug discovery against tuberculosis

Structural diversity in the six-fold redundant set of acyl-CoA carboxyltransferases in Mycobacterium tuberculosis

Expression, purification, crystallization and preliminary crystallographic analysis of the mouse transcription factor MafB in complex with its DNA-recognition motif Cmare

Structure of Mesorhizobium loti arylamine N-acetyltransferase 1

Abstract 980: BAY-299, a novel chemical probe for in-depth analysis of the function of the bromodomain proteins BRPF2 and TAF1

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