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Gastprofessor/in, Biologie - Mikrobiologie II
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Gastwissenschaftler/in, Biologie - Mikrobiologie II
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Professor/in, Mikrobiologie II
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Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.
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A Photocaged N-Phosphonopiperidinone as a Selective Photo-Cleavable DPP8/9 InhibitorIn: ChemBioChem, Jg. 26, 2025, Nr. 19, e202500558DOI (Open Access)
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High resolution analysis of proteolytic substrate processingIn: The Journal of Biological Chemistry (JBC), Jg. 300, 2024, Nr. 11, 107812DOI, Online Volltext (Open Access)
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Rational correction of pathogenic conformational defects in HTRA1In: Nature Communications, Jg. 15, 2024, Nr. 1, 5944DOI (Open Access)
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Facile Multicomponent Synthesis of Oxazolidinones from Primary Amines and Cesium (Hydrogen)CarbonateIn: European Journal of Organic Chemistry, Jg. 26, 2023, Nr. 27, e202300135DOI (Open Access)
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Hemophagocytic lymphohistiocytosis : Like hyperinflammation due to a de novo mutation in DPP9In: The Journal of Allergy and Clinical Immunology, Jg. 152, 2023, Nr. 5, S. 1336 – 1344.e5DOI, Online Volltext (Open Access)
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Chemoproteomics‐Enabled Identification of 4‐Oxo‐β‐Lactams as Inhibitors of Dipeptidyl Peptidases 8 and 9In: Angewandte Chemie International Edition, Jg. 61, 2022, Nr. 47, e202210498DOI (Open Access)
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Dipeptidyl peptidase 9 triggers BRCA2 degradation and promotes DNA damage repairIn: EMBO Reports, Jg. 23, 2022, Nr. 10, e54136DOI (Open Access)
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Aerosol-based ligand soaking of reservoir-free protein crystalsIn: Journal of Applied Crystallography, Jg. 54, 2021, Nr. 3, S. 895 – 902DOI (Open Access)
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Structural basis for the regulation of nucleosome recognition and HDAC activity by histone deacetylase assembliesIn: Science Advances, Jg. 7, 2021, Nr. 2, S. eabd4413DOI (Open Access)
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A precisely positioned MED12 activation helix stimulates CDK8 kinase activityIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 117, 2020, Nr. 6, S. 2894 – 2905DOI, Online Volltext (Open Access)
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Activation by substoichiometric inhibitionIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 117, 2020, Nr. 3, S. 1414 – 1418DOI, Online Volltext (Open Access)
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Crystal structure and mechanism of human carboxypeptidase O : Insights into its specific activity for acidic residuesIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 115, 2018, Nr. 17, S. E3932 – E3939DOI, Online Volltext (Open Access)
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Structures and mechanism of dipeptidyl peptidases 8 and 9, important players in cellular homeostasis and cancerIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 115, 2018, Nr. 7, S. E1437 – E1445DOI (Open Access)
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Structure of the unliganded form of the proprotein convertase furin suggests activation by a substrate-induced mechanismIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 113, 2016, Nr. 40, S. 11196 – 11201DOI (Open Access)
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Design, Synthesis, and Biological Evaluation of Quercetagetin Analogues as JNK1 InhibitorsIn: Chemistry - A European Journal, Jg. 21, 2015, Nr. 47, S. 16887 – 16894
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Flt3 is a target of coumestrol in protecting against UVB-induced skin photoagingIn: Biochemical Pharmacology, Jg. 98, 2015, Nr. 3, S. 473 – 483
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Cerebral small vessel disease-related protease HtrA1 processes latent TGF-β binding protein 1 and facilitates TGF-β signalingIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 111, 2014, Nr. 46, S. 16496 – 16501
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Differential global structural changes in the core particle of yeast and mouse proteasome induced by ligand bindingIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 111, 2014, Nr. 26, S. 9479 – 9484
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IR laser-induced protein crystal transformationIn: Acta Crystallographica Section D: Biological Crystallography, Jg. D70, 2014, Nr. 5, S. 1224 – 1232DOI (Open Access)
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Structural analysis of the human fibroblast growth factor receptor 4 kinaseIn: Journal of Molecular Biology (JMB), Jg. 426, 2014, Nr. 22, S. 3744 – 3756
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Structural and Functional Analysis of the Natural JNK1 Inhibitor QuercetagetinIn: Journal of Molecular Biology (JMB), Jg. 425, 2013, Nr. 2, S. 411 – 423DOI, Online Volltext (Open Access)
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Structure-kinetic relationship study of CDK8/CycC specific compoundsIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 110, 2013, Nr. 20, S. 8081 – 8086
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“How I Chose Research on Proteases or, More Correctly, How it Chose Me”In: Angewandte Chemie International Edition, Jg. 52, 2013, Nr. 1, S. 68 – 73
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Chemical Biology Approaches Reveal Conserved Features of a C-Terminal Processing PDZ ProteaseIn: ChemBioChem, Jg. 13, 2012, Nr. 3, S. 402 – 408
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Human high temperature requirement serine protease A1 (HTRA1) degrades tau protein aggregatesIn: The Journal of Biological Chemistry (JBC), Jg. 287, 2012, Nr. 25, S. 20931 – 20941
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Hydroxyureas as noncovalent proteasome inhibitorsIn: Angewandte Chemie International Edition, Jg. 51, 2012, Nr. 1, S. 247 – 249
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Structure of the stapled p53 peptide bound to Mdm2In: Journal of the American Chemical Society: JACS, Jg. 134, 2012, Nr. 1, S. 103 – 106
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Elucidation of the α-keto-aldehyde binding mechanism : A lead structure motif for proteasome inhibitionIn: Angewandte Chemie International Edition, Jg. 50, 2011, Nr. 2, S. 542 – 544
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HTRA proteases : regulated proteolysis in protein quality controlIn: Nature Reviews Molecular Cell Biology, Jg. 12, 2011, Nr. 3, S. 152 – 162
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Molecular architecture of the Spire-actin nucleus and its implication for actin filament assemblyIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 108, 2011, Nr. 49, S. 19575 – 19580DOI, Online Volltext (Open Access)
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Protein quality control in the bacterial periplasmIn: Annual Review of Microbiology, Jg. 65, 2011, S. 149 – 168
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The structure of CDK8/CycC implicates specificity in the CDK/cyclin family and reveals interaction with a deep pocket binderIn: Journal of Molecular Biology (JMB), Jg. 412, 2011, Nr. 2, S. 251 – 266
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Convergent synthesis and biological evaluation of syringolin a and derivatives as eukaryotic 20S proteasome inhibitorsIn: European Journal of Organic Chemistry, 2010, Nr. 21, S. 3991 – 4003
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Conversion of a regulatory into a degradative proteaseIn: Journal of Molecular Biology (JMB), Jg. 397, 2010, Nr. 4, S. 957 – 966
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Determinants of structural and functional plasticity of a widely conserved protease chaperone complexIn: Nature Structural & Molecular Biology, Jg. 17, 2010, Nr. 7, S. 837 – 843
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HtrA proteases have a conserved activation mechanism that can be triggered by distinct molecular cuesIn: Nature Structural & Molecular Biology, Jg. 17, 2010, Nr. 7, S. 844 – 852
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Structures of actin-bound Wiskott-Aldrich syndrome protein homology 2 (WH2) domains of Spire and the implication for filament nucleationIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 107, 2010, Nr. 26, S. 11757 – 11762DOI, Online Volltext (Open Access)
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Structural basis for Ca2+-independence and activation by homodimerization of tomato subtilase 3In: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 106, 2009, Nr. 40, S. 17223 – 17228
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Structure, function and regulation of the conserved serine proteases DegP and DegS of Escherichia coliIn: Research in Microbiology, Jg. 160, 2009, Nr. 9, S. 660 – 666
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Synthetic and structural studies on Syringolin A and B reveal critical determinants for selectivity and potency of proteasome inhibitionIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 106, 2009, Nr. 16, S. 6507 – 6512
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Syringolin A selectively labels the 20S proteasome in murine EL4 and wildtype and bortezomib adapted leukemic cell linesIn: ChemBioChem, Jg. 10, 2009, Nr. 16, S. 2638 – 2643
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A plant pathogen virulence factor inhibits the eukaryotic proteasome by a novel mechanismIn: Nature, Jg. 452, 2008, S. 755 – 758
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Interplay of PDZ and protease domain of DegP ensures efficient elimination of misfolded proteinsIn: Proceedings of the National Academy of Sciences of the United States of America (PNAS), Jg. 22, 2008, S. 7702 – 7707
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Binding mode of TMC-95A analogues to eukaryotic 20S proteasomeIn: ChemBioChem, Jg. 5, 2004, Nr. 9, S. 1256 – 1266
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Navigation inside a protease: Substrate selection and product exit in the tricorn protease from Thermoplasma acidophilumIn: Journal of Molecular Biology (JMB), Jg. 324, 2002, Nr. 5, S. 1041 – 1050
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The Core Structure of TMC-95A Is a Promising Lead for Reversible Proteasome InhibitionIn: Angewandte Chemie International Edition, Jg. 41, 2002, Nr. 5, S. 780 – 783
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ProteolysisIn: Brenner's Encyclopedia of Genetics: Second Edition / Maloy, Stanley R.; Hughes, Kelly T.. Amsterdam: Elsevier, 2013, S. 501 – 503
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Structural determinants for 20S proteasome inhibition by TMC-95AIn: Peptides 2004 : bridges between disciplines ; proceedings of the Third International and Twenty-Eighth European Peptide Symposium, September 5 - 10, 2004, Prague, Czech Republic / Flegel, Martin (Hrsg.). Geneva, Switzerland: Kenes International, 2004, S. 657 – 658