D. Lindenblatt

发表

Design of CK2β‐Mimicking Peptides as Tools To Study the CK2α/CK2β Interaction in Cancer Cells

C. Götz, M. Pietsch, K. Niefind, 2019, ChemMedChem.

De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway

Tzung-Chien Hsieh, N. Fleischer, P. Krawitz, 2022, HGG advances.

Structural and mechanistic basis of the inhibitory potency of selected 2-aminothiazole compounds on protein kinase CK2.

J. Jose, K. Niefind, D. Lindenblatt, 2020, Journal of medicinal chemistry.

Development of a high-throughput screening-compatible assay to identify inhibitors of the CK2α/CK2β interaction.

C. Götz, O. Issinger, V. Helms, 2015, Analytical biochemistry.

Impact of process stress on protein stability in highly-loaded solid protein/PEG formulations from small-scale melt extrusion

K. Wagner, C. Werner, D. Lindenblatt, 2022, International journal of pharmaceutics: X.

Unexpected Binding Mode of a Potent Indeno[1,2-b]indole-Type Inhibitor of Protein Kinase CK2 Revealed by Complex Structures with the Catalytic Subunit CK2α and Its Paralog CK2α′

J. Jose, K. Niefind, D. Lindenblatt, 2017, Pharmaceuticals.

Molecular Plasticity of Crystalline CK2α' Leads to KN2, a Bivalent Inhibitor of Protein Kinase CK2 with Extraordinary Selectivity.

C. Götz, J. Jose, K. Niefind, 2021, Journal of medicinal chemistry.

Diacritic Binding of an Indenoindole Inhibitor by CK2α Paralogs Explored by a Reliable Path to Atomic Resolution CK2α′ Structures

J. Jose, K. Niefind, D. Lindenblatt, 2019, ACS omega.

Structural and Enzymological Evidence for an Altered Substrate Specificity in Okur-Chung Neurodevelopmental Syndrome Mutant CK2αLys198Arg

J. Jose, K. Niefind, D. Lindenblatt, 2022, Frontiers in Molecular Biosciences.

Synthesis, biological properties and structural study of new halogenated azolo[4,5-b]pyridines as inhibitors of CK2 kinase.

K. Niefind, D. Lindenblatt, C. Toelzer, 2020, Bioorganic chemistry.

Unexpected Binding Mode of a Potent Indeno[1,2-b]indole-Type Inhibitor of Protein Kinase CK2 Revealed by Complex Structures with the Catalytic Subunit CK2α and Its Paralog CK2α′

J. Jose, K. Niefind, D. Lindenblatt, 2017, Pharmaceuticals.

Discovery and Exploration of Protein Kinase CK2 Binding Sites Using CK2α′Cys336Ser as an Exquisite Crystallographic Tool

K. Niefind, A. Uri, Kaido Viht, 2023, Kinases and Phosphatases.