Cargando…
Competition between electrostatic interactions and halogen bonding in the protein–ligand system: structural and thermodynamic studies of 5,6-dibromobenzotriazole-hCK2α complexes
CK2 is a member of the CMGC group of eukaryotic protein kinases and a cancer drug target. It can be efficiently inhibited by halogenated benzotriazoles and benzimidazoles. Depending on the scaffold, substitution pattern, and pH, these compounds are either neutral or anionic. Their binding poses are...
Autores principales: | Winiewska-Szajewska, Maria, Czapinska, Honorata, Kaus-Drobek, Magdalena, Fricke, Anna, Mieczkowska, Kinga, Dadlez, Michał, Bochtler, Matthias, Poznański, Jarosław |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641685/ https://www.ncbi.nlm.nih.gov/pubmed/36347916 http://dx.doi.org/10.1038/s41598-022-23611-0 |
Ejemplares similares
-
Halogen Atoms in the Protein–Ligand System.
Structural and Thermodynamic Studies of the Binding of Bromobenzotriazoles
by the Catalytic Subunit of Human Protein Kinase CK2
por: Czapinska, Honorata, et al.
Publicado: (2021) -
Synthesis of Novel Halogenated Heterocycles Based on o-Phenylenediamine and Their Interactions with the Catalytic Subunit of Protein Kinase CK2
por: Winiewska-Szajewska, Maria, et al.
Publicado: (2021) -
Structural basis of the methylation specificity of R.DpnI
por: Mierzejewska, Karolina, et al.
Publicado: (2014) -
Rational drug-design approach supported with thermodynamic studies — a peptide leader for the efficient bi-substrate inhibitor of protein kinase CK2
por: Winiewska-Szajewska, Maria, et al.
Publicado: (2019) -
Restriction endonuclease MvaI is a monomer that recognizes its target sequence asymmetrically
por: Kaus-Drobek, Magdalena, et al.
Publicado: (2007)