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Addressing the Glycine-Rich Loop of Protein Kinases by a Multi-Facetted Interaction Network: Inhibition of PKA and a PKB MimicScreening and Design of Inhibitor Scaffolds for the Antibiotic Resistance Oxacillinase-48 (OXA-48) through Surface Plasmon Resonance ScreeningA high-throughput, restriction-free cloning and screening strategy based on ccdB-gene replacement.Structural origins of AGC protein kinase inhibitor selectivities: PKA as a drug discovery tool.Dissemination and Characteristics of a Novel Plasmid-Encoded Carbapenem-Hydrolyzing Class D β-Lactamase, OXA-436 from Four Patients Involving Six Different Hospitals in Denmark.A focused fragment library targeting the antibiotic resistance enzyme - Oxacillinase-48: Synthesis, structural evaluation and inhibitor design.Structure, activity and thermostability investigations of OXA-163, OXA-181 and OXA-245 using biochemical analysis, crystal structures and differential scanning calorimetry analysisThe biological assembly of OXA-48 reveals a dimer interface with high charge complementarity and very high affinity
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description
hulumtues
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հետազոտող
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Bjarte Aarmo Lund
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Bjarte Aarmo Lund
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Bjarte Aarmo Lund
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0000-0001-9141-0555