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Crystal structure of the PIM2 kinase in complex with an organoruthenium inhibitorStructure of the CaMKIIdelta/calmodulin complex reveals the molecular mechanism of CaMKII kinase activationCrystal structure of the tetrameric Mad1-Mad2 core complex: implications of a 'safety belt' binding mechanism for the spindle checkpointStructures of the human eIF4E homologous protein, h4EHP, in its m7GTP-bound and unliganded formsA small-molecule inhibitor of Haspin alters the kinetochore functions of Aurora BSelective inhibition of BET bromodomainsBromodomain-containing protein 4 (BRD4) regulates RNA polymerase II serine 2 phosphorylation in human CD4+ T cellsCrystal structures and inhibitor identification for PTPN5, PTPRR and PTPN7: a family of human MAPK-specific protein tyrosine phosphatasesStructure of the human protein kinase MPSK1 reveals an atypical activation loop architectureActivation segment dimerization: a mechanism for kinase autophosphorylation of non-consensus sitesHistone recognition and large-scale structural analysis of the human bromodomain familyLarge-scale structural analysis of the classical human protein tyrosine phosphatomeThe structure of P-TEFb (CDK9/cyclin T1), its complex with flavopiridol and regulation by phosphorylationRestoring p53 function in human melanoma cells by inhibiting MDM2 and cyclin B1/CDK1-phosphorylated nuclear iASPPDNA damage in oocytes induces a switch of the quality control factor TAp63α from dimer to tetramerPIM serine/threonine kinases in the pathogenesis and therapy of hematologic malignancies and solid cancersSmall-molecule inhibition of BRDT for male contraception.Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressivaStructural genomics of histone tail recognitionProtein production and purificationCrystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-Met and its complex with the microbial alkaloid K-252aThe crystal structure of human receptor protein tyrosine phosphatase kappa phosphatase domain 1Structural coupling of SH2-kinase domains links Fes and Abl substrate recognition and kinase activationExploration of type II binding mode: A privileged approach for kinase inhibitor focused drug discovery?Structure and regulation of the human Nek2 centrosomal kinaseCrystal Structures of the p21-Activated Kinases PAK4, PAK5, and PAK6 Reveal Catalytic Domain Plasticity of Active Group II PAKsStructural analysis identifies imidazo[1,2-b]pyridazines as PIM kinase inhibitors with in vitro antileukemic activityStructural and Functional Characterization of the Human Protein Kinase ASK1Structure of the SOCS4-ElonginB/C Complex Reveals a Distinct SOCS Box Interface and the Molecular Basis for SOCS-Dependent EGFR DegradationA systematic interaction map of validated kinase inhibitors with Ser/Thr kinasesSimilar Biological Activities of Two Isostructural Ruthenium and Osmium ComplexesExtremely Tight Binding of a Ruthenium Complex to Glycogen Synthase Kinase 3Structure of the Pseudokinase VRK3 Reveals a Degraded Catalytic Site, a Highly Conserved Kinase Fold, and a Putative Regulatory Binding SiteKinase Domain Insertions Define Distinct Roles of CLK Kinases in SR Protein PhosphorylationStructure of dystrophia myotonica protein kinaseStructural Determinants of G-protein Subunit Selectivity by Regulator of G-protein Signaling 2 (RGS2)Synthesis, kinase inhibitory potencies, and in vitro antiproliferative evaluation of new Pim kinase inhibitorsStructure and functional characterization of the atypical human kinase haspinSmall-molecule kinase inhibitors provide insight into Mps1 cell cycle functionNew potent dual inhibitors of CK2 and Pim kinases: discovery and structural insights
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P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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Stefan Knapp
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Stefan Knapp
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Stefan Knapp
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Stefan Knapp
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Stefan Knapp
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Stefan Knapp
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S. Knapp
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Stefan Knapp
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Stefan Knapp
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Stefan Knapp
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Stefan Knapp
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Stefan Knapp
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P69
P106
P21
P31
P496
0000-0001-5995-6494