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Displaying 20 of 272 results for "MAPKAPK5"
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Dataset Title Dataset ID Primary Publications Keywords
Crystal Structure of the Complex of Human Mitogen Activated Protein Kinase Kinase 5 Phox Domain (MAP2K5-phox) with Human Mitogen Activated Protein Kinase Kinase Kinase 3 (MAP3K3B-phox) PDB:2O2V Crystal Structure of the Complex of Human Mitogen Activated Protein Kinase Kinase 5 Phox Domain (MAP2K5-phox) with Human Mitogen Activated Protein Kinase Kinase Kinase 3 (MAP3K3B-phox)
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mitogen activated protein kinase kinase 5 MAP kinase 5 mitogen activated protein kinase kinase kinas...
Crystal Structure of the complex of human mitogen activated protein kinase kinase 5 phox domain (MAP2K5-phox) with human mitogen activated protein kinase kinase kinase 2 phox domain (MAP3K2-phox) PDB:2NPT Crystal Structure of the complex of human mitogen activated protein kinase kinase 5 phox domain (MAP2K5-phox) with human mitogen activated protein kinase kinase kinase 2 phox domain (MAP3K2-phox)
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mitogen activated protein kinase kinase 5 MAP kinase kinase 5 mitogen activated protein kinase kinas...
Solution structure of the PB1 domain of mouse mitogen activated protein kinase kinase 5 (MAP2K5) PDB:1WI0 Solution structure of the PB1 domain of mouse mitogen activated protein kinase kinase 5 (MAP2K5)
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protein-protein interaction site
STRUCTURE OF MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 5 PDB:2CLQ Structural and Functional Characterization of the Human Protein Kinase Ask1.
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TRANSFERASE
TRANSFERASE
METAL-BINDING
APOPTOSIS
Unphosphorylated Mitogen Activated Protein Kinase ERK2 in Complex with (4-{[5-Carbamoyl-4-(3-Methylanilino)Pyrimidin 2-Yl]Amino}Phenyl)Acetic Acid PDB:2Z7L Identification of a key element for hydrogen-bonding patterns between protein kinases and their inhibitors
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SERINE/THREONINE-PROTEIN KINASE
Crystal structure of mitogen-activated protein kinase 14 (P38-H5) complex with 2-(2-CHLOROPHENYL)-N-(5-(CYCLOPROPYLCARBAMOYL)-2-METHYLPHENYL)-1,3-THIAZOLE-5-CARBOXAMIDE PDB:4KIP The Identification of Novel P38-Alpha Isoform Selective Kinase Inhibitors Having an Unprecedented P38-Alpha Binding Mode
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SERINE/THREONINE-PROTEIN KINASE KINASE P38 MAP KINASE
Crystal structure of mitogen-activated protein kinase 14 (P38-H5) complex with ETHYL 6-((5-(CYCLOPROPYLCARBAMOYL)-2-METHYLPHENYL)CARBAMOYL)-1H-INDOLE-1-CARBOXYLATE PDB:4KIQ The Identification of Novel P38-Alpha Isoform Selective Kinase Inhibitors Having an Unprecedented P38-Alpha Binding Mode
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SERINE/THREONINE-PROTEIN KINASE KINASE P38 MAP KINASE
Crystal structure of mitogen-activated protein kinase 14 (P38-H5) complex with 5-(2-CHLOROPHENYL)-N-(5-(CYCLOPROPYLCARBAMOYL)-2-METHYLPHENYL)-2-THIOPHENECARBOXAMIDE PDB:4KIN The Identification of Novel P38-Alpha Isoform Selective Kinase Inhibitors Having an Unprecedented P38-Alpha Binding Mode
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SERINE/THREONINE-PROTEIN KINASE KINASE P38 MAP KINASE
X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in a complex with ligand and MgATP PDB:2P55 4-anilino-5-carboxamido-2-pyridone derivatives as noncompetitive inhibitors of mitogen-activated protein kinase kinase.
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protein kinase structure; Mitogen activated protein kinase kinase; signal transduction; ligand co-co...
Phenylalanine pyrrolotriazine p38 alpha map kinase inhibitor compound 11B PDB:2RG5 Design, Synthesis, and Anti-inflammatory Properties of Orally Active 4-(Phenylamino)-pyrrolo[2,1-f][1,2,4]triazine p38alpha Mitogen-Activated Protein Kinase Inhibitors
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SERINE/THREONINE-PROTEIN KINASE KINASE P38 MAP KINASE
Mitogen-Activated Protein Kinase Kinase (MEK1) bound to G805 PDB:4U7Z Structure based design of novel 6,5 heterobicyclic mitogen-activated protein kinase kinase (MEK) inhibitors leading to the discovery of imidazo[1,5-a] pyrazine G-479.
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Kinase
Phenylalanine pyrrolotriazine p38 alpha map kinase inhibitor compound 11J PDB:2RG6 Design, Synthesis, and Anti-inflammatory Properties of Orally Active 4-(Phenylamino)-pyrrolo[2,1-f][1,2,4]triazine p38alpha Mitogen-Activated Protein Kinase Inhibitors
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SERINE/THREONINE-PROTEIN KINASE KINASE P38 MAP KINASE
X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in complex with an inhibitor and MgATP PDB:3VVH X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in complex with an inhibitor and MgATP
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kinase domain kinase
X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in a complex with ligand and MgATP PDB:3EQB 2-Alkylamino- and alkoxy-substituted 2-amino-1,3,4-oxadiazoles-O-Alkyl benzohydroxamate esters replacements retain the desired inhibition and selectivity against MEK (MAP ERK kinase).
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PROTEIN KINASE STRUCTURE MITOGEN ACTIVATED PROTEIN KINASE KINASE TERNARY CO-COMPLEX WITH KINASE NON-...
Structural basis of autoactivation of p38 alpha induced by TAB1 (Tetragonal crystal form with bound sulphate) PDB:4LOQ Mechanism and consequence of the autoactivation of p38 alpha mitogen-activated protein kinase promoted by TAB1.
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protein kinase kinase-regulatory protein complex
Human p38 MAP Kinase in Complex with a Dibenzosuberone Derivative PDB:3UVQ Dibenzosuberones as p38 mitogen-activated protein kinase inhibitors with low ATP competitiveness and outstanding whole blood activity.
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protein kinase
MITOGEN ACTIVATED PROTEIN KINASE 7 IN COMPLEX WITH INHIBITOR PDB:4ZSG Discovery of a novel allosteric inhibitor-binding site in ERK5: comparison with the canonical kinase hinge ATP-binding site.
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KINASE KINASE
Human p38 MAP Kinase in Complex with Skepinone-L PDB:3QUE Skepinone-L is a selective p38 mitogen-activated protein kinase inhibitor.
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Kinase Domain
MITOGEN ACTIVATED PROTEIN KINASE 7 IN COMPLEX WITH INHIBITOR PDB:4ZSL Discovery of a novel allosteric inhibitor-binding site in ERK5: comparison with the canonical kinase hinge ATP-binding site.
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KINASE
MITOGEN ACTIVATED PROTEIN KINASE 7 IN COMPLEX WITH INHIBITOR PDB:4ZSJ Discovery of a novel allosteric inhibitor-binding site in ERK5: comparison with the canonical kinase hinge ATP-binding site.
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KINASE