Atomic structure of the MAP kinase ERK2 at 2.3 A resolution

Zhang, Faming, Strand, Arne, Robbins, David, Cobb, Melanie H., Goldsmith, Elizabeth J.·1994·Nature

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  55. signaling pathway required for germ cell survival GLA-3 is a novel component of the MAP kinase MPK-1
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  56. Dissecting mitogen-activated protein kinase cascades involving arabidopsis MKK6
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  57. Inhibition Of Vascular Endothelial Growth Factor ( Vegf) And Stem- Cell Factor ( Scf) Receptor Kinases As Therapeutic Targets For The Treatment Of Human Diseases
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  61. Propofol-induced changes in neurotrophic signaling in 14-day-old rat forebrain
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  98. BindingDB Entry 50007037: Structure-based design of a potent, selective, and irreversible inhibitor of the catalytic domain of the erbB receptor subfamily of protein tyrosine kinases.
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  99. BindingDB Entry 50016960: Crystal structure of human ERK2 complexed with a pyrazolo[3,4-c]pyridazine derivative.
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  100. BindingDB Entry 50006430: Tyrosine kinase inhibitors. 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth factor receptor.
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