subject area of
- Activation of JNK3 alpha 1 requires both MKK4 and MKK7: Kinetic characterization of in vitro phosphorylated JNK3 alpha 1 Academic Article
- Beta-arrestin 2: a receptor-regulated MAPK scaffold for the activation of JNK3 Academic Article
- Design and synthesis of 1-aryl-5-anilinoindazoles as c-Jun N-terminal kinase inhibitors Academic Article
- Design and synthesis of highly potent and isoform selective JNK3 inhibitors: SAR studies on aminopyrazole derivatives Academic Article
- Identification of a motif in the carboxyl terminus of β-arrestin2 responsible for activation of JNK3 Academic Article
- Kinetic mechanism and inhibitor characterization for c-jun-N-terminal kinase 3 alpha 1 Academic Article
- Structural basis and biological consequences for JNK2/3 isoform selective aminopyrazoles Academic Article
- Structural mechanisms of allostery and autoinhibition in JNK family kinases Academic Article
- Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-jun N-terminal kinase 3 (JNK3) over p38 Academic Article
- Substituting c-jun n-terminal kinase-3 (jnk3) atp-binding site amino acid residues with their p38 counterparts affects binding of jnk- and p38-selective inhibitors Academic Article
- The structure of jnk3 in complex with small molecule inhibitors: Structural basis for potency and selectivity Academic Article