1jnk: THE C-JUN N-TERMINAL KINASE (JNK3S) COMPLEXED WITH MGAMP-PNP
1pmn: Crystal structure of JNK3 in complex with an imidazole-pyrimidine inhibitor
1pmq: The structure of JNK3 in complex with an imidazole-pyrimidine inhibitor
1pmu: The crystal structure of JNK3 in complex with a phenantroline inhibitor
1pmv: The structure of JNK3 in complex with a dihydroanthrapyrazole inhibitor
1ukh: Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
1uki: Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
2b1p: inhibitor complex of JNK3
2exc: Inhibitor complex of JNK3
2g01: Pyrazoloquinolones as Novel, Selective JNK1 inhibitors
2gmx: Selective Aminopyridine-Based C-Jun N-terminal Kinase inhibitors with cellular activity
2h96: Discovery of Potent, Highly Selective, and Orally Bioavailable Pyridine Carboxamide C-jun NH2-terminal Kinase Inhibitors
2no3: Novel 4-anilinopyrimidines as potent JNK1 Inhibitors
2o0u: Crystal structure of human JNK3 complexed with N-{3-cyano-6-[3-(1-piperidinyl)propanoyl]-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-2-yl}-1-naphthalenecarboxamide
2o2u: Crystal structure of human JNK3 complexed with N-(3-cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)-2-fluorobenzamide
2ok1: Crystal structure of JNK3 bound to N-benzyl-4-(4-(3-chlorophenyl)-1H-pyrazol-3-yl)-1H-pyrrole-2-carboxamide