Template:PDB Gallery/5602

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