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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

Summary for 2O0U
Entry DOI10.2210/pdb2o0u/pdb
DescriptorMitogen-activated protein kinase 10, N-{3-CYANO-6-[3-(1-PIPERIDINYL)PROPANOYL]-4,5,6,7-TETRAHYDROTHIENO[2,3-C]PYRIDIN-2-YL}1-NAPHTHALENECARBOXAMIDE (3 entities in total)
Functional Keywordskinase fold, transferase
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm : P53779
Total number of polymer chains1
Total formula weight42532.28
Authors
Rowland, P.,Somers, D. (deposition date: 2006-11-28, release date: 2007-02-27, Last modification date: 2023-12-27)
Primary citationAngell, R.M.,Atkinson, F.L.,Brown, M.J.,Chuang, T.T.,Christopher, J.A.,Cichy-Knight, M.,Dunn, A.K.,Hightower, K.E.,Malkakorpi, S.,Musgrave, J.R.,Neu, M.,Rowland, P.,Shea, R.L.,Smith, J.L.,Somers, D.O.,Thomas, S.A.,Thompson, G.,Wang, R.
N-(3-Cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)amides as potent, selective, inhibitors of JNK2 and JNK3.
Bioorg.Med.Chem.Lett., 17:1296-1301, 2007
Cited by
PubMed: 17194588
DOI: 10.1016/j.bmcl.2006.12.003
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

218853

數據於2024-04-24公開中

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