2H96
Discovery of Potent, Highly Selective, and Orally Bioavailable Pyridine Carboxamide C-jun NH2-terminal Kinase Inhibitors
Summary for 2H96
Entry DOI | 10.2210/pdb2h96/pdb |
Related | 2g01 2gmx |
Descriptor | Mitogen-activated protein kinase 8, C-jun-amino-terminal kinase-interacting protein 1, SULFATE ION, ... (5 entities in total) |
Functional Keywords | jnk1, c-jun n-terminal kinase, protein kinase jnk1 inhibitors, pyridine carboxamide inhibitors, transcription |
Biological source | Homo sapiens (human) More |
Cellular location | Cytoplasm (By similarity): Q9UQF2 |
Total number of polymer chains | 4 |
Total formula weight | 89781.50 |
Authors | Abad-Zapatero, C. (deposition date: 2006-06-09, release date: 2006-07-25, Last modification date: 2023-08-30) |
Primary citation | Zhao, H.,Serby, M.D.,Xin, Z.,Szczepankiewicz, B.G.,Liu, M.,Kosogof, C.,Liu, B.,Nelson, L.T.,Johnson, E.F.,Wang, S.,Pederson, T.,Gum, R.J.,Clampit, J.E.,Haasch, D.L.,Abad-Zapatero, C.,Fry, E.H.,Rondinone, C.,Trevillyan, J.M.,Sham, H.L.,Liu, G. Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitors. J.Med.Chem., 49:4455-4458, 2006 Cited by PubMed: 16854050DOI: 10.1021/jm060465l PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3 Å) |
Structure validation
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