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TitleBenzothiazole based inhibitors of p38alpha MAP kinase.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 1874-1879, Year 2008
Publish dateFeb 1, 2008 (structure data deposition date)
AuthorsLiu, C. / Lin, J. / Pitt, S. / Zhang, R.F. / Sack, J.S. / Kiefer, S.E. / Kish, K. / Doweyko, A.M. / Zhang, H. / Marathe, P.H. ...Liu, C. / Lin, J. / Pitt, S. / Zhang, R.F. / Sack, J.S. / Kiefer, S.E. / Kish, K. / Doweyko, A.M. / Zhang, H. / Marathe, P.H. / Trzaskos, J. / Mckinnon, M. / Dodd, J.H. / Barrish, J.C. / Schieven, G.L. / Leftheris, K.
External linksBioorg. Med. Chem. Lett. / PubMed:18296051
MethodsX-ray diffraction
Resolution2.8 Å
Structure data

PDB-3c5u:
P38 ALPHA map kinase complexed with a benzothiazole based inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.8 Å

Chemicals

ChemComp-P41:
6-[4-(2-fluorophenyl)-1,3-oxazol-5-yl]-N-(1-methylethyl)-1,3-benzothiazol-2-amine

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / SERINE/THREONINE-PROTEIN KINASE / KINASE / P38 MAP KINASE / Alternative splicing / ATP-binding / Cytoplasm / Nucleotide-binding / Nucleus / Phosphoprotein

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