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Structure paper

TitleStructure-Based Design of Novel Potent Protein Kinase CK2 (CK2) Inhibitors with Phenyl-azole Scaffolds
Journal, issue, pagesJ. Med. Chem., Vol. 55, Page 2899-2903, Year 2012
Publish dateApr 18, 2011 (structure data deposition date)
AuthorsHou, Z. / Nakanishi, I. / Kinoshita, T. / Takei, Y. / Yasue, M. / Misu, R. / Suzuki, Y. / Nakamura, S. / Kure, T. / Ohno, H. ...Hou, Z. / Nakanishi, I. / Kinoshita, T. / Takei, Y. / Yasue, M. / Misu, R. / Suzuki, Y. / Nakamura, S. / Kure, T. / Ohno, H. / Murata, K. / Kitaura, K. / Hirasawa, A. / Tsujimoto, G. / Oishi, S. / Fujii, N.
External linksJ. Med. Chem. / PubMed:22339433
MethodsX-ray diffraction
Resolution2.5 Å
Structure data

PDB-3axw:
Crystal structure of human CK2alpha complexed with a potent inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

Chemicals

ChemComp-TID:
4-(5-amino-1,3,4-thiadiazol-2-yl)benzoic acid

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / kinase domain / serine/threonine kinase / TRANSFERASE-TRANSFERASE INHIBITOR complex

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