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Structure paper

TitleA detailed thermodynamic profile of cyclopentyl and isopropyl derivatives binding to CK2 kinase
Journal, issue, pagesMol. Cell. Biochem., Vol. 356, Page 97-105, Year 2011
Publish dateDec 23, 2010 (structure data deposition date)
AuthorsKinoshita, T. / Sekiguchi, Y. / Fukada, H. / Nakaniwa, T. / Tada, T. / Nakamura, S. / Kitaura, K. / Ohno, H. / Suzuki, Y. / Hirasawa, A. ...Kinoshita, T. / Sekiguchi, Y. / Fukada, H. / Nakaniwa, T. / Tada, T. / Nakamura, S. / Kitaura, K. / Ohno, H. / Suzuki, Y. / Hirasawa, A. / Nakanishi, I. / Tsujimoto, G.
External linksMol. Cell. Biochem. / PubMed:21735094
MethodsX-ray diffraction
Resolution1.6 - 2.6 Å
Structure data

PDB-3at2:
Crystal structure of CK2alpha
Method: X-RAY DIFFRACTION / Resolution: 1.6 Å

PDB-3at3:
Crystal structure of CK2alpha with pyradine derivative
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

PDB-3at4:
Crystal structure of CK2alpha with pyradine derivertive
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-HOH:
WATER

ChemComp-ATK:
(1-{6-[6-(cyclopentylamino)-1H-indazol-1-yl]pyrazin-2-yl}-1H-pyrrol-3-yl)acetic acid

ChemComp-CCK:
[1-(6-{6-[(1-methylethyl)amino]-1H-indazol-1-yl}pyrazin-2-yl)-1H-pyrrol-3-yl]acetic acid

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / CK2 / kinase / TRANSFERASE/TRANSFERASE INHIBITOR / TRANSFERASE-TRANSFERASE INHIBITOR complex

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