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Structure paper

TitleAntitumor activity of pyridocarbazole and benzopyridoindole derivatives that inhibit protein kinase CK2.
Journal, issue, pagesCancer Res., Vol. 70, Page 9865-9874, Year 2010
Publish dateSep 20, 2010 (structure data deposition date)
AuthorsPrudent, R. / Moucadel, V. / Nguyen, C.H. / Barette, C. / Schmidt, F. / Florent, J.C. / Lafanechere, L. / Sautel, C.F. / Duchemin-Pelletier, E. / Spreux, E. ...Prudent, R. / Moucadel, V. / Nguyen, C.H. / Barette, C. / Schmidt, F. / Florent, J.C. / Lafanechere, L. / Sautel, C.F. / Duchemin-Pelletier, E. / Spreux, E. / Filhol, O. / Reiser, J.B. / Cochet, C.
External linksCancer Res. / PubMed:21118972
MethodsX-ray diffraction
Resolution1.8 - 2.1 Å
Structure data

PDB-3owj:
Human CK2 catalytic domain in complex with a pyridocarbazole derivative inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.85 Å

PDB-3owk:
Human CK2 catalytic domain in complex with a benzopyridoindole derivative inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

PDB-3owl:
Human CK2 catalytic domain in complex with a benzopyridoindole derivative inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-1EL:
9-hydroxy-5,11-dimethyl-4,6-dihydro-1H-pyrido[4,3-b]carbazol-1-one

ChemComp-HOH:
WATER

ChemComp-18E:
7-chloro-10-methyl-11H-benzo[g]pyrido[4,3-b]indol-3-ol

ChemComp-SO4:
SULFATE ION

ChemComp-19E:
11-chloro-8-methyl-7H-benzo[e]pyrido[4,3-b]indol-3-ol

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / SERINE/THREONINE-PROTEIN KINASE / CK2 / inhibitor / pyridocarbazole / ellipticine / TRANSFERASE / TRANSFERASE-TRANSFERASE INHIBITOR complex / benzopyridoindole / pyridocarbazol

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