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Structure paper

TitleCrystal structure of human CDC7 kinase in complex with its activator DBF4.
Journal, issue, pagesNat. Struct. Mol. Biol., Vol. 19, Page 1101-1107, Year 2012
Publish dateMay 18, 2012 (structure data deposition date)
AuthorsHughes, S. / Elustondo, F. / Di Fonzo, A. / Leroux, F.G. / Wong, A.C. / Snijders, A.P. / Matthews, S.J. / Cherepanov, P.
External linksNat. Struct. Mol. Biol. / PubMed:23064647
MethodsX-ray diffraction
Resolution2.08 - 2.5 Å
Structure data

PDB-4f99:
Human CDC7 kinase in complex with DBF4 and nucleotide
Method: X-RAY DIFFRACTION / Resolution: 2.33 Å

PDB-4f9a:
Human CDC7 kinase in complex with DBF4 and nucleotide
Method: X-RAY DIFFRACTION / Resolution: 2.17 Å

PDB-4f9b:
Human CDC7 kinase in complex with DBF4 and PHA767491
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

PDB-4f9c:
Human CDC7 kinase in complex with DBF4 and XL413
Method: X-RAY DIFFRACTION / Resolution: 2.08 Å

Chemicals

ChemComp-ADP:
ADENOSINE-5'-DIPHOSPHATE / ADP, energy-carrying molecule*YM

ChemComp-MG:
Unknown entry

ChemComp-ZN:
Unknown entry

ChemComp-HOH:
WATER

ChemComp-0SY:
2-(pyridin-4-yl)-1,5,6,7-tetrahydro-4H-pyrrolo[3,2-c]pyridin-4-one

ChemComp-0SX:
8-chloro-2-[(2S)-pyrrolidin-2-yl][1]benzofuro[3,2-d]pyrimidin-4(3H)-one

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / SER/THR PROTEIN KINASE / PHOSPHORYLATION / CELL CYCLE / CELL DIVISION / MITOSIS / S PHASE / SERINE/THREONINE-PROTEIN KINASE / DBF4-dependent kinase / DDK / ATP-BINDING / NUCLEOTIDE-BINDING / ZINC-BINDING / NUCLEUS / TRANSFERASE/TRANSFERASE INHIBITOR / TRANSFERASE-TRANSFERASE INHIBITOR complex

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