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Structure paper

TitleToward understanding the structural basis of cyclin-dependent kinase 6 specific inhibition.
Journal, issue, pagesJ. Med. Chem., Vol. 49, Page 3826-3831, Year 2006
Publish dateOct 28, 2005 (structure data deposition date)
AuthorsLu, H. / Schulze-Gahmen, U.
External linksJ. Med. Chem. / PubMed:16789739
MethodsX-ray diffraction
Resolution2.8 - 3 Å
Structure data

PDB-2euf:
X-ray structure of human CDK6-Vcyclin in complex with the inhibitor PD0332991
Method: X-RAY DIFFRACTION / Resolution: 3 Å

PDB-2f2c:
X-ray structure of human CDK6-Vcyclinwith the inhibitor aminopurvalanol
Method: X-RAY DIFFRACTION / Resolution: 2.8 Å

Chemicals

ChemComp-CA:
Unknown entry

ChemComp-ACT:
ACETATE ION

ChemComp-LQQ:
6-ACETYL-8-CYCLOPENTYL-5-METHYL-2-[(5-PIPERAZIN-1-YLPYRIDIN-2-YL)AMINO]PYRIDO[2,3-D]PYRIMIDIN-7(8H)-ONE / medication, inhibitor*YM

ChemComp-DMS:
DIMETHYL SULFOXIDE / DMSO, precipitant*YM

ChemComp-HOH:
WATER

ChemComp-SO4:
SULFATE ION

ChemComp-AP9:
(2S)-2-({6-[(3-AMINO-5-CHLOROPHENYL)AMINO]-9-ISOPROPYL-9H-PURIN-2-YL}AMINO)-3-METHYLBUTAN-1-OL

Source
  • herpesvirus saimiri (strain 11)
  • homo sapiens (human)
KeywordsCELL CYCLE/TRANSFERASE / inhibitor complex of human cyclin-dependent kinase 6 / CELL CYCLE-TRANSFERASE COMPLEX / Small molecule inhibitor bound between N-terminal and C-terminal domain of kinase

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