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TitleDiscovery of Oral Polo-Like Kinase (Plk) Inhibitors with Enhanced Selectivity Profile Using Residue Targeted Drug Design
Journal, issue, pagesTo be Published
Publish dateAug 14, 2012 (structure data deposition date)
AuthorsBrown, K. / Charrier, J.D. / Durrant, S. / Griffiths, M. / Hudson, C. / Kay, D. / Knegtel, R. / Odonnell, M. / Pierard, F. / Twin, H. ...Brown, K. / Charrier, J.D. / Durrant, S. / Griffiths, M. / Hudson, C. / Kay, D. / Knegtel, R. / Odonnell, M. / Pierard, F. / Twin, H. / Weber, P. / Young, S.
External linksSearch PubMed
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-4b6l:
Discovery of Oral Polo-Like Kinase (PLK) Inhibitors with Enhanced Selectivity Profile using Residue Targeted Drug Design
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-9ZP:
4-[[(4R)-5-cyclopentyl-4-ethyl-3a,4-dihydro-3H-[1,2,4]triazolo[4,3-f]pteridin-7-yl]amino]-N-cyclopropyl-3-methoxy-benzamide

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / KINASE INHIBITORS / WATER-MEDIATED H-BOND

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