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Structure paper

TitleSpecific inhibition of an anticancer target, polo-like kinase 1, by allosterically dismantling its mechanism of substrate recognition.
Journal, issue, pagesProc. Natl. Acad. Sci. USA, Vol. 120, Page e2305037120-e2305037120, Year 2023
Publish dateMar 8, 2023 (structure data deposition date)
AuthorsPark, J.E. / Kirsch, K. / Lee, H. / Oliva, P. / Ahn, J.I. / Ravishankar, H. / Zeng, Y. / Fox, S.D. / Kirby, S.A. / Badhwar, P. ...Park, J.E. / Kirsch, K. / Lee, H. / Oliva, P. / Ahn, J.I. / Ravishankar, H. / Zeng, Y. / Fox, S.D. / Kirby, S.A. / Badhwar, P. / Andresson, T. / Jacobson, K.A. / Lee, K.S.
External linksProc. Natl. Acad. Sci. USA / PubMed:37603740
MethodsX-ray diffraction
Resolution1.65 Å
Structure data

PDB-8crc:
Structure of human Plk1 PBD in complex with Allopole-A
Method: X-RAY DIFFRACTION / Resolution: 1.65 Å

Chemicals

ChemComp-GOL:
GLYCEROL

ChemComp-VIH:
7-chloro-4-(cyclopropylmethyl)-1-thioxo-2,4-dihydrothieno[2,3-e][1,2,4]triazolo[4,3-a]pyrimidin-5(1H)-one

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / KINASE / SERINE/THREONINE PROTEIN KINASE / SMALL MOLECULE / ALLOSTERIC INHIBITOR / CELL CYCLE / LOCALIZATION / CELL DIVISION / MITOSIS / NUCLEUS / PHOSPHOPROTEIN / PHOSPHOPEPTIDE BINDING DOMAIN / TRANSFERASE-INHIBITOR COMPLEX

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