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Structure paper

TitleDihydroxylphenyl amides as inhibitors of the Hsp90 molecular chaperone.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 6273-6278, Year 2008
Publish dateSep 19, 2008 (structure data deposition date)
AuthorsKung, P.P. / Funk, L. / Meng, J. / Collins, M. / Zhou, J.Z. / Johnson, M.C. / Ekker, A. / Wang, J. / Mehta, P. / Yin, M.J. ...Kung, P.P. / Funk, L. / Meng, J. / Collins, M. / Zhou, J.Z. / Johnson, M.C. / Ekker, A. / Wang, J. / Mehta, P. / Yin, M.J. / Rodgers, C. / Davies, J.F. / Bayman, E. / Smeal, T. / Maegley, K.A. / Gehring, M.R.
External linksBioorg. Med. Chem. Lett. / PubMed:18929486
MethodsX-ray diffraction
Resolution1.55 - 2 Å
Structure data

PDB-3eko:
Dihydroxylphenyl amides as inhibitors of the Hsp90 molecular chaperone
Method: X-RAY DIFFRACTION / Resolution: 1.55 Å

PDB-3ekr:
Dihydroxylphenyl amides as inhibitors of the Hsp90 molecular chaperone
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-PYU:
2-(1H-pyrrol-1-ylcarbonyl)benzene-1,3,5-triol

ChemComp-PO4:
PHOSPHATE ION

ChemComp-HOH:
WATER

ChemComp-PY9:
4-{[(2R)-2-(2-methylphenyl)pyrrolidin-1-yl]carbonyl}benzene-1,3-diol

Source
  • homo sapiens (human)
KeywordsCHAPERONE / HSP90 inhibitors / Alternative splicing / ATP-binding / Cytoplasm / Nucleotide-binding / Phosphoprotein / Stress response

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