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TitleSpecies-selective targeting of pathogens revealed by the atypical structure and active site of Trypanosoma cruzi histone deacetylase DAC2.
Journal, issue, pagesCell Rep, Vol. 37, Page 110129-110129, Year 2021
Publish dateOct 18, 2021 (structure data deposition date)
AuthorsMarek, M. / Ramos-Morales, E. / Picchi-Constante, G.F.A. / Bayer, T. / Norstrom, C. / Herp, D. / Sales-Junior, P.A. / Guerra-Slompo, E.P. / Hausmann, K. / Chakrabarti, A. ...Marek, M. / Ramos-Morales, E. / Picchi-Constante, G.F.A. / Bayer, T. / Norstrom, C. / Herp, D. / Sales-Junior, P.A. / Guerra-Slompo, E.P. / Hausmann, K. / Chakrabarti, A. / Shaik, T.B. / Merz, A. / Troesch, E. / Schmidtkunz, K. / Goldenberg, S. / Pierce, R.J. / Mourao, M.M. / Jung, M. / Schultz, J. / Sippl, W. / Zanchin, N.I.T. / Romier, C.
External linksCell Rep / PubMed:34936867
MethodsX-ray diffraction
Resolution1.75 - 2.3 Å
Structure data

PDB-7q1b:
Crystal structure of Trypanosoma cruzi histone deacetylase DAC2 complexed with Quisinostat
Method: X-RAY DIFFRACTION / Resolution: 1.75 Å

PDB-7q1c:
Crystal structure of Trypanosoma cruzi histone deacetylase DAC2 complexed with a hydroxamate inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-K:
Unknown entry

ChemComp-GOK:
2-[4-[[(1-methylindol-3-yl)methylamino]methyl]piperidin-1-yl]-~{N}-oxidanyl-pyrimidine-5-carboxamide / antineoplastic, inhibitor*YM

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

ChemComp-T56:
(E)-3-dibenzofuran-4-yl-N-oxidanyl-prop-2-enamide

Source
  • trypanosoma cruzi (eukaryote)
KeywordsHYDROLASE / Epigenetics / Trypanosoma cruzi / Histone deacetylase / DAC2 / Pathogen

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