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-Structure paper
Title | Multitarget, Selective Compound Design Yields Potent Inhibitors of a Kinetoplastid Pteridine Reductase 1. |
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Journal, issue, pages | J. Med. Chem., Vol. 65, Page 9011-9033, Year 2022 |
Publish date | Jun 7, 2019 (structure data deposition date) |
Authors | Pohner, I. / Quotadamo, A. / Panecka-Hofman, J. / Luciani, R. / Santucci, M. / Linciano, P. / Landi, G. / Di Pisa, F. / Dello Iacono, L. / Pozzi, C. ...Pohner, I. / Quotadamo, A. / Panecka-Hofman, J. / Luciani, R. / Santucci, M. / Linciano, P. / Landi, G. / Di Pisa, F. / Dello Iacono, L. / Pozzi, C. / Mangani, S. / Gul, S. / Witt, G. / Ellinger, B. / Kuzikov, M. / Santarem, N. / Cordeiro-da-Silva, A. / Costi, M.P. / Venturelli, A. / Wade, R.C. |
External links | J. Med. Chem. / PubMed:35675511 |
Methods | X-ray diffraction |
Resolution | 1.11 - 2.1 Å |
Structure data | PDB-6rx0: PDB-6rx5: PDB-6rx6: PDB-6rxc: |
Chemicals | ChemComp-NAP: ChemComp-ACT: ChemComp-KM5: ChemComp-GOL: ChemComp-HOH: ChemComp-FE1: ChemComp-KMK: ChemComp-NDP: |
Source |
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Keywords | OXIDOREDUCTASE / Trypanosoma brucei / pteridine reductase / PTR1 / TbPTR1 / pteridine based inhibitors / Leishmania major / LmPTR1 |