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Structure paper

TitlePlasma metabolites-based drug design: Discovery of novel and highly selective phosphodiesterase 5 inhibitors
Journal, issue, pagesChin. Chem. Lett., Page 111236-, Year 2025
Publish dateFeb 4, 2025 (structure data deposition date)
AuthorsWu, D. / Ma, Q. / Chen, Y. / Yang, G. / Zhang, F. / Jiang, M. / Wang, X. / Liu, X. / Zhou, Q. / Huang, Y.Y. ...Wu, D. / Ma, Q. / Chen, Y. / Yang, G. / Zhang, F. / Jiang, M. / Wang, X. / Liu, X. / Zhou, Q. / Huang, Y.Y. / Li, Z. / Luo, H.B.
External linksChin. Chem. Lett. / Search PubMed
MethodsX-ray diffraction
Resolution2.5 - 2.7 Å
Structure data

PDB-9lsl:
The crystal structure of PDE5A with L1
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

PDB-9lsm:
The crystal structure of PDE5A with L9
Method: X-RAY DIFFRACTION / Resolution: 2.7 Å

Chemicals

PDB-1elj:
THE CRYSTAL STRUCTURE OF LIGANDED MALTODEXTRIN-BINDING PROTEIN FROM PYROCOCCUS FURIOSUS

ChemComp-ZN:
Unknown entry

ChemComp-MG:
Unknown entry

ChemComp-HOH:
WATER

PDB-1elc:
Analogous inhibitors of elastase do not always bind analogously

ChemComp-SO4:
SULFATE ION

Source
  • homo sapiens (human)
KeywordsHYDROLASE / PDE5A

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