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  3. JAK2 JH2 Fluorescence Polarization Assay and Crystal Structures for Complexes with Three Small Molecules

JAK2 JH2 Fluorescence Polarization Assay and Crystal Structures for Complexes with Three Small Molecules

  • ACS Med Chem Lett. 2017 May 17;8(6):614-617. doi: 10.1021/acsmedchemlett.7b00154.
Ana S Newton 1,  Luca Deiana 1,  David E Puleo 2,  José A Cisneros 1,  Kara J Cutrona 1,  Joseph Schlessinger 2,  William L Jorgensen 1
Affiliations

Affiliations

  • 1 Department of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.
  • 2 Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.
PMID: 28626520 DOI: 10.1021/acsmedchemlett.7b00154
Abstract

A competitive fluorescence polarization (FP) assay is reported for determining binding affinities of probe molecules with the pseudokinase JAK2 JH2 allosteric site. The syntheses of the fluorescent 5 and 6 used in the assay are reported as well as Kd results for 10 compounds, including JNJ7706621, NVP-BSK805, and filgotinib (GLPG0634). X-ray crystal structures of JAK2 JH2 in complex with NVP-BSK805, filgotinib, and diaminopyrimidine 8 elucidate the binding poses.

Keywords

FP; Filgotinib (GLPG0634); Fluorescence polarization; JAK2; JAK2 JH2; JNJ7706621; Janus Kinase 2; NVP-BSK805; Protein crystallography; Pseudokinase domain.

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