John T. Evans

ORCID: 0000-0003-1007-9675
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About
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Research Areas
  • Protein Kinase Regulation and GTPase Signaling
  • Cellular transport and secretion
  • Erythrocyte Function and Pathophysiology
  • Cell death mechanisms and regulation
  • Biochemical and Molecular Research
  • Pancreatic function and diabetes
  • PI3K/AKT/mTOR signaling in cancer

University of Victoria
2022-2024

Class IB phosphoinositide 3-kinase (PI3Kγ) is activated in immune cells and can form two distinct complexes (p110γ-p84 p110γ-p101), which are differentially by G protein-coupled receptors (GPCRs) Ras. Using a combination of X-ray crystallography, hydrogen deuterium exchange mass spectrometry (HDX-MS), electron microscopy, molecular modeling, single-molecule imaging, activity assays, we identify differences between p110γ-p84 p110γ-p101 that explain their differential membrane recruitment...

10.1016/j.celrep.2023.112172 article EN cc-by-nc-nd Cell Reports 2023-02-26

The formation of complexes between Rab11 and its effectors regulates multiple aspects membrane trafficking, including recycling ciliogenesis. WD repeat–containing protein 44 (WDR44) is a structurally uncharacterized effector that ciliogenesis by competing with prociliogenesis factors for binding. Here, we present detailed biochemical biophysical characterization the WDR44–Rab11 complex define specific residues mediating Using AlphaFold2 modeling hydrogen/deuterium exchange mass spectrometry,...

10.1016/j.jbc.2022.102764 article EN cc-by Journal of Biological Chemistry 2022-12-01
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