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To initially locate the most abundant phosphorylation sites within ArfGAP1, we conducted in vitro radioactive kinase assays using [ 33 P]--ATP together with immunopurified recombinant full-length FLAG-tagged human LRRK2 (WT, G2019S or D1994A) and a series of GST-tagged ArfGAP1 protein fragments (residues 1-136, 137-415, 137-251, 252-359 and 360-415) ( Fig

2 Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA

doi: 10.1016/j.biopsych.2009.10.030 44 St-OngeVWattsAAbizaidA

Mechanistic insights into hyperuricemia-associated renal abnormalities with special emphasis on epithelial-to-mesenchymal transition: Pathologic implications and putative pharmacologic targets

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doi: 10.1371/journal.pone.0132589 130 LiM.WangB.ZhangM.RantalainenM.WangS.ZhouH.et al (2008)