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1 PI4K-IIIalpha co-localized with NS5A and double-stranded
2 y, Vps74 (the orthologue of human GOLPH3), a PI4K effector required to maintain residence of a subset
4 onist-induced phospholipase C activation and PI4K inhibition, but not isolated PtdIns(4,5)P(2) deplet
6 rum (Pf) phosphatidylinositol-4-kinase beta (PI4K), identified 1,5-naphthyridines with basic groups a
7 versely, lowering PIP2 synthesis by blocking PI4K or using the PIP2 scavengers polylysine or bovine s
9 er-studied phosphoinositide kinase families, PI4K and PIPK, focusing on their functions and relevance
10 l 4-kinase beta (PI4KB) is one of four human PI4K enzymes that generate phosphatidylinositol 4-phosph
13 t of subtype-specific inhibitors of type-III PI4Ks and help to better understand the significance of
15 ibits phosphatidylinositol 4-kinase IIIbeta (PI4K) in the human malaria parasite Plasmodium, demonstr
16 chemically distinct agents known to inhibit PI4K, resulted in both an inhibition of agonist-induced
17 , neither LIS1 nor phosphoinositol-4 kinase (PI4K) were detected in any of the purified tagged 3A sam
22 wo classes of phosphatidylinositol 4-kinase (PI4K), designated as Types II and III, that phosphorylat
28 nlike PI3Ks, phosphatidylinositol 4-kinases (PI4Ks) and phosphatidylinositol phosphate kinases (PIPKs
31 hat distinct phosphatidylinositol 4-kinases (PI4Ks) play important roles at multiple steps in the tra
32 vesicles by phosphatidylinositol 4-kinases (PI4Ks) that produce phosphatidylinositol 4-phosphate (Pt
35 parison of type II and type III PI4-kinases, PI4Ks were not required for HCV entry, and only PI4K-III
36 respect to the kinetic effects of modulating PI4K activity on polarized biosynthetic traffic in MDCK
37 IIalpha, which also accounts for the bulk of PI4K activity in brain extracts, is concentrated at syna
41 ailed study of novel selective inhibitors of PI4K IIIbeta, which exert antiviral activity against a p
48 tidylinositol 4-kinases (PtdIns 4-kinases or PI4Ks) are at the apex of the phosphoinsitide cascade.
51 ups at 8-position, which retained Plasmodium PI4K inhibitory activity but switched primary mode of ac
55 initial HCV RNA translation, suggesting that PI4K-IIIalpha functions at a posttranslational stage.
56 l binding protein (Osbp) or knockdown of the PI4K four wheel drive (fwd) exacerbates the Vps54KO/KO p
59 ts under dynamic conditions and that various PI4Ks regulate PI(4)P synthesis in distinct cellular com