1 ction as a phosphatidylinositol 4-phosphate (PtdIns(4)P) 5-kinase ().

2 (4,5)P(2) because of robust up-regulation of PtdIns4P 5-kinases.

3 ynthesis by phosphorylating and inactivating PtdIns(4)P 5-kinase.

4 n by Cki1 in vitro decreases the activity of PtdIns(4)P 5-kinase.

5 ctions as a coincidence detector of the Mss4 PtdIns(4)P 5-kinase and PtdIns(4,5)P(2) and serves as a

6  of PtdIns(4,5)P2 and in a lower activity of PtdIns(4)P 5-kinase associated with the plasma membrane.

7           Phosphatidylinositol ()P 5-kinase (PtdIns(4)P 5-kinase) catalyzes the last step in the synt

8 ction, purification, and characterization of PtdIns(4)P 5-kinase from the plasma membranes of Schizos

9 ons in phosphoinositide-modifying enzymes (a PtdIns(4)P-5-kinase in S. pombe and a PI-4-kinase in D.

10  demonstrate a role for PtdIns 4-kinases and PtdIns4P 5-kinases in selective and nonselective types o

11                   These results suggest that PtdIns(4)P 5-kinase is a target of Cki1 in S. pombe and

12                We also provide evidence that PtdIns(4)P 5-kinase is phosphorylated and inactivated by

13 ab1p homologues or mammalian Type I PIPkins (PtdIns4P 5-kinases) make PtdIns(3,5)P(2) in vivo.

14  4,5-bisphosphate [PtdIns(4,5)P2] as well as PtdIns4P 5-kinases mediating their interconversion, are

15 nase Stt4 and the plasma membrane-associated PtdIns4P 5-kinase Mss4 (but not the Golgi-associated Ptd

16 nd selective types of autophagy, whereas the PtdIns4P 5-kinase Mss4 is specifically involved in mitop

17                   We show that the conserved PtdIns(4)P 5-kinase, Mss4, forms dynamic, oligomeric str

18                                          The PtdIns(4)P 5-kinase, Mss4p, also is essential for spore

19                                          The PtdIns4P 5-kinases PIP5K1 and PIP5K2 are redundantly req

20 ype Igamma phosphatidylinositol 4-phosphate (PtdIns(4)P) 5-kinase (PIPKIgamma) and inositol polyphosp