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1 ma and internal Na+ via mechanisms requiring phosphatidylinositol phosphates.
2 a likely binding site for the head groups of phosphatidylinositol phosphates.
3 tify a functional role for enigmatic nuclear phosphatidylinositol phosphates.
4 o isolated granule membranes and do not bind phosphatidylinositol phosphates.
5 reviously been used in headgroup analysis of phosphatidylinositol phosphates.
6 phosphorus chemical shifts in NMR spectra of phosphatidylinositol phosphates.
7 gy (PX) domains selectively bind to specific phosphatidylinositol phosphates.
8 ctor, whereas the PH domain binds to various phosphatidylinositol-phosphates.
9 ly activating the beta isoform of the type I phosphatidylinositol phosphate 5-kinase (PIP5Kbeta) thro
10                            Overexpression of phosphatidylinositol phosphate 5-kinase (PIP5KI) isoform
11                     Overexpression of type I phosphatidylinositol phosphate 5-kinase (PIP5KI), which
12 us to infect CV1 cells with the mouse type I phosphatidylinositol phosphate 5-kinase alpha (PIP5KI),
13                            Overexpression of phosphatidylinositol phosphate 5-kinase alpha (PIP5KIalp
14                      Cells expressing type I phosphatidylinositol phosphate 5-kinase and Dyn2-GFP rev
15        Here, we demonstrate that type Igamma phosphatidylinositol phosphate 5-kinase i5 (PIPKIgammai5
16              Here, we show that type I gamma phosphatidylinositol phosphate 5-kinase i5 (PIPKIgammai5
17        Here we demonstrate that type I gamma phosphatidylinositol phosphate 5-kinase i5 (PIPKIgammai5
18 wever, we demonstrate here that type I gamma phosphatidylinositol phosphate 5-kinase i5 (PIPKIgammai5
19 h motile vesicles in cells expressing type I phosphatidylinositol phosphate 5-kinases.
20 hat hydrolyze 5-phosphates from a variety of phosphatidylinositol phosphate and inositol phosphate su
21            There is evidence suggesting that phosphatidylinositol phosphate and nucleic acid are esse
22 acylglycerol and concomitant accumulation of phosphatidylinositol phosphate and phosphatidylinositol
23 n the PTEN N-terminus, we tested all natural phosphatidylinositol phosphates and found preferential b
24                            GSDMD-NT binds to phosphatidylinositol phosphates and phosphatidylserine (
25  full-length form, its preference to bind to phosphatidylinositol phosphates and sulfatides, and the
26 ol, phosphatidic acid, phosphatidylinositol, phosphatidylinositol phosphate, and phosphatidylinositol
27 hosphatidylglycerols, phosphatidylinositols, phosphatidylinositol-phosphates, and sulfatides) were sc
28 include lipid kinases with the generation of phosphatidylinositol phosphates as second messengers, al
29                  Binding assays confirm that phosphatidylinositol phosphates bind the PH domain, but
30 stored by expression of wild-type ORP1S or a phosphatidylinositol phosphate-binding mutant but not by
31 ongin domains 2/3 of Mon1 and functions as a phosphatidylinositol phosphate-binding site, explaining
32                  Additionally, we identified phosphatidylinositol phosphate biosynthesis and choleste
33 framework to strengthen our understanding of phosphatidylinositol-phosphate biosynthesis in the conte
34 nal framework to understand the mechanism of phosphatidylinositol-phosphate biosynthesis.
35                                              Phosphatidylinositol phosphates can act on both lipid re
36 ghly regulated through a network of distinct phosphatidylinositol phosphates consisting of seven grou
37                            Newly synthesized phosphatidylinositol phosphates have been implicated in
38 o phosphatase activity, but it can recognize phosphatidylinositol phosphate head groups.
39              We have now studied the role of phosphatidylinositol phosphates in synaptic vesicle exoc
40 ility; however, the highest-ranking lipid is phosphatidylinositol phosphate, in line with its propose
41 tes but can dephosphorylate a broad range of phosphatidylinositol phosphates, including phosphatidyli
42                      Activation of Kir2.1 by phosphatidylinositol phosphates is also highly selective
43                                       Type I phosphatidylinositol phosphate kinase (PIP5K1) phosphory
44 hreonine protein kinase (PK) and type IIbeta phosphatidylinositol phosphate kinase (PIPK) structures
45 pe and mutant p53 is regulated by the type I phosphatidylinositol phosphate kinase (PIPKI-alpha (also
46                Here we show that type Igamma phosphatidylinositol phosphate kinase (PIPKIgamma) direc
47                                  Type Igamma phosphatidylinositol phosphate kinase (PIPKIgamma) regul
48                                  Type Igamma phosphatidylinositol phosphate kinase (PIPKIgamma), a ph
49 vation of PIP2-producing enzyme, type Igamma phosphatidylinositol phosphate kinase (PIPKIgamma), by a
50  we show that phosphorylation of type Igamma phosphatidylinositol phosphate kinase (PIPKIgamma661) on
51                                      Type II phosphatidylinositol phosphate kinase (PIPKII) is an enz
52                 We show that the type Igamma phosphatidylinositol phosphate kinase 661 (PIPKIgamma661
53  signalling, increasing both the activity of phosphatidylinositol phosphate kinase and its associatio
54                     Here, we identify type I phosphatidylinositol phosphate kinase beta (PIPKIbeta),
55 uded that the flattened face of type II beta phosphatidylinositol phosphate kinase binds to membranes
56 mma (PIPKIgamma90) is a member of the type I phosphatidylinositol phosphate kinase family that has be
57  function of NRF2 is regulated by the type I phosphatidylinositol phosphate kinase gamma (PIPKIgamma)
58   This new protein, which we have designated phosphatidylinositol phosphate kinase homolog (PIPKH), i
59     Our research has identified type I gamma phosphatidylinositol phosphate kinase i5 (PIPKIgammai5)
60    Analytical ultracentrifugation shows that phosphatidylinositol phosphate kinase is a dimer in solu
61                                 Type II beta phosphatidylinositol phosphate kinase is a representativ
62                 Here we show that the type I phosphatidylinositol phosphate kinase isoform-gamma 661
63 nositol phosphate kinase is a representative phosphatidylinositol phosphate kinase that is active aga
64                                              Phosphatidylinositol phosphate kinase type 1 gamma (PtdI
65                                              Phosphatidylinositol phosphate kinase type 1gamma (PIPKI
66 tyrosine kinase Src phosphorylates Tyr644 on phosphatidylinositol phosphate kinase type I (PIPKI) gam
67                          Extended isoform of phosphatidylinositol phosphate kinase type I gamma (PIPK
68 retion in chromaffin cells from mice lacking phosphatidylinositol phosphate kinase type I gamma, the
69                    Here, we demonstrate that phosphatidylinositol phosphate kinase type Igamma (PIPKI
70 alin binds to a short C-terminal sequence in phosphatidylinositol phosphate kinase type Igamma (PIPKI
71                               We report that phosphatidylinositol phosphate kinase type Igamma (PIPKI
72  another non-integrin talin-binding protein, phosphatidylinositol phosphate kinase type Igamma-90, al
73 he structure of one such enzyme, type IIbeta phosphatidylinositol phosphate kinase, reveals a protein
74          Antibodies directed against type II phosphatidylinositol-phosphate kinase (phosphatidylinosi
75 ts of micromolar wortmannin and anti-type II phosphatidylinositol-phosphate kinase antibodies were ad
76 embers of one of these families, the type II phosphatidylinositol phosphate kinases (PIP kinases), ar
77 l G protein and upstream regulator of type I phosphatidylinositol phosphate kinases (PIP5Ks) and PM P
78 he 5 position of the inositol ring by type I phosphatidylinositol phosphate kinases (PIPK): PIPKIalph
79         PI(4,5)P(2) is synthesized by type I phosphatidylinositol phosphate kinases (PIPKI).
80                          It is unclear which phosphatidylinositol phosphate kinases (PIPkins) are res
81 nding proteins and is produced by the type I phosphatidylinositol phosphate kinases (PIPKIs).
82                               In animals the phosphatidylinositol phosphate kinases (PIPKs) are assoc
83                       The type I B family of phosphatidylinositol phosphate kinases (PIPKs) contain a
84 , phosphatidylinositol 4-kinases (PI4Ks) and phosphatidylinositol phosphate kinases (PIPKs) do not us
85                 We demonstrate that distinct phosphatidylinositol phosphate kinases (PIPKs), the type
86 te is synthesized by two distinct classes of phosphatidylinositol phosphate kinases (PIPKs), the type
87        These pathways require two classes of phosphatidylinositol phosphate kinases, termed type I an
88 yrosine-binding domain specifically binds to phosphatidylinositol phosphates known to be produced dur
89 teractions between the cytoplasmic tails and phosphatidylinositol phosphate lipids in the inner membr
90  suggest a model whereby local production of phosphatidylinositol phosphates may trigger the binding
91 icantly reduced binding to liposomes lacking phosphatidylinositol phosphates or cholesterol, liposome
92 mologue deleted on chromosome 10 (PTEN) is a phosphatidylinositol phosphate phosphatase and is freque
93                               PTEN encodes a phosphatidylinositol phosphate phosphatase specific for
94 t is lost in many human tumors and encodes a phosphatidylinositol phosphate phosphatase specific for
95                               Binding of the phosphatidylinositol phosphate PI5P to the PBR of UHRF1
96         Both a murine monoclonal antibody to phosphatidylinositol phosphate (PIP) and a human monoclo
97                         Imaging of different phosphatidylinositol phosphate (PIP) and organelle marke
98 tive method to detect, identify and quantify phosphatidylinositol phosphate (PIP) and phosphatidylino
99 ts of about 100 pmol, and the D3 isoforms of phosphatidylinositol phosphate (PIP) and PIP(2) are dete
100                             Here we describe phosphatidylinositol phosphate (PIP) binding by these pr
101 o pivotal features of Jps1: dimerization and phosphatidylinositol phosphate (PIP) binding.
102 to PI(4,5)P2 and its generating enzymes, the phosphatidylinositol phosphate (PIP) kinases (PIPKs).
103 also shows significant homology to mammalian phosphatidylinositol phosphate (PIP) kinases and we show
104                           Type I and type II phosphatidylinositol phosphate (PIP) kinases generate th
105            Organelle membranes have specific phosphatidylinositol phosphate (PIP) lipid enrichment li
106 ys by binding second messenger lipids of the phosphatidylinositol phosphate (PIP) lipid family.
107                                              Phosphatidylinositol phosphate (PIP) lipids are low-abun
108 Rs simulated, in particular, cholesterol and phosphatidylinositol phosphate (PIP) lipids, but the num
109 y important in these signaling processes are phosphatidylinositol phosphate (PIP) lipids, which are d
110 ruit proteins to membranes by recognition of phosphatidylinositol phosphate (PIP) lipids.
111  provide evidence for the phosphorylation of phosphatidylinositol phosphate (PIP) metabolic enzymes a
112  protein-membrane interactions by binding to phosphatidylinositol phosphate (PIP) molecules.
113 ruption of Ptpmt1, a mitochondrial Pten-like phosphatidylinositol phosphate (PIP) phosphatase, result
114 phosphorylated inositol polar head groups of phosphatidylinositol phosphate (PIP) phospholipids.
115            Mono-, di-, and triphosphorylated phosphatidylinositol phosphate (PIP) species as well as
116 d fluorescence-based assays to demonstrate a phosphatidylinositol phosphate (PIP)-selective mechanism
117 le for the conversion of bacterially-derived phosphatidylinositol phosphate (PIP-DAG) to phosphatidyl
118 ar phosphatase involved in the regulation of phosphatidylinositol phosphates (PIP's).
119          Like the yeast Sec14p, CPSFL1 binds phosphatidylinositol phosphates (PIPs) and phosphatidic
120                                              Phosphatidylinositol phosphates (PIPs) are membrane phos
121 ile ring behavior but not mislocalization of phosphatidylinositol phosphates (PIPs) at the plasma mem
122 tricate network of signalling pathways, with phosphatidylinositol phosphates (PIPs) having a central
123 the most widespread, binding specifically to phosphatidylinositol phosphates (PIPs) in cell membranes
124                                              Phosphatidylinositol phosphates (PIPs) perform central f
125                                              Phosphatidylinositol phosphates (PIPs) profoundly antago
126 of Dok7 associates with membranes containing phosphatidylinositol phosphates (PIPs) via interactions
127 residues that are predicted to interact with phosphatidylinositol phosphate (PtdInsP) head groups.
128  apparently due to specific interaction with phosphatidylinositol phosphates (PtdInsP).
129 its PH domain preferentially interacted with phosphatidylinositol phosphates showing strongest affini
130                                          The phosphatidylinositol phosphate signaling pathway is invo
131     Conserved basic residues form a putative phosphatidylinositol phosphate specificity site.
132  tris- and bis-, but not mono-phosphorylated phosphatidylinositol phosphate substrates containing a 5
133 cy altered mitochondrial metabolism and that phosphatidylinositol phosphate substrates of PTPMT1 dire
134 idine diphosphate-alcohol phosphotransferase phosphatidylinositol-phosphate synthase (PIPS), an essen
135 port the structures of a related enzyme, the phosphatidylinositol-phosphate synthase from Renibacteri
136  PTEN/MMAC dephosphorylates 3-phosphorylated phosphatidylinositol phosphates that activate AKT/protei
137 ic binding to anionic phospholipids, such as phosphatidylinositol phosphates that are essential for i
138 acylglycerol and inositol-phosphate to yield phosphatidylinositol-phosphate, the immediate precursor

 
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