scholarly article | Q13442814 |
P50 | author | Sheena Claire Li | Q42559176 |
Wandi Zhu | Q85919719 | ||
P2093 | author name string | Lois S Weisman | |
Tao Xu | |||
Maureen Tarsio | |||
Patricia M Kane | |||
Theodore T Diakov | |||
Sergio Couoh-Cardel | |||
P2860 | cites work | PIKfyve Controls Fluid Phase Endocytosis but Not Recycling/Degradation of Endocytosed Receptors or Sorting of Procathepsin D by Regulating Multivesicular Body Morphogenesis | Q24297560 |
VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse | Q24318746 | ||
Regulation of Fab1 phosphatidylinositol 3-phosphate 5-kinase pathway by Vac7 protein and Fig4, a polyphosphoinositide phosphatase family member. | Q24515262 | ||
The phosphoinositide kinase PIKfyve/Fab1p regulates terminal lysosome maturation in Caenorhabditis elegans | Q24548664 | ||
The phosphoinositide kinase PIKfyve is vital in early embryonic development: preimplantation lethality of PIKfyve-/- embryos but normality of PIKfyve+/- mice | Q24618677 | ||
Assembly of a Fab1 phosphoinositide kinase signaling complex requires the Fig4 phosphoinositide phosphatase | Q24643186 | ||
Structure of the yeast vacuolar ATPase | Q24645117 | ||
Fab1 phosphatidylinositol 3-phosphate 5-kinase controls trafficking but not silencing of endocytosed receptors | Q24671705 | ||
Loss of Vac14, a regulator of the signaling lipid phosphatidylinositol 3,5-bisphosphate, results in neurodegeneration in mice. | Q24678783 | ||
The Vac14p-Fig4p complex acts independently of Vac7p and couples PI3,5P2 synthesis and turnover | Q24683845 | ||
Crystal Structure of the Cytoplasmic N-Terminal Domain of Subunit I, a Homolog of Subunit a, of V-ATPase | Q27670991 | ||
Two-Site Recognition of Phosphatidylinositol 3-Phosphate by PROPPINs in Autophagy | Q27681186 | ||
Phosphoinositides in cell regulation and membrane dynamics | Q27861051 | ||
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q27861085 | ||
Osmotic stress-induced increase of phosphatidylinositol 3,5-bisphosphate requires Vac14p, an activator of the lipid kinase Fab1p | Q27930743 | ||
Fab1p Is Essential for PtdIns(3)P 5-Kinase Activity and the Maintenance of Vacuolar Size and Membrane Homeostasis | Q27931112 | ||
Vac14 controls PtdIns(3,5)P(2) synthesis and Fab1-dependent protein trafficking to the multivesicular body | Q27932192 | ||
Novel Vacuolar H+-ATPase Complexes Resulting from Overproduction of Vma5p and Vma13p | Q27932640 | ||
Role of vacuolar acidification in protein sorting and zymogen activation: a genetic analysis of the yeast vacuolar proton-translocating ATPase | Q27933484 | ||
Synthesis and function of membrane phosphoinositides in budding yeast, Saccharomyces cerevisiae | Q36768641 | ||
PIP2 is a necessary cofactor for ion channel function: how and why? | Q37197976 | ||
The vacuolar proton pump, V-ATPase, is required for notch signaling and endosomal trafficking in Drosophila | Q37378404 | ||
Regulation by salt of vacuolar H+-ATPase and H+-pyrophosphatase activities and Na+/H+ exchange | Q37612731 | ||
Phosphatidylinositol-3,5-bisphosphate: no longer the poor PIP2. | Q37898748 | ||
PIKfyve and its Lipid Products in Health and in Sickness | Q38053955 | ||
On the physiological roles of PIP(2) at cardiac Na+ Ca2+ exchangers and K(ATP) channels: a long journey from membrane biophysics into cell biology | Q38573614 | ||
Structural Basis for Endosomal Targeting by FYVE Domains | Q40620748 | ||
Phosphoinositides as regulators in membrane traffic | Q40968891 | ||
Structure of the vacuolar-type ATPase from Saccharomyces cerevisiae at 11-Å resolution | Q41792129 | ||
A different conformation for EGC stator subcomplex in solution and in the assembled yeast V-ATPase: possible implications for regulatory disassembly | Q41792154 | ||
Stimulus-induced phosphorylation of vacuolar H(+)-ATPase by protein kinase A. | Q42031982 | ||
Weak acid and alkali stress regulate phosphatidylinositol bisphosphate synthesis in Saccharomyces cerevisiae | Q42128054 | ||
Regulation of vacuolar H+-ATPase activity by the Cdc42 effector Ste20 in Saccharomyces cerevisiae | Q42559102 | ||
Atg18 phosphoregulation controls organellar dynamics by modulating its phosphoinositide-binding activity | Q42560292 | ||
Phosphatidic acid is a pH biosensor that links membrane biogenesis to metabolism. | Q42924633 | ||
Methods for studying the yeast vacuole | Q44041860 | ||
Three-dimensional structure of the vacuolar ATPase proton channel by electron microscopy | Q44077049 | ||
Partial assembly of the yeast vacuolar H(+)-ATPase in mutants lacking one subunit of the enzyme. | Q45092115 | ||
Activity of tonoplast proton pumps and Na+/H+ exchange in potato cell cultures is modulated by salt. | Q46123589 | ||
RAVE is essential for the efficient assembly of the C subunit with the vacuolar H(+)-ATPase | Q80595390 | ||
Vacuole Size Control: Regulation of PtdIns(3,5)P2Levels by the Vacuole-associated Vac14-Fig4 Complex, a PtdIns(3,5)P2-specific Phosphatase | Q27933521 | ||
The amino-terminal domain of the vacuolar proton-translocating ATPase a subunit controls targeting and in vivo dissociation, and the carboxyl-terminal domain affects coupling of proton transport and ATP hydrolysis. | Q27939014 | ||
Assembly and targeting of peripheral and integral membrane subunits of the yeast vacuolar H(+)-ATPase | Q27939259 | ||
The stress-activated phosphatidylinositol 3-phosphate 5-kinase Fab1p is essential for vacuole function in S. cerevisiae | Q27939343 | ||
The VPH1 gene encodes a 95-kDa integral membrane polypeptide required for in vivo assembly and activity of the yeast vacuolar H(+)-ATPase | Q27939895 | ||
The H subunit (Vma13p) of the yeast V-ATPase inhibits the ATPase activity of cytosolic V1 complexes | Q28142904 | ||
Cryo-electron microscopy of the vacuolar ATPase motor reveals its mechanical and regulatory complexity | Q28236433 | ||
Disassembly and reassembly of the yeast vacuolar H(+)-ATPase in vivo | Q28294160 | ||
Biochemical and biophysical properties of interactions between subunits of the peripheral stalk region of human V-ATPase | Q28486120 | ||
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J | Q28511673 | ||
PI(3,5)P2 controls membrane trafficking by direct activation of mucolipin Ca2+ release channels in the endolysosome | Q29543488 | ||
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q29546523 | ||
A guided tour into subcellular colocalization analysis in light microscopy | Q29547199 | ||
Vacuolar ATPases: rotary proton pumps in physiology and pathophysiology | Q29614686 | ||
Membrane recognition by phospholipid-binding domains | Q29614848 | ||
Mutation of FIG4 causes a rapidly progressive, asymmetric neuronal degeneration | Q30489465 | ||
Lysosome dysfunction triggers Atg7-dependent neural apoptosis | Q33796094 | ||
Phosphatidylinositol 3,5-bisphosphate: a novel lipid that links stress responses to membrane trafficking events | Q33985634 | ||
Regulation of vacuolar proton-translocating ATPase activity and assembly by extracellular pH | Q34025366 | ||
Domain characterization and interaction of the yeast vacuolar ATPase subunit C with the peripheral stator stalk subunits E and G. | Q34042638 | ||
Structural and functional separation of the N- and C-terminal domains of the yeast V-ATPase subunit H. | Q34348713 | ||
A genomic screen for yeast vacuolar membrane ATPase mutants | Q34348722 | ||
Osmotic stress activates phosphatidylinositol-3,5-bisphosphate synthesis | Q34446025 | ||
Phosphoinositide 5-phosphatase Fig 4p is required for both acute rise and subsequent fall in stress-induced phosphatidylinositol 3,5-bisphosphate levels | Q34512579 | ||
Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS. | Q34913669 | ||
Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2. | Q35005794 | ||
Vacuolar H+-ATPase works in parallel with the HOG pathway to adapt Saccharomyces cerevisiae cells to osmotic stress | Q35804688 | ||
Phosphoinositides in constitutive membrane traffic. | Q35842974 | ||
Subunit Interactions at the V1-Vo Interface in Yeast Vacuolar ATPase | Q35921635 | ||
Sorting of the yeast vacuolar-type, proton-translocating ATPase enzyme complex (V-ATPase): identification of a necessary and sufficient Golgi/endosomal retention signal in Stv1p | Q36003848 | ||
Regulation of ion channels by phosphatidylinositol 4,5-bisphosphate | Q36142866 | ||
SOS2 promotes salt tolerance in part by interacting with the vacuolar H+-ATPase and upregulating its transport activity | Q36315865 | ||
The where, when, and how of organelle acidification by the yeast vacuolar H+-ATPase | Q36416690 | ||
Critical roles of type III phosphatidylinositol phosphate kinase in murine embryonic visceral endoderm and adult intestine | Q36583080 | ||
Function and subunit interactions of the N-terminal domain of subunit a (Vph1p) of the yeast V-ATPase | Q36744179 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 8 | |
P304 | page(s) | 1251-1262 | |
P577 | publication date | 2014-02-12 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | The signaling lipid PI(3,5)P₂ stabilizes V₁-V(o) sector interactions and activates the V-ATPase | |
P478 | volume | 25 |
Q37626840 | A cell-permeable tool for analysing APP intracellular domain function and manipulation of PIKfyve activity. |
Q64272039 | Acidifying Endolysosomes Prevented Low-Density Lipoprotein-Induced Amyloidogenesis |
Q30379694 | Affinity Purification and Structural Features of the Yeast Vacuolar ATPase Vo Membrane Sector. |
Q89046974 | Arabidopsis VAC14 Is Critical for Pollen Development through Mediating Vacuolar Organization |
Q48189738 | Biolayer interferometry of lipid nanodisc-reconstituted yeast vacuolar H+ -ATPase |
Q52315057 | Control of vacuole membrane homeostasis by a resident PI-3,5-kinase inhibitor. |
Q48131243 | DepHining membrane identity |
Q46334211 | Direct interaction of the Golgi V-ATPase a-subunit isoform with PI(4)P drives localization of Golgi V-ATPases in yeast |
Q48241853 | Early protection to stress mediated by CDK-dependent PI3,5P2 signaling from the vacuole/lysosome. |
Q36310514 | Early to Late Endosome Trafficking Controls Secretion and Zymogen Activation in Rodent and Human Pancreatic Acinar Cells |
Q47909119 | Evidence for ESCRT- and clathrin-dependent microautophagy. |
Q38560548 | Lipids implicated in the journey of a secretory granule: from biogenesis to fusion |
Q91747205 | Lysosomal size matters |
Q58298746 | PI(3,5)P controls vacuole potassium transport to support cellular osmoregulation |
Q39182894 | PI5P and PI(3,5)P2: Minor, but Essential Phosphoinositides. |
Q38600541 | PIKfyve activity regulates reformation of terminal storage lysosomes from endolysosomes |
Q64261450 | PIKfyve/Fab1 is required for efficient V-ATPase and hydrolase delivery to phagosomes, phagosomal killing, and restriction of Legionella infection |
Q36282823 | Perturbation of the Vacuolar ATPase: A NOVEL CONSEQUENCE OF INOSITOL DEPLETION |
Q38819806 | Phosphatidylinositol 3,5-Bisphosphate-Rich Membrane Domains in Endosomes and Lysosomes |
Q48028332 | Phosphatidylinositol 3,5-bisphosphate is involved in methylglyoxal-induced activation of the Mpk1 mitogen-activated protein kinase cascade in Saccharomyces cerevisiae |
Q64934872 | Phosphatidylinositol 3,5-bisphosphate regulates the transition between trans-SNARE complex formation and vacuole membrane fusion |
Q36812142 | Phosphatidylinositol 3,5-bisphosphate: regulation of cellular events in space and time |
Q49547382 | Phosphoinositide conversion in endocytosis and the endolysosomal system |
Q38684254 | Proton Transport and pH Control in Fungi |
Q38593788 | Recent Insights into the Structure, Regulation, and Function of the V-ATPases |
Q97528993 | Regulation of V-ATPase Activity and Organelle pH by Phosphatidylinositol Phosphate Lipids |
Q57109591 | Regulation of V-ATPase Assembly in Nutrient Sensing and Function of V-ATPases in Breast Cancer Metastasis |
Q38746834 | Regulation of V-ATPase assembly and function of V-ATPases in tumor cell invasiveness |
Q38922191 | Regulation of autophagy by mitochondrial phospholipids in health and diseases. |
Q38202559 | Saccharomyces cerevisiae vacuolar H+-ATPase regulation by disassembly and reassembly: one structure and multiple signals |
Q30396376 | Structure of the Lipid Nanodisc-reconstituted Vacuolar ATPase Proton Channel: DEFINITION OF THE INTERACTION OF ROTOR AND STATOR AND IMPLICATIONS FOR ENZYME REGULATION BY REVERSIBLE DISSOCIATION. |
Q60053070 | TOR-autophagy branch signaling via Imp1 dictates plant-microbe biotrophic interface longevity |
Q38846161 | Target of rapamycin signaling mediates vacuolar fragmentation |
Q27314340 | The Fab1/PIKfyve phosphoinositide phosphate kinase is not necessary to maintain the pH of lysosomes and of the yeast vacuole. |
Q60944020 | The Phosphoinositide Kinase PIKfyve Promotes Cathepsin-S-Mediated Major Histocompatibility Complex Class II Antigen Presentation |
Q38768292 | The signaling lipid phosphatidylinositol-3,5-bisphosphate targets plant CLC-a anion/H+ exchange activity. |
Q36399070 | The yeast protein kinase Sch9 adjusts V-ATPase assembly/disassembly to control pH homeostasis and longevity in response to glucose availability |
Q34925693 | What are the roles of V-ATPases in membrane fusion? |
Q50316174 | pH homeostasis links the nutrient sensing PKA/TORC1/Sch9 ménage-à-trois to stress tolerance and longevity. |
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