PHO8/YDR481C Literature Guide Help

Other names published for PHO8: phoH, YDR481C

PHO8 - Cellular Location (23)

ReferenceOther Genes Addressed
Logan MR, et al.  (2011) Functional analysis of RhoGDI inhibitory activity on vacuole membrane fusion. Biochem J 434(3):445-57
Mendl N, et al.  (2011) Mitophagy in yeast is independent of mitochondrial fission and requires the stress response gene WHI2. J Cell Sci 124(Pt 8):1339-50
Anand VC, et al.  (2009) Genome-wide analysis of AP-3-dependent protein transport in yeast. Mol Biol Cell 20(5):1592-604
Dancourt J and Barlowe C  (2009) Erv26p-dependent export of alkaline phosphatase from the ER requires lumenal domain recognition. Traffic 10(8):1006-18
Mitsui K, et al.  (2009) Saccharomyces cerevisiae Na+/H+ antiporter Nha1p associates with lipid rafts and requires sphingolipid for stable localization to the plasma membrane. J Biochem 145(6):709-20
Muthusamy BP, et al.  (2009) Control of protein and sterol trafficking by antagonistic activities of a type IV P-type ATPase and oxysterol binding protein homologue. Mol Biol Cell 20(12):2920-31
Qiao W, et al.  (2009) Zinc status and vacuolar zinc transporters control alkaline phosphatase accumulation and activity in Saccharomyces cerevisiae. Mol Microbiol 72(2):320-34
Wiederhold E, et al.  (2009) The yeast vacuolar membrane proteome. Mol Cell Proteomics 8(2):380-92
Sarry JE, et al.  (2007) Analysis of the vacuolar luminal proteome of Saccharomyces cerevisiae. FEBS J 274(16):4287-305
Bue CA, et al.  (2006) Erv26p Directs Pro-Alkaline Phosphatase into Endoplasmic Reticulum-derived Coat Protein Complex II Transport Vesicles. Mol Biol Cell 17(11):4780-9
Wen W, et al.  (2006) Identification of the Yeast R-SNARE Nyv1p as a Novel Longin Domain-containing Protein. Mol Biol Cell 17(10):4282-99
Johnston HD, et al.  (2005) Golgi-to-late endosome trafficking of the yeast pheromone processing enzyme Ste13p is regulated by a phosphorylation site in its cytosolic domain. Mol Biol Cell 16(3):1456-68
Nothwehr SF, et al.  (2000) Sorting of yeast membrane proteins into an endosome-to-Golgi pathway involves direct interaction of their cytosolic domains with Vps35p. J Cell Biol 151(2):297-310
Fischer von Mollard G and Stevens TH  (1999) The Saccharomyces cerevisiae v-SNARE Vti1p is required for multiple membrane transport pathways to the vacuole. Mol Biol Cell 10(6):1719-32
Rehling P, et al.  (1999) Formation of AP-3 transport intermediates requires Vps41 function. Nat Cell Biol 1(6):346-53
Campbell CL and Thorsness PE  (1998) Escape of mitochondrial DNA to the nucleus in yme1 yeast is mediated by vacuolar-dependent turnover of abnormal mitochondrial compartments. J Cell Sci 111 ( Pt 16)():2455-64
Vowels JJ and Payne GS  (1998) A dileucine-like sorting signal directs transport into an AP-3-dependent, clathrin-independent pathway to the yeast vacuole. EMBO J 17(9):2482-93
Stepp JD, et al.  (1997) The yeast adaptor protein complex, AP-3, is essential for the efficient delivery of alkaline phosphatase by the alternate pathway to the vacuole. J Cell Biol 139(7):1761-74
Kohrer K and Emr SD  (1993) The yeast VPS17 gene encodes a membrane-associated protein required for the sorting of soluble vacuolar hydrolases. J Biol Chem 268(1):559-69
Klionsky DJ and Emr SD  (1989) Membrane protein sorting: biosynthesis, transport and processing of yeast vacuolar alkaline phosphatase. EMBO J 8(8):2241-50
Mitchell JK, et al.  (1981) A particulate form of alkaline phosphatase in the yeast, Saccharomyces cerevisiae. Biochim Biophys Acta 657(2):482-94
Bauer H and Sigarlakie E  (1975) Localization of alkaline phosphatase in Saccharomyces cerevisiae by means of ultrathin frozen sections. J Ultrastruct Res 50(2):208-15
Patching JW and Rose AH  (1971) Cold osmotic shock in Saccharomyces cerevisiae. J Bacteriol 108(1):451-8