Mutation of a tyrosine localization signal in the cytosolic tail of yeast Kex2 protease disrupts Golgi retention and results in default transport to the vacuole.
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Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: a novel mechanism of regulated traffickingTwo independent targeting signals in the cytoplasmic domain determine trans-Golgi network localization and endosomal trafficking of the proprotein convertase furinIntracellular trafficking and activation of the furin proprotein convertase: localization to the TGN and recycling from the cell surfaceVma21p is a yeast membrane protein retained in the endoplasmic reticulum by a di-lysine motif and is required for the assembly of the vacuolar H(+)-ATPase complexDistinct domains within Vps35p mediate the retrieval of two different cargo proteins from the yeast prevacuolar/endosomal compartmentA membrane coat complex essential for endosome-to-Golgi retrograde transport in yeastThe isoforms of proprotein convertase PC5 are sorted to different subcellular compartmentsSorting of yeast membrane proteins into an endosome-to-Golgi pathway involves direct interaction of their cytosolic domains with Vps35pCrystal structure of the yeast Phox homology (PX) domain protein Grd19p complexed to phosphatidylinositol-3-phosphateSla1p serves as the targeting signal recognition factor for NPFX(1,2)D-mediated endocytosis.The iron transporter Fth1p forms a complex with the Fet5 iron oxidase and resides on the vacuolar membrane.Novel Golgi to vacuole delivery pathway in yeast: identification of a sorting determinant and required transport component.Allele-specific suppression of a defective trans-Golgi network (TGN) localization signal in Kex2p identifies three genes involved in localization of TGN transmembrane proteins.Ric1p and the Ypt6p GTPase function in a common pathway required for localization of trans-Golgi network membrane proteinsThe yeast proprotein convertase encoded by YAP3 is a glycophosphatidylinositol-anchored protein that localizes to the plasma membrane.Review: biosynthesis and function of yeast vacuolar proteases.Vps52p, Vps53p, and Vps54p form a novel multisubunit complex required for protein sorting at the yeast late GolgiRetrograde transport of the mannosyltransferase Och1p to the early Golgi requires a component of the COG transport complex.Mutants in trs120 disrupt traffic from the early endosome to the late Golgi.Pep3p/Pep5p complex: a putative docking factor at multiple steps of vesicular transport to the vacuole of Saccharomyces cerevisiaeShared functions in vivo of a glycosyl-phosphatidylinositol-linked aspartyl protease, Mkc7, and the proprotein processing protease Kex2 in yeast.Cdk1-dependent control of membrane-trafficking dynamics.The newly identified yeast GRD genes are required for retention of late-Golgi membrane proteins.Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p.Ypt31/32 GTPases and their novel F-box effector protein Rcy1 regulate protein recyclingProtein kinases Fpk1p and Fpk2p are novel regulators of phospholipid asymmetry.Localization and targeting of the Saccharomyces cerevisiae Kre2p/Mnt1p alpha 1,2-mannosyltransferase to a medial-Golgi compartmentMorphological classification of the yeast vacuolar protein sorting mutants: evidence for a prevacuolar compartment in class E vps mutants.Two syntaxin homologues in the TGN/endosomal system of yeastNovel genes involved in endosomal traffic in yeast revealed by suppression of a targeting-defective plasma membrane ATPase mutantNovel syntaxin homologue, Pep12p, required for the sorting of lumenal hydrolases to the lysosome-like vacuole in yeast.Vacuole biogenesis in Saccharomyces cerevisiae: protein transport pathways to the yeast vacuoleSOI1 encodes a novel, conserved protein that promotes TGN-endosomal cycling of Kex2p and other membrane proteins by modulating the function of two TGN localization signals.Vps10p cycles between the late-Golgi and prevacuolar compartments in its function as the sorting receptor for multiple yeast vacuolar hydrolases.Retrieval of resident late-Golgi membrane proteins from the prevacuolar compartment of Saccharomyces cerevisiae is dependent on the function of Grd19p.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.Endosome to Golgi retrieval of the vacuolar protein sorting receptor, Vps10p, requires the function of the VPS29, VPS30, and VPS35 gene products.Soi3p/Rav1p functions at the early endosome to regulate endocytic trafficking to the vacuole and localization of trans-Golgi network transmembrane proteinsEndocytic recycling in yeast is regulated by putative phospholipid translocases and the Ypt31p/32p-Rcy1p pathway.Clathrin-dependent localization of alpha 1,3 mannosyltransferase to the Golgi complex of Saccharomyces cerevisiae
P2860
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P2860
Mutation of a tyrosine localization signal in the cytosolic tail of yeast Kex2 protease disrupts Golgi retention and results in default transport to the vacuole.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Mutation of a tyrosine localiz ...... ault transport to the vacuole.
@en
type
label
Mutation of a tyrosine localiz ...... ault transport to the vacuole.
@en
prefLabel
Mutation of a tyrosine localiz ...... ault transport to the vacuole.
@en
P2093
P2860
P356
P1476
Mutation of a tyrosine localiz ...... ault transport to the vacuole.
@en
P2093
P2860
P304
P356
10.1091/MBC.3.12.1353
P577
1992-12-01T00:00:00Z