scholarly article | Q13442814 |
P2093 | author name string | T H Stevens | |
N J Bryant | |||
P2860 | cites work | Mutational analysis of the human KDEL receptor: distinct structural requirements for Golgi retention, ligand binding and retrograde transport | Q24564552 |
Two independent targeting signals in the cytoplasmic domain determine trans-Golgi network localization and endosomal trafficking of the proprotein convertase furin | Q24568252 | ||
Rapid and efficient site-specific mutagenesis without phenotypic selection | Q27860628 | ||
Immunoisolation of Kex2p-containing organelles from yeast demonstrates colocalisation of three processing proteinases to a single Golgi compartment | Q27929930 | ||
Compartmental organization of Golgi-specific protein modification and vacuolar protein sorting events defined in a yeast sec18 (NSF) mutant | Q27932509 | ||
The newly identified yeast GRD genes are required for retention of late-Golgi membrane proteins. | Q27934905 | ||
Yeast Vps45p is a Sec1p-like protein required for the consumption of vacuole-targeted, post-Golgi transport vesicles | Q27935404 | ||
Localization and targeting of the Saccharomyces cerevisiae Kre2p/Mnt1p alpha 1,2-mannosyltransferase to a medial-Golgi compartment | Q27936583 | ||
Morphological classification of the yeast vacuolar protein sorting mutants: evidence for a prevacuolar compartment in class E vps mutants | Q27936883 | ||
Novel syntaxin homologue, Pep12p, required for the sorting of lumenal hydrolases to the lysosome-like vacuole in yeast | Q27937502 | ||
Membrane protein sorting: biosynthesis, transport and processing of yeast vacuolar alkaline phosphatase | Q27938078 | ||
Vps10p cycles between the late-Golgi and prevacuolar compartments in its function as the sorting receptor for multiple yeast vacuolar hydrolases. | Q27938475 | ||
The sorting receptor for yeast vacuolar carboxypeptidase Y is encoded by the VPS10 gene | Q27939402 | ||
The VPH1 gene encodes a 95-kDa integral membrane polypeptide required for in vivo assembly and activity of the yeast vacuolar H(+)-ATPase | Q27939895 | ||
Localization of components involved in protein transport and processing through the yeast Golgi apparatus | Q27940278 | ||
Mechanisms of intracellular protein transport | Q28131681 | ||
Coat proteins and vesicle budding | Q28645867 | ||
VPS27 controls vacuolar and endocytic traffic through a prevacuolar compartment in Saccharomyces cerevisiae | Q29620184 | ||
Ligand-induced redistribution of a human KDEL receptor from the Golgi complex to the endoplasmic reticulum | Q34233252 | ||
Structure and function of the mannose 6-phosphate/insulinlike growth factor II receptors | Q34236758 | ||
Retention of a cis Golgi protein requires polar residues on one face of a predicted alpha-helix in the transmembrane domain | Q34438261 | ||
Sorting of yeast alpha 1,3 mannosyltransferase is mediated by a lumenal domain interaction, and a transmembrane domain signal that can confer clathrin-dependent Golgi localization to a secreted protein | Q34449760 | ||
The cytoplasmic tail domain of the vacuolar protein sorting receptor Vps10p and a subset of VPS gene products regulate receptor stability, function, and localization | Q34451174 | ||
The membrane spanning domain of beta-1,4-galactosyltransferase specifies trans Golgi localization | Q35934419 | ||
Membrane protein retention in the yeast Golgi apparatus: dipeptidyl aminopeptidase A is retained by a cytoplasmic signal containing aromatic residues | Q36232915 | ||
Localization of TGN38 to the trans-Golgi network: involvement of a cytoplasmic tyrosine-containing sequence | Q36233082 | ||
Golgi and vacuolar membrane proteins reach the vacuole in vps1 mutant yeast cells via the plasma membrane. | Q36235242 | ||
Immunolocalization of Kex2 protease identifies a putative late Golgi compartment in the yeast Saccharomyces cerevisiae | Q36529667 | ||
Posttranslational processing of the prohormone-cleaving Kex2 protease in the Saccharomyces cerevisiae secretory pathway | Q36530340 | ||
Membrane protein sorting in the yeast secretory pathway: evidence that the vacuole may be the default compartment | Q36531936 | ||
A Golgi retention signal in a membrane-spanning domain of coronavirus E1 protein | Q36532876 | ||
The functioning of the yeast Golgi apparatus requires an ER protein encoded by ANP1, a member of a new family of genes affecting the secretory pathway | Q36726376 | ||
Localization of cathepsin D in endosomes: characterization and biological importance | Q37041768 | ||
Alternative pathways for the sorting of soluble vacuolar proteins in yeast: a vps35 null mutant missorts and secretes only a subset of vacuolar hydrolases | Q37372170 | ||
An acidic sequence within the cytoplasmic domain of furin functions as a determinant of trans-Golgi network localization and internalization from the cell surface | Q37623766 | ||
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 | Q40241598 | ||
Sorting of membrane proteins in the yeast secretory pathway | Q40734090 | ||
Sorting of membrane proteins in the secretory pathway | Q40781366 | ||
Cholesterol and the Golgi apparatus | Q40840990 | ||
TGN38 is maintained in the trans-Golgi network by a tyrosine-containing motif in the cytoplasmic domain | Q40872991 | ||
Sequences within and adjacent to the transmembrane segment of alpha-2,6-sialyltransferase specify Golgi retention | Q41083198 | ||
Localization of furin to the trans-Golgi network and recycling from the cell surface involves Ser and Tyr residues within the cytoplasmic domain. | Q41269334 | ||
Localization of the signal for rapid internalization of the bovine cation-independent mannose 6-phosphate/insulin-like growth factor-II receptor to amino acids 24-29 of the cytoplasmic tail | Q41690827 | ||
Localization of a yeast early Golgi mannosyltransferase, Och1p, involves retrograde transport | Q41982832 | ||
Yeast Kex1p is a Golgi-associated membrane protein: deletions in a cytoplasmic targeting domain result in mislocalization to the vacuolar membrane | Q43108600 | ||
Dynamic retention of TGN membrane proteins in Saccharomyces cerevisiae | Q46349111 | ||
Involvement of Ypt7p, a small GTPase, in traffic from late endosome to the vacuole in yeast | Q57179731 | ||
The SXYQRL sequence in the cytoplasmic domain of TGN38 plays a major role in trans-Golgi network localization | Q72571291 | ||
Kin recognition. A model for the retention of Golgi enzymes | Q72921207 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | membrane protein | Q423042 |
P1104 | number of pages | 11 | |
P304 | page(s) | 287-297 | |
P577 | publication date | 1997-01-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | Two separate signals act independently to localize a yeast late Golgi membrane protein through a combination of retrieval and retention | |
P478 | volume | 136 |
Q34982485 | A di-leucine sequence and a cluster of acidic amino acids are required for dynamic retention in the endosomal recycling compartment of fibroblasts |
Q33948272 | A novel mechanism for localizing membrane proteins to yeast trans-Golgi network requires function of synaptojanin-like protein |
Q36381155 | A subset of yeast vacuolar protein sorting mutants is blocked in one branch of the exocytic pathway |
Q33914545 | Alternative protein sorting pathways |
Q27930206 | An effector of Ypt6p binds the SNARE Tlg1p and mediates selective fusion of vesicles with late Golgi membranes |
Q29642793 | Bi-cycling the furin pathway: from TGN localization to pathogen activation and embryogenesis |
Q28354036 | Biosynthesis and subcellular localization of a lepidopteran insect alpha 1,2-mannosidase |
Q27938198 | Btn3 is a negative regulator of Btn2-mediated endosomal protein trafficking and prion curing in yeast |
Q45057171 | Cell-free reconstitution of transport from the trans-golgi network to the late endosome/prevacuolar compartment |
Q36274874 | Cell-free transport to distinct Golgi cisternae is compartment specific and ARF independent |
Q34405959 | Crystal structure of human vacuolar protein sorting protein 29 reveals a phosphodiesterase/nuclease-like fold and two protein-protein interaction sites. |
Q36608402 | Direct binding of the Kex2p cytosolic tail to the VHS domain of yeast Gga2p facilitates TGN to prevacuolar compartment transport and is regulated by phosphorylation |
Q46334211 | Direct interaction of the Golgi V-ATPase a-subunit isoform with PI(4)P drives localization of Golgi V-ATPases in yeast |
Q27933441 | Disruption of YHC8, a member of the TSR1 gene family, reveals its direct involvement in yeast protein translocation |
Q24657977 | Distinct domains within Vps35p mediate the retrieval of two different cargo proteins from the yeast prevacuolar/endosomal compartment |
Q40504718 | Endosomal sorting of GLUT4 and Gap1 is conserved between yeast and insulin-sensitive cells. |
Q27939459 | Endosome to Golgi retrieval of the vacuolar protein sorting receptor, Vps10p, requires the function of the VPS29, VPS30, and VPS35 gene products |
Q35757387 | Ent3p and Ent5p exhibit cargo-specific functions in trafficking proteins between the trans-Golgi network and the endosomes in yeast |
Q27936769 | Global analysis of yeast endosomal transport identifies the vps55/68 sorting complex |
Q33914482 | Golgi-to-late endosome trafficking of the yeast pheromone processing enzyme Ste13p is regulated by a phosphorylation site in its cytosolic domain |
Q33851952 | Identification of two sequences in the cytoplasmic tail of the human immunodeficiency virus type 1 envelope glycoprotein that inhibit cell surface expression |
Q35153097 | Insulin-regulated trafficking of GLUT4 requires ubiquitination |
Q36256386 | Integral membrane protein sorting to vacuoles in plant cells: evidence for two pathways. |
Q35131675 | Intracellular sorting and transport of proteins |
Q77136123 | Multiple sorting pathways between the late Golgi and the vacuole in yeast |
Q73511692 | Pep12p is a multifunctional yeast syntaxin that controls entry of biosynthetic, endocytic and retrograde traffic into the prevacuolar compartment |
Q36650539 | Plant prevacuolar/endosomal compartments |
Q39636885 | Precursor B cell receptor signaling activity can be uncoupled from surface expression |
Q27938823 | Retrieval of resident late-Golgi membrane proteins from the prevacuolar compartment of Saccharomyces cerevisiae is dependent on the function of Grd19p. |
Q36288266 | Retrograde traffic out of the yeast vacuole to the TGN occurs via the prevacuolar/endosomal compartment |
Q29617826 | Retrograde transport from endosomes to the trans-Golgi network |
Q27932804 | Retrograde transport of the mannosyltransferase Och1p to the early Golgi requires a component of the COG transport complex |
Q27931535 | Retromer and the sorting nexins Snx4/41/42 mediate distinct retrieval pathways from yeast endosomes |
Q27931624 | Ric1p and the Ypt6p GTPase function in a common pathway required for localization of trans-Golgi network membrane proteins |
Q27938174 | SOI1 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 |
Q34694822 | Separation of Golgi and endosomal compartments |
Q27939568 | Soi3p/Rav1p functions at the early endosome to regulate endocytic trafficking to the vacuole and localization of trans-Golgi network transmembrane proteins |
Q36003848 | 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 |
Q24677799 | Sorting of yeast membrane proteins into an endosome-to-Golgi pathway involves direct interaction of their cytosolic domains with Vps35p |
Q27937968 | Specific retrieval of the exocytic SNARE Snc1p from early yeast endosomes |
Q36824414 | Structural features of vps35p involved in interaction with other subunits of the retromer complex |
Q41585861 | Structural requirements for the activity of the MirB ferrisiderophore transporter of Aspergillus fumigatus |
Q36768641 | Synthesis and function of membrane phosphoinositides in budding yeast, Saccharomyces cerevisiae |
Q36294202 | The Tlg SNARE complex is required for TGN homotypic fusion |
Q27939014 | 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. |
Q36117565 | The clathrin adaptor complex 1 directly binds to a sorting signal in Ste13p to reduce the rate of its trafficking to the late endosome of yeast |
Q36276391 | The membrane protein alkaline phosphatase is delivered to the vacuole by a route that is distinct from the VPS-dependent pathway. |
Q34784061 | The sodium/proton exchanger Nhx1p is required for endosomal protein trafficking in the yeast Saccharomyces cerevisiae |
Q34924926 | The synaptojanin-like protein Inp53/Sjl3 functions with clathrin in a yeast TGN-to-endosome pathway distinct from the GGA protein-dependent pathway |
Q38614318 | The syntaxin Tlg1p mediates trafficking of chitin synthase III to polarized growth sites in yeast |
Q91853466 | The t-SNARE protein FgPep12, associated with FgVam7, is essential for ascospore discharge and plant infection by trafficking Ca2+ ATPase FgNeo1 between Golgi and endosome/vacuole in Fusarium graminearum |
Q36955558 | The yeast GRD20 gene is required for protein sorting in the trans-Golgi network/endosomal system and for polarization of the actin cytoskeleton |
Q36255062 | The yeast adaptor protein complex, AP-3, is essential for the efficient delivery of alkaline phosphatase by the alternate pathway to the vacuole |
Q27936300 | The yeast clathrin adaptor protein complex 1 is required for the efficient retention of a subset of late Golgi membrane proteins |
Q27939153 | Tlg2p, a yeast syntaxin homolog that resides on the Golgi and endocytic structures |
Q36351035 | Topological analysis of a plant vacuolar Na + /H + antiporter reveals a luminal C terminus that regulates antiporter cation selectivity |
Q27936482 | Traffic into the prevacuolar/endosomal compartment of Saccharomyces cerevisiae: a VPS45-dependent intracellular route and a VPS45-independent, endocytic route |
Q39592132 | Trafficking of varicella-zoster virus glycoprotein gI: T(338)-dependent retention in the trans-Golgi network, secretion, and mannose 6-phosphate-inhibitable uptake of the ectodomain |
Q27937369 | Two syntaxin homologues in the TGN/endosomal system of yeast |
Q58480871 | Ubiquitin Sorts Proteins into the Intralumenal Degradative Compartment of the Late-Endosome/Vacuole |
Q27938062 | Vacuole biogenesis in Saccharomyces cerevisiae: protein transport pathways to the yeast vacuole |
Q34984669 | Vps10p transport from the trans-Golgi network to the endosome is mediated by clathrin-coated vesicles |
Q27932636 | Vps52p, Vps53p, and Vps54p form a novel multisubunit complex required for protein sorting at the yeast late Golgi |
Q37073871 | Yeast Gga coat proteins function with clathrin in Golgi to endosome transport |
Q35613387 | Yeast P4-ATPases Drs2p and Dnf1p are essential cargos of the NPFXD/Sla1p endocytic pathway. |
Q35153461 | Ykt6p is a multifunctional yeast R-SNARE that is required for multiple membrane transport pathways to the vacuole. |