scholarly article | Q13442814 |
P2093 | author name string | Guendalina Rossi | |
Patrick Brennwald | |||
P2860 | cites work | The Exocyst is a multiprotein complex required for exocytosis in Saccharomyces cerevisiae | Q24561799 |
The Rho GTPase Rho3 has a direct role in exocytosis that is distinct from its role in actin polarity | Q24647386 | ||
Structure of the yeast polarity protein Sro7 reveals a SNARE regulatory mechanism | Q27644268 | ||
Ypt32 recruits the Sec4p guanine nucleotide exchange factor, Sec2p, to secretory vesicles; evidence for a Rab cascade in yeast | Q27931218 | ||
The COOH-terminal domain of Myo2p, a yeast myosin V, has a direct role in secretory vesicle targeting | Q27932330 | ||
Structurally conserved interaction of Lgl family with SNAREs is critical to their cellular function | Q27932466 | ||
The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles | Q27932839 | ||
Sec9 is a SNAP-25-like component of a yeast SNARE complex that may be the effector of Sec4 function in exocytosis | Q27933277 | ||
The yeast lgl family member Sro7p is an effector of the secretory Rab GTPase Sec4p | Q27933359 | ||
The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis | Q27934654 | ||
The CORVET subunit Vps8 cooperates with the Rab5 homolog Vps21 to induce clustering of late endosomal compartments | Q27935566 | ||
Yeast homologues of tomosyn and lethal giant larvae function in exocytosis and are associated with the plasma membrane SNARE, Sec9 | Q27935690 | ||
Tropomyosin-containing actin cables direct the Myo2p-dependent polarized delivery of secretory vesicles in budding yeast | Q27935856 | ||
Mlc1p is a light chain for the unconventional myosin Myo2p in Saccharomyces cerevisiae | Q27936373 | ||
Analysis of a yeast SNARE complex reveals remarkable similarity to the neuronal SNARE complex and a novel function for the C terminus of the SNAP-25 homolog, Sec9. | Q27936879 | ||
Sec2p mediates nucleotide exchange on Sec4p and is involved in polarized delivery of post-Golgi vesicles | Q27939177 | ||
The molecular motor toolbox for intracellular transport | Q28211349 | ||
Elucidation of the interaction of calmodulin with the IQ motifs of IQGAP1 | Q28215755 | ||
Rabs and their effectors: achieving specificity in membrane traffic | Q29619989 | ||
A GTP-binding protein required for secretion rapidly associates with secretory vesicles and the plasma membrane in yeast | Q29620584 | ||
Transport-vesicle targeting: tethers before SNAREs | Q33772639 | ||
Functional cross-talk between Rab14 and Rab4 through a dual effector, RUFY1/Rabip4. | Q34029364 | ||
Calmodulin signaling via the IQ motif | Q34120325 | ||
Ypt/rab gtpases: regulators of protein trafficking | Q34386638 | ||
Vesicles carry most exocyst subunits to exocytic sites marked by the remaining two subunits, Sec3p and Exo70p | Q34553174 | ||
Rho GTPase regulation of exocytosis in yeast is independent of GTP hydrolysis and polarization of the exocyst complex | Q34560143 | ||
The yeast kinesin-related protein Smy1p exerts its effects on the class V myosin Myo2p via a physical interaction | Q34686464 | ||
Vesicle transport: a close collaboration of Rabs and effectors | Q35623425 | ||
Myosins: tails (and heads) of functional diversity | Q36197820 | ||
The Sec15 protein responds to the function of the GTP binding protein, Sec4, to control vesicular traffic in yeast | Q36221387 | ||
The role of Myo2, a yeast class V myosin, in vesicular transport | Q36235470 | ||
Lethal giant larvae proteins interact with the exocyst complex and are involved in polarized exocytosis | Q36320849 | ||
Secretory vesicle transport velocity in living cells depends on the myosin-V lever arm length | Q36324635 | ||
The role of the COOH terminus of Sec2p in the transport of post-Golgi vesicles | Q36328209 | ||
Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud | Q36380043 | ||
The terminal tail region of a yeast myosin-V mediates its attachment to vacuole membranes and sites of polarized growth | Q36754969 | ||
Direct interaction between a myosin V motor and the Rab GTPases Ypt31/32 is required for polarized secretion | Q36914328 | ||
Sro7p, a Saccharomyces cerevisiae counterpart of the tumor suppressor l(2)gl protein, is related to myosins in function | Q38334814 | ||
Reconstitution of Rab- and SNARE-dependent membrane fusion by synthetic endosomes. | Q39848704 | ||
Yeast lacking the SRO7/SOP1-encoded tumor suppressor homologue show increased susceptibility to apoptosis-like cell death on exposure to NaCl stress | Q40648776 | ||
The tumour-suppressor genes lgl and dlg regulate basal protein targeting in Drosophila neuroblasts | Q42497218 | ||
The Saccharomyces cerevisiae SOP1 and SOP2 genes, which act in cation homeostasis, can be functionally substituted by the Drosophila lethal(2)giant larvae tumor suppressor gene | Q42687279 | ||
Interactions of three domains distinguishing the Ras-related GTP-binding proteins Ypt1 and Sec4. | Q54310462 | ||
Distinct roles of myosin Va in membrane remodeling and exocytosis of secretory granules | Q82867465 | ||
P433 | issue | 6 | |
P921 | main subject | exocytosis | Q323426 |
P304 | page(s) | 842-857 | |
P577 | publication date | 2011-01-19 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | Yeast homologues of lethal giant larvae and type V myosin cooperate in the regulation of Rab-dependent vesicle clustering and polarized exocytosis | |
P478 | volume | 22 |
Q44036219 | Apical myosin XI anticipates F-actin during polarized growth of Physcomitrella patens cells. |
Q30524660 | Arabidopsis Myosin XI-K Localizes to the Motile Endomembrane Vesicles Associated with F-actin |
Q30550022 | Bem3, a Cdc42 GTPase-activating protein, traffics to an intracellular compartment and recruits the secretory Rab GTPase Sec4 to endomembranes |
Q37490408 | Dynamic Partitioning of Synaptic Vesicle Pools by the SNARE-Binding Protein Tomosyn. |
Q47991408 | Frontline Science: Tumor necrosis factor-α stimulation and priming of human neutrophil granule exocytosis |
Q24322633 | Identification and characterization of multiple novel Rab-myosin Va interactions |
Q34801730 | In vitro reconstitution of Rab GTPase-dependent vesicle clustering by the yeast lethal giant larvae/tomosyn homolog, Sro7. |
Q45069611 | Lipid-dependent regulation of exocytosis in S. cerevisiae by OSBP homolog (Osh) 4. |
Q38021975 | Mechanisms of cytokinesis in budding yeast. |
Q35621765 | Myosin V transports secretory vesicles via a Rab GTPase cascade and interaction with the exocyst complex |
Q30528813 | Myosin Vs organize actin cables in fission yeast |
Q41993334 | Quantitative analysis of membrane trafficking in regulation of Cdc42 polarity |
Q89896520 | The Role of Secretory Pathways in Candida albicans Pathogenesis |
Q38819431 | The Sec1/Munc18 Protein Groove Plays a Conserved Role in Interaction with Sec9p/SNAP-25. |
Q88396882 | The tomosyn homologue, Sro7, is a direct effector of the Rab GTPase, Sec4, in post-Golgi vesicle tethering |
Q47263177 | The ubiquitin-proteasome system functionally links neuronal Tomosyn-1 to dendritic morphology |
Q41137742 | Tomosyn associates with secretory vesicles in neurons through its N- and C-terminal domains. |
Q27310147 | Tracking individual secretory vesicles during exocytosis reveals an ordered and regulated process |
Q35102466 | α-Synuclein and ALPS motifs are membrane curvature sensors whose contrasting chemistry mediates selective vesicle binding. |
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