scholarly article | Q13442814 |
P50 | author | Randy Schekman | Q740638 |
P2093 | author name string | Edina Harsay | |
P2860 | cites work | Prediction and Functional Analysis of Native Disorder in Proteins from the Three Kingdoms of Life | Q22061741 |
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 | ||
Protein kinase D regulates the fission of cell surface destined transport carriers from the trans-Golgi network | Q24290905 | ||
Farnesyltransferase inhibitors disrupt EGF receptor traffic through modulation of the RhoB GTPase | Q24298206 | ||
Essential role of Hrs in a recycling mechanism mediating functional resensitization of cell signaling. | Q33893544 | ||
Protein complexes in transport vesicle targeting | Q33913418 | ||
Genealogy of principal strains of the yeast genetic stock center | Q33951962 | ||
Transmission electron microscopy of yeast | Q34136196 | ||
Cooperation of GGAs and AP-1 in packaging MPRs at the trans-Golgi network | Q34148158 | ||
Principles for the buffering of genetic variation | Q34171380 | ||
The role of phosphoinositides in membrane transport | Q34309086 | ||
Maintenance of the diacylglycerol level in the Golgi apparatus by the Nir2 protein is critical for Golgi secretory function. | Q34396325 | ||
Synthetic genetic interactions with temperature-sensitive clathrin in Saccharomyces cerevisiae. Roles for synaptojanin-like Inp53p and dynamin-related Vps1p in clathrin-dependent protein sorting at the trans-Golgi network | Q34608593 | ||
The synaptojanin-like protein Inp53/Sjl3 functions with clathrin in a yeast TGN-to-endosome pathway distinct from the GGA protein-dependent pathway | Q34924926 | ||
Chs5/6 complex: a multiprotein complex that interacts with and conveys chitin synthase III from the trans-Golgi network to the cell surface | Q35128222 | ||
Phosphoinositides in constitutive membrane traffic. | Q35842974 | ||
Characteristics of endoplasmic reticulum-derived transport vesicles | Q36234617 | ||
Kinetic analysis of secretory protein traffic and characterization of golgi to plasma membrane transport intermediates in living cells | Q36256009 | ||
Phospholipase D stimulates release of nascent secretory vesicles from the trans-Golgi network | Q36276378 | ||
Modulation of life and death by the tumor necrosis factor receptor-associated factors (TRAFs). | Q36296922 | ||
Correlative light-electron microscopy reveals the tubular-saccular ultrastructure of carriers operating between Golgi apparatus and plasma membrane | Q36301626 | ||
Actin dynamics coupled to clathrin-coated vesicle formation at the trans-Golgi network | Q36322509 | ||
Recycling endosomes can serve as intermediates during transport from the Golgi to the plasma membrane of MDCK cells | Q36322619 | ||
Complexes of syndapin II with dynamin II promote vesicle formation at the trans-Golgi network | Q24309352 | ||
DENN, a novel human gene differentially expressed in normal and neoplastic cells | Q24311875 | ||
Hrs regulates multivesicular body formation via ESCRT recruitment to endosomes | Q24313594 | ||
MADD, a novel death domain protein that interacts with the type 1 tumor necrosis factor receptor and activates mitogen-activated protein kinase | Q24315104 | ||
CART: an Hrs/actinin-4/BERP/myosin V protein complex required for efficient receptor recycling | Q24523519 | ||
The BAR domain proteins: molding membranes in fission, fusion, and phagy | Q24544126 | ||
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 | ||
The Pfam protein families database | Q24599089 | ||
Protein kinase D regulates basolateral membrane protein exit from trans-Golgi network | Q24605796 | ||
The GTP/GDP cycling of rho GTPase TCL is an essential regulator of the early endocytic pathway | Q24607678 | ||
MUSCLE: multiple sequence alignment with high accuracy and high throughput | Q24613456 | ||
The Rho GTPase Rho3 has a direct role in exocytosis that is distinct from its role in actin polarity | Q24647386 | ||
Distribution and function of AP-1 clathrin adaptor complexes in polarized epithelial cells | Q24670526 | ||
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
Confidence Limits on Phylogenies: an Approach using the Bootstrap | Q26778379 | ||
The use of lead citrate at high pH as an electron-opaque stain in electron microscopy | Q26778439 | ||
BAR domains as sensors of membrane curvature: the amphiphysin BAR structure | Q27642663 | ||
Protein secondary structure prediction based on position-specific scoring matrices | Q27860483 | ||
Fitting a mixture model by expectation maximization to discover motifs in biopolymers | Q27860556 | ||
A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae | Q27860636 | ||
The PSIPRED protein structure prediction server | Q27860953 | ||
T-Coffee: A novel method for fast and accurate multiple sequence alignment | Q27860999 | ||
A comprehensive two-hybrid analysis to explore the yeast protein interactome | Q27861093 | ||
A role for Vps1p, actin, and the Myo2p motor in peroxisome abundance and inheritance in Saccharomyces cerevisiae | Q27929921 | ||
Role for Drs2p, a P-type ATPase and potential aminophospholipid translocase, in yeast late Golgi function | Q27930668 | ||
Cdc42 interacts with the exocyst and regulates polarized secretion. | Q27931224 | ||
Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway | Q27931724 | ||
The yeast phosphatidylinositol-4-OH kinase pik1 regulates secretion at the Golgi | Q27931832 | ||
Mutants in trs120 disrupt traffic from the early endosome to the late Golgi | Q27932894 | ||
The yeast lgl family member Sro7p is an effector of the secretory Rab GTPase Sec4p | Q27933359 | ||
Genetic analysis of the Saccharomyces cerevisiae RHO3 gene, encoding a rho-type small GTPase, provides evidence for a role in bud formation | Q27933966 | ||
Role of formins in actin assembly: nucleation and barbed-end association | Q27934072 | ||
Phenotypic analysis of temperature-sensitive yeast actin mutants | Q27934481 | ||
Global mapping of the yeast genetic interaction network | Q27934987 | ||
The vesicular transport protein Cgp1p/Vps54p/Tcs3p/Luv1p is required for the integrity of the actin cytoskeleton. | Q27935812 | ||
Tropomyosin-containing actin cables direct the Myo2p-dependent polarized delivery of secretory vesicles in budding yeast | Q27935856 | ||
The yeast clathrin adaptor protein complex 1 is required for the efficient retention of a subset of late Golgi membrane proteins | Q27936300 | ||
Adaptor complex-independent clathrin function in yeast | Q27936498 | ||
Protein translocation mutants defective in the insertion of integral membrane proteins into the endoplasmic reticulum | Q27937605 | ||
Mutual control of membrane fission and fusion proteins. | Q27937640 | ||
A counterselection for the tryptophan pathway in yeast: 5-fluoroanthranilic acid resistance | Q27937641 | ||
Drs2p-coupled aminophospholipid translocase activity in yeast Golgi membranes and relationship to in vivo function | Q27937731 | ||
Protein sorting in Saccharomyces cerevisiae: isolation of mutants defective in the delivery and processing of multiple vacuolar hydrolases | Q27937990 | ||
YOR129c, a new element interacting with Cnm67p, a component of the spindle pole body of Saccharomyces cerevisiae | Q27938399 | ||
An essential role for a phospholipid transfer protein in yeast Golgi function | Q27938456 | ||
An actin nucleation mechanism mediated by Bni1 and profilin | Q27938654 | ||
Exomer: A coat complex for transport of select membrane proteins from the trans-Golgi network to the plasma membrane in yeast | Q27938814 | ||
Direct involvement of phosphatidylinositol 4-phosphate in secretion in the yeast Saccharomyces cerevisiae | Q27939346 | ||
Formin-dependent actin assembly is regulated by distinct modes of Rho signaling in yeast | Q27939574 | ||
Yeast RHO3 and RHO4 ras superfamily genes are necessary for bud growth, and their defect is suppressed by a high dose of bud formation genes CDC42 and BEM1 | Q27939713 | ||
Role of actin and Myo2p in polarized secretion and growth of Saccharomyces cerevisiae. | Q27940123 | ||
Arf1p, Chs5p and the ChAPs are required for export of specialized cargo from the Golgi | Q27940204 | ||
Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications | Q28131600 | ||
Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccharomyces cerevisiae | Q28131615 | ||
High efficiency transformation of intact yeast cells using single stranded nucleic acids as a carrier | Q28131646 | ||
A protein interaction map of Drosophila melanogaster | Q28131783 | ||
Expression of an isoform of the novel signal transduction protein ST5 is linked to cell morphology | Q28143063 | ||
Clathrin | Q28145011 | ||
Deletion of the COOH terminus converts the ST5 p70 protein from an inhibitor of RAS signaling to an activator with transforming activity in NIH-3T3 cells | Q28145521 | ||
Arf and its many interactors | Q28191279 | ||
The root of the eukaryote tree pinpointed | Q28205101 | ||
Secretory vesicle transport velocity in living cells depends on the myosin-V lever arm length | Q36324635 | ||
Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud | Q36380043 | ||
A subset of yeast vacuolar protein sorting mutants is blocked in one branch of the exocytic pathway | Q36381155 | ||
Parallel secretory pathways to the cell surface in yeast | Q36382718 | ||
Actin dynamics at the Golgi complex in mammalian cells. | Q36401070 | ||
Depolarization of the actin cytoskeleton is a specific phenotype in Saccharomyces cerevisiae. | Q36627925 | ||
Continued functioning of the secretory pathway is essential for ribosome synthesis | Q36650192 | ||
Modulation of the Golgi apparatus in Saccharomyces cerevisiae sec7 mutants as seen by three-dimensional electron microscopy | Q36763001 | ||
Transformations of membrane-bound organelles in sec 14 mutants of the yeasts Saccharomyces cerevisiae and Yarrowia lipolytica | Q36818959 | ||
Isolation and characterization of a GDP/GTP exchange protein specific for the Rab3 subfamily small G proteins | Q36844977 | ||
The yeast GRD20 gene is required for protein sorting in the trans-Golgi network/endosomal system and for polarization of the actin cytoskeleton | Q36955558 | ||
MesA, a novel fungal protein required for the stabilization of polarity axes in Aspergillus nidulans | Q37031693 | ||
Clathrin, adaptors, and sorting | Q37902930 | ||
cdc42 regulates the exit of apical and basolateral proteins from the trans-Golgi network | Q39645140 | ||
MADD/DENN splice variant of the IG20 gene is necessary and sufficient for cancer cell survival | Q40282319 | ||
Cdc42 controls secretory and endocytic transport to the basolateral plasma membrane of MDCK cells | Q40918582 | ||
Dual-color visualization of trans-Golgi network to plasma membrane traffic along microtubules in living cells. | Q40990237 | ||
A putative GTP binding protein homologous to interferon-inducible Mx proteins performs an essential function in yeast protein sorting | Q43862545 | ||
Spontaneous cell polarization through actomyosin-based delivery of the Cdc42 GTPase | Q44298545 | ||
Weighted neighbor joining: a likelihood-based approach to distance-based phylogeny reconstruction | Q44809305 | ||
aex-3 encodes a novel regulator of presynaptic activity in C. elegans | Q47069011 | ||
Involvement of the late secretory pathway in actin regulation and mRNA transport in yeast | Q47359029 | ||
Isolation and characterization of two novel ras superfamily genes in Saccharomyces cerevisiae | Q48174766 | ||
A transition probability model for amino acid substitutions from blocks. | Q51023305 | ||
A membrane transport defect leads to a rapid attenuation of translation initiation in Saccharomyces cerevisiae. | Q51034012 | ||
uDENN, DENN, and dDENN: indissociable domains in Rab and MAP kinases signaling pathways. | Q52054969 | ||
'Marker swap' plasmids: convenient tools for budding yeast molecular genetics. | Q52526054 | ||
Drs2p-dependent formation of exocytic clathrin-coated vesicles in vivo. | Q52547804 | ||
De Novo Prediction of Three-dimensional Structures for Major Protein Families | Q56999399 | ||
Improved recognition of native-like protein structures using a combination of sequence-dependent and sequence-independent features of proteins | Q56999449 | ||
CtBP3/BARS drives membrane fission in dynamin-independent transport pathways | Q57369587 | ||
Multiple Roles for Phosphatidylinositol 4-Kinase in Biosynthetic Transport in Polarized Madin-Darby Canine Kidney Cells | Q57372009 | ||
Transformations of membrane-bound organelles insec14 mutants of the yeastsSaccharomyces cerevisiae andYarrowia lipolytica | Q58382130 | ||
Genetic analysis of the mitotic transmission of minichromosomes | Q69881458 | ||
Vectors for expression of cloned genes in yeast: regulation, overproduction, and underproduction | Q70120823 | ||
Confidence Limits on Phylogenies: an Approach using the Bootstrap | Q104205453 | ||
Phospholipase D | Q28253553 | ||
Combining evidence using p-values: application to sequence homology searches | Q28265811 | ||
Protein kinase D regulates vesicular transport by phosphorylating and activating phosphatidylinositol-4 kinase IIIbeta at the Golgi complex | Q28267260 | ||
Prediction of CASP6 structures using automated Robetta protocols | Q28274221 | ||
The GGA proteins: key players in protein sorting at the trans-Golgi network | Q28290298 | ||
Actin and Arf1-dependent recruitment of a cortactin-dynamin complex to the Golgi regulates post-Golgi transport | Q28581970 | ||
Prediction of protein secondary structure at better than 70% accuracy | Q29547323 | ||
SMART 4.0: towards genomic data integration | Q29547824 | ||
Hidden Markov models for detecting remote protein homologies | Q29614396 | ||
Adaptable adaptors for coated vesicles | Q29614827 | ||
Bi-directional protein transport between the ER and Golgi | Q29615233 | ||
Isolation of yeast mutants defective in protein targeting to the vacuole | Q29615734 | ||
3D-Jury: a simple approach to improve protein structure predictions | Q29615989 | ||
Getting started with yeast | Q29618025 | ||
ARF proteins: roles in membrane traffic and beyond | Q29618078 | ||
76 β-d-Fructofuranoside fructohydrolase from yeast | Q29618502 | ||
Use of a screen for synthetic lethal and multicopy suppressee mutants to identify two new genes involved in morphogenesis in Saccharomyces cerevisiae | Q29618599 | ||
Actin Assembly and Endocytosis: From Yeast to Mammals | Q29620135 | ||
Induction of mutant dynamin specifically blocks endocytic coated vesicle formation | Q29620182 | ||
A ras-like protein is required for a post-Golgi event in yeast secretion | Q29620275 | ||
Protein sorting in yeast: mutants defective in vacuole biogenesis mislocalize vacuolar proteins into the late secretory pathway | Q29620577 | ||
Vps27 recruits ESCRT machinery to endosomes during MVB sorting | Q29620778 | ||
Dynamin and its role in membrane fission | Q30168695 | ||
Combining local-structure, fold-recognition, and new fold methods for protein structure prediction. | Q30336231 | ||
Automated structure prediction of weakly homologous proteins on a genomic scale | Q30341442 | ||
Protein structure prediction and analysis using the Robetta server. | Q30341988 | ||
Mechanism of constitutive export from the golgi: bulk flow via the formation, protrusion, and en bloc cleavage of large trans-golgi network tubular domains. | Q30486978 | ||
Actin dependence of polarized receptor recycling in Madin-Darby canine kidney cell endosomes | Q30857070 | ||
Construction of a GAL1-regulated yeast cDNA expression library and its application to the identification of genes whose overexpression causes lethality in yeast | Q31033635 | ||
Cell polarity in yeast | Q33804326 | ||
CtBP/BARS induces fission of Golgi membranes by acylating lysophosphatidic acid | Q33882728 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
Avl9p YLR114C | Q27551971 | ||
P304 | page(s) | 1203-19 | |
P577 | publication date | 2007-04-01 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | Avl9p, a member of a novel protein superfamily, functions in the late secretory pathway | |
P478 | volume | 18 |
Q90419746 | A Humanized Yeast Phenomic Model of Deoxycytidine Kinase to Predict Genetic Buffering of Nucleoside Analog Cytotoxicity |
Q33585902 | A chemical genetic screen for modulators of exocytic transport identifies inhibitors of a transport mechanism linked to GTR2 function |
Q36587948 | A conserved regulatory mode in exocytic membrane fusion revealed by Mso1p membrane interactions |
Q33576087 | A high-throughput screen for chemical inhibitors of exocytic transport in yeast |
Q38117545 | Actin acting at the Golgi. |
Q43116437 | Cancer driver candidate genes AVL9, DENND5A and NUPL1 contribute to MDCK cystogenesis. |
Q37598464 | Cancer driver-passenger distinction via sporadic human and dog cancer comparison: a proof-of-principle study with colorectal cancer. |
Q24298712 | Crystal structure of folliculin reveals a hidDENN function in genetically inherited renal cancer |
Q37844335 | DENN domain proteins: regulators of Rab GTPases |
Q30624208 | DENND2B activates Rab13 at the leading edge of migrating cells and promotes metastatic behavior |
Q24302350 | Family-wide characterization of the DENN domain Rab GDP-GTP exchange factors |
Q58801934 | Hypoxia-regulated lncRNA CRPAT4 promotes cell migration via regulating AVL9 in clear cell renal cell carcinomas |
Q45069611 | Lipid-dependent regulation of exocytosis in S. cerevisiae by OSBP homolog (Osh) 4. |
Q24323182 | Rab14 and its exchange factor FAM116 link endocytic recycling and adherens junction stability in migrating cells |
Q42571521 | Sec1p and Mso1p C-terminal tails cooperate with the SNAREs and Sec4p in polarized exocytosis |
Q34980423 | Segregation of sphingolipids and sterols during formation of secretory vesicles at the trans-Golgi network |
Q24643414 | Swf1p, a member of the DHHC-CRD family of palmitoyltransferases, regulates the actin cytoskeleton and polarized secretion independently of its DHHC motif |
Q28504575 | The Connecdenn DENN domain: a GEF for Rab35 mediating cargo-specific exit from early endosomes |
Q38819431 | The Sec1/Munc18 Protein Groove Plays a Conserved Role in Interaction with Sec9p/SNAP-25. |
Q40075586 | The connecdenn family, Rab35 guanine nucleotide exchange factors interfacing with the clathrin machinery. |
Q58493545 | The role of the cytoskeleton in the structure and function of the Golgi apparatus |
Q37071739 | The synaptobrevin homologue Snc2p recruits the exocyst to secretory vesicles by binding to Sec6p |
Q30381017 | Yeast Sec1p functions before and after vesicle docking. |
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