scholarly article | Q13442814 |
P2093 | author name string | Charles Barlowe | |
Polina Shindiapina | |||
P2860 | cites work | Identification of pleckstrin-homology-domain-containing proteins with novel phosphoinositide-binding specificities | Q24290290 |
Sphingomyelin synthase-related protein SMSr controls ceramide homeostasis in the ER | Q24337469 | ||
Diacylglycerol kinase delta suppresses ER-to-Golgi traffic via its SAM and PH domains | Q24555039 | ||
Maintenance of Golgi structure and function depends on the integrity of ER export | Q24653507 | ||
Sec16 defines endoplasmic reticulum exit sites and is required for secretory cargo export in mammalian cells | Q24670130 | ||
Transformation of intact yeast cells treated with alkali cations | Q24672708 | ||
Two mammalian Sec16 homologues have nonredundant functions in endoplasmic reticulum (ER) export and transitional ER organization | Q24685724 | ||
SNARE selectivity of the COPII coat | Q27641907 | ||
Structural studies examining the substrate specificity profiles of PC-PLCBc protein variants | Q27643912 | ||
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q27861085 | ||
Coupled ER to Golgi transport reconstituted with purified cytosolic proteins | Q27929807 | ||
COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum | Q27930804 | ||
Surface structure of the COPII-coated vesicle | Q27931455 | ||
Specific requirements for the ER to Golgi transport of GPI-anchored proteins in yeast | Q27931471 | ||
Requirement for a GTPase-activating protein in vesicle budding from the endoplasmic reticulum | Q27931640 | ||
Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway | Q27931724 | ||
Golgi structure correlates with transitional endoplasmic reticulum organization in Pichia pastoris and Saccharomyces cerevisiae | Q27931787 | ||
Yeast homologue of neuronal frequenin is a regulator of phosphatidylinositol-4-OH kinase | Q27932258 | ||
Asymmetric requirements for a Rab GTPase and SNARE proteins in fusion of COPII vesicles with acceptor membranes | Q27932451 | ||
The yeast integral membrane protein Apq12 potentially links membrane dynamics to assembly of nuclear pore complexes | Q27932688 | ||
The Sec13p complex and reconstitution of vesicle budding from the ER with purified cytosolic proteins | Q27933342 | ||
Distinct roles for the yeast phosphatidylinositol 4-kinases, Stt4p and Pik1p, in secretion, cell growth, and organelle membrane dynamics | Q27933485 | ||
Erv41p and Erv46p: new components of COPII vesicles involved in transport between the ER and Golgi complex | Q27934087 | ||
Dual prenylation is required for Rab protein localization and function | Q27934323 | ||
Sec16p potentiates the action of COPII proteins to bud transport vesicles | Q27935297 | ||
Multiple cargo binding sites on the COPII subunit Sec24p ensure capture of diverse membrane proteins into transport vesicles | Q27935680 | ||
Evidence for overlapping and distinct functions in protein transport of coat protein Sec24p family members | Q27936142 | ||
SNARE-mediated retrograde traffic from the Golgi complex to the endoplasmic reticulum | Q27937494 | ||
SEC12 encodes a guanine-nucleotide-exchange factor essential for transport vesicle budding from the ER. | Q27937857 | ||
The dynamics of golgi protein traffic visualized in living yeast cells | Q27938880 | ||
Dynamics of the COPII coat with GTP and stable analogues | Q27939261 | ||
A role for Yip1p in COPII vesicle biogenesis | Q27939417 | ||
Dissection of COPII subunit-cargo assembly and disassembly kinetics during Sar1p-GTP hydrolysis | Q27939504 | ||
Construction of a set of convenient Saccharomyces cerevisiae strains that are isogenic to S288C | Q28131625 | ||
Reconstitution of SEC gene product-dependent intercompartmental protein transport | Q28295130 | ||
The mammalian guanine nucleotide exchange factor mSec12 is essential for activation of the Sar1 GTPase directing endoplasmic reticulum export | Q28568377 | ||
COPI-coated ER-to-Golgi transport complexes segregate from COPII in close proximity to ER exit sites | Q28645792 | ||
Dynamics of transitional endoplasmic reticulum sites in vertebrate cells | Q28645796 | ||
Bi-directional protein transport between the ER and Golgi | Q29615233 | ||
Multiple genes are required for proper insertion of secretory proteins into the endoplasmic reticulum in yeast | Q29618500 | ||
Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway | Q29618501 | ||
Rapid transbilayer diffusion of 1,2-diacylglycerol and its relevance to control of membrane curvature | Q59076619 | ||
The specificity of phospholipase A2 and phospholipase C in a mixed micellar system | Q67266249 | ||
47 Phosphatidylinositol-specific phospholipases C from Bacillus cereus and Bacillus thuringiensis | Q68240609 | ||
Phosphatidylinositol-specific phospholipase C from Bacillus cereus combines intrinsic phosphotransferase and cyclic phosphodiesterase activities: a 31P NMR study | Q68490241 | ||
The action mechanism of cerulenin. I. Effect of cerulenin on sterol and fatty acid biosynthesis in yeast | Q69204010 | ||
Functional characteristics of phosphatidylinositol-specific phospholipases C from Bacillus cereus and Bacillus thuringiensis | Q69363158 | ||
The choline binding site of phospholipase C (Bacillus cereus): insights into substrate specificity | Q73570972 | ||
De novo formation of transitional ER sites and Golgi structures in Pichia pastoris | Q78315009 | ||
De novo formation, fusion and fission of mammalian COPII-coated endoplasmic reticulum exit sites | Q30476542 | ||
Adaptation of endoplasmic reticulum exit sites to acute and chronic increases in cargo load | Q30483089 | ||
Organisation of human ER-exit sites: requirements for the localisation of Sec16 to transitional ER. | Q30489454 | ||
Macroscopic consequences of the action of phospholipase C on giant unilamellar liposomes | Q30837435 | ||
Morphogenesis and dynamics of the yeast Golgi apparatus | Q31869432 | ||
Dynamics of COPII vesicles and the Golgi apparatus in cultured Nicotiana tabacum BY-2 cells provides evidence for transient association of Golgi stacks with endoplasmic reticulum exit sites. | Q33213541 | ||
COPII under the microscope | Q33293899 | ||
Yeast Sec23p acts in the cytoplasm to promote protein transport from the endoplasmic reticulum to the Golgi complex in vivo and in vitro. | Q33566208 | ||
Nm23H2 facilitates coat protein complex II assembly and endoplasmic reticulum export in mammalian cells | Q33763879 | ||
Erv14p directs a transmembrane secretory protein into COPII-coated transport vesicles | Q34011746 | ||
Structure of the Sec13/31 COPII coat cage | Q34483894 | ||
Mammalian Sec16/p250 plays a role in membrane traffic from the endoplasmic reticulum | Q34618297 | ||
Sar1 promotes vesicle budding from the endoplasmic reticulum but not Golgi compartments | Q34662584 | ||
A novel GTP-binding protein, Sar1p, is involved in transport from the endoplasmic reticulum to the Golgi apparatus. | Q36222049 | ||
The organization of endoplasmic reticulum export complexes | Q36237498 | ||
Identification of a gene required for membrane protein retention in the early secretory pathway. | Q36515193 | ||
Distinct biochemical requirements for the budding, targeting, and fusion of ER-derived transport vesicles | Q36530046 | ||
Sec12p-dependent membrane binding of the small GTP-binding protein Sar1p promotes formation of transport vesicles from the ER. | Q36532755 | ||
GTP/GDP exchange by Sec12p enables COPII vesicle bud formation on synthetic liposomes | Q37592808 | ||
Mammalian Sec23p homologue is restricted to the endoplasmic reticulum transitional cytoplasm | Q37599174 | ||
Phosphatidylinositol 4-phosphate formation at ER exit sites regulates ER export | Q40212158 | ||
Isolation and biochemical characterization of organelles from the yeast, Saccharomyces cerevisiae | Q40465413 | ||
GPI anchor attachment is required for Gas1p transport from the endoplasmic reticulum in COP II vesicles | Q41063582 | ||
Sterols regulate ER-export dynamics of secretory cargo protein ts-O45-G. | Q41455784 | ||
A cytoskeleton-related gene, uso1, is required for intracellular protein transport in Saccharomyces cerevisiae | Q41839314 | ||
Genome-wide analysis reveals inositol, not choline, as the major effector of Ino2p-Ino4p and unfolded protein response target gene expression in yeast | Q42010811 | ||
A novel role for dp115 in the organization of tER sites in Drosophila | Q42136020 | ||
Inositol induces a profound alteration in the pattern and rate of synthesis and turnover of membrane lipids in Saccharomyces cerevisiae | Q42496875 | ||
Erv25p, a component of COPII-coated vesicles, forms a complex with Emp24p that is required for efficient endoplasmic reticulum to Golgi transport | Q42643149 | ||
Drosophila Sec16 mediates the biogenesis of tER sites upstream of Sar1 through an arginine-rich motif | Q43007174 | ||
Differential effects of a GTP-restricted mutant of Sar1p on segregation of cargo during export from the endoplasmic reticulum | Q44976926 | ||
Regulation of intracellular phosphatidylinositol-4-phosphate by the Sac1 lipid phosphatase | Q45212986 | ||
COPII-cargo interactions direct protein sorting into ER-derived transport vesicles | Q46046050 | ||
Concentration of GPI-anchored proteins upon ER exit in yeast | Q46215537 | ||
Secretory cargo regulates the turnover of COPII subunits at single ER exit sites | Q46907625 | ||
The transitional ER localization mechanism of Pichia pastoris Sec12. | Q47640214 | ||
Dynamics of Golgi matrix proteins after the blockage of ER to Golgi transport. | Q47871174 | ||
Sec16 is a determinant of transitional ER organization | Q48124825 | ||
Determination of the kinetic parameters for phospholipase C (Bacillus cereus) on different phospholipid substrates using a chromogenic assay based on the quantitation of inorganic phosphate. | Q50527138 | ||
Cerulenin-resistant mutants of Saccharomyces cerevisiae with an altered fatty acid synthase gene. | Q54199525 | ||
The GTP-binding Sar1 protein is localized to the early compartment of the yeast secretory pathway. | Q54694535 | ||
Structural and mechanistic comparison of prokaryotic and eukaryotic phosphoinositide-specific phospholipases C | Q57648131 | ||
Golgi maturation visualized in living yeast | Q59058669 | ||
P433 | issue | 9 | |
P921 | main subject | endoplasmic reticulum | Q79927 |
Saccharomyces cerevisiae | Q719725 | ||
P304 | page(s) | 1530-1545 | |
P577 | publication date | 2010-03-03 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | Requirements for transitional endoplasmic reticulum site structure and function in Saccharomyces cerevisiae | |
P478 | volume | 21 |
Q37429816 | A family of membrane-shaping proteins at ER subdomains regulates pre-peroxisomal vesicle biogenesis. |
Q34729599 | A stress assembly that confers cell viability by preserving ERES components during amino-acid starvation |
Q37078360 | COPII - a flexible vesicle formation system |
Q37947559 | COPII and COPI traffic at the ER-Golgi interface |
Q37970881 | COPII and the regulation of protein sorting in mammals |
Q41881232 | COPII machinery cooperates with ER-localized Hsp40 to sequester misfolded membrane proteins into ER-associated compartments |
Q26744484 | Coat/Tether Interactions-Exception or Rule? |
Q34414972 | Contact of cis-Golgi with ER exit sites executes cargo capture and delivery from the ER |
Q38959427 | Coordinate Regulation of Yeast Sterol Regulatory Element-binding Protein (SREBP) and Mga2 Transcription Factors |
Q40991389 | ER arrival sites for COPI vesicles localize to hotspots of membrane trafficking. |
Q37167928 | ER exit sites are physical and functional core autophagosome biogenesis components |
Q30560940 | Golgi enlargement in Arf-depleted yeast cells is due to altered dynamics of cisternal maturation |
Q27935407 | Insights into structural and regulatory roles of Sec16 in COPII vesicle formation at ER exit sites |
Q27938069 | Involvement of the penta-EF-hand protein Pef1p in the Ca2+-dependent regulation of COPII subunit assembly in Saccharomyces cerevisiae |
Q61135386 | Lipid droplet and peroxisome biogenesis occur at the same ER subdomains |
Q55266563 | Lysophospholipids Facilitate COPII Vesicle Formation. |
Q44977067 | MAIGO5 functions in protein export from Golgi-associated endoplasmic reticulum exit sites in Arabidopsis. |
Q38659514 | Microscopy analysis of reconstituted COPII coat polymerization and Sec16 dynamics |
Q41135155 | New Insights In Intestinal Sar1B GTPase Regulation and Role in Cholesterol Homeostasis |
Q41543991 | Phosphorylation of Chs2p regulates interaction with COPII. |
Q50276545 | Regulation of ER-Golgi Transport Dynamics by GTPases in Budding Yeast. |
Q34020488 | Regulation of coat assembly--sorting things out at the ER. |
Q38318878 | Role of phosphatidylserine in phospholipid flippase-mediated vesicle transport in Saccharomyces cerevisiae |
Q46782581 | SEC16 in COPII coat dynamics at ER exit sites |
Q41285549 | Sar1 localizes at the rims of COPII-coated membranes in vivo. |
Q28480558 | Sec12 binds to Sec16 at transitional ER sites |
Q27679874 | Sec16 influences transitional ER sites by regulating rather than organizing COPII. |
Q27930159 | Sec23 homolog Nel1 is a novel GTPase-activating protein for Sar1 but does not function as a subunit of the coat protein complex II (COPII) coat |
Q41911008 | Sec24 phosphorylation regulates autophagosome abundance during nutrient deprivation |
Q38080412 | Secretory protein biogenesis and traffic in the early secretory pathway |
Q89896520 | The Role of Secretory Pathways in Candida albicans Pathogenesis |
Q30495976 | The yeast GRASP Grh1 colocalizes with COPII and is dispensable for organizing the secretory pathway. |
Q34237397 | The yeast Golgi apparatus |
Q53001273 | Three-dimensional and immune electron microscopic analysis of the secretory pathway in Saccharomyces cerevisiae. |
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