| scholarly article | Q13442814 |
| P50 | author | Catherine Rabouille | Q47158649 |
| P2093 | author name string | Joep Sprangers | |
| P2860 | cites work | Leucine-rich repeat kinase 2 regulates Sec16A at ER exit sites to allow ER-Golgi export | Q24303851 |
| PCTAIRE protein kinases interact directly with the COPII complex and modulate secretory cargo transport | Q24314410 | ||
| Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells | Q24315632 | ||
| Sec16 defines endoplasmic reticulum exit sites and is required for secretory cargo export in mammalian cells | Q24670130 | ||
| Two mammalian Sec16 homologues have nonredundant functions in endoplasmic reticulum (ER) export and transitional ER organization | Q24685724 | ||
| Structure of the Sec13–Sec16 edge element, a template for assembly of the COPII vesicle coat | Q27664006 | ||
| Sec16 influences transitional ER sites by regulating rather than organizing COPII. | Q27679874 | ||
| Yeast SEC16 gene encodes a multidomain vesicle coat protein that interacts with Sec23p | Q27931226 | ||
| COPII subunit interactions in the assembly of the vesicle coat | Q27931462 | ||
| 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 | ||
| Autophagosome requires specific early Sec proteins for its formation and NSF/SNARE for vacuolar fusion | Q27934199 | ||
| Sec16p potentiates the action of COPII proteins to bud transport vesicles | Q27935297 | ||
| Insights into structural and regulatory roles of Sec16 in COPII vesicle formation at ER exit sites | Q27935407 | ||
| SED4 encodes a yeast endoplasmic reticulum protein that binds Sec16p and participates in vesicle formation | Q27938513 | ||
| Dynamics of the COPII coat with GTP and stable analogues | Q27939261 | ||
| Sec12 binds to Sec16 at transitional ER sites | Q28480558 | ||
| Bi-directional protein transport between the ER and Golgi | Q29615233 | ||
| COPII-coated vesicle formation reconstituted with purified coat proteins and chemically defined liposomes | Q29616856 | ||
| Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer | Q29618155 | ||
| Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway | Q29618501 | ||
| COPII-Golgi protein interactions regulate COPII coat assembly and Golgi size | Q30480431 | ||
| 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 | ||
| Requirements for transitional endoplasmic reticulum site structure and function in Saccharomyces cerevisiae | Q30494268 | ||
| Comparative genomic evidence for a complete nuclear pore complex in the last eukaryotic common ancestor. | Q33719317 | ||
| MAPK signaling to the early secretory pathway revealed by kinase/phosphatase functional screening | Q33916063 | ||
| Regulation of coat assembly--sorting things out at the ER. | Q34020488 | ||
| A comprehensive comparison of transmembrane domains reveals organelle-specific properties | Q34083658 | ||
| Characterization of human Sec16B: indications of specialized, non-redundant functions | Q34256181 | ||
| CK2 phosphorylates Sec31 and regulates ER-To-Golgi trafficking | Q34563010 | ||
| Mammalian Sec16/p250 plays a role in membrane traffic from the endoplasmic reticulum | Q34618297 | ||
| A stress assembly that confers cell viability by preserving ERES components during amino-acid starvation | Q34729599 | ||
| ERK7 is a negative regulator of protein secretion in response to amino-acid starvation by modulating Sec16 membrane association | Q35214896 | ||
| Sec24p and Sec16p cooperate to regulate the GTP cycle of the COPII coat | Q35759972 | ||
| The organization of endoplasmic reticulum export complexes | Q36237498 | ||
| ER exit sites are physical and functional core autophagosome biogenesis components | Q37167928 | ||
| The EM structure of the TRAPPIII complex leads to the identification of a requirement for COPII vesicles on the macroautophagy pathway. | Q37353153 | ||
| COPII coat subunit interactions: Sec24p and Sec23p bind to adjacent regions of Sec16p | Q37383426 | ||
| Phosphatidylinositol 4-phosphate formation at ER exit sites regulates ER export | Q40212158 | ||
| Fine mapping of autophagy-related proteins during autophagosome formation in Saccharomyces cerevisiae | Q41792153 | ||
| TFG-1 function in protein secretion and oncogenesis | Q42056487 | ||
| The role of molecular microtubule motors and the microtubule cytoskeleton in stress granule dynamics | Q42065558 | ||
| Drosophila Sec16 mediates the biogenesis of tER sites upstream of Sar1 through an arginine-rich motif | Q43007174 | ||
| Sec16 determines the size and functioning of the Golgi in the protist parasite, Trypanosoma brucei | Q43650592 | ||
| Sec16 is a determinant of transitional ER organization | Q48124825 | ||
| Akt phosphorylates Sec24: new clues into the regulation of ER-to-Golgi trafficking. | Q51771330 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 97-103 | |
| P577 | publication date | 2015-02-01 | |
| P1433 | published in | Biochemical Society Transactions | Q864226 |
| P1476 | title | SEC16 in COPII coat dynamics at ER exit sites | |
| P478 | volume | 43 |
| Q58708488 | COPII vesicles can affect the activity of antisense oligonucleotides by facilitating the release of oligonucleotides from endocytic pathways |
| Q92455023 | Cellular stress leads to the formation of membraneless stress assemblies in eukaryotic cells |
| Q26767385 | GRASP: A Multitasking Tether |
| Q26773168 | Golgi Fragmentation in ALS Motor Neurons. New Mechanisms Targeting Microtubules, Tethers, and Transport Vesicles |
| Q96305093 | Identification of Plasmodium falciparum HSP70-2 as a resident of the Plasmodium export compartment |
| Q42362081 | In vivo vizualisation of mono-ADP-ribosylation by dPARP16 upon amino-acid starvation |
| Q93016366 | Membrane-Bound Meet Membraneless in Health and Disease |
| Q39220061 | Membrane-bound organelles versus membrane-less compartments and their control of anabolic pathways in Drosophila |
| Q52316968 | Modulation of the secretory pathway by amino-acid starvation. |
| Q48024686 | Phospho-Rasputin Stabilization by Sec16 Is Required for Stress Granule Formation upon Amino Acid Starvation |
| Q27964823 | Proteins interacting with CreA and CreB in the carbon catabolite repression network in Aspergillus nidulans |
| Q41852907 | ROS-independent Nrf2 activation in prostate cancer |
| Q41526609 | Regulation of the Sar1 GTPase Cycle Is Necessary for Large Cargo Secretion from the Endoplasmic Reticulum |
| Q50296294 | SEC16 complex binds SAR1B:GTP:SEC23:SEC24 |
| Q37063757 | SEC16A is a RAB10 effector required for insulin-stimulated GLUT4 trafficking in adipocytes |
| Q42365219 | Sec16 alternative splicing dynamically controls COPII transport efficiency |
| Q39119334 | Sec16 in conventional and unconventional exocytosis: Working at the interface of membrane traffic and secretory autophagy? |
| Q38820136 | TANGO1 recruits Sec16 to coordinately organize ER exit sites for efficient secretion |
| Q41790373 | The link between autophagy and secretion: a story of multitasking proteins |
| Q39422970 | Transport from the endoplasmic reticulum to the Golgi in plants: Where are we now? |
Search more.