scholarly article | Q13442814 |
P2093 | author name string | Robert C Piper | |
Younghoon Kee | |||
Jihui Ren | |||
Jon M Huibregtse | |||
P2860 | cites work | Possible involvement of a novel STAM-associated molecule "AMSH" in intracellular signal transduction mediated by cytokines | Q22010172 |
The E3 ubiquitin ligase AIP4 mediates ubiquitination and sorting of the G protein-coupled receptor CXCR4 | Q24299260 | ||
The ubiquitin isopeptidase UBPY regulates endosomal ubiquitin dynamics and is essential for receptor down-regulation | Q24306674 | ||
Growth factors induce differential phosphorylation profiles of the Hrs-STAM complex: a common node in signalling networks with signal-specific properties | Q24532853 | ||
AMSH is an endosome-associated ubiquitin isopeptidase | Q24676880 | ||
The C2 domain of the Rsp5 ubiquitin ligase binds membrane phosphoinositides and directs ubiquitination of endosomal cargo | Q24677536 | ||
Functional profiling of the Saccharomyces cerevisiae genome | Q27860544 | ||
Global analysis of protein expression in yeast | Q27860658 | ||
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q27861085 | ||
A generic protein purification method for protein complex characterization and proteome exploration | Q27861087 | ||
A comprehensive two-hybrid analysis to explore the yeast protein interactome | Q27861093 | ||
Four permeases import proline and the toxic proline analogue azetidine-2-carboxylate into yeast | Q27930049 | ||
A combined experimental and computational strategy to define protein interaction networks for peptide recognition modules | Q27930492 | ||
The iron transporter Fth1p forms a complex with the Fet5 iron oxidase and resides on the vacuolar membrane | Q27931127 | ||
A transmembrane ubiquitin ligase required to sort membrane proteins into multivesicular bodies | Q27931399 | ||
Functional domains of the Rsp5 ubiquitin-protein ligase. | Q27931992 | ||
Permease Recycling and Ubiquitination Status Reveal a Particular Role for Bro1 in the Multivesicular Body Pathway | Q27933496 | ||
The Rsp5 ubiquitin ligase is coupled to and antagonized by the Ubp2 deubiquitinating enzyme | Q27933628 | ||
Physiological regulation of membrane protein sorting late in the secretory pathway of Saccharomyces cerevisiae | Q27933680 | ||
GGA proteins bind ubiquitin to facilitate sorting at the trans-Golgi network | Q27934125 | ||
Components of a ubiquitin ligase complex specify polyubiquitination and intracellular trafficking of the general amino acid permease | Q27935024 | ||
Protein-protein interactions of ESCRT complexes in the yeast Saccharomyces cerevisiae. | Q27935665 | ||
Zim17, a novel zinc finger protein essential for protein import into mitochondria | Q27935898 | ||
Transferrin receptor-like proteins control the degradation of a yeast metal transporter | Q27935937 | ||
The Doa4 deubiquitinating enzyme is functionally linked to the vacuolar protein-sorting and endocytic pathways | Q27936688 | ||
Morphological classification of the yeast vacuolar protein sorting mutants: evidence for a prevacuolar compartment in class E vps mutants | Q27936883 | ||
Domains of the Rsp5 ubiquitin-protein ligase required for receptor-mediated and fluid-phase endocytosis | Q27936947 | ||
The Vps27p Hse1p complex binds ubiquitin and mediates endosomal protein sorting. | Q27937143 | ||
Multivesicular body sorting: ubiquitin ligase Rsp5 is required for the modification and sorting of carboxypeptidase S. | Q27937366 | ||
end3 and end4: two mutants defective in receptor-mediated and fluid-phase endocytosis in Saccharomyces cerevisiae | Q27938116 | ||
Vps10p cycles between the late-Golgi and prevacuolar compartments in its function as the sorting receptor for multiple yeast vacuolar hydrolases. | Q27938475 | ||
Ubiquitin-dependent sorting into the multivesicular body pathway requires the function of a conserved endosomal protein sorting complex, ESCRT-I. | Q27939053 | ||
Bsd2 binds the ubiquitin ligase Rsp5 and mediates the ubiquitination of transmembrane proteins. | Q27939068 | ||
The PY-motif of Bul1 protein is essential for growth of Saccharomyces cerevisiae under various stress conditions. | Q27939323 | ||
Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications | Q28131600 | ||
Receptor downregulation and multivesicular-body sorting | Q28131720 | ||
A deubiquitinating enzyme UBPY interacts with the Src homology 3 domain of Hrs-binding protein via a novel binding motif PX(V/I)(D/N)RXXKP | Q28138440 | ||
STAM and Hrs are subunits of a multivalent ubiquitin-binding complex on early endosomes | Q28205230 | ||
A deubiquitinating enzyme UBPY regulates the level of protein ubiquitination on endosomes | Q28245757 | ||
Hrs, a tyrosine kinase substrate with a conserved double zinc finger domain, is localized to the cytoplasmic surface of early endosomes | Q28245945 | ||
WW domains of Rsp5p define different functions: determination of roles in fluid phase and uracil permease endocytosis in Saccharomyces cerevisiae | Q28345570 | ||
A novel active site-directed probe specific for deubiquitylating enzymes reveals proteasome association of USP14 | Q28359750 | ||
Regulation of epidermal growth factor receptor down-regulation by UBPY-mediated deubiquitination at endosomes | Q28511379 | ||
Fab1p PtdIns(3)P 5-kinase function essential for protein sorting in the multivesicular body | Q29547922 | ||
A single motif responsible for ubiquitin recognition and monoubiquitination in endocytic proteins | Q29616733 | ||
A second set of loxP marker cassettes for Cre-mediated multiple gene knockouts in budding yeast | Q29616852 | ||
c-Cbl/Sli-1 regulates endocytic sorting and ubiquitination of the epidermal growth factor receptor | Q29618661 | ||
Regulation of Membrane Protein Transport by Ubiquitin and Ubiquitin-Binding Proteins | Q29619145 | ||
Expression cloning of a cDNA encoding a retinoblastoma-binding protein with E2F-like properties | Q29620009 | ||
Structural basis for the binding of proline-rich peptides to SH3 domains | Q29620408 | ||
The biogenesis of multivesicular endosomes | Q29620561 | ||
Activation of the endosome-associated ubiquitin isopeptidase AMSH by STAM, a component of the multivesicular body-sorting machinery | Q30159944 | ||
A nonconserved Ala401 in the yeast Rsp5 ubiquitin ligase is involved in degradation of Gap1 permease and stress-induced abnormal proteins | Q33193077 | ||
Localization of the Rsp5p ubiquitin-protein ligase at multiple sites within the endocytic pathway | Q33559052 | ||
Ubiquitin-mediated targeting of a mutant plasma membrane ATPase, Pma1-7, to the endosomal/vacuolar system in yeast | Q33693280 | ||
The GAT domains of clathrin-associated GGA proteins have two ubiquitin binding motifs | Q34026517 | ||
Chemistry-based functional proteomics reveals novel members of the deubiquitinating enzyme family | Q34156341 | ||
Protein sorting into multivesicular endosomes | Q34218897 | ||
Regulation of ubiquitin-binding proteins by monoubiquitination | Q34486954 | ||
Direct sorting of the yeast uracil permease to the endosomal system is controlled by uracil binding and Rsp5p-dependent ubiquitylation. | Q35803062 | ||
The Hrs/STAM complex in the downregulation of receptor tyrosine kinases | Q36043224 | ||
Riding the DUBway: regulation of protein trafficking by deubiquitylating enzymes. | Q36117513 | ||
Ubiquitin and endocytic protein sorting | Q36297842 | ||
Starvation induces vacuolar targeting and degradation of the tryptophan permease in yeast | Q36301450 | ||
Vps27-Hse1 and ESCRT-I complexes cooperate to increase efficiency of sorting ubiquitinated proteins at the endosome. | Q36324529 | ||
Role of ubiquitylation in cellular membrane transport | Q36443011 | ||
Antagonistic roles of ESCRT and Vps class C/HOPS complexes in the recycling of yeast membrane proteins | Q37497187 | ||
Regulation of epidermal growth factor receptor degradation by heterotrimeric Galphas protein | Q37657338 | ||
Cis- and trans-acting functions required for endocytosis of the yeast pheromone receptors | Q42769697 | ||
Ligand-induced lysosomal epidermal growth factor receptor (EGFR) degradation is preceded by proteasome-dependent EGFR de-ubiquitination | Q42800213 | ||
Ubiquitination and proteasomal activity is required for transport of the EGF receptor to inner membranes of multivesicular bodies | Q42917525 | ||
c-Cbl ubiquitinates the EGF receptor at the plasma membrane and remains receptor associated throughout the endocytic route | Q43700308 | ||
Ubiquitin is required for sorting to the vacuole of the yeast general amino acid permease, Gap1. | Q43704241 | ||
Expression of an enzymatically active parasite molecule in Escherichia coli: Schistosoma japonicum glutathione S-transferase | Q58039618 | ||
Ubiquitin Sorts Proteins into the Intralumenal Degradative Compartment of the Late-Endosome/Vacuole | Q58480871 | ||
The evolutionarily conserved N-terminal region of Cbl is sufficient to enhance down-regulation of the epidermal growth factor receptor | Q73316781 | ||
Ubiquitination of the PEST-like endocytosis signal of the yeast a-factor receptor | Q73538505 | ||
The deubiquitinating enzyme Ubp2 modulates Rsp5-dependent Lys63-linked polyubiquitin conjugates in Saccharomyces cerevisiae | Q79209223 | ||
A single PXY motif located within the carboxyl terminus of Spt23p and Mga2p mediates a physical and functional interaction with ubiquitin ligase Rsp5p | Q80825563 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | multivesicular body | Q14878286 |
P304 | page(s) | 324-335 | |
P577 | publication date | 2006-11-01 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | Hse1, a component of the yeast Hrs-STAM ubiquitin-sorting complex, associates with ubiquitin peptidases and a ligase to control sorting efficiency into multivesicular bodies | |
P478 | volume | 18 |
Q34580742 | A concentric circle model of multivesicular body cargo sorting. |
Q35998598 | A dual role for K63-linked ubiquitin chains in multivesicular body biogenesis and cargo sorting |
Q35210801 | A single ubiquitin is sufficient for cargo protein entry into MVBs in the absence of ESCRT ubiquitination |
Q33810229 | An ubiquitin-dependent balance between mitofusin turnover and fatty acids desaturation regulates mitochondrial fusion. |
Q24601502 | Biogenesis and function of multivesicular bodies |
Q27934992 | DOA1/UFD3 plays a role in sorting ubiquitinated membrane proteins into multivesicular bodies |
Q37329815 | Deubiquitinase activity is required for the proteasomal degradation of misfolded cytosolic proteins upon heat-stress |
Q33632446 | Deubiquitinating enzymes Ubp2 and Ubp15 regulate endocytosis by limiting ubiquitination and degradation of ARTs |
Q27937377 | Direct binding to Rsp5 mediates ubiquitin-independent sorting of Sna3 via the multivesicular body pathway. |
Q37707470 | ESCRT & Co. |
Q24646021 | ESCRT complexes and the biogenesis of multivesicular bodies |
Q27931999 | ESCRT ubiquitin-binding domains function cooperatively during MVB cargo sorting |
Q34684750 | ESCRT-0 assembles as a heterotetrameric complex on membranes and binds multiple ubiquitinylated cargoes simultaneously. |
Q27935349 | Efficient mRNA polyadenylation requires a ubiquitin-like domain, a zinc knuckle, and a RING finger domain, all contained in the Mpe1 protein |
Q37145116 | Endosomal sorting complex required for transport proteins in cancer pathogenesis, vesicular transport, and non-endosomal functions |
Q47909119 | Evidence for ESCRT- and clathrin-dependent microautophagy. |
Q33827329 | Homoserine toxicity in Saccharomyces cerevisiae and Candida albicans homoserine kinase (thr1Delta) mutants |
Q37896711 | How ubiquitin functions with ESCRTs |
Q34155287 | Hrs controls sorting of the epithelial Na+ channel between endosomal degradation and recycling pathways |
Q27654065 | Hybrid Structural Model of the Complete Human ESCRT-0 Complex |
Q43686642 | Identification of phosphatase 2A-like Sit4-mediated signalling and ubiquitin-dependent protein sorting as modulators of caffeine sensitivity in S. cerevisiae |
Q27934554 | Interaction of the deubiquitinating enzyme Ubp2 and the e3 ligase Rsp5 is required for transporter/receptor sorting in the multivesicular body pathway |
Q33719095 | Intracellular trafficking and signaling in development |
Q37401247 | Membrane protein targeting to the MVB/lysosome |
Q35738601 | Molecular mechanisms of ubiquitin-dependent membrane traffic |
Q53369064 | Multiple proteins and phosphorylations regulate Saccharomyces cerevisiae Cdc24p localization. |
Q30010172 | Novel roles for the E3 ubiquitin ligase atrophin-interacting protein 4 and signal transduction adaptor molecule 1 in G protein-coupled receptor signaling. |
Q55052724 | Origin and evolution of fungal HECT ubiquitin ligases. |
Q36017039 | Plasticity of polyubiquitin recognition as lysosomal targeting signals by the endosomal sorting machinery |
Q37703481 | Quality control: quality control at the plasma membrane: one mechanism does not fit all |
Q24621192 | Regulation of Epidermal Growth Factor Receptor Ubiquitination and Trafficking by the USP8·STAM Complex |
Q36714155 | Regulation of catalytic activities of HECT ubiquitin ligases |
Q28308073 | Regulation of endocytic sorting by ESCRT-DUB-mediated deubiquitination |
Q35310258 | Routing misfolded proteins through the multivesicular body (MVB) pathway protects against proteotoxicity |
Q58558639 | Rsp5 Ubiquitin ligase-mediated quality control system clears membrane proteins mistargeted to the vacuole membrane |
Q35947104 | Split-ubiquitin two-hybrid assay to analyze protein-protein interactions at the endosome: application to Saccharomyces cerevisiae Bro1 interacting with ESCRT complexes, the Doa4 ubiquitin hydrolase, and the Rsp5 ubiquitin ligase |
Q36744498 | The Budding Yeast Ubiquitin Protease Ubp7 Is a Novel Component Involved in S Phase Progression |
Q24569667 | The Deubiquitinating Enzyme USP8 Promotes Trafficking and Degradation of the Chemokine Receptor 4 at the Sorting Endosome |
Q49887941 | The E3 ubiquitin ligase NEDD4 mediates cell migration signaling of EGFR in lung cancer cells. |
Q24569709 | The ESCRT complexes |
Q26849199 | The ESCRT machinery: from the plasma membrane to endosomes and back again |
Q33553868 | The HECT domain of the ubiquitin ligase Rsp5 contributes to substrate recognition |
Q27645148 | The Vps27/Hse1 Complex Is a GAT Domain-Based Scaffold for Ubiquitin-Dependent Sorting |
Q29620787 | The emerging shape of the ESCRT machinery |
Q36844591 | The spatial and temporal organization of ubiquitin networks |
Q37812727 | Ubiquitin: Same Molecule, Different Degradation Pathways |
Q27932816 | Ubp2 regulates Rsp5 ubiquitination activity in vivo and in vitro |
Q34774715 | Versatile roles of k63-linked ubiquitin chains in trafficking |
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