| 1 |
2023 |
Arabidopsis clathrin adaptor EPSIN1 but not MODIFIED TRANSPORT TO THE VACOULE1 contributes to effective plant immunity against pathogenic Pseudomonas bacteria. |
AtEPS1, AtFLS2, EE, PM, Pto, TGN |
| 2 |
2021 |
A continuum membrane model can predict curvature sensing by helix insertion. |
--- |
| 3 |
2020 |
Complimentary action of structured and unstructured domains of epsin supports clathrin-mediated endocytosis at high tension. |
CCSs, CME, IDP |
| 4 |
2020 |
ESCRT-dependent protein sorting is required for the viability of yeast clathrin-mediated endocytosis mutants. |
CME, ESCRT, PM |
| 5 |
2020 |
Proteomic Exploration of Membrane Curvature Sensors Using a Series of Spherical Supported Lipid Bilayers. |
BAR, MCS, NHDF, SSLB |
| 6 |
2019 |
Single-Nanometer Changes in Nanopore Geometry Influence Curvature, Local Properties, and Protein Localization in Membrane Simulations. |
--- |
| 7 |
2018 |
AP180 N-Terminal Homology (ANTH) and Epsin N-Terminal Homology (ENTH) Domains: Physiological Functions and Involvement in Disease. |
--- |
| 8 |
2017 |
Structure and evolution of ENTH and VHS/ENTH-like domains in tepsin. |
AP4, TGN |
| 9 |
2017 |
To a better understanding of the giardial ENTH protein function. |
epsinR |
| 10 |
2016 |
Vestiges of Ent3p/Ent5p function in the giardial epsin homolog. |
--- |
| 11 |
2014 |
Btn3 regulates the endosomal sorting function of the yeast Ent3 epsin, an adaptor for SNARE proteins. |
--- |
| 12 |
2013 |
Crystallographic analysis of the ENTH domain from yeast epsin Ent2 that induces a cell division phenotype. |
--- |
| 13 |
2013 |
Dual role of BAR domain-containing proteins in regulating vesicle release catalyzed by the GTPase, dynamin-2. |
Dyn2, EAPs, PRD, SH3 |
| 14 |
2012 |
Membrane binding and self-association of the epsin N-terminal homology domain. |
CG, MD |
| 15 |
2012 |
Single molecule kinetics of ENTH binding to lipid membranes. |
TIRFM |
| 16 |
2011 |
Epsin N-terminal homology domains bind on opposite sides of two SNAREs. |
--- |
| 17 |
2011 |
Liquid facets-related (lqfR) is required for egg chamber morphogenesis during Drosophila oogenesis. |
CLINT1, lqfR |
| 18 |
2010 |
Analysis of the development of a morphological phenotype as a function of protein concentration in budding yeast. |
--- |
| 19 |
2010 |
Curvature sensing by the epsin N-terminal homology domain measured on cylindrical lipid membrane tethers. |
--- |
| 20 |
2010 |
Dissecting Ent3p: the ENTH domain binds different SNAREs via distinct amino acid residues while the C-terminus is sufficient for retrograde transport from endosomes. |
GFP |
| 21 |
2010 |
The epsin family of endocytic adaptors promotes fibrosarcoma migration and invasion. |
--- |
| 22 |
2009 |
Drosophila liquid facets-Related encodes Golgi epsin and is an essential gene required for cell proliferation, growth, and patterning. |
epsinR, lqfR |
| 23 |
2009 |
Molecular basis of the potent membrane-remodeling activity of the epsin 1 N-terminal homology domain. |
--- |
| 24 |
2009 |
The single ENTH-domain protein of trypanosomes; endocytic functions and evolutionary relationship with epsin. |
epsinR, T. brucei, UIM |
| 25 |
2009 |
The yeast endocytic protein Epsin 2 functions in a cell-division signaling pathway. |
Ent2 |
| 26 |
2007 |
EpsinR2 interacts with clathrin, adaptor protein-3, AtVTI12, and phosphatidylinositol-3-phosphate. Implications for EpsinR2 function in protein trafficking in plant cells. |
--- |
| 27 |
2006 |
Epsin N-terminal homology domains perform an essential function regulating Cdc42 through binding Cdc42 GTPase-activating proteins. |
--- |
| 28 |
2006 |
Membrane topology of helix 0 of the Epsin N-terminal homology domain. |
EPR |
| 29 |
2005 |
Sequence analysis of Arabidopsis thaliana E/ANTH-domain-containing proteins: membrane tethers of the clathrin-dependent vesicle budding machinery. |
E/ANTH |
| 30 |
2004 |
Accelerated screening of phage-display output with alkaline phosphatase fusions. |
AP, LIC |
| 31 |
2004 |
HIP1 and HIP1r stabilize receptor tyrosine kinases and bind 3-phosphoinositides via epsin N-terminal homology domains. |
HIP1, HIP1R |
| 32 |
2003 |
A role for epsin N-terminal homology/AP180 N-terminal homology (ENTH/ANTH) domains in tubulin binding. |
--- |
| 33 |
2003 |
Contrasting membrane interaction mechanisms of AP180 N-terminal homology (ANTH) and epsin N-terminal homology (ENTH) domains. |
--- |
| 34 |
2003 |
Either part of a Drosophila epsin protein, divided after the ENTH domain, functions in endocytosis of delta in the developing eye. |
Dl, Lqf |
| 35 |
2003 |
Ent3p Is a PtdIns(3,5)P2 effector required for protein sorting to the multivesicular body. |
MVB |
| 36 |
2003 |
ENTH/ANTH proteins and clathrin-mediated membrane budding. |
E/ANTH |
| 37 |
2003 |
Potential role for a novel AP180-related protein during endocytosis in MDCK cells. |
MDCK |
| 38 |
2003 |
Solution structure of the epsin N-terminal homology (ENTH) domain of human epsin. |
--- |
| 39 |
2003 |
Specific interaction between SNAREs and epsin N-terminal homology (ENTH) domains of epsin-related proteins in trans-Golgi network to endosome transport. |
--- |
| 40 |
2002 |
Phosphoinositide-binding domains: Functional units for temporal and spatial regulation of intracellular signalling. |
PH, PX |
| 41 |
2002 |
The ENTH domain. |
--- |
| 42 |
2002 |
Yeast epsin-related proteins required for Golgi-endosome traffic define a gamma-adaptin ear-binding motif. |
CCVs, TGN |
| 43 |
2001 |
Clathrin- and AP-2-binding sites in HIP1 uncover a general assembly role for endocytic accessory proteins. |
HIP1 |
| 44 |
2001 |
Role of the ENTH domain in phosphatidylinositol-4,5-bisphosphate binding and endocytosis. |
--- |
| 45 |
2001 |
The Phox homology (PX) domain, a new player in phosphoinositide signalling. |
PH, PX |
| 46 |
1999 |
Yeast epsins contain an essential N-terminal ENTH domain, bind clathrin and are required for endocytosis. |
--- |
A Search Service for Abbreviation / Long Form
