scholarly article | Q13442814 |
P2093 | author name string | Marino Arroyo | |
Juan M Vanegas | |||
P2860 | cites work | 3D pressure field in lipid membranes and membrane-protein complexes. | Q51788823 |
An improved united atom force field for simulation of mixed lipid bilayers. | Q51798189 | ||
Molecular dissection of the large mechanosensitive ion channel (MscL) of E. coli: mutants with altered channel gating and pressure sensitivity. | Q54567112 | ||
Definition and testing of the GROMOS force-field versions 54A7 and 54B7 | Q56225271 | ||
CHARMM-GUI: a web-based graphical user interface for CHARMM | Q80900573 | ||
Lipid-protein interactions | Q84157392 | ||
The determinants of hydrophobic mismatch response for transmembrane helices | Q85004924 | ||
Importance of Force Decomposition for Local Stress Calculations in Biomembrane Molecular Simulations | Q86720961 | ||
Crystal structure of the human two-pore domain potassium channel K2P1 | Q24303649 | ||
Membrane-protein interactions in mechanosensitive channels | Q24538186 | ||
Revisiting hydrophobic mismatch with free energy simulation studies of transmembrane helix tilt and rotation | Q24623070 | ||
Mechanosensitive channels: what can they do and how do they do it? | Q24633554 | ||
Analytic models for mechanotransduction: gating a mechanosensitive channel | Q24633961 | ||
CHARMM: the biomolecular simulation program | Q24658108 | ||
Hierarchies, multiple energy barriers, and robustness govern the fracture mechanics of alpha-helical and beta-sheet protein domains | Q24678577 | ||
Crystal structure of rhodopsin: A G protein-coupled receptor | Q27625972 | ||
Structure of the Human Dopamine D3 Receptor in Complex with a D2/D3 Selective Antagonist | Q27666030 | ||
Structural Basis for Molecular Recognition at Serotonin Receptors | Q27676926 | ||
UCSF Chimera--a visualization system for exploratory research and analysis | Q27860666 | ||
GROMACS 4: Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation | Q27860944 | ||
Generation and evaluation of a large mutational library from the Escherichia coli mechanosensitive channel of large conductance, MscL: implications for channel gating and evolutionary design | Q28188123 | ||
The gating mechanism of the large mechanosensitive channel MscL | Q28202124 | ||
Structural models of the MscL gating mechanism | Q28207726 | ||
Physical principles underlying the transduction of bilayer deformation forces during mechanosensitive channel gating | Q28217366 | ||
Loss-of-function mutations at the rim of the funnel of mechanosensitive channel MscL | Q28252469 | ||
Structure of the MscL homolog from Mycobacterium tuberculosis: a gated mechanosensitive ion channel | Q28291702 | ||
Single residue substitutions that change the gating properties of a mechanosensitive channel in Escherichia coli | Q28293902 | ||
Structure and mechanism in prokaryotic mechanosensitive channels | Q30311180 | ||
Energetics of hydrogen bonds in peptides. | Q30336189 | ||
Gating of the mechanosensitive channel protein MscL: the interplay of membrane and protein | Q30367265 | ||
g_membed: Efficient insertion of a membrane protein into an equilibrated lipid bilayer with minimal perturbation | Q30387289 | ||
Membrane proteins diffuse as dynamic complexes with lipids. | Q30389145 | ||
The gating mechanism of the bacterial mechanosensitive channel MscL revealed by molecular dynamics simulations: from tension sensing to channel opening | Q30423526 | ||
Water clusters: untangling the mysteries of the liquid, one molecule at a time | Q31964801 | ||
Hydrophobic mismatch of mobile transmembrane helices: Merging theory and experiments | Q33353021 | ||
VORO++: a three-dimensional voronoi cell library in C++. | Q33522732 | ||
Lysophospholipids open the two-pore domain mechano-gated K(+) channels TREK-1 and TRAAK. | Q33896398 | ||
Release of content through mechano-sensitive gates in pressurized liposomes | Q34147450 | ||
An improved open-channel structure of MscL determined from FRET confocal microscopy and simulation | Q34161460 | ||
Gating of MscL Studied by Steered Molecular Dynamics | Q34182988 | ||
Probing the relation between force--lifetime--and chemistry in single molecular bonds | Q34243206 | ||
Force-dependent chemical kinetics of disulfide bond reduction observed with single-molecule techniques | Q34624392 | ||
Curvature and hydrophobic forces drive oligomerization and modulate activity of rhodopsin in membranes. | Q35606672 | ||
Three routes to modulate the pore size of the MscL channel/nanovalve | Q35788552 | ||
Sensing and responding to membrane tension: the bacterial MscL channel as a model system. | Q36105316 | ||
Membrane mechanics as a probe of ion-channel gating mechanisms. | Q36395029 | ||
Three-dimensional stress field around a membrane protein: atomistic and coarse-grained simulation analysis of gramicidin A. | Q36518513 | ||
Chimeras reveal a single lipid-interface residue that controls MscL channel kinetics as well as mechanosensitivity | Q36673509 | ||
On the structure of the N-terminal domain of the MscL channel: helical bundle or membrane interface | Q36838841 | ||
Dynamics of protein-protein interactions at the MscL periplasmic-lipid interface | Q37533546 | ||
Assessment of potential stimuli for mechano-dependent gating of MscL: effects of pressure, tension, and lipid headgroups | Q39362425 | ||
Interactions of phospholipids with the potassium channel KcsA. | Q40215125 | ||
Modulation of rhodopsin function by properties of the membrane bilayer | Q40655644 | ||
Different effects of lipid chain length on the two sides of a membrane and the lipid annulus of MscL. | Q42592729 | ||
Contributions of the different extramembranous domains of the mechanosensitive ion channel MscL to its response to membrane tension. | Q42616686 | ||
Anionic phospholipids affect the rate and extent of flux through the mechanosensitive channel of large conductance MscL. | Q43202528 | ||
Mechanosensitive ion channels of E. coli activated by amphipaths. | Q45044862 | ||
Hydration properties of mechanosensitive channel pores define the energetics of gating | Q47319724 | ||
Opposite modulation of NMDA receptors by lysophospholipids and arachidonic acid: common features with mechanosensitivity | Q48355564 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e113947 | |
P577 | publication date | 2014-01-01 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Force transduction and lipid binding in MscL: a continuum-molecular approach | |
P478 | volume | 9 |
Q90640032 | Allosteric activation of an ion channel triggered by modification of mechanosensitive nano-pockets |
Q53122328 | Channel disassembled: Pick, tweak, and soak parts to soften. |
Q64245550 | Computational Modeling of Realistic Cell Membranes |
Q38725688 | Continuum descriptions of membranes and their interaction with proteins: Towards chemically accurate models. |
Q38928950 | From membrane tension to channel gating: A principal energy transfer mechanism for mechanosensitive channels |
Q51420842 | Gating mechanism of mechanosensitive channel of large conductance: a coupled continuum mechanical-continuum solvation approach. |
Q35961203 | Gating of a mechanosensitive channel due to cellular flows |
Q37690319 | High-Throughput Simulations Reveal Membrane-Mediated Effects of Alcohols on MscL Gating. |
Q26798390 | Molecular Simulations of Gram-Negative Bacterial Membranes: A Vignette of Some Recent Successes |
Q63547192 | Multiscale Simulations of Biological Membranes: The Challenge To Understand Biological Phenomena in a Living Substance |
Q53717221 | Nonuniqueness of local stress of three-body potentials in molecular simulations. |
Q41577849 | Pulling MscL open via N-terminal and TM1 helices: A computational study towards engineering an MscL nanovalve |
Q59801457 | Structure of the hyperosmolality-gated calcium-permeable channel OSCA1.2 |
Q35950796 | The Combined Effect of Hydrophobic Mismatch and Bilayer Local Bending on the Regulation of Mechanosensitive Ion Channels |
Q92732450 | The plasma membrane as a mechanochemical transducer |
Q27342278 | The role of MscL amphipathic N terminus indicates a blueprint for bilayer-mediated gating of mechanosensitive channels |
Search more.