scholarly article | Q13442814 |
P2093 | author name string | Harry W Schroeder | |
Yale E Goldman | |||
Kazuaki Homma | |||
Mitsuo Ikebe | |||
John F Beausang | |||
Yujie Sun | |||
P2860 | cites work | Myosin-V is a processive actin-based motor | Q22003739 |
Myosin VI is an actin-based motor that moves backwards | Q22010643 | ||
Three myosin V structures delineate essential features of chemo-mechanical transduction | Q24310086 | ||
Myosin VI is a processive motor with a large step size | Q24555089 | ||
Three conformational states of scallop myosin S1 | Q27627289 | ||
The crystal structure of uncomplexed actin in the ADP state | Q27633714 | ||
X-ray structure of the magnesium(II).ADP.vanadate complex of the Dictyostelium discoideum myosin motor domain to 1.9 A resolution | Q27732650 | ||
Crystal structure of a vertebrate smooth muscle myosin motor domain and its complex with the essential light chain: visualization of the pre-power stroke state | Q27765344 | ||
Myosin VI: two distinct roles in endocytosis | Q28191412 | ||
The myosin power stroke | Q28216645 | ||
Molecular motors: structural adaptations to cellular functions | Q28251722 | ||
Structure of the actin-myosin complex and its implications for muscle contraction | Q28259888 | ||
Myosin V walks hand-over-hand: single fluorophore imaging with 1.5-nm localization | Q29615477 | ||
A homobifunctional rhodamine for labeling proteins with defined orientations of a fluorophore | Q30430189 | ||
Unconstrained steps of myosin VI appear longest among known molecular motors | Q30476442 | ||
Measurement of single macromolecule orientation by total internal reflection fluorescence polarization microscopy | Q30476746 | ||
Adaptability of myosin V studied by simultaneous detection of position and orientation | Q30477232 | ||
The power stroke of myosin VI and the basis of reverse directionality | Q30478493 | ||
Twirling of actin by myosins II and V observed via polarized TIRF in a modified gliding assay. | Q30484986 | ||
The structure of the myosin VI motor reveals the mechanism of directionality reversal | Q30490997 | ||
Assembly dynamics of microtubules at molecular resolution | Q30818762 | ||
Myosin VI: roles for a minus end-directed actin motor in cells | Q34038023 | ||
Protein structural dynamics by single-molecule fluorescence polarization | Q34099035 | ||
Interhead distance measurements in myosin VI via SHRImP support a simplified hand-over-hand model | Q34350508 | ||
Myosin VI: cellular functions and motor properties | Q34357378 | ||
Role of the lever arm in the processive stepping of myosin V. | Q34392475 | ||
Flexible light-chain and helical structure of F-actin explain the movement and step size of myosin-VI. | Q35128923 | ||
The unique insert at the end of the myosin VI motor is the sole determinant of directionality | Q35575273 | ||
Myosin VI: a structural role in actin organization important for protein and organelle localization and trafficking | Q35804828 | ||
Rotational motions of macro-molecules by single-molecule fluorescence microscopy | Q36200123 | ||
Porcine myosin-VI: characterization of a new mammalian unconventional myosin | Q36234743 | ||
What can myosin VI do in cells? | Q36686696 | ||
The unique insert in myosin VI is a structural calcium-calmodulin binding site. | Q37415026 | ||
Mechanism of nucleotide binding to actomyosin VI: evidence for allosteric head-head communication | Q40536919 | ||
A monomeric myosin VI with a large working stroke | Q40573331 | ||
Class VI myosin moves processively along actin filaments backward with large steps | Q40758767 | ||
Orientation of the myosin light chain region by single molecule total internal reflection fluorescence polarization microscopy | Q42124824 | ||
Cargo-binding makes a wild-type single-headed myosin-VI move processively | Q42128939 | ||
Bacterial expression and characterization of proteins derived from the chicken calmodulin cDNA and a calmodulin processed gene | Q43473529 | ||
Kinetic mechanism and regulation of myosin VI. | Q43651972 | ||
Three-dimensional structural dynamics of myosin V by single-molecule fluorescence polarization | Q44379280 | ||
Calcium functionally uncouples the heads of myosin VI. | Q44394472 | ||
The mechanism of myosin VI translocation and its load-induced anchoring | Q44790017 | ||
Myosin VI walks hand-over-hand along actin | Q45001874 | ||
A flexible domain is essential for the large step size and processivity of myosin VI. | Q47391271 | ||
Fluorescence imaging with one nanometer accuracy: application to molecular motors. | Q50761313 | ||
Two-headed binding of a processive myosin to F-actin. | Q52863984 | ||
Purification of muscle actin | Q70410249 | ||
Brain myosin-V is a two-headed unconventional myosin with motor activity | Q70488210 | ||
Myosin VI steps via a hand-over-hand mechanism with its lever arm undergoing fluctuations when attached to actin | Q80341101 | ||
Full-length myosin VI dimerizes and moves processively along actin filaments upon monomer clustering | Q82457987 | ||
P433 | issue | 6 | |
P304 | page(s) | 954-964 | |
P577 | publication date | 2007-12-01 | |
P1433 | published in | Molecular Cell | Q3319468 |
P1476 | title | Myosin VI walks "wiggly" on actin with large and variable tilting | |
P478 | volume | 28 |
Q35556327 | A conformational transition in the myosin VI converter contributes to the variable step size |
Q99579416 | Advances of super-resolution fluorescence polarization microscopy and its applications in life sciences |
Q47833103 | Brownian search-and-catch mechanism for myosin-VI steps |
Q30499937 | Cargo binding activates myosin VIIA motor function in cells |
Q33842753 | Contribution of the myosin VI tail domain to processive stepping and intramolecular tension sensing |
Q48047394 | Cryo-EM structures reveal specialization at the myosin VI-actin interface and a mechanism of force sensitivity |
Q34494423 | Detailed tuning of structure and intramolecular communication are dispensable for processive motion of myosin VI. |
Q26770569 | Eccentric contraction: unraveling mechanisms of force enhancement and energy conservation |
Q35990181 | Engineered myosin VI motors reveal minimal structural determinants of directionality and processivity. |
Q34626433 | Enhancement of single-molecule fluorescence signals by colloidal silver nanoparticles in studies of protein translation |
Q41976915 | Filopodia formation and endosome clustering induced by mutant plus-end-directed myosin VI. |
Q37802709 | Fluorescence anisotropy and resonance energy transfer: powerful tools for measuring real time protein dynamics in a physiological environment |
Q44871950 | Kinematics of the lever arm swing in myosin VI. |
Q28743071 | Lever-arm mechanics of processive myosins |
Q36740061 | Long single alpha-helical tail domains bridge the gap between structure and function of myosin VI. |
Q36318743 | Membrane-induced lever arm expansion allows myosin VI to walk with large and variable step sizes |
Q39310881 | Mesoscopic analysis of motion and conformation of cross-bridges |
Q36542334 | Myosin VI has a one track mind versus myosin Va when moving on actin bundles or at an intersection |
Q42787195 | Myosin VI lever arm rotation: fixed or variable? |
Q30491564 | Myosin VI undergoes a 180 degrees power stroke implying an uncoupling of the front lever arm. |
Q33809113 | Myosin VI: an innovative motor that challenged the swinging lever arm hypothesis |
Q81358717 | Nanotechnology in biology: big collaborations for a small world |
Q34307078 | Nucleotide-Dependent Shape Changes in the Reverse Direction Motor, Myosin VI |
Q41833832 | Parallax: high accuracy three-dimensional single molecule tracking using split images |
Q27671822 | Processive Steps in the Reverse Direction Require Uncoupling of the Lead Head Lever Arm of Myosin VI |
Q93496498 | Reply to Sun et al.: Myosin VI movement: Wiggly or straight? |
Q33780128 | Reverse conformational changes of the light chain-binding domain of myosin V and VI processive motor heads during and after hydrolysis of ATP by small-angle X-ray solution scattering |
Q30398533 | Single molecule optical measurements of orientation and rotations of biological macromolecules |
Q91765323 | Single-molecule in vitro reconstitution assay for kinesin-1-driven membrane dynamics |
Q30494681 | Single-molecule stepping and structural dynamics of myosin X. |
Q90754188 | Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy |
Q85045885 | Switch between Large Hand-Over-Hand and Small Inchworm-like Steps in Myosin VI |
Q35719960 | The azimuthal path of myosin V and its dependence on lever-arm length |
Q41825148 | The path to visualization of walking myosin V by high-speed atomic force microscopy |
Q34635825 | Tilting and wobble of myosin V by high-speed single-molecule polarized fluorescence microscopy |
Q42263121 | Twirling motion of actin filaments in gliding assays with nonprocessive Myosin motors |
Q30484986 | Twirling of actin by myosins II and V observed via polarized TIRF in a modified gliding assay. |
Q34262470 | Use of fluorescent techniques to study the in vitro movement of myosins |
Q36803485 | Using electrical and optical tweezers to facilitate studies of molecular motors |
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