| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2001PNAS...9813655R |
| P356 | DOI | 10.1073/PNAS.191512398 |
| P932 | PMC publication ID | 61096 |
| P698 | PubMed publication ID | 11707568 |
| P5875 | ResearchGate publication ID | 11646641 |
| P2093 | author name string | A L Wells | |
| H L Sweeney | |||
| J A Spudich | |||
| R S Rock | |||
| T J Purcell | |||
| S E Rice | |||
| P2860 | cites work | Myosin-V is a processive actin-based motor | Q22003739 |
| The localization of myosin VI at the golgi complex and leading edge of fibroblasts and its phosphorylation and recruitment into membrane ruffles of A431 cells after growth factor stimulation | Q22008538 | ||
| Myosin VI is an actin-based motor that moves backwards | Q22010643 | ||
| Myosin VI isoform localized to clathrin-coated vesicles with a role in clathrin-mediated endocytosis | Q24291429 | ||
| Molecular motors: structural adaptations to cellular functions | Q28251722 | ||
| The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells | Q28513409 | ||
| Spare the rod, spoil the regulation: necessity for a myosin rod. | Q30454447 | ||
| Use of optical traps in single-molecule study of nonprocessive biological motors | Q32015212 | ||
| Getting to the point with myosin VI. | Q33912767 | ||
| Bead movement by single kinesin molecules studied with optical tweezers | Q33957127 | ||
| A new direction for myosin | Q33960462 | ||
| Myosin learns to walk | Q34330237 | ||
| Single myosin molecule mechanics: piconewton forces and nanometre steps | Q34338098 | ||
| Myosin-V stepping kinetics: a molecular model for processivity | Q35207228 | ||
| A large step for myosin | Q36110560 | ||
| Processivity of the motor protein kinesin requires two heads | Q36255126 | ||
| An unconventional myosin heavy chain gene from Drosophila melanogaster | Q36532145 | ||
| The core of the motor domain determines the direction of myosin movement | Q40784283 | ||
| Reversible unfolding of single RNA molecules by mechanical force | Q43590684 | ||
| Kinetic mechanism and regulation of myosin VI. | Q43651972 | ||
| Movement of microtubules by single kinesin molecules | Q46085669 | ||
| In vitro assays of processive myosin motors | Q46420532 | ||
| Transport of cytoplasmic particles catalysed by an unconventional myosin in living Drosophila embryos | Q47070706 | ||
| Two-headed binding of a processive myosin to F-actin. | Q52863984 | ||
| Micromechanics and ultrastructure of actin filament networks crosslinked by human fascin: a comparison with alpha-actinin. | Q55034914 | ||
| A single myosin head moves along an actin filament with regular steps of 5.3 nanometres | Q59063267 | ||
| Inner-arm dynein c of Chlamydomonas flagella is a single-headed processive motor | Q59085733 | ||
| Single molecule imaging of fluorophores and enzymatic reactions achieved by objective-type total internal reflection fluorescence microscopy | Q73442854 | ||
| Direct observation of processive movement by individual myosin V molecules | Q73838381 | ||
| Kinetic tuning of myosin via a flexible loop adjacent to the nucleotide binding pocket | Q74299321 | ||
| P433 | issue | 24 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 13655-9 | |
| P577 | publication date | 2001-11-20 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Myosin VI is a processive motor with a large step size | |
| P478 | volume | 98 |
| Q44428760 | A Kinetic Mechanism for the Fast Movement of Chara Myosin |
| Q35556327 | A conformational transition in the myosin VI converter contributes to the variable step size |
| Q43847147 | A crossbridge too far. |
| Q33223012 | A force-dependent state controls the coordination of processive myosin V |
| Q34687221 | A hearing loss-associated myo1c mutation (R156W) decreases the myosin duty ratio and force sensitivity |
| Q30841286 | A microRNA-initiated DNAzyme motor operating in living cells. |
| Q40573331 | A monomeric myosin VI with a large working stroke |
| Q30494542 | A mutant heterodimeric myosin with one inactive head generates maximal displacement |
| Q30482736 | A myosin motor that selects bundled actin for motility |
| Q30500251 | A nonsense mutation in the gene encoding a zebrafish myosin VI isoform causes defects in hair-cell mechanotransduction |
| Q34221079 | A novel myosin heavy chain gene in human chromosome 19q13.3. |
| Q36448190 | A one-headed class V myosin molecule develops multiple large (approximately 32-nm) steps successively |
| Q30492389 | A peptide tag system for facile purification and single-molecule immobilization |
| Q30832160 | A programmable DNA origami nanospring that reveals force-induced adjacent binding of myosin VI heads |
| Q34180584 | A simple kinetic model describes the processivity of myosin-v |
| Q24317526 | A unique mechanism for the processive movement of single-headed myosin-IX |
| Q37802543 | Actin dynamics in plant cells: a team effort from multiple proteins orchestrates this very fast-paced game |
| Q44654217 | An electromechanical model of myosin molecular motors |
| Q85726930 | Biological machines: Molecular motor teamwork |
| Q44394472 | Calcium functionally uncouples the heads of myosin VI. |
| Q42128939 | Cargo-binding makes a wild-type single-headed myosin-VI move processively |
| Q52684724 | Cell adhesion molecule Echinoid associates with unconventional myosin VI/Jaguar motor to regulate cell morphology during dorsal closure in Drosophila. |
| Q27339563 | Cellobiohydrolase 1 from Trichoderma reesei degrades cellulose in single cellobiose steps |
| Q28566322 | Characterization of the motor activity of mammalian myosin VIIA |
| Q90113102 | Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss |
| Q30477041 | Coiled-coil nanomechanics and uncoiling and unfolding of the superhelix and alpha-helices of myosin |
| Q37035184 | Coiled-coil-mediated dimerization is not required for myosin VI to stabilize actin during spermatid individualization in Drosophila melanogaster |
| Q26786679 | Collective dynamics of processive cytoskeletal motors |
| Q33842753 | Contribution of the myosin VI tail domain to processive stepping and intramolecular tension sensing |
| Q44790011 | Converting a motor to an anchor |
| Q40975610 | Coordinated force generation of skeletal myosins in myofilaments through motor coupling |
| Q39747692 | Coordination of molecular motors: from in vitro assays to intracellular dynamics |
| Q37387839 | Coupled myosin VI motors facilitate unidirectional movement on an F-actin network |
| Q50354277 | Creation of functional micro/nano systems through top-down and bottom-up approaches |
| Q34185646 | Cross-bridge number, position, and angle in target zones of cryofixed isometrically active insect flight muscle |
| Q47251095 | Crosslinkers both drive and brake cytoskeletal remodeling and furrowing in cytokinesis |
| Q37698266 | Cytoskeletal mechanisms for breaking cellular symmetry |
| Q34494423 | Detailed tuning of structure and intramolecular communication are dispensable for processive motion of myosin VI. |
| Q24299160 | Determination of human myosin III as a motor protein having a protein kinase activity |
| Q39752625 | Dictyostelium myosin-5b is a conditional processive motor. |
| Q28573622 | Different degrees of lever arm rotation control myosin step size |
| Q30481554 | Different subcellular localizations and functions of Arabidopsis myosin VIII |
| Q36646228 | Differential gene expression profiles of gastric cancer cells established from primary tumour and malignant ascites |
| Q35009659 | Do longer oars row farther? |
| Q33203151 | Does the myosin V neck region act as a lever? |
| Q46895770 | Drosophila myosin VIIA is a high duty ratio motor with a unique kinetic mechanism |
| Q36869856 | Dynamic charge interactions create surprising rigidity in the ER/K alpha-helical protein motif |
| Q46645141 | Dynamic compartmentalization of protein tyrosine phosphatase receptor Q at the proximal end of stereocilia: implication of myosin VI-based transport |
| Q36385806 | Dynamic exchange of myosin VI on endocytic structures |
| Q28570749 | Dynamic imaging of cannabinoid receptor 1 vesicular trafficking in cultured astrocytes |
| Q27320510 | Electron Tomography of Cryofixed, Isometrically Contracting Insect Flight Muscle Reveals Novel Actin-Myosin Interactions |
| Q59230010 | Electrospray ionization mass spectrometry studies of noncovalent myosin VI complexes reveal a new specific calmodulin binding site |
| Q35990181 | Engineered myosin VI motors reveal minimal structural determinants of directionality and processivity. |
| Q31155712 | Engineering Dictyostelium discoideum myosin II for the introduction of site-specific fluorescence probes. |
| Q42005922 | Engineering myosins for long-range transport on actin filaments |
| Q36653751 | Exploring mechanochemical processes in the cell with optical tweezers |
| Q35070360 | Extension of a three-helix bundle domain of myosin VI and key role of calmodulins |
| Q21562391 | Fast benchtop fabrication of laminar flow chambers for advanced microscopy techniques |
| Q24677668 | Filopodia act as phagocytic tentacles and pull with discrete steps and a load-dependent velocity. |
| Q35128923 | Flexible light-chain and helical structure of F-actin explain the movement and step size of myosin-VI. |
| Q26827691 | Force generation by kinesin and myosin cytoskeletal motor proteins |
| Q34190781 | Force-dependent stepping kinetics of myosin-V. |
| Q33777174 | Force-induced bidirectional stepping of cytoplasmic dynein |
| Q42580509 | Formation of Salt Bridges Mediates Internal Dimerization of Myosin VI Medial Tail Domain |
| Q34699313 | Free energy of conformational transition paths in biomolecules: the string method and its application to myosin VI. |
| Q30497272 | Functional adaptation of the switch-2 nucleotide sensor enables rapid processive translocation by myosin-5. |
| Q33667075 | Functional diversity among a family of human skeletal muscle myosin motors |
| Q33264887 | Functional studies of individual myosin molecules |
| Q30495863 | Head of myosin IX binds calmodulin and moves processively toward the plus-end of actin filaments |
| Q30501806 | High-resolution, single-molecule measurements of biomolecular motion |
| Q34794210 | Higher plant myosin XI moves processively on actin with 35 nm steps at high velocity |
| Q24658390 | How are the cellular functions of myosin VI regulated within the cell? |
| Q35837057 | How myosin VI coordinates its heads during processive movement |
| Q38567972 | How myosin motors power cellular functions: an exciting journey from structure to function: based on a lecture delivered at the 34th FEBS Congress in Prague, Czech Republic, July 2009 |
| Q43177905 | How single molecule detection measures the dynamic actions of life |
| Q44881249 | Human deafness mutation of myosin VI (C442Y) accelerates the ADP dissociation rate |
| Q34388623 | Improved hidden Markov models for molecular motors, part 1: basic theory |
| Q79446000 | Insight into the mechanism of fast movement of myosin from Chara corallina |
| Q30390486 | Insights into human beta-cardiac myosin function from single molecule and single cell studies |
| Q34350508 | Interhead distance measurements in myosin VI via SHRImP support a simplified hand-over-hand model |
| Q37204300 | Interrogating biology with force: single molecule high-resolution measurements with optical tweezers |
| Q41774300 | Intramolecular strain coordinates kinesin stepping behavior along microtubules |
| Q38963256 | Investigations of human myosin VI targeting using optogenetically controlled cargo loading |
| Q27325433 | Ionic imbalance, in addition to molecular crowding, abates cytoskeletal dynamics and vesicle motility during hypertonic stress. |
| Q44871950 | Kinematics of the lever arm swing in myosin VI. |
| Q42085347 | Kinesins with extended neck linkers: a chemomechanical model for variable-length stepping |
| Q35998868 | Lever arms and necks: a common mechanistic theme across the myosin superfamily |
| Q28743071 | Lever-arm mechanics of processive myosins |
| Q36693901 | Load-dependent ADP binding to myosins V and VI: implications for subunit coordination and function |
| Q36740061 | Long single alpha-helical tail domains bridge the gap between structure and function of myosin VI. |
| Q27311401 | Mechanical coordination in motor ensembles revealed using engineered artificial myosin filaments. |
| Q37408634 | Mechanical design of translocating motor proteins |
| Q38803208 | Mechanics and Activation of Unconventional Myosins |
| Q37283513 | Mechanism of muscle contraction based on stochastic properties of single actomyosin motors observed in vitro |
| Q40536919 | Mechanism of nucleotide binding to actomyosin VI: evidence for allosteric head-head communication |
| Q36318743 | Membrane-induced lever arm expansion allows myosin VI to walk with large and variable step sizes |
| Q46505682 | Methods in statistical kinetics |
| Q35109708 | Molecular motors |
| Q34228870 | Molecular motors: forty years of interdisciplinary research |
| Q88537108 | Motor Proteins |
| Q28585827 | Mouse myosin-19 is a plus-end-directed, high-duty ratio molecular motor |
| Q44748338 | Muscle activation described with a differential equation model for large ensembles of locally coupled molecular motors |
| Q42410029 | Muscle contraction mechanism based on single molecule measurements |
| Q35580794 | Myosin V motor proteins: marching stepwise towards a mechanism |
| Q28588566 | Myosin V: regulation by calcium, calmodulin, and the tail domain |
| Q27656923 | Myosin VI Dimerization Triggers an Unfolding of a Three-Helix Bundle in Order to Extend Its Reach |
| Q46044406 | Myosin VI altered at threonine 406 stabilizes actin filaments in vivo |
| Q33957293 | Myosin VI contributes to synaptic transmission and development at the Drosophila neuromuscular junction. |
| Q35212474 | Myosin VI deafness mutation prevents the initiation of processive runs on actin |
| Q36542334 | Myosin VI has a one track mind versus myosin Va when moving on actin bundles or at an intersection |
| Q38962635 | Myosin VI must dimerize and deploy its unusual lever arm in order to perform its cellular roles. |
| Q34731167 | Myosin VI reduces proliferation, but not differentiation, in pluripotent P19 cells |
| Q34662188 | Myosin VI stabilizes an actin network during Drosophila spermatid individualization |
| Q30491564 | Myosin VI undergoes a 180 degrees power stroke implying an uncoupling of the front lever arm. |
| Q42149706 | Myosin VI walks "wiggly" on actin with large and variable tilting |
| Q45001874 | Myosin VI walks hand-over-hand along actin |
| Q33809113 | Myosin VI: an innovative motor that challenged the swinging lever arm hypothesis |
| Q30503692 | Myosin Va and myosin VI coordinate their steps while engaged in an in vitro tug of war during cargo transport |
| Q46551350 | Myosin X is a high duty ratio motor |
| Q30574594 | Myosin lever arm directs collective motion on cellular actin network |
| Q33607079 | Myosin-10 produces its power-stroke in two phases and moves processively along a single actin filament under low load |
| Q87929283 | Myosin-Driven Intracellular Transport |
| Q27004163 | Myosins in cell junctions |
| Q36197820 | Myosins: tails (and heads) of functional diversity |
| Q34187072 | Nanometer localization of single green fluorescent proteins: evidence that myosin V walks hand-over-hand via telemark configuration |
| Q55036346 | Native Myosin-IXb is a plus-, not a minus-end-directed motor. |
| Q60307553 | Non-Syndromic Hearing Loss and High-Throughput Strategies to Decipher Its Genetic Heterogeneity |
| Q24301373 | Nuclear myosin VI enhances RNA polymerase II-dependent transcription |
| Q24669585 | Optical trapping |
| Q30388659 | Optical traps to study properties of molecular motors |
| Q24300284 | Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis |
| Q30513401 | Plus-end directed myosins accelerate actin filament sliding by single-headed myosin VI. |
| Q27334526 | Precise positioning of myosin VI on endocytic vesicles in vivo |
| Q27671822 | Processive Steps in the Reverse Direction Require Uncoupling of the Lead Head Lever Arm of Myosin VI |
| Q38216570 | Processive cytoskeletal motors studied with single-molecule fluorescence techniques. |
| Q92153545 | Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting |
| Q36856422 | Regular gaits and optimal velocities for motor proteins |
| 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 |
| Q35433502 | Robust Mechanosensing and Tension Generation by Myosin VI |
| Q27666772 | Role of Insert-1 of Myosin VI in Modulating Nucleotide Affinity |
| Q34392475 | Role of the lever arm in the processive stepping of myosin V. |
| Q63194496 | Shifting gears with light |
| Q33323668 | Single molecule measurements and molecular motors |
| Q83500618 | Single-Virus Tracking: From Imaging Methodologies to Virological Applications |
| Q30391342 | Single-molecule dual-beam optical trap analysis of protein structure and function |
| Q35760214 | Single-molecule fluorescence spectroscopy and microscopy of biomolecular motors. |
| Q36897487 | Single-molecule fluorescence to study molecular motors. |
| Q30494681 | Single-molecule stepping and structural dynamics of myosin X. |
| Q41775117 | Statistical kinetics of macromolecular dynamics |
| Q46446808 | Step-size analyses of the mitochondrial Hsp70 import motor reveal the Brownian ratchet in operation |
| Q30479459 | Stepwise movements in vesicle transport of HER2 by motor proteins in living cells |
| Q44624681 | Stochastic processes in nano-biomachines revealed by single molecule detection |
| Q43863354 | Stretching the lever-arm theory. |
| Q37779877 | Stretchy proteins on stretchy substrates: the important elements of integrin-mediated rigidity sensing |
| Q38722191 | Structural Basis of Cargo Recognition by Unconventional Myosins in Cellular Trafficking |
| Q34421180 | Structural attributes for the recognition of weak and anomalous regions in coiled-coils of myosins and other motor proteins |
| Q33943892 | Structure of the light chain-binding domain of myosin V |
| Q30496161 | Structured post-IQ domain governs selectivity of myosin X for fascin-actin bundles |
| Q85045885 | Switch between Large Hand-Over-Hand and Small Inchworm-like Steps in Myosin VI |
| Q35651183 | Systematic control of protein interaction using a modular ER/K α-helix linker |
| Q36883114 | Temperature dependent measurements reveal similarities between muscle and non-muscle myosin motility |
| Q34134758 | The Stepping Pattern of Myosin X Is Adapted for Processive Motility on Bundled Actin |
| Q38155160 | The cortical acto-Myosin network: from diffusion barrier to functional gateway in the transport of neurosecretory vesicles to the plasma membrane |
| Q35580325 | The kinetic properties of smooth muscle: how a little extra weight makes myosin faster |
| Q44790017 | The mechanism of myosin VI translocation and its load-induced anchoring |
| Q41825148 | The path to visualization of walking myosin V by high-speed atomic force microscopy |
| Q30478493 | The power stroke of myosin VI and the basis of reverse directionality |
| Q52857621 | The predicted coiled-coil domain of myosin 10 forms a novel elongated domain that lengthens the head. |
| Q34324028 | The sliding filament model: 1972-2004. |
| Q30490997 | The structure of the myosin VI motor reveals the mechanism of directionality reversal |
| Q48442387 | The tail domain of myosin Va modulates actin binding to one head |
| Q35575273 | The unique insert at the end of the myosin VI motor is the sole determinant of directionality |
| Q37415026 | The unique insert in myosin VI is a structural calcium-calmodulin binding site. |
| Q60361517 | Tracking enzymatic steps of DNA topoisomerases using single-molecule micromanipulation |
| Q35227173 | Tuning myosin-driven sorting on cellular actin networks |
| Q30579400 | Uncoated endocytic vesicles require the unconventional myosin, Myo6, for rapid transport through actin barriers |
| Q30476442 | Unconstrained steps of myosin VI appear longest among known molecular motors |
| Q92156441 | Unconventional Myosins: How Regulation Meets Function |
| Q30488428 | Unconventional myosin traffic in cells reveals a selective actin cytoskeleton |
| Q34074389 | Unconventional processive mechanics of non-muscle myosin IIB. |
| 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 |
| Q33223992 | Vertebrate myosin VIIb is a high duty ratio motor adapted for generating and maintaining tension |
| Q37380209 | Walking the walk: how kinesin and dynein coordinate their steps |
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