review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | K M Trybus | |
P2860 | cites work | Myosin-V is a processive actin-based motor | Q22003739 |
Bmf: a proapoptotic BH3-only protein regulated by interaction with the myosin V actin motor complex, activated by anoikis | Q24291662 | ||
A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport | Q24295585 | ||
Myosin Vb is required for trafficking of the cystic fibrosis transmembrane conductance regulator in Rab11a-specific apical recycling endosomes in polarized human airway epithelial cells | Q24304047 | ||
In vitro reconstitution of a transport complex containing Rab27a, melanophilin and myosin Va | Q24307247 | ||
Three myosin V structures delineate essential features of chemo-mechanical transduction | Q24310086 | ||
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) | Q24313435 | ||
Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice | Q24555217 | ||
Intracellular actin-based transport: how far you go depends on how often you switch | Q24561914 | ||
Myosin vb is associated with plasma membrane recycling systems | Q24633656 | ||
Two distinct myosin light chain structures are induced by specific variations within the bound IQ motifs-functional implications | Q27640371 | ||
A structural state of the myosin V motor without bound nucleotide | Q27642224 | ||
Crystal structure of apo-calmodulin bound to the first two IQ motifs of myosin V reveals essential recognition features | Q27643231 | ||
Calcium-induced conformational transition revealed by the solution structure of apo calmodulin | Q27729469 | ||
Solution structure of calcium-free calmodulin | Q27729471 | ||
Regulated degradation of a class V myosin receptor directs movement of the yeast vacuole | Q27936360 | ||
Interaction of the postsynaptic density-95/guanylate kinase domain-associated protein complex with a light chain of myosin-V and dynein | Q28145916 | ||
Slac2-a/melanophilin, the missing link between Rab27 and myosin Va: implications of a tripartite protein complex for melanosome transport | Q28202672 | ||
Effect of ADP and ionic strength on the kinetic and motile properties of recombinant mouse myosin V | Q28369753 | ||
Identification of an organelle receptor for myosin-Va | Q28504759 | ||
Melanophilin and myosin Va track the microtubule plus end on EB1 | Q28507496 | ||
The structural basis of myosin V processive movement as revealed by electron cryomicroscopy | Q28509931 | ||
Myosin V exhibits a high duty cycle and large unitary displacement | Q28512626 | ||
Myosin-Va regulates exocytosis through the submicromolar Ca2+-dependent binding of syntaxin-1A. | Q28565862 | ||
Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations | Q28587966 | ||
Myosin V: regulation by calcium, calmodulin, and the tail domain | Q28588566 | ||
Novel myosin heavy chain encoded by murine dilute coat colour locus | Q28590446 | ||
Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner | Q28592127 | ||
A mutation in Rab27a causes the vesicle transport defects observed in ashen mice | Q28594384 | ||
Identification of a minimal myosin Va binding site within an intrinsically unstructured domain of melanophilin | Q28910206 | ||
Myosin V walks hand-over-hand: single fluorophore imaging with 1.5-nm localization | Q29615477 | ||
Tracking melanosomes inside a cell to study molecular motors and their interaction | Q30479179 | ||
Myosin Va maneuvers through actin intersections and diffuses along microtubules | Q30479183 | ||
Myosin Vb interacts with Rab8a on a tubular network containing EHD1 and EHD3. | Q30479902 | ||
Rab27a enables myosin Va-dependent melanosome capture by recruiting the myosin to the organelle. | Q32066956 | ||
Differential labeling of myosin V heads with quantum dots allows direct visualization of hand-over-hand processivity | Q33212840 | ||
A force-dependent state controls the coordination of processive myosin V | Q33223012 | ||
Myosin V walks by lever action and Brownian motion | Q33285750 | ||
Myosin V movement: lessons from molecular dynamics studies of IQ peptides in the lever arm. | Q33306092 | ||
Class V myosins. | Q33866590 | ||
Structure of the light chain-binding domain of myosin V | Q33943892 | ||
Human myosin-Vc is a novel class V myosin expressed in epithelial cells | Q34116426 | ||
Rab11 family interacting protein 2 associates with Myosin Vb and regulates plasma membrane recycling | Q34155849 | ||
Melanosomes transported by myosin-V in Xenopus melanophores perform slow 35 nm steps | Q34352932 | ||
Role of the lever arm in the processive stepping of myosin V. | Q34392475 | ||
Structural basis for myosin V discrimination between distinct cargoes. | Q34410967 | ||
The cargo-binding domain regulates structure and activity of myosin 5 | Q35752269 | ||
RNA localization in yeast: moving towards a mechanism | Q35985189 | ||
A bent monomeric conformation of myosin from smooth muscle | Q36315546 | ||
Myosin V attachment to cargo requires the tight association of two functional subdomains. | Q36321353 | ||
Interactions and regulation of molecular motors in Xenopus melanophores | Q36324176 | ||
Secretory vesicle transport velocity in living cells depends on the myosin-V lever arm length | Q36324635 | ||
Two distinct regions in a yeast myosin-V tail domain are required for the movement of different cargoes | Q36328460 | ||
Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo | Q36328552 | ||
Walking with myosin V. | Q36354001 | ||
The kinetic mechanism of myosin V. | Q36700327 | ||
Regulation and recycling of myosin V. | Q36701558 | ||
Myosin V processivity: multiple kinetic pathways for head-to-head coordination | Q37681953 | ||
Alternatively spliced exon B of myosin Va is essential for binding the tail-associated light chain shared by dynein | Q40222323 | ||
The globular tail domain of myosin Va functions as an inhibitor of the myosin Va motor | Q40270903 | ||
Ca2+-induced activation of ATPase activity of myosin Va is accompanied with a large conformational change | Q40587730 | ||
Engineering the processive run length of Myosin V. | Q42032567 | ||
Cell cycle regulation of myosin-V by calcium/calmodulin-dependent protein kinase II. | Q43710205 | ||
The gated gait of the processive molecular motor, myosin V. | Q43820585 | ||
Kinetic characterization of the weak binding states of myosin V. | Q44039546 | ||
Functional role of loop 2 in myosin V. | Q44781712 | ||
Slac2-a/melanophilin contains multiple PEST-like sequences that are highly sensitive to proteolysis | Q44897879 | ||
Kinetics of ADP dissociation from the trail and lead heads of actomyosin V following the power stroke | Q44933308 | ||
A model of myosin V processivity | Q44978572 | ||
Mechanochemical coupling of two substeps in a single myosin V motor | Q45001867 | ||
Molecular motors: a tale of two filaments | Q46053061 | ||
Load-dependent kinetics of myosin-V can explain its high processivity | Q46650611 | ||
Dynamics of the unbound head during myosin V processive translocation | Q46692109 | ||
Myosin-V makes two brownian 90 degrees rotations per 36-nm step | Q46985077 | ||
Step-size is determined by neck length in myosin V. | Q47358625 | ||
Regulated conformation of myosin V. | Q47368896 | ||
Identification of the single specific IQ motif of myosin V from which calmodulin dissociates in the presence of Ca2+. | Q48419013 | ||
Kinesin undergoes a 9 S to 6 S conformational transition | Q48491444 | ||
Enzymatic characterization and functional domain mapping of brain myosin-V. | Q48962038 | ||
The light chain composition of chicken brain myosin-Va: calmodulin, myosin-II essential light chains, and 8-kDa dynein light chain/PIN. | Q52144362 | ||
Two-headed binding of a processive myosin to F-actin. | Q52863984 | ||
Structural basis for the interaction of the myosin light chain Mlc1p with the myosin V Myo2p IQ motifs. | Q53590717 | ||
Brain myosin-V is a two-headed unconventional myosin with motor activity | Q70488210 | ||
Conformational states of smooth muscle myosin. Effects of light chain phosphorylation and ionic strength | Q71010590 | ||
Actin and light chain isoform dependence of myosin V kinetics | Q73212750 | ||
Regulation of myosin V processivity by calcium at the single molecule level | Q80141852 | ||
The binding of DYNLL2 to myosin Va requires alternatively spliced exon B and stabilizes a portion of the myosin's coiled-coil domain | Q80280712 | ||
Organelle targeting of myosin XI is mediated by two globular tail subdomains with separate cargo binding sites | Q80328535 | ||
Effect of calcium on calmodulin bound to the IQ motifs of myosin V | Q80465025 | ||
Activation of myosin Va function by melanophilin, a specific docking partner of myosin Va | Q81508526 | ||
Processivity of chimeric class V myosins | Q82081618 | ||
Three-dimensional structure of the myosin V inhibited state by cryoelectron tomography | Q83177861 | ||
P433 | issue | 9 | |
P304 | page(s) | 1378-1389 | |
P577 | publication date | 2008-05-01 | |
P1433 | published in | Cellular and Molecular Life Sciences | Q5058352 |
P1476 | title | Myosin V from head to tail | |
P478 | volume | 65 |
Q42109184 | A Myosin V Inhibitor Based on Privileged Chemical Scaffolds |
Q99596488 | A Novel Labeling Strategy Reveals That Myosin Va and Myosin Vb Bind the Same Dendritically Polarized Vesicle Population |
Q41978648 | A novel form of motility in filopodia revealed by imaging myosin-X at the single-molecule level |
Q55281306 | Allosteric binding sites in Rab11 for potential drug candidates. |
Q30524660 | Arabidopsis Myosin XI-K Localizes to the Motile Endomembrane Vesicles Associated with F-actin |
Q38019540 | Assembly of mRNA-protein complexes for directional mRNA transport in eukaryotes--an overview |
Q52659621 | Bilobal architecture is a requirement for calmodulin signaling to CaV1.3 channels. |
Q30501053 | Characterization of Mug33 reveals complementary roles for actin cable-dependent transport and exocyst regulators in fission yeast exocytosis |
Q43004259 | Class XI myosins are required for development, cell expansion, and F-Actin organization in Arabidopsis |
Q30417695 | Coarse-grained simulation of myosin-V movement |
Q36201901 | Collective dynamics of elastically coupled myosin V motors |
Q90286423 | Converter domain mutations in myosin alter structural kinetics and motor function |
Q27304842 | Dense granule trafficking in Toxoplasma gondii requires a unique class 27 myosin and actin filaments |
Q42929677 | Differential patterns of myosin Va expression during the ontogenesis of the rat hippocampus |
Q36914328 | Direct interaction between a myosin V motor and the Rab GTPases Ypt31/32 is required for polarized secretion |
Q27321597 | Direct observation of the myosin Va recovery stroke that contributes to unidirectional stepping along actin |
Q37642018 | Divergent Soybean Calmodulins Respond Similarly to Calcium Transients: Insight into Differential Target Regulation |
Q37263304 | Drunk or sober? Myosin V walks the (quantum) dotted line in cells |
Q93367899 | Duplicated Myosin V Genes in Teleosts Show Evolutionary Rate Variations among the Motor and Cargo-Binding Domains |
Q37262205 | Essential features of the class V myosin from budding yeast for ASH1 mRNA transport |
Q27315873 | Flexural Stiffness of Myosin Va Subdomains as Measured from Tethered Particle Motion |
Q36071935 | Force-dependent detachment of kinesin-2 biases track switching at cytoskeletal filament intersections. |
Q30505111 | Full-length myosin Va exhibits altered gating during processive movement on actin |
Q37213744 | Functions of class V myosins in neurons |
Q99616838 | Fusion partners of NTRK3 affect subcellular localization of the fusion kinase and cytomorphology of melanocytes |
Q28392110 | Genome-Wide Meta-Analysis of Sciatica in Finnish Population |
Q42001346 | Genomics: Of monarchs and migration |
Q39440818 | Hypertrophic cardiomyopathy and the myosin mesa: viewing an old disease in a new light |
Q30560522 | In vitro reconstitution of an mRNA-transport complex reveals mechanisms of assembly and motor activation |
Q30390486 | Insights into human beta-cardiac myosin function from single molecule and single cell studies |
Q50422621 | Interacting-heads motif has been conserved as a mechanism of myosin II inhibition since before the origin of animals |
Q28743071 | Lever-arm mechanics of processive myosins |
Q47661261 | Loss of Myosin Vb in colorectal cancer is a strong prognostic factor for disease recurrence |
Q58585938 | MARCKS (Myristoylated Alanine-Rich C Kinase Substrate) and Lung Disease |
Q47269140 | MYO5B, STX3 and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update |
Q33288865 | Mammalian Kinesin-3 motors are dimeric in vivo and move by processive motility upon release of autoinhibition. |
Q35956491 | Mechanism of evenness interrupted (Evi)-exosome release at synaptic boutons |
Q26829426 | Mitochondrial inheritance in yeast |
Q57049996 | Molecular mechanisms of the interhead coordination by interhead tension in cytoplasmic dyneins |
Q34228870 | Molecular motors: forty years of interdisciplinary research |
Q37226089 | More than just a cargo adapter, melanophilin prolongs and slows processive runs of myosin Va |
Q28571755 | Muscle cells engage Rab8A and myosin Vb in insulin-dependent GLUT4 translocation |
Q38962635 | Myosin VI must dimerize and deploy its unusual lever arm in order to perform its cellular roles. |
Q33809113 | Myosin VI: an innovative motor that challenged the swinging lever arm hypothesis |
Q64077575 | Myosin Va and spermine synthase: partners in exosome transport |
Q64074584 | Myosin Va interacts with the exosomal protein spermine synthase |
Q37371351 | Myosin Va is developmentally regulated and expressed in the human cerebellum from birth to old age. |
Q30499108 | Myosin Va is required for P body but not stress granule formation |
Q30354407 | Myosin Va molecular motors manoeuvre liposome cargo through suspended actin filament intersections in vitro. |
Q35216754 | Myosin Va plays a key role in nitrergic neurotransmission by transporting nNOSα to enteric varicosity membrane |
Q92986379 | Myosin Va transport of liposomes in three-dimensional actin networks is modulated by actin filament density, position, and polarity |
Q28117478 | Myosin Vc is a molecular motor that functions in secretory granule trafficking |
Q30528813 | Myosin Vs organize actin cables in fission yeast |
Q26770575 | Myosin isoforms and the mechanochemical cross-bridge cycle |
Q30574594 | Myosin lever arm directs collective motion on cellular actin network |
Q34985570 | Myosin motor function: the ins and outs of actin-based membrane protrusions. |
Q27336880 | Myosin motor isoforms direct specification of actomyosin function by tropomyosins |
Q42000419 | Myosin--a monarch of pigment transport? |
Q35656527 | Myosin-5, kinesin-1 and myosin-17 cooperate in secretion of fungal chitin synthase |
Q34800260 | Myosin5a tail associates directly with Rab3A-containing compartments in neurons |
Q35995640 | Myosins FaMyo2B and Famyo2 Affect Asexual and Sexual Development, Reduces Pathogenicity, and FaMyo2B Acts Jointly with the Myosin Passenger Protein FaSmy1 to Affect Resistance to Phenamacril in Fusarium asiaticum |
Q51377017 | Myosins: Domain Organisation, Motor Properties, Physiological Roles and Cellular Functions. |
Q38284527 | Of social molecules: The interactive assembly of ASH1 mRNA-transport complexes in yeast |
Q37967198 | Principles of mRNA transport in yeast |
Q37884613 | Principles of unconventional myosin function and targeting |
Q41785586 | Purification, crystallization and preliminary crystallographic analysis of the globular domain of the human type V myosin Myo5a |
Q60915261 | Regulation of Myosin-5b by Rab11a and the Rab11 family interacting protein 2 |
Q39449551 | Regulation of class V myosin. |
Q45250242 | Role of myosin Va in neuritogenesis of chick dorsal root ganglia nociceptive neurons |
Q35849429 | Role of myosin Va in purinergic vesicular neurotransmission in the gut |
Q33727604 | Simultaneous Observation of Tail and Head Movements of Myosin V during Processive Motion |
Q37008302 | Spatial diffusivity and availability of intracellular calmodulin |
Q27680148 | Structural Insights into Functional Overlapping and Differentiation among Myosin V Motors |
Q90044150 | Structural basis for power stroke vs. Brownian ratchet mechanisms of motor proteins |
Q91905280 | Structural mechanism for versatile cargo recognition by the yeast class V myosin Myo2 |
Q64992797 | Suo Quan Wan Protects Mouse From Early Diabetic Bladder Dysfunction by Mediating Motor Protein Myosin Va and Transporter Protein SLC17A9. |
Q34671790 | Surface dynamics in allosteric regulation of protein-protein interactions: modulation of calmodulin functions by Ca2+. |
Q27654477 | Sus1, Cdc31, and the Sac3 CID Region Form a Conserved Interaction Platform that Promotes Nuclear Pore Association and mRNA Export |
Q27007553 | The axonal transport of mitochondria |
Q37683931 | The molecular motor Myosin Va interacts with the cilia-centrosomal protein RPGRIP1L. |
Q37941546 | The myosin family: unconventional roles of actin-dependent molecular motors in immune cells. |
Q35156995 | The myosin-related motor protein Myo2 is an essential mediator of bud-directed mitochondrial movement in yeast |
Q37942354 | The nucleoskeleton as a genome-associated dynamic 'network of networks'. |
Q36604050 | Tropomyosin is essential for processive movement of a class V myosin from budding yeast |
Q37297090 | Tropomyosin isoforms bias actin track selection by vertebrate myosin Va |
Q35227173 | Tuning myosin-driven sorting on cellular actin networks |
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