review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Natalia Fili | Q92156436 |
Christopher P. Toseland | Q49406828 | ||
P2860 | cites work | Activation of myosin Va function by melanophilin, a specific docking partner of myosin Va | Q81508526 |
The actin-binding interface of a myosin III is phosphorylated in vivo in response to signals from a circadian clock | Q81571539 | ||
Full-length myosin VI dimerizes and moves processively along actin filaments upon monomer clustering | Q82457987 | ||
Three-dimensional structure of the myosin V inhibited state by cryoelectron tomography | Q83177861 | ||
Competition between two high- and low-affinity protein-binding sites in myosin VI controls its cellular function | Q91343838 | ||
Kinetics of the interaction of myo1c with phosphoinositides | Q37431105 | ||
Myosin VI rewrites the rules for myosin motors | Q37755563 | ||
Principles of unconventional myosin function and targeting | Q37884613 | ||
Nuclear actin and myosins: life without filaments | Q37952090 | ||
Myosin VI and its cargo adaptors - linking endocytosis and autophagy | Q38115519 | ||
Cargo recognition and cargo-mediated regulation of unconventional myosins | Q38250419 | ||
Structural Basis of Cargo Recognition by Unconventional Myosins in Cellular Trafficking | Q38722191 | ||
How Myosin Generates Force on Actin Filaments | Q38975414 | ||
Myosin VI is required for sorting of AP-1B-dependent cargo to the basolateral domain in polarized MDCK cells | Q39735805 | ||
Myosin Va phosphorylated on Ser1650 is found in nuclear speckles and redistributes to nucleoli upon inhibition of transcription | Q40004114 | ||
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 | ||
MYO6 is targeted by Salmonella virulence effectors to trigger PI3-kinase signaling and pathogen invasion into host cells. | Q40276496 | ||
TEDS rule: a molecular rationale for differential regulation of myosins by phosphorylation of the heavy chain head | Q40410613 | ||
A monomeric myosin VI with a large working stroke | Q40573331 | ||
Ca2+-induced activation of ATPase activity of myosin Va is accompanied with a large conformational change | Q40587730 | ||
Class VI myosin moves processively along actin filaments backward with large steps | Q40758767 | ||
The localization and sequence of the phosphorylation sites of Acanthamoeba myosins I. An improved method for locating the phosphorylated amino acid | Q41266974 | ||
Myosin I can act as a molecular force sensor. | Q41334383 | ||
The motor function of Drosophila melanogaster myosin-5 is activated by calcium and cargo-binding protein dRab11. | Q41998305 | ||
Kinetic properties and small-molecule inhibition of human myosin-6. | Q42032109 | ||
Magnesium impacts myosin V motor activity by altering key conformational changes in the mechanochemical cycle. | Q42073159 | ||
Comparative kinetic and functional characterization of the motor domains of human nonmuscle myosin-2C isoforms | Q42093317 | ||
Myosin VI targeting to clathrin-coated structures and dimerization is mediated by binding to Disabled-2 and PtdIns(4,5)P2. | Q42155473 | ||
Phosphorylation of the kinase domain regulates autophosphorylation of myosin IIIA and its translocation in microvilli | Q42173398 | ||
The Rab interacting lysosomal protein (RILP) homology domain functions as a novel effector domain for small GTPase Rab36: Rab36 regulates retrograde melanosome transport in melanocytes. | Q42323966 | ||
Membrane-bound myo1c powers asymmetric motility of actin filaments | Q42554416 | ||
Effect of phosphorylation in the motor domain of human myosin IIIA on its ATP hydrolysis cycle | Q43146291 | ||
Ste20-kinase-dependent TEDS-site phosphorylation modulates the dynamic localisation and endocytic function of the fission yeast class I myosin, Myo1. | Q43266175 | ||
Kinetic mechanism and regulation of myosin VI. | Q43651972 | ||
Cell cycle regulation of myosin-V by calcium/calmodulin-dependent protein kinase II. | Q43710205 | ||
Crosstalk between PI(4,5)P₂and CK2 modulates actin polymerization during endocytic uptake | Q44110982 | ||
Calcium functionally uncouples the heads of myosin VI. | Q44394472 | ||
The mechanism of myosin VI translocation and its load-induced anchoring | Q44790017 | ||
Magnesium regulates ADP dissociation from myosin V. | Q45173714 | ||
Changes in Mg2+ ion concentration and heavy chain phosphorylation regulate the motor activity of a class I myosin | Q45173722 | ||
A chemical-genetic strategy implicates myosin-1c in adaptation by hair cells. | Q45712448 | ||
Myosin VI altered at threonine 406 stabilizes actin filaments in vivo | Q46044406 | ||
She3p binds to the rod of yeast myosin V and prevents it from dimerizing, forming a single-headed motor complex | Q46822902 | ||
Dictyostelium myosin-IE is a fast molecular motor involved in phagocytosis | Q46917024 | ||
Myosin VI is required for structural integrity of the apical surface of sensory hair cells in zebrafish | Q47073856 | ||
NDP52 activates nuclear myosin VI to enhance RNA polymerase II transcription. | Q47140521 | ||
Regulated conformation of myosin V. | Q47368896 | ||
Frontline Science: Tumor necrosis factor-α stimulation and priming of human neutrophil granule exocytosis | Q47991408 | ||
Myosin-1C uses a novel phosphoinositide-dependent pathway for nuclear localization | Q48251880 | ||
Myosin VI-Dependent Actin Cages Encapsulate Parkin-Positive Damaged Mitochondria | Q49339871 | ||
Ca2+-Induced Rigidity Change of the Myosin VIIa IQ Motif-Single α Helix Lever Arm Extension. | Q51110298 | ||
Structure of myosin-1c tail bound to calmodulin provides insights into calcium-mediated conformational coupling | Q52159623 | ||
Phospholipid-dependent regulation of the motor activity of myosin X. | Q52612413 | ||
The predicted coiled-coil domain of myosin 10 forms a novel elongated domain that lengthens the head. | Q52857621 | ||
A tissue-specific exon of myosin Va is responsible for selective cargo binding in melanocytes. | Q53788055 | ||
The motor protein myosin-I produces its working stroke in two steps | Q56894963 | ||
Dissecting myosin-5B mechanosensitivity and calcium regulation at the single molecule level | Q61135840 | ||
Brain myosin-V is a two-headed unconventional myosin with motor activity | Q70488210 | ||
The interaction of F-actin with phosphorylated and unphosphorylated myosins IA and IB from Acanthamoeba castellanii | Q72559861 | ||
Kinetic analyses of a truncated mammalian myosin I suggest a novel isomerization event preceding nucleotide binding | Q73712699 | ||
Localization of myosin-Ibeta near both ends of tip links in frog saccular hair cells | Q77458696 | ||
Myosin Va becomes a low duty ratio motor in the inhibited form | Q79960802 | ||
The binding of DYNLL2 to myosin Va requires alternatively spliced exon B and stabilizes a portion of the myosin's coiled-coil domain | Q80280712 | ||
Effect of calcium on calmodulin bound to the IQ motifs of myosin V | Q80465025 | ||
Motility of myosin V regulated by the dissociation of single calmodulin | Q81308489 | ||
Myosin va mediates docking of secretory granules at the plasma membrane | Q81358009 | ||
Drawing the tree of eukaryotic life based on the analysis of 2,269 manually annotated myosins from 328 species | Q21092862 | ||
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 isoform localized to clathrin-coated vesicles with a role in clathrin-mediated endocytosis | Q24291429 | ||
MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes | Q24294793 | ||
A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport | Q24295585 | ||
Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis | Q24300284 | ||
Myo1e binds anionic phospholipids with high affinity | Q24300535 | ||
Nuclear myosin VI enhances RNA polymerase II-dependent transcription | Q24301373 | ||
A new compartment at stereocilia tips defined by spatial and temporal patterns of myosin IIIa expression | Q24305683 | ||
Myosin 1G (Myo1G) is a haematopoietic specific myosin that localises to the plasma membrane and regulates cell elasticity | Q24336738 | ||
Rab27a is an essential component of melanosome receptor for myosin Va | Q24524137 | ||
Myosin VI is a processive motor with a large step size | Q24555089 | ||
Myo1c is designed for the adaptation response in the inner ear | Q24610102 | ||
A millennial myosin census | Q24633678 | ||
T6BP and NDP52 are myosin VI binding partners with potential roles in cytokine signalling and cell adhesion | Q24650918 | ||
Myosin Vb mobilizes recycling endosomes and AMPA receptors for postsynaptic plasticity | Q24655632 | ||
Identification, characterization and cloning of myr 1, a mammalian myosin-I | Q24674123 | ||
Calcium can mobilize and activate myosin-VI | Q27317433 | ||
Precise positioning of myosin VI on endocytic vesicles in vivo | Q27334526 | ||
Myosin VI Dimerization Triggers an Unfolding of a Three-Helix Bundle in Order to Extend Its Reach | Q27656923 | ||
Myosin VI undergoes cargo-mediated dimerization | Q27656929 | ||
Antiparallel coiled-coil-mediated dimerization of myosin X | Q27673659 | ||
Structural basis of the myosin X PH1N-PH2-PH1C tandem as a specific and acute cellular PI(3,4,5)P3 sensor | Q27674679 | ||
Structural basis of cargo recognitions for class V myosins | Q27678783 | ||
Structural basis of myosin V Rab GTPase-dependent cargo recognition | Q27680629 | ||
A vertebrate myosin-I structure reveals unique insights into myosin mechanochemical tuning | Q27681483 | ||
Crystal structure of human myosin 1c--the motor in GLUT4 exocytosis: implications for Ca2+ regulation and 14-3-3 binding | Q27689527 | ||
Human myosin V gene produces different transcripts in a cell type-specific manner | Q28117452 | ||
Slac2-a/melanophilin, the missing link between Rab27 and myosin Va: implications of a tripartite protein complex for melanosome transport | Q28202672 | ||
Coupled myosin VI motors facilitate unidirectional movement on an F-actin network | Q37387839 | ||
Transient kinetic analysis of the 130-kDa myosin I (MYR-1 gene product) from rat liver. A myosin I designed for maintenance of tension? | Q28369644 | ||
Identification of an organelle receptor for myosin-Va | Q28504759 | ||
Molecular genetic dissection of mouse unconventional myosin-VA: tail region mutations | Q28507012 | ||
Binding of internalized receptors to the PDZ domain of GIPC/synectin recruits myosin VI to endocytic vesicles | Q28511953 | ||
Mouse class III myosins: kinase activity and phosphorylation sites | Q28512769 | ||
Localization of myosin 1b to actin protrusions requires phosphoinositide binding | Q28566730 | ||
Biochemical and motile properties of Myo1b splice isoforms | Q28570970 | ||
Control of myosin-I force sensing by alternative splicing | Q28577567 | ||
Regulation of myosin-VI targeting to endocytic compartments | Q28580721 | ||
Role of myosin VI in the differentiation of cochlear hair cells | Q28585164 | ||
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 | ||
Localization of ASH1 mRNA particles in living yeast | Q29614818 | ||
A FERM domain autoregulates Drosophila myosin 7a activity | Q30157340 | ||
Fast adaptation in vestibular hair cells requires myosin-1c activity | Q30437793 | ||
Myo1c binds phosphoinositides through a putative pleckstrin homology domain | Q30478257 | ||
Myosin Vb interacts with Rab8a on a tubular network containing EHD1 and EHD3. | Q30479902 | ||
Calcium sensitivity of the cross-bridge cycle of Myo1c, the adaptation motor in the inner ear | Q30481688 | ||
Control of cell membrane tension by myosin-I. | Q30489048 | ||
Cargo binding activates myosin VIIA motor function in cells | Q30499937 | ||
Myosin VI small insert isoform maintains exocytosis by tethering secretory granules to the cortical actin | Q30534452 | ||
Unconventional myosin Myo1c promotes membrane fusion in a regulated exocytic pathway | Q30592846 | ||
TEDS site phosphorylation of the yeast myosins I is required for ligand-induced but not for constitutive endocytosis of the G protein-coupled receptor Ste2p. | Q33233910 | ||
Myosin-Vb functions as a dynamic tether for peripheral endocytic compartments during transferrin trafficking | Q33358549 | ||
Myosin 1G is an abundant class I myosin in lymphocytes whose localization at the plasma membrane depends on its ancient divergent pleckstrin homology (PH) domain (Myo1PH). | Q33726416 | ||
Cloning and chromosomal localization of a human class III myosin | Q33913130 | ||
Myosin-X, a novel myosin with pleckstrin homology domains, associates with regions of dynamic actin. | Q33917620 | ||
Leveraging the membrane - cytoskeleton interface with myosin-1. | Q33965456 | ||
Evidence that myosin activity opposes microtubule-based axonal transport of mitochondria | Q33998992 | ||
Myosin VI: roles for a minus end-directed actin motor in cells | Q34038023 | ||
Dual regulation of mammalian myosin VI motor function | Q34087728 | ||
Human myosin-Vc is a novel class V myosin expressed in epithelial cells | Q34116426 | ||
Magnesium modulates actin binding and ADP release in myosin motors | Q34141150 | ||
Genome structure and differential expression of two isoforms of a novel PDZ-containing myosin (MysPDZ) (Myo18A). | Q34199087 | ||
Intermolecular autophosphorylation regulates myosin IIIa activity and localization in parallel actin bundles. | Q34285278 | ||
Nucleotide-Dependent Shape Changes in the Reverse Direction Motor, Myosin VI | Q34307078 | ||
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 | ||
Kinetic mechanism of human myosin IIIA. | Q34577832 | ||
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing. | Q34634062 | ||
Myosin VI stabilizes an actin network during Drosophila spermatid individualization | Q34662188 | ||
Myo3A, one of two class III myosin genes expressed in vertebrate retina, is localized to the calycal processes of rod and cone photoreceptors and is expressed in the sacculus | Q34813453 | ||
New insights into myosin evolution and classification | Q34944007 | ||
Myosin-X: a MyTH-FERM myosin at the tips of filopodia | Q35576442 | ||
Two single-headed myosin V motors bound to a tetrameric adapter protein form a processive complex | Q35670601 | ||
Melanophilin Stimulates Myosin-5a Motor Function by Allosterically Inhibiting the Interaction between the Head and Tail of Myosin-5a | Q35679335 | ||
The cargo-binding domain regulates structure and activity of myosin 5 | Q35752269 | ||
Myosin 5a is an insulin-stimulated Akt2 (protein kinase Bbeta) substrate modulating GLUT4 vesicle translocation | Q35949606 | ||
Calmodulin bound to the first IQ motif is responsible for calcium-dependent regulation of myosin 5a | Q35956753 | ||
p21-activated kinase has substrate specificity similar to Acanthamoeba myosin I heavy chain kinase and activates Acanthamoeba myosin I | Q35987694 | ||
Myo4p is a monomeric myosin with motility uniquely adapted to transport mRNA | Q36119329 | ||
Myosin VI and vinculin cooperate during the morphogenesis of cadherin cell cell contacts in mammalian epithelial cells | Q36119767 | ||
Membrane-induced lever arm expansion allows myosin VI to walk with large and variable step sizes | Q36318743 | ||
Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo | Q36328552 | ||
The globular tail domain puts on the brake to stop the ATPase cycle of myosin Va. | Q36446088 | ||
Long single alpha-helical tail domains bridge the gap between structure and function of myosin VI. | Q36740061 | ||
Various Themes of Myosin Regulation | Q36880297 | ||
Class VI unconventional myosin is required for spermatogenesis in Drosophila | Q36956898 | ||
Loop 2 of limulus myosin III is phosphorylated by protein kinase A and autophosphorylation | Q36966889 | ||
Myosin light chains: Teaching old dogs new tricks | Q37021389 | ||
Alternative splicing in class V myosins determines association with Rab10. | Q37036487 | ||
Single-molecule reconstitution of mRNA transport by a class V myosin | Q37076266 | ||
Diverse functions of myosin VI elucidated by an isoform-specific α-helix domain | Q37135682 | ||
The tail binds to the head-neck domain, inhibiting ATPase activity of myosin VIIA | Q37208900 | ||
More than just a cargo adapter, melanophilin prolongs and slows processive runs of myosin Va | Q37226089 | ||
Calmodulin in complex with the first IQ motif of myosin-5a functions as an intact calcium sensor. | Q37323208 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 1 | |
P577 | publication date | 2019-12-20 | |
P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
P1476 | title | Unconventional Myosins: How Regulation Meets Function | |
P478 | volume | 21 |
Q110697472 | Dynamics of the orphan myosin MyoF over Trypanosoma cruzi life cycle and along the endocytic pathway |
Q101403005 | Nonmuscle myosin IIB regulates Parkin-mediated mitophagy associated with amyotrophic lateral sclerosis-linked TDP-43 |
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