scholarly article | Q13442814 |
P356 | DOI | 10.1074/JBC.M504887200 |
P698 | PubMed publication ID | 16030012 |
P50 | author | Kavitha Thirumurugan | Q39734845 |
Michelle Peckham | Q41530215 | ||
P2093 | author name string | Fei Wang | |
Arnout P Kalverda | |||
Walter F Stafford | |||
James R Sellers | |||
Peter J Knight | |||
Yuhui Xu | |||
P2860 | cites work | Myosin VI is a processive motor with a large step size | Q24555089 |
A millennial myosin census | Q24633678 | ||
Improving coiled-coil stability by optimizing ionic interactions | Q27639132 | ||
Predicting coiled coils from protein sequences | Q27861097 | ||
Relationship between nuclear magnetic resonance chemical shift and protein secondary structure | Q28252147 | ||
Effect of ADP and ionic strength on the kinetic and motile properties of recombinant mouse myosin V | Q28369753 | ||
SMART 4.0: towards genomic data integration | Q29547824 | ||
Predicting coiled coils by use of pairwise residue correlations | Q29616472 | ||
Helix stabilization by Glu-...Lys+ salt bridges in short peptides of de novo design | Q34376818 | ||
Unconventional myosins in cell movement, membrane traffic, and signal transduction | Q41687083 | ||
An exceptionally stable helix from the ribosomal protein L9: implications for protein folding and stability | Q42661355 | ||
Sequence-dependent correction of random coil NMR chemical shifts | Q43677693 | ||
Designing heterodimeric two-stranded alpha-helical coiled-coils: the effect of chain length on protein folding, stability and specificity | Q43989540 | ||
Neck length and processivity of myosin V. | Q44436395 | ||
Shape and flexibility of the myosin molecule | Q45145980 | ||
Assembly of Acanthamoeba myosin-II minifilaments. Definition of C-terminal residues required to form coiled-coils, dimers, and octamers | Q45168186 | ||
A flexible domain is essential for the large step size and processivity of myosin VI. | Q47391271 | ||
Analysis of heterologous interacting systems by sedimentation velocity: curve fitting algorithms for estimation of sedimentation coefficients, equilibrium and kinetic constants | Q47884569 | ||
DICHROWEB: an interactive website for the analysis of protein secondary structure from circular dichroism spectra. | Q52046718 | ||
Protein volumes and hydration effects. The calculations of partial specific volumes, neutron scattering matchpoints and 280-nm absorption coefficients for proteins and glycoproteins from amino acid sequences. | Q52641055 | ||
An autonomous folding unit mediates the assembly of two-stranded coiled coils | Q36790232 | ||
Computer modelling of the alpha-helical coiled coil: packing of side-chains in the inner core | Q38572632 | ||
A monomeric myosin VI with a large working stroke | Q40573331 | ||
Use of negative stain and single-particle image processing to explore dynamic properties of flexible macromolecules | Q41628059 | ||
P433 | issue | 41 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 34702-34708 | |
P577 | publication date | 2005-07-18 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | The predicted coiled-coil domain of myosin 10 forms a novel elongated domain that lengthens the head. | |
P478 | volume | 280 |
Q30826156 | A Combination of Diffusion and Active Translocation Localizes Myosin 10 to the Filopodial Tip |
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Q27306218 | Actin structure-dependent stepping of myosin 5a and 10 during processive movement |
Q30841590 | Activated full-length myosin-X moves processively on filopodia with large steps toward diverse two-dimensional directions |
Q27673659 | Antiparallel coiled-coil-mediated dimerization of myosin X |
Q37366472 | Cargo binding induces dimerization of myosin VI. |
Q41861222 | Characterization of long and stable de novo single alpha-helix domains provides novel insight into their stability |
Q36201824 | Cloning, expression, and characterization of a novel molecular motor, Leishmania myosin-XXI. |
Q37936477 | Coiled coils and SAH domains in cytoskeletal molecular motors |
Q30383024 | Combining single-molecule optical trapping and small-angle x-ray scattering measurements to compute the persistence length of a protein ER/K alpha-helix. |
Q37000324 | Competition between Coiled-Coil Structures and the Impact on Myosin-10 Bundle Selection |
Q51359862 | Consensus Prediction of Charged Single Alpha-Helices with CSAHserver. |
Q54981565 | Critical buckling length versus persistence length: what governs biofilament conformation? |
Q33795702 | Design of active transport must be highly intricate: a possible role of myosin and Ena/VASP for G-actin transport in filopodia |
Q30514794 | Differential regulation of myosin X movements by its cargos, DCC and neogenin. |
Q30477237 | Dimerized Drosophila myosin VIIa: a processive motor |
Q36331997 | Distribution and evolution of stable single α-helices (SAH domains) in myosin motor proteins |
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 |
Q61821271 | Dynamic ion pair behavior stabilizes single alpha helices in proteins |
Q42580509 | Formation of Salt Bridges Mediates Internal Dimerization of Myosin VI Medial Tail Domain |
Q39498964 | Functional and Structural Characterization of Novel Type of Linker Connecting Capsid and Nucleocapsid Protein Domains in Murine Leukemia Virus. |
Q24306911 | Functional characterization of the human myosin-7a motor domain |
Q30365100 | Harnessing the unique structural properties of isolated α-helices. |
Q36127036 | Headless Myo10 is a negative regulator of full-length Myo10 and inhibits axon outgrowth in cortical neurons |
Q41148281 | Helicity of short E‐R/K peptides |
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 |
Q42800641 | Human myosin VIIa is a very slow processive motor protein on various cellular actin structures |
Q36092974 | Interactions of Yeast Dynein with Dynein Light Chain and Dynactin: GENERAL IMPLICATIONS FOR INTRINSICALLY DISORDERED DUPLEX SCAFFOLDS IN MULTIPROTEIN ASSEMBLIES |
Q38756098 | Kinetic Adaptations of Myosins for Their Diverse Cellular Functions |
Q28743071 | Lever-arm mechanics of processive myosins |
Q41460366 | Local and macroscopic electrostatic interactions in single α-helices. |
Q36740061 | Long single alpha-helical tail domains bridge the gap between structure and function of myosin VI. |
Q38803208 | Mechanics and Activation of Unconventional Myosins |
Q28575899 | Modification of loop 1 affects the nucleotide binding properties of Myo1c, the adaptation motor in the inner ear |
Q89674062 | Modulating the Stiffness of the Myosin VI Single α-Helical Domain |
Q33861746 | Multiple Myo4 motors enhance ASH1 mRNA transport in Saccharomyces cerevisiae |
Q37515120 | MyTH4-FERM myosins have an ancient and conserved role in filopod formation |
Q34459239 | Myo1c mutations associated with hearing loss cause defects in the interaction with nucleotide and actin. |
Q27656923 | Myosin VI Dimerization Triggers an Unfolding of a Three-Helix Bundle in Order to Extend Its Reach |
Q38962635 | Myosin VI must dimerize and deploy its unusual lever arm in order to perform its cellular roles. |
Q34662188 | Myosin VI stabilizes an actin network during Drosophila spermatid individualization |
Q33809113 | Myosin VI: an innovative motor that challenged the swinging lever arm hypothesis |
Q36378456 | Myosin X dimerization and its impact on cellular functions |
Q30493830 | Myosin X regulates sealing zone patterning in osteoclasts through linkage of podosomes and microtubules |
Q33540368 | Myosin individualized: single nucleotide polymorphisms in energy transduction |
Q34985570 | Myosin motor function: the ins and outs of actin-based membrane protrusions. |
Q41530183 | Myosin tails and single α-helical domains |
Q33607079 | Myosin-10 produces its power-stroke in two phases and moves processively along a single actin filament under low load |
Q26825835 | Myosin-X and disease |
Q30494868 | Myosin-X induces filopodia by multiple elongation mechanism |
Q24299253 | Myosin-X is a molecular motor that functions in filopodia formation |
Q47139973 | Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation. |
Q35576442 | Myosin-X: a MyTH-FERM myosin at the tips of filopodia |
Q36415686 | Myosinome: a database of myosins from select eukaryotic genomes to facilitate analysis of sequence-structure-function relationships |
Q47140521 | NDP52 activates nuclear myosin VI to enhance RNA polymerase II transcription. |
Q34307078 | Nucleotide-Dependent Shape Changes in the Reverse Direction Motor, Myosin VI |
Q90702016 | Optimized filopodia formation requires myosin tail domain cooperation |
Q52612413 | Phospholipid-dependent regulation of the motor activity of myosin X. |
Q38042929 | Plant-Specific Myosin XI, a Molecular Perspective |
Q92048491 | Post-ER Stress Biogenesis of Golgi Is Governed by Giantin |
Q45969530 | Production of recombinant human tektin 1, 2, and 4 and in vitro assembly of human tektin 1. |
Q37936474 | Regulation of myosin 5a and myosin 7a. |
Q92222204 | Remarkable Rigidity of the Single α-Helical Domain of Myosin-VI As Revealed by NMR Spectroscopy |
Q30494681 | Single-molecule stepping and structural dynamics of myosin X. |
Q30588808 | Stable single α-helices are constant force springs in proteins |
Q38722191 | Structural Basis of Cargo Recognition by Unconventional Myosins in Cellular Trafficking |
Q41540386 | Structural flexibility of CaV1.2 and CaV2.2 I-II proximal linker fragments in solution. |
Q35837241 | Structure and Regulation of the Movement of Human Myosin VIIA. |
Q30496161 | Structured post-IQ domain governs selectivity of myosin X for fascin-actin bundles |
Q27023615 | Structures of usher syndrome 1 proteins and their complexes |
Q30376716 | The Inner Centromere Protein (INCENP) Coil Is a Single α-Helix (SAH) Domain That Binds Directly to Microtubules and Is Important for Chromosome Passenger Complex (CPC) Localization and Function in Mitosis. |
Q37477144 | The SAH domain extends the functional length of the myosin lever |
Q34134758 | The Stepping Pattern of Myosin X Is Adapted for Processive Motility on Bundled Actin |
Q34685505 | The kinetic mechanism of mouse myosin VIIA |
Q30480576 | The motor activity of myosin-X promotes actin fiber convergence at the cell periphery to initiate filopodia formation. |
Q27333243 | The myosin X motor is optimized for movement on actin bundles |
Q27011868 | The myosin superfamily at a glance. |
Q41825148 | The path to visualization of walking myosin V by high-speed atomic force microscopy |
Q37208900 | The tail binds to the head-neck domain, inhibiting ATPase activity of myosin VIIA |
Q37629911 | To understand muscle you must take it apart |
Q64253417 | Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition |
Q92156441 | Unconventional Myosins: How Regulation Meets Function |
Q34262470 | Use of fluorescent techniques to study the in vitro movement of myosins |
Q36599315 | Usher syndrome: molecular links of pathogenesis, proteins and pathways |
Q50000382 | Waggawagga-CLI: A command-line tool for predicting stable single α-helices (SAH-domains), and the SAH-domain distribution across eukaryotes |
Q44273438 | Waggawagga: comparative visualization of coiled-coil predictions and detection of stable single α-helices (SAH domains). |
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