scholarly article | Q13442814 |
P356 | DOI | 10.1038/35036357 |
P698 | PubMed publication ID | 11025663 |
P2093 | author name string | C F Schmidt | |
R J Stewart | |||
L A Clarke | |||
M J deCastro | |||
R M Fondecave | |||
P2860 | cites work | Kinesin-II, a membrane traffic motor in axons, axonemes, and spindles | Q24671932 |
Direction determination in the minus-end-directed kinesin motor ncd | Q27765757 | ||
Reversal in the direction of movement of a molecular motor | Q28248501 | ||
A structural change in the kinesin motor protein that drives motility | Q29617533 | ||
Two-dimensional tracking of ncd motility by back focal plane interferometry | Q30539074 | ||
Interference model for back-focal-plane displacement detection in optical tweezers. | Q33310600 | ||
The road less traveled: emerging principles of kinesin motor utilization | Q33804309 | ||
Antagonistic microtubule-sliding motors position mitotic centrosomes in Drosophila early embryos | Q33880076 | ||
Kinetics processivity and the direction of motion of Ncd. | Q34171109 | ||
Single myosin molecule mechanics: piconewton forces and nanometre steps | Q34338098 | ||
A processive single-headed motor: kinesin superfamily protein KIF1A. | Q34502365 | ||
Flexural rigidity of microtubules and actin filaments measured from thermal fluctuations in shape | Q36383049 | ||
Direct observation of kinesin stepping by optical trapping interferometry | Q36774439 | ||
Signals and noise in micromechanical measurements | Q36888831 | ||
The stiffness of rabbit skeletal actomyosin cross-bridges determined with an optical tweezers transducer. | Q40128502 | ||
Three-dimensional structure of functional motor proteins on microtubules | Q41633942 | ||
Identification and characterization of a gene encoding a kinesin-like protein in Drosophila | Q44542698 | ||
The Ncd tail domain promotes microtubule assembly and stability | Q44860144 | ||
A 35-A movement of smooth muscle myosin on ADP release. | Q46023129 | ||
Movement of microtubules by single kinesin molecules | Q46085669 | ||
Crystal structure of the motor domain of the kinesin-related motor ncd. | Q46107252 | ||
The directional preference of kinesin motors is specified by an element outside of the motor catalytic domain | Q46232085 | ||
Highly processive motility is not a general feature of the kinesins | Q47737078 | ||
Nucleotide-dependent structural changes in dimeric NCD molecules complexed to microtubules. | Q48454533 | ||
The kinesin-like ncd protein of Drosophila is a minus end-directed microtubule motor. | Q52239281 | ||
The Drosophila claret segregation protein is a minus-end directed motor molecule. | Q52449568 | ||
Determinants of kinesin motor polarity. | Q52565252 | ||
The motor protein myosin-I produces its working stroke in two steps | Q56894963 | ||
Motor domains of kinesin and ncd interact with microtubule protofilaments with the same binding geometry | Q57873906 | ||
Kinetic studies of dimeric Ncd: evidence that Ncd is not processive | Q73454499 | ||
Motility of dimeric ncd on a metal-chelating surfactant: evidence that ncd is not processive | Q77357821 | ||
Equilibrium binding studies of non-claret disjunctional protein (Ncd) reveal cooperative interactions between the motor domains | Q77696902 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 724-9 | |
P577 | publication date | 2000-10-01 | |
P1433 | published in | Nature Cell Biology | Q1574111 |
P1476 | title | Working strokes by single molecules of the kinesin-related microtubule motor ncd | |
P478 | volume | 2 |
Q34313753 | A bidirectional kinesin motor in live Drosophila embryos. |
Q27663120 | A kinesin motor in a force-producing conformation |
Q33777127 | A lever-arm rotation drives motility of the minus-end-directed kinesin Ncd. |
Q33692223 | A mechanistic model for the organization of microtubule asters by motor and non-motor proteins in a mammalian mitotic extract. |
Q34698969 | Backtracking by single RNA polymerase molecules observed at near-base-pair resolution |
Q31138317 | Biased binding of single molecules and continuous movement of multiple molecules of truncated single-headed kinesin |
Q30492106 | Bidirectional membrane tube dynamics driven by nonprocessive motors |
Q34398580 | Bidirectional power stroke by ncd kinesin |
Q31134487 | Building and using optical traps to study properties of molecular motors |
Q47648869 | Changes in microtubule overlap length regulate kinesin-14-driven microtubule sliding |
Q41610112 | Common mechanistic themes for the powerstroke of kinesin-14 motors |
Q34132747 | Conformational changes during kinesin motility. |
Q35671035 | Coordination between motor domains in processive kinesins |
Q33226257 | Detection of forces and displacements along the axial direction in an optical trap |
Q55473913 | Diffusive tail anchorage determines velocity and force produced by kinesin-14 between crosslinked microtubules. |
Q34495160 | Directionality and processivity of molecular motors. |
Q39939101 | Directionality of individual kinesin-5 Cin8 motors is modulated by loop 8, ionic strength and microtubule geometry. |
Q33412379 | Dissection of kinesin's processivity |
Q35253269 | Eg5 steps it up! |
Q38052151 | Functional asymmetry in kinesin and dynein dimers |
Q35187663 | Hysteresis-based mechanism for the directed motility of the Ncd motor |
Q24669545 | Individual dimers of the mitotic kinesin motor Eg5 step processively and support substantial loads in vitro |
Q37204300 | Interrogating biology with force: single molecule high-resolution measurements with optical tweezers |
Q27681395 | Kar3Vik1, a member of the kinesin-14 superfamily, shows a novel kinesin microtubule binding pattern |
Q30539509 | Kinesin KIFC1 actively transports bare double-stranded DNA. |
Q35310192 | Kinesin Kar3Cik1 ATPase pathway for microtubule cross-linking. |
Q34182907 | Kinesins at a glance |
Q30532351 | Measuring collective transport by defined numbers of processive and nonprocessive kinesin motors |
Q30165102 | Microscopic evidence for a minus-end-directed power stroke in the kinesin motor ncd. |
Q33840045 | Microtubule organization by the antagonistic mitotic motors kinesin-5 and kinesin-14 |
Q88662698 | Mitotic kinesins in action: diffusive searching, directional switching, and ensemble coordination |
Q37843437 | Moving into the cell: single-molecule studies of molecular motors in complex environments. |
Q33568380 | Nonprocessive motor dynamics at the microtubule membrane tube interface |
Q30388659 | Optical traps to study properties of molecular motors |
Q34805354 | Probing the kinesin reaction cycle with a 2D optical force clamp |
Q44532919 | Processivity of the single-headed kinesin KIF1A through biased binding to tubulin |
Q36060057 | Regulation of bi-directional movement of single kinesin-5 Cin8 molecules |
Q33257540 | Resource Letter: LBOT-1: Laser-based optical tweezers |
Q44226110 | The ATPase cross-bridge cycle of the Kar3 motor domain. Implications for single head motility |
Q36347634 | The ATPase pathway that drives the kinesin-14 Kar3Vik1 powerstroke. |
Q24550989 | The human chromokinesin Kid is a plus end-directed microtubule-based motor |
Q27329125 | The origin of minus-end directionality and mechanochemistry of Ncd motors |
Q34822805 | Two-state displacement by the kinesin-14 Ncd stalk |
Q84918554 | Ultrafast force-clamp spectroscopy of single molecules reveals load dependence of myosin working stroke |
Q37379633 | Working stroke of the kinesin-14, ncd, comprises two substeps of different direction |
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