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Items: 1 to 20 of 90

1.

The human chromokinesin Kid is a plus end-directed microtubule-based motor.

Yajima J, Edamatsu M, Watai-Nishii J, Tokai-Nishizumi N, Yamamoto T, Toyoshima YY.

EMBO J. 2003 Mar 3;22(5):1067-74.

2.

The second microtubule-binding site of monomeric kid enhances the microtubule affinity.

Shiroguchi K, Ohsugi M, Edamatsu M, Yamamoto T, Toyoshima YY.

J Biol Chem. 2003 Jun 20;278(25):22460-5. Epub 2003 Apr 12.

3.

Microtubule movements on the arms of mitotic chromosomes: polar ejection forces quantified in vitro.

Brouhard GJ, Hunt AJ.

Proc Natl Acad Sci U S A. 2005 Sep 27;102(39):13903-8. Epub 2005 Sep 20.

4.
6.

The spindle protein CHICA mediates localization of the chromokinesin Kid to the mitotic spindle.

Santamaria A, Nagel S, Sillje HH, Nigg EA.

Curr Biol. 2008 May 20;18(10):723-9. doi: 10.1016/j.cub.2008.04.041.

7.

NuSAP governs chromosome oscillation by facilitating the Kid-generated polar ejection force.

Li C, Xue C, Yang Q, Low BC, Liou YC.

Nat Commun. 2016 Feb 3;7:10597. doi: 10.1038/ncomms10597.

8.

Kid, a novel kinesin-like DNA binding protein, is localized to chromosomes and the mitotic spindle.

Tokai N, Fujimoto-Nishiyama A, Toyoshima Y, Yonemura S, Tsukita S, Inoue J, Yamamota T.

EMBO J. 1996 Feb 1;15(3):457-67.

9.

The chromokinesin Kid is required for maintenance of proper metaphase spindle size.

Tokai-Nishizumi N, Ohsugi M, Suzuki E, Yamamoto T.

Mol Biol Cell. 2005 Nov;16(11):5455-63. Epub 2005 Sep 21.

10.

A processive single-headed motor: kinesin superfamily protein KIF1A.

Okada Y, Hirokawa N.

Science. 1999 Feb 19;283(5405):1152-7.

11.

A kinesin-like motor inhibits microtubule dynamic instability.

Bringmann H, Skiniotis G, Spilker A, Kandels-Lewis S, Vernos I, Surrey T.

Science. 2004 Mar 5;303(5663):1519-22.

12.

Arabidopsis thaliana protein, ATK1, is a minus-end directed kinesin that exhibits non-processive movement.

Marcus AI, Ambrose JC, Blickley L, Hancock WO, Cyr RJ.

Cell Motil Cytoskeleton. 2002 Jul;52(3):144-50.

PMID:
12112142
13.

A functional relationship between NuMA and kid is involved in both spindle organization and chromosome alignment in vertebrate cells.

Levesque AA, Howard L, Gordon MB, Compton DA.

Mol Biol Cell. 2003 Sep;14(9):3541-52. Epub 2003 Jun 13.

14.

Protein friction limits diffusive and directed movements of kinesin motors on microtubules.

Bormuth V, Varga V, Howard J, Schäffer E.

Science. 2009 Aug 14;325(5942):870-3. doi: 10.1126/science.1174923.

15.

Kinetic and mechanistic basis of the nonprocessive Kinesin-3 motor NcKin3.

Adio S, Bloemink M, Hartel M, Leier S, Geeves MA, Woehlke G.

J Biol Chem. 2006 Dec 8;281(49):37782-93. Epub 2006 Oct 1.

16.

Kinetic studies of dimeric Ncd: evidence that Ncd is not processive.

Foster KA, Gilbert SP.

Biochemistry. 2000 Feb 22;39(7):1784-91.

PMID:
10677228
17.

The microtubule-binding and coiled-coil domains of Kid are required to turn off the polar ejection force at anaphase.

Soeda S, Yamada-Nomoto K, Ohsugi M.

J Cell Sci. 2016 Oct 1;129(19):3609-3619. Epub 2016 Aug 22.

18.

Decoupling of nucleotide- and microtubule-binding sites in a kinesin mutant.

Song H, Endow SA.

Nature. 1998 Dec 10;396(6711):587-90.

PMID:
9859995
19.

Temperature dependence of force, velocity, and processivity of single kinesin molecules.

Kawaguchi K, Ishiwata S.

Biochem Biophys Res Commun. 2000 Jun 16;272(3):895-9.

PMID:
10860848
20.

A non-motor microtubule binding site is essential for the high processivity and mitotic function of kinesin-8 Kif18A.

Mayr MI, Storch M, Howard J, Mayer TU.

PLoS One. 2011;6(11):e27471. doi: 10.1371/journal.pone.0027471. Epub 2011 Nov 10.

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