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Items: 19

1.

Rab6 regulation of the kinesin family KIF1C motor domain contributes to Golgi tethering.

Lee PL, Ohlson MB, Pfeffer SR.

Elife. 2015 Mar 30;4. doi: 10.7554/eLife.06029.

2.

Catalytic strategy used by the myosin motor to hydrolyze ATP.

Kiani FA, Fischer S.

Proc Natl Acad Sci U S A. 2014 Jul 22;111(29):E2947-56. doi: 10.1073/pnas.1401862111. Epub 2014 Jul 8.

3.

Robustness of the rotary catalysis mechanism of F1-ATPase.

Watanabe R, Matsukage Y, Yukawa A, Tabata KV, Noji H.

J Biol Chem. 2014 Jul 11;289(28):19331-40. doi: 10.1074/jbc.M114.569905. Epub 2014 May 29.

4.

Stabilization of the ADP/metaphosphate intermediate during ATP hydrolysis in pre-power stroke myosin: quantitative anatomy of an enzyme.

Kiani FA, Fischer S.

J Biol Chem. 2013 Dec 6;288(49):35569-80. doi: 10.1074/jbc.M113.500298. Epub 2013 Oct 28.

5.

Myosin-1c regulates the dynamic stability of E-cadherin-based cell-cell contacts in polarized Madin-Darby canine kidney cells.

Tokuo H, Coluccio LM.

Mol Biol Cell. 2013 Sep;24(18):2820-33. doi: 10.1091/mbc.E12-12-0884. Epub 2013 Jul 17.

6.

Mammalian myosin-18A, a highly divergent myosin.

Guzik-Lendrum S, Heissler SM, Billington N, Takagi Y, Yang Y, Knight PJ, Homsher E, Sellers JR.

J Biol Chem. 2013 Mar 29;288(13):9532-48. doi: 10.1074/jbc.M112.441238. Epub 2013 Feb 4.

7.

Cargo binding activates myosin VIIA motor function in cells.

Sakai T, Umeki N, Ikebe R, Ikebe M.

Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):7028-33. doi: 10.1073/pnas.1009188108. Epub 2011 Apr 11.

8.

A hearing loss-associated myo1c mutation (R156W) decreases the myosin duty ratio and force sensitivity.

Lin T, Greenberg MJ, Moore JR, Ostap EM.

Biochemistry. 2011 Mar 22;50(11):1831-8. doi: 10.1021/bi1016777. Epub 2011 Feb 15.

9.

Myo1c mutations associated with hearing loss cause defects in the interaction with nucleotide and actin.

Adamek N, Geeves MA, Coluccio LM.

Cell Mol Life Sci. 2011 Jan;68(1):139-50. doi: 10.1007/s00018-010-0448-x. Epub 2010 Jul 17.

10.

Insights into the importance of hydrogen bonding in the gamma-phosphate binding pocket of myosin: structural and functional studies of serine 236.

Frye JJ, Klenchin VA, Bagshaw CR, Rayment I.

Biochemistry. 2010 Jun 15;49(23):4897-907. doi: 10.1021/bi1001344.

11.

Switch 1 mutation S217A converts myosin V into a low duty ratio motor.

Forgacs E, Sakamoto T, Cartwright S, Belknap B, Kovács M, Tóth J, Webb MR, Sellers JR, White HD.

J Biol Chem. 2009 Jan 23;284(4):2138-49. doi: 10.1074/jbc.M805530200. Epub 2008 Nov 12.

12.

Impacts of Usher syndrome type IB mutations on human myosin VIIa motor function.

Watanabe S, Umeki N, Ikebe R, Ikebe M.

Biochemistry. 2008 Sep 9;47(36):9505-13. doi: 10.1021/bi8007142. Epub 2008 Aug 13.

13.

Extensive conformational transitions are required to turn on ATP hydrolysis in myosin.

Yang Y, Yu H, Cui Q.

J Mol Biol. 2008 Sep 19;381(5):1407-20. doi: 10.1016/j.jmb.2008.06.071. Epub 2008 Jul 1.

14.
15.

Molecular dynamics analysis of structural factors influencing back door pi release in myosin.

Lawson JD, Pate E, Rayment I, Yount RG.

Biophys J. 2004 Jun;86(6):3794-803.

16.

Theoretical studies of the ATP hydrolysis mechanism of myosin.

Okimoto N, Yamanaka K, Ueno J, Hata M, Hoshino T, Tsuda M.

Biophys J. 2001 Nov;81(5):2786-94.

17.

Myosin I mutants with only 1% of wild-type actin-activated MgATPase activity retain essential in vivo function(s).

Liu X, Osherov N, Yamashita R, Brzeska H, Korn ED, May GS.

Proc Natl Acad Sci U S A. 2001 Jul 31;98(16):9122-7. Epub 2001 Jul 17.

18.

On the tryptophan residue of smooth muscle myosin that responds to binding of nucleotide.

Onishi H, Konishi K, Fujiwara K, Hayakawa K, Tanokura M, Martinez HM, Morales MF.

Proc Natl Acad Sci U S A. 2000 Oct 10;97(21):11203-8.

19.
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