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Items: 14


Parkin-mediated ubiquitylation redistributes MITOL/March5 from mitochondria to peroxisomes.

Koyano F, Yamano K, Kosako H, Kimura Y, Kimura M, Fujiki Y, Tanaka K, Matsuda N.

EMBO Rep. 2019 Oct 10:e47728. doi: 10.15252/embr.201947728. [Epub ahead of print]


Parkin recruitment to impaired mitochondria for nonselective ubiquitylation is facilitated by MITOL.

Koyano F, Yamano K, Kosako H, Tanaka K, Matsuda N.

J Biol Chem. 2019 Jun 28;294(26):10300-10314. doi: 10.1074/jbc.RA118.006302. Epub 2019 May 20.


Parkinson's disease-related DJ-1 functions in thiol quality control against aldehyde attack in vitro.

Matsuda N, Kimura M, Queliconi BB, Kojima W, Mishima M, Takagi K, Koyano F, Yamano K, Mizushima T, Ito Y, Tanaka K.

Sci Rep. 2017 Oct 9;7(1):12816. doi: 10.1038/s41598-017-13146-0.


Unexpected mitochondrial matrix localization of Parkinson's disease-related DJ-1 mutants but not wild-type DJ-1.

Kojima W, Kujuro Y, Okatsu K, Bruno Q, Koyano F, Kimura M, Yamano K, Tanaka K, Matsuda N.

Genes Cells. 2016 Jul;21(7):772-88. doi: 10.1111/gtc.12382. Epub 2016 Jun 8. Erratum in: Genes Cells. 2017 Jan;22(1):124.


Site-specific Interaction Mapping of Phosphorylated Ubiquitin to Uncover Parkin Activation.

Yamano K, Queliconi BB, Koyano F, Saeki Y, Hirokawa T, Tanaka K, Matsuda N.

J Biol Chem. 2015 Oct 16;290(42):25199-211. doi: 10.1074/jbc.M115.671446. Epub 2015 Aug 10.


Phosphorylated ubiquitin chain is the genuine Parkin receptor.

Okatsu K, Koyano F, Kimura M, Kosako H, Saeki Y, Tanaka K, Matsuda N.

J Cell Biol. 2015 Apr 13;209(1):111-28. doi: 10.1083/jcb.201410050. Epub 2015 Apr 6.


Molecular mechanisms underlying PINK1 and Parkin catalyzed ubiquitylation of substrates on damaged mitochondria.

Koyano F, Matsuda N.

Biochim Biophys Acta. 2015 Oct;1853(10 Pt B):2791-6. doi: 10.1016/j.bbamcr.2015.02.009. Epub 2015 Feb 18. Review.


[How E3 activity of Parkin is enhanced by damaged mitochondria].

Koyano F, Matsuda N.

Seikagaku. 2014 Oct;86(5):676-82. Review. Japanese. No abstract available.


Ubiquitin is phosphorylated by PINK1 to activate parkin.

Koyano F, Okatsu K, Kosako H, Tamura Y, Go E, Kimura M, Kimura Y, Tsuchiya H, Yoshihara H, Hirokawa T, Endo T, Fon EA, Trempe JF, Saeki Y, Tanaka K, Matsuda N.

Nature. 2014 Jun 5;510(7503):162-6. doi: 10.1038/nature13392. Epub 2014 Jun 4.


A dimeric PINK1-containing complex on depolarized mitochondria stimulates Parkin recruitment.

Okatsu K, Uno M, Koyano F, Go E, Kimura M, Oka T, Tanaka K, Matsuda N.

J Biol Chem. 2013 Dec 20;288(51):36372-84. doi: 10.1074/jbc.M113.509653. Epub 2013 Nov 4.


Parkin-catalyzed ubiquitin-ester transfer is triggered by PINK1-dependent phosphorylation.

Iguchi M, Kujuro Y, Okatsu K, Koyano F, Kosako H, Kimura M, Suzuki N, Uchiyama S, Tanaka K, Matsuda N.

J Biol Chem. 2013 Jul 26;288(30):22019-32. doi: 10.1074/jbc.M113.467530. Epub 2013 Jun 10.


The principal PINK1 and Parkin cellular events triggered in response to dissipation of mitochondrial membrane potential occur in primary neurons.

Koyano F, Okatsu K, Ishigaki S, Fujioka Y, Kimura M, Sobue G, Tanaka K, Matsuda N.

Genes Cells. 2013 Aug;18(8):672-81. doi: 10.1111/gtc.12066. Epub 2013 Jun 10.


Mitochondrial hexokinase HKI is a novel substrate of the Parkin ubiquitin ligase.

Okatsu K, Iemura S, Koyano F, Go E, Kimura M, Natsume T, Tanaka K, Matsuda N.

Biochem Biophys Res Commun. 2012 Nov 9;428(1):197-202. doi: 10.1016/j.bbrc.2012.10.041. Epub 2012 Oct 13.


PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria.

Okatsu K, Oka T, Iguchi M, Imamura K, Kosako H, Tani N, Kimura M, Go E, Koyano F, Funayama M, Shiba-Fukushima K, Sato S, Shimizu H, Fukunaga Y, Taniguchi H, Komatsu M, Hattori N, Mihara K, Tanaka K, Matsuda N.

Nat Commun. 2012;3:1016. doi: 10.1038/ncomms2016.

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