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Effects of age and calorie restriction on tryptophan nitration, protein content, and activity of succinyl-CoA:3-ketoacid CoA transferase in rat kidney mitochondria.

Brégère C, Rebrin I, Gallaher TK, Sohal RS.

Free Radic Biol Med. 2010 Feb 15;48(4):609-18. doi: 10.1016/j.freeradbiomed.2009.12.009. Epub 2009 Dec 16.


Nitration of tryptophan 372 in succinyl-CoA:3-ketoacid CoA transferase during aging in rat heart mitochondria.

Rebrin I, Brégère C, Kamzalov S, Gallaher TK, Sohal RS.

Biochemistry. 2007 Sep 4;46(35):10130-44. Epub 2007 Aug 8.


Nitration of succinyl-CoA:3-oxoacid CoA-transferase in rats after endotoxin administration.

Marcondes S, Turko IV, Murad F.

Proc Natl Acad Sci U S A. 2001 Jun 19;98(13):7146-51.


Diabetes-associated nitration of tyrosine and inactivation of succinyl-CoA:3-oxoacid CoA-transferase.

Turko IV, Marcondes S, Murad F.

Am J Physiol Heart Circ Physiol. 2001 Dec;281(6):H2289-94.


The nitrated proteome in heart mitochondria of the db/db mouse model: characterization of nitrated tyrosine residues in SCOT.

Wang Y, Peng F, Tong W, Sun H, Xu N, Liu S.

J Proteome Res. 2010 Aug 6;9(8):4254-63. doi: 10.1021/pr100349g.


Metallothionein prevents diabetes-induced cardiac pathological changes, likely via the inhibition of succinyl-CoA:3-ketoacid coenzyme A transferase-1 nitration at Trp(374).

Cong W, Ma W, Zhao T, Zhu Z, Wang Y, Tan Y, Li X, Jin L, Cai L.

Am J Physiol Endocrinol Metab. 2013 Apr 15;304(8):E826-35. doi: 10.1152/ajpendo.00570.2012. Epub 2013 Feb 19.


Monitoring succinyl-CoA:3-oxoacid CoA transferase nitration in mitochondria using monoclonal antibodies.

Sun H, He J, Ru Y, Yin S, Xie Y, Yin L, Wei H, Wu L, Liu S.

Biochem Biophys Res Commun. 2011 Nov 18;415(2):239-44. doi: 10.1016/j.bbrc.2011.10.014. Epub 2011 Oct 12.


Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase.

Orii KE, Fukao T, Song XQ, Mitchell GA, Kondo N.

Tohoku J Exp Med. 2008 Jul;215(3):227-36.


Lower succinyl-CoA:3-ketoacid-CoA transferase (SCOT) and ATP citrate lyase in pancreatic islets of a rat model of type 2 diabetes: knockdown of SCOT inhibits insulin release in rat insulinoma cells.

Hasan NM, Longacre MJ, Seed Ahmed M, Kendrick MA, Gu H, Ostenson CG, Fukao T, MacDonald MJ.

Arch Biochem Biophys. 2010 Jul;499(1-2):62-8. doi: 10.1016/ Epub 2010 May 9.


Successful adaptation to ketosis by mice with tissue-specific deficiency of ketone body oxidation.

Cotter DG, Schugar RC, Wentz AE, d'Avignon DA, Crawford PA.

Am J Physiol Endocrinol Metab. 2013 Feb 15;304(4):E363-74. doi: 10.1152/ajpendo.00547.2012. Epub 2012 Dec 11.


Detection and characterization of in vivo nitration and oxidation of tryptophan residues in proteins.

Bregere C, Rebrin I, Sohal RS.

Methods Enzymol. 2008;441:339-49. doi: 10.1016/S0076-6879(08)01219-6. Review.


Cloning and characterization of a human orthologue of testis-specific succinyl CoA: 3-oxo acid CoA transferase (Scot-t) cDNA.

Tanaka H, Kohroki J, Iguchi N, Onishi M, Nishimune Y.

Mol Hum Reprod. 2002 Jan;8(1):16-23.


Elevated neuronal nitric oxide synthase expression during ageing and mitochondrial energy production.

Lam PY, Yin F, Hamilton RT, Boveris A, Cadenas E.

Free Radic Res. 2009 May;43(5):431-9. doi: 10.1080/10715760902849813.


Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency.

Song XQ, Fukao T, Mitchell GA, Kassovska-Bratinova S, Ugarte M, Wanders RJ, Hirayama K, Shintaku H, Churchill P, Watanabe H, Orii T, Kondo N.

Biochim Biophys Acta. 1997 Apr 12;1360(2):151-6.


Patients homozygous for the T435N mutation of succinyl-CoA:3-ketoacid CoA Transferase (SCOT) do not show permanent ketosis.

Fukao T, Shintaku H, Kusubae R, Zhang GX, Nakamura K, Kondo M, Kondo N.

Pediatr Res. 2004 Dec;56(6):858-63. Epub 2004 Oct 20.


Detection and characterization of peroxynitrite-induced modifications of tyrosine, tryptophan, and methionine residues by tandem mass spectrometry.

Rebrin I, Bregere C, Gallaher TK, Sohal RS.

Methods Enzymol. 2008;441:283-94. doi: 10.1016/S0076-6879(08)01215-9. Review.


A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.

Shafqat N, Kavanagh KL, Sass JO, Christensen E, Fukao T, Lee WH, Oppermann U, Yue WW.

J Inherit Metab Dis. 2013 Nov;36(6):983-7. doi: 10.1007/s10545-013-9589-z. Epub 2013 Feb 19.


Differential expression of succinyl CoA transferase (SCOT) genes in somatic and germline cells of the mouse testis.

Tanaka H, Iguchi N, Miyagawa Y, Koga M, Kohroki J, Nishimune Y.

Int J Androl. 2003 Feb;26(1):52-6.


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