| 1 | MSUDMV, PPM1K
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| A novel regulatory defect in the branched-chain α-keto acid dehydrogenase complex due to a mutation in the PPM1K gene causes a mild variant phenotype of maple syrup urine disease.
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| Oyarzabal A, Martínez-Pardo M, Merinero B, Navarrete R, Desviat LR, Ugarte M, Rodríguez-Pombo P.
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| Hum Mutat 34(2):355-62. doi: 10.1002/humu.22242. Epub 2012 Dec 12.
2013
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| 2 | PPM1K
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| Tissue-specific and nutrient regulation of the branched-chain α-keto acid dehydrogenase phosphatase, protein phosphatase 2Cm (PP2Cm).
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| Zhou M, Lu G, Gao C, Wang Y, Sun H.
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| J Biol Chem 287(28):23397-406. doi: 10.1074/jbc.M112.351031. Epub 2012 May 15.
2012
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| 3 | PPM1K
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| Structural and biochemical characterization of human mitochondrial branched-chain α-ketoacid dehydrogenase phosphatase.
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| Wynn RM, Li J, Brautigam CA, Chuang JL, Chuang DT.
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| J Biol Chem 287(12):9178-92. doi: 10.1074/jbc.M111.314963. Epub 2012 Jan 30.
2012
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| 4 | PPM1K
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| Identification of a novel PP2C-type mitochondrial phosphatase.
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| Joshi M, Jeoung NH, Popov KM, Harris RA.
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| Biochem Biophys Res Commun 356(1):38-44. Epub 2007 Feb 28. Erratum in: Biochem Biophys Res Commun. 2007 Oct 5;361(4):1061.
2007
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| 5 | PPM1K
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| Characterization of a novel human protein phosphatase 2C family member, PP2Ckappa.
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| Dai J, Zhang J, Sun Y, Wu Q, Sun L, Ji C, Gu S, Feng C, Xie Y, Mao Y.
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| Int J Mol Med 17(6):1117-23.
2006
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