Sequence of AGK_HUMAN

ceramide kinase

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The DNA sequence of human chromosome 7.

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The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Genome Res.

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Bektas M.,Payne S.G.,Liu H.,Goparaju S.,Milstien S.,Spiegel S.

A novel acylglycerol kinase that produces lysophosphatidic acid modulates cross talk with EGFR in prostate cancer cells.

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Choudhary C.,Kumar C.,Gnad F.,Nielsen M.L.,Rehman M.,Walther T.C.,Olsen J.V.,Mann M.

Lysine acetylation targets protein complexes and co-regulates major cellular functions.

Science

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Burkard T.R.,Planyavsky M.,Kaupe I.,Breitwieser F.P.,Buerckstuemmer T.,Bennett K.L.,Superti-Furga G.,Colinge J.

Initial characterization of the human central proteome.

BMC Syst. Biol.

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Mayr J.A.,Haack T.B.,Graf E.,Zimmermann F.A.,Wieland T.,Haberberger B.,Superti-Furga A.,Kirschner J.,Steinmann B.,Baumgartner M.R.,Moroni I.,Lamantea E.,Zeviani M.,Rodenburg R.J.,Smeitink J.,Strom T.M.,Meitinger T.,Sperl W.,Prokisch H.

Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome.

Am. J. Hum. Genet.

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3068

Aldahmesh M.A.,Khan A.O.,Mohamed J.Y.,Alghamdi M.H.,Alkuraya F.S.

Identification of a truncation mutation of acylglycerol kinase (AGK) gene in a novel autosomal recessive cataract locus.

Hum. Mutat.

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3069

Van Damme P.,Lasa M.,Polevoda B.,Gazquez C.,Elosegui-Artola A.,Kim D.S.,De Juan-Pardo E.,Demeyer K.,Hole K.,Larrea E.,Timmerman E.,Prieto J.,Arnesen T.,Sherman F.,Gevaert K.,Aldabe R.

N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.

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Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.

Sci. Transl. Med.

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Bian Y.,Song C.,Cheng K.,Dong M.,Wang F.,Huang J.,Sun D.,Wang L.,Ye M.,Zou H.

An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

J. Proteomics

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Vaca Jacome A.S.,Rabilloud T.,Schaeffer-Reiss C.,Rompais M.,Ayoub D.,Lane L.,Bairoch A.,Van Dorsselaer A.,Carapito C.

N-terminome analysis of the human mitochondrial proteome.

Proteomics

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Vukotic M.,Nolte H.,Koenig T.,Saita S.,Ananjew M.,Krueger M.,Tatsuta T.,Langer T.

Acylglycerol kinase mutated in Sengers Syndrome is a subunit of the TIM22 protein translocase in mitochondria.

Mol. Cell

0

0-0

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3074

Kang Y.,Stroud D.A.,Baker M.J.,De Souza D.P.,Frazier A.E.,Liem M.,Tull D.,Mathivanan S.,McConville M.J.,Thorburn D.R.,Ryan M.T.,Stojanovski D.

Sengers syndrome-associated mitochondrial acylglycerol kinase is a subunit of the human TIM22 protein import complex.

Mol. Cell

0

0-0

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Siriwardena K.,Mackay N.,Levandovskiy V.,Blaser S.,Raiman J.,Kantor P.F.,Ackerley C.,Robinson B.H.,Schulze A.,Cameron J.M.

Mitochondrial citrate synthase crystals: novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations.

Mol. Genet. Metab.

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Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients.

Orphanet J. Rare Dis.

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2014