Literature DB >> 29290639

Protein moonlighting in inborn errors of metabolism: the case of the mitochondrial acylglycerol kinase.

Sander M Houten1.   

Abstract

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Year:  2017        PMID： 29290639      PMCID： PMC5743438          DOI： 10.1007/s10545-017-0090-y

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  6 in total

1.  Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex.

Authors:  Yilin Kang; David A Stroud; Michael J Baker; David P De Souza; Ann E Frazier; Michael Liem; Dedreia Tull; Suresh Mathivanan; Malcolm J McConville; David R Thorburn; Michael T Ryan; Diana Stojanovski
Journal:  Mol Cell       Date:  2017-07-14       Impact factor: 17.970

2.  Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria.

Authors:  Milena Vukotic; Hendrik Nolte; Tim König; Shotaro Saita; Maria Ananjew; Marcus Krüger; Takashi Tatsuta; Thomas Langer
Journal:  Mol Cell       Date:  2017-07-14       Impact factor: 17.970

3.  RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme.

Authors:  Johann Holzmann; Peter Frank; Esther Löffler; Keiryn L Bennett; Christopher Gerner; Walter Rossmanith
Journal:  Cell       Date:  2008-10-31       Impact factor: 41.582

4.  Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcripts.

Authors:  Andrea J Deutschmann; Albert Amberger; Claudia Zavadil; Herbert Steinbeisser; Johannes A Mayr; René G Feichtinger; Stephanie Oerum; Wyatt W Yue; Johannes Zschocke
Journal:  Hum Mol Genet       Date:  2014-02-18       Impact factor: 6.150

5.  2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene.

Authors:  Rob Ofman; Jos P N Ruiter; Marike Feenstra; Marinus Duran; Bwee Tien Poll-The; Johannes Zschocke; Regina Ensenauer; Willy Lehnert; Jörn Oliver Sass; Wolfgang Sperl; Ronald J A Wanders
Journal:  Am J Hum Genet       Date:  2003-04-14       Impact factor: 11.025

6.  Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome.

Authors:  Johannes A Mayr; Tobias B Haack; Elisabeth Graf; Franz A Zimmermann; Thomas Wieland; Birgit Haberberger; Andrea Superti-Furga; Janbernd Kirschner; Beat Steinmann; Matthias R Baumgartner; Isabella Moroni; Eleonora Lamantea; Massimo Zeviani; Richard J Rodenburg; Jan Smeitink; Tim M Strom; Thomas Meitinger; Wolfgang Sperl; Holger Prokisch
Journal:  Am J Hum Genet       Date:  2012-01-26       Impact factor: 11.025
  6 in total
  1 in total

1.  Protein moonlighting elucidates the essential human pathway catalyzing lipoic acid assembly on its cognate enzymes.

Authors:  Xinyun Cao; Lei Zhu; Xuejiao Song; Zhe Hu; John E Cronan
Journal:  Proc Natl Acad Sci U S A       Date:  2018-07-09       Impact factor: 11.205
  1 in total

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