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TitleDefects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
Journal, issue, pagesYear 2019 Dec
Publish dateMar 26, 2017 (data collection date)
AuthorsArrondel C / Missoury S / Snoek R / Patat J / Menara G / Collinet B / Liger D / Durand D / Gribouval O / Boyer O ...Arrondel C / Missoury S / Snoek R / Patat J / Menara G / Collinet B / Liger D / Durand D / Gribouval O / Boyer O / Buscara L / Martin G / Machuca E / Nevo F / Lescop E / Braun D / Boschat A / Sanquer S / Guerrera I / Revy P / Parisot M / Masson C / Boddaert N / Charbit M / Decramer S / Novo R / Macher M / Ranchin B / Bacchetta J / Laurent A / Collardeau-Frachon S / van Eerde A / Hildebrandt F / Magen D / Antignac C / van Tilbeurgh H
External linksPublisher's page / Search PubMed
MethodsSAS (X-ray synchrotron)
Structure data

SASDFK8: GON7, the fifth subunit of human KEOPS (EKC/KEOPS complex subunit GON7, GON7)
Method: SAXS/SANS

SASDFL8:
GON7, the fifth subunit of human KEOPS, bound to LAGE3-OSGEP (EKC/KEOPS complex subunit:Probable tRNA N6-adenosine threonylcarbamoyltransferase)
Method: SAXS/SANS

SASDFM8: GON7, the fifth subunit of human KEOPS, bound to the EKC/KEOPS complex subunit, LAGE3
Method: SAXS/SANS

Source
  • Homo sapiens (human)

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