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-Structure paper
タイトル | Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome |
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ジャーナル・号・ページ | Year 2019 Dec |
掲載日 | 2017年3月26日 (データ計測日) |
![]() | Arrondel 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 |
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手法 | SAS (X-ray synchrotron) |
構造データ | ![]() SASDFK8: GON7, the fifth subunit of human KEOPS (EKC/KEOPS complex subunit GON7, GON7) ![]() SASDFL8: ![]() SASDFM8: GON7, the fifth subunit of human KEOPS, bound to the EKC/KEOPS complex subunit, LAGE3 |
由来 |
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