Protein O-GlcNAcylation: emerging mechanisms and functions (vol 18, pg 452, 2017)
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作者:
Yang, Xiaoyong
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机构:Program in Integrative Cell Signaling and Neurobiology of Metabolism, Department of Comparative Medicine, Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, 06510, CT
Yang, Xiaoyong
Qian, Kevin
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机构:Program in Integrative Cell Signaling and Neurobiology of Metabolism, Department of Comparative Medicine, Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, 06510, CT
Qian, Kevin
机构:
[1] Program in Integrative Cell Signaling and Neurobiology of Metabolism, Department of Comparative Medicine, Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, 06510, CT
O-GlcNAcylation-the attachment of O-linked N-acetylglucosamine (O-GlcNAc) moieties to cytoplasmic, nuclear and mitochondrial proteins - is a post-translational modification that regulates fundamental cellular processes in metazoans. A single pair of enzymes - O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA) - controls the dynamic cycling of this protein modification in a nutrient-and stress-responsive manner. Recent years have seen remarkable advances in our understanding of O-GlcNAcylation at levels that range from structural and molecular biology to cell signalling and gene regulation to physiology and disease. New mechanisms and functions of O-GlcNAcylation that are emerging from these recent developments enable us to begin constructing a unified conceptual framework through which the significance of this modification in cellular and organismal physiology can be understood.
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Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USAUniv Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
Zhang, Jianchao
Wang, Yanzhuang
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Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
Univ Michigan, Sch Med, Dept Neurol, Ann Arbor, MI 48109 USAUniv Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
机构:
Univ Dundee, Div Biol Chem & Drug Discovery, Coll Life Sci, Dundee DD1 5EH, ScotlandUniv Dundee, Div Biol Chem & Drug Discovery, Coll Life Sci, Dundee DD1 5EH, Scotland
Hurtado-Guerrero, Ramon
Dorfmueller, Helge C.
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Univ Dundee, Div Biol Chem & Drug Discovery, Coll Life Sci, Dundee DD1 5EH, ScotlandUniv Dundee, Div Biol Chem & Drug Discovery, Coll Life Sci, Dundee DD1 5EH, Scotland
Dorfmueller, Helge C.
Van Aalten, Daan Mf
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Univ Dundee, Div Biol Chem & Drug Discovery, Coll Life Sci, Dundee DD1 5EH, ScotlandUniv Dundee, Div Biol Chem & Drug Discovery, Coll Life Sci, Dundee DD1 5EH, Scotland
机构:
Yonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South KoreaYonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South Korea
Kim, Eunah
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Kang, Jeong Gu
Jho, Eek-hoon
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Yonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South Korea
Univ Seoul, Dept Life Sci, 163 Seoulsiripdae Ro, Seoul 02504, South KoreaYonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South Korea
Jho, Eek-hoon
Yang, Won Ho
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Yonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South Korea
Yonsei Univ, Coll Life Sci & Biotechnol, Dept Syst Biol, 50 Yonsei Ro, Seoul 03722, South KoreaYonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South Korea
Yang, Won Ho
Cho, Jin Won
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Yonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South KoreaYonsei Univ, Glycosylat Network Res Ctr, 50 Yonsei Ro, Seoul 03722, South Korea