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Molecular Basis for Multiple Sulfatase Deficiency and Mechanism for Formylglycine Generation of the Human Formylglycine-Generating Enzyme

机译：多种硫酸酯酶缺乏的分子基础和人类甲酰甘氨酸生成酶的甲酰甘氨酸生成机理。

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Dierks Thomas; Dickmanns Achim; Preusser-Kunze Andrea; Schmidt Bernhard; Mariappan Malaiyalam; von Figura Kurt; Ficner Ralf; Rudolph Markus Georg;
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1. Structural distortions due to missense mutations in human formylglycine-generating enzyme leading to multiple sulfatase deficiency [J] . Meshach Paul D, Tania Chadah, Senthilkumar B, Journal of Biomolecular Structure and Dynamics . 2018,第13a14期

机译：人甲酰甘氨酸生成酶中的畸形突变引起的结构扭曲导致多种硫酸酶缺乏
2. Rapid degradation of an active formylglycine generating enzyme variant leads to a late infantile severe form of multiple sulfatase deficiency [J] . SchlotawaL., RadhakrishnanK., BaumgartnerM., European journal of human genetics: EJHG . 2013,第9期

机译：活性甲酰基甘氨酸生成酶变异体的快速降解导致晚期婴幼儿严重的多种硫酸酯酶缺乏症
3. SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency. [J] . Schlotawa L, Ennemann EC, Radhakrishnan K, European journal of human genetics: EJHG . 2011,第3期

机译：SUMF1突变影响甲酰甘氨酸生成酶的稳定性和活性，预测多种硫酸酯酶缺乏症的临床结果。
4. The Molecular Basis of Common HDL Deficiency States [C] . World Association for Laser Therapy . 2002

机译：常见HDL缺乏态的分子基础
5. Sulfatases and the formylglycine generating enzyme applications in protein engineering. [D] . Rush, Jason Samuel. 2009

机译：硫酸酯酶和甲酰甘氨酸生成酶在蛋白质工程中的应用。
6. A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme [O] . Dirk Roeser, Andrea Preusser-Kunze, Bernhard Schmidt, 2006

机译：甲酰基甘氨酸生成酶对所有人类硫酸酯酶的一般结合机制
7. Molecular analysis ofSUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency [O] . Lars Schlotawa, Robert Steinfeld, Kurt von Figura, 2007

机译：Sumf1突变的分子分析：突变型甲酰基甘氨酸生成酶的稳定性和残留活性确定多种硫酸酶缺乏的疾病严重程度
8. Regulation of 4F2 Heavy-Chain Gene Expression during Normal Human T-Cell Activation Can Be Mediated by Multiple Distinct Molecular Mechanisms [R] . Lindsten, T., June, C. H., Thompson, C. B., 1988

机译：正常人T细胞活化过程中4F2重链基因表达的调节可以通过多种不同的分子机制介导

Molecular Basis for Multiple Sulfatase Deficiency and Mechanism for Formylglycine Generation of the Human Formylglycine-Generating Enzyme

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