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Comparative analysis of pyrimidine substituted aminoacyl-sulfamoyl nucleosides as potential inhibitors targeting class I aminoacyl-tRNA synthetases

机译：嘧啶取代的氨基酰基 - 磺酰核苷的对比分析为靶向I类氨基酰基-TRNA合成酶的潜在抑制剂

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Manesh Nautiyal; Steff De Graef; Luping Pang; Bharat Gadakh; Sergei V. Strelkov; Stephen D. Weeks; Arthur Van Aerschot;
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年度 2019
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1. Comparative analysis of pyrimidine substituted aminoacyl-sulfamoyl nucleosides as potential inhibitors targeting class I aminoacyl-tRNA synthetases [J] . Nautiyal Manesh, De Graef Steff, Pang Luping, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2019,第期

机译：嘧啶取代的氨基酰基 - 磺酰核苷的对比分析为靶向I类氨基酰基-TRNA合成酶的潜在抑制剂
2. Structural Insights into the Binding of Natural Pyrimidine-Based Inhibitors of Class II Aminoacyl-tRNA Synthetases [J] . Pang Luping, Nautiyal Manesh, De Graef Steff, ACS Chemical Biology . 2020,第2期

机译：结构洞察II类氨基酰基-TRNA合成酶的天然嘧啶基抑制剂的结合
3. Six Rossmannoid folds, including the Class I aminoacyl-tRNA synthetases, share a partial core with the anti-codon-binding domain of a Class II aminoacyl-tRNA synthetase [J] . Cammer, Stephen, Carter, Charles W. Jr. Bioinformatics . 2010,第6期

机译：六类Rossmannoid折叠，包括I类氨酰基-tRNA合成酶，与II类氨酰基-tRNA合成酶的反密码子结合域共享部分核心
4. Electrochemical Impedance Evaluation of Uracil and Thymine Pyrimidine Derivatives and its Nucleosides Compounds as a Non-toxic Corrosion Inhibitors of Steels in 1M HCl [C] . Araceli Espinoza-Vazquez, Guillermo E. Negron-Silva, Deyanira Angeles Beltran, MES 26: Electrochemistry as a tool for sustainable development . 2011

机译：尿嘧啶和胸腺嘧啶嘧啶衍生物及其核苷化合物作为钢在1M HCl中的无毒腐蚀抑制剂的电化学阻抗评估
5. Histidine triad nucleotide binding proteins (Hints): Nucleoside phosphoramidases and potential regulators of aminoacyl-tRNA synthetases [D] . Chou, Tsui-Fen. 2006

机译：组氨酸三联体核苷酸结合蛋白（提示）：核苷磷酸酰胺酶和氨基酰基-tRNA合成酶的潜在调节剂
6. Six Rossmannoid folds including the Class I aminoacyl-tRNA synthetases share a partial core with the anti-codon-binding domain of a Class II aminoacyl-tRNA synthetase [O] . Stephen Cammer, Charles W. Carter Jr -1

机译：六类Rossmannoid折叠包括I类氨酰基-tRNA合成酶与II类氨酰基-tRNA合成酶的反密码子结合域共享部分核心
7. Structural Insights into the Binding of Natural Pyrimidine-Based Inhibitors of Class II Aminoacyl-tRNA Synthetases [O] . -1

机译：结构见解阶层氨基酰基-TRNA合成酶的天然嘧啶抑制剂的结合

Comparative analysis of pyrimidine substituted aminoacyl-sulfamoyl nucleosides as potential inhibitors targeting class I aminoacyl-tRNA synthetases

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