Structural analyses of a human lysyl-tRNA synthetase mutant associated with autosomal recessive nonsyndromic hearing impairment.
第一作者:
Siqi,Wu
第一单位:
State Key Laboratory of Bioorganic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China.
作者:
主题词
氨基酰化(Aminoacylation);反密码子(Anticodon);结晶学, X线(Crystallography, X-Ray);聋(Deafness);疾病遗传易感性(Genetic Predisposition to Disease);人类(Humans);赖氨酸tRNA连接酶(Lysine-tRNA Ligase);线粒体(Mitochondria);突变蛋白质类(Mutant Proteins);突变(Mutation);蛋白质生物合成(Protein Biosynthesis);RNA, 转移(RNA, Transfer)
DOI
10.1016/j.bbrc.2021.03.093
PMID
33784510
发布时间
2021-07-12
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