...
机译:活性位点的完整性需要Mulv逆转录酶的赖氨酸152
Department of Biochemistry and Molecular Biology University of Medicine and Dentistry of New Jersey Medical School Newark New Jersey 07103;
Department of Biochemistry and Molecular Biology University of Medicine and Dentistry of New Jersey Medical School Newark New Jersey 07103;
Department of Biochemistry and Molecular Biology University of Medicine and Dentistry of New Jersey Medical School Newark New Jersey 07103;
Department of Biochemistry and Molecular Biology University of Medicine and Dentistry of New Jersey Medical School Newark New Jersey 07103;
Department of Biochemsitry and Molecular Biology University of Medicine and Dentistry of New Jersey Medical School Newark New Jersey 07103;
机译:活性位点的完整性需要Mulv逆转录酶的赖氨酸152
机译:对同型二聚体EIAV p51 / 51逆转录酶的聚合动力学分析表明,形成了与异二聚体EIAV p66 / 51逆转录酶相同的聚合酶活性位点
机译:EFDA / MK-8591的高遗传屏障源于与耐药HIV-1逆转录酶的活性位点的强相互作用
机译:HIV-1核衣壳蛋白对单分子显微镜揭示的逆转录酶停顿位点的影响
机译:研究活性位点赖氨酸在核糖核酸酶活性位点中的催化作用
机译:端粒酶逆转录酶(hTERT)基因的转录抑制需要赖氨酸特定的脱甲基酶1(LSD1)。
机译:千分比下降至DNTPS是在一步RT-PCR测定中进行有效的cDNA合成所需的必要性M-Mulv逆转录酶采用