Modolell J, Cabrer B, Parmeggiani A, Vazquez D
Proc Natl Acad Sci U S A. 1971 Aug;68(8):1796-800. doi: 10.1073/pnas.68.8.1796.
Siomycin, a peptide antibiotic that interacts with the 50S ribosomal subunit and inhibits binding of factor G, is shown also to inhibit binding of aminoacyl-tRNA; however, it does not impair binding of fMet-tRNA and completion of the initiation complex. Moreover, unlike other inhibitors of aminoacyl-tRNA binding (tetracycline, sparsomycin, and streptogramin A), siomycin completely abolishes the GTPase activity associated with the binding of aminoacyl-tRNA catalyzed by factor T(u). A single-site interaction of siomycin appears to be responsible for its effect on both the binding of the aminoacyl-tRNA-T(u)-GTP complex and that of factor G.
西霉素是一种与50S核糖体亚基相互作用并抑制因子G结合的肽抗生素,它还被证明能抑制氨酰基-tRNA的结合;然而,它并不损害甲酰甲硫氨酰-tRNA的结合以及起始复合物的形成。此外,与其他氨酰基-tRNA结合抑制剂(四环素、稀疏霉素和链阳性菌素A)不同,西霉素完全消除了与因子T(u)催化的氨酰基-tRNA结合相关的GTPase活性。西霉素的单点相互作用似乎是其对氨酰基-tRNA-T(u)-GTP复合物和因子G结合产生影响的原因。