一种碳环嘌呤霉素类似物对体外蛋白质合成的抑制作用。 - Suppr

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超能文献

Inhibition of in vitro protein synthesis by a carbocyclic puromycin analog.

作者信息

Vince R, Daluge S, Palm M

出版信息

Biochem Biophys Res Commun. 1972 Jan 31;46(2):866-70. doi: 10.1016/s0006-291x(72)80221-3.

DOI:10.1016/s0006-291x(72)80221-3

PMID:4550700

Abstract

摘要

相似文献

Inhibition of in vitro protein synthesis by a carbocyclic puromycin analog.一种碳环嘌呤霉素类似物对体外蛋白质合成的抑制作用。

Biochem Biophys Res Commun. 1972 Jan 31;46(2):866-70. doi: 10.1016/s0006-291x(72)80221-3.

Reversibility of chloramphenicol inhibition of the poly U directed polyphenylalanine synthesis by G factor and GTP.氯霉素对多聚尿嘧啶指导的聚苯丙氨酸合成的抑制作用可被G因子和鸟苷三磷酸逆转。

Biochem Biophys Res Commun. 1970 Sep 30;40(6):1331-9. doi: 10.1016/0006-291x(70)90012-4.

A cell-free amino acid incorporating system from Azotobacter vinelandii.一种来自棕色固氮菌的无细胞氨基酸掺入系统。

Arch Biochem Biophys. 1969 Jan;129(1):228-41. doi: 10.1016/0003-9861(69)90170-2.

[Specific and non-specific inhibition of cell-free protein synthesis with polyanions].[多聚阴离子对无细胞蛋白质合成的特异性和非特异性抑制作用]

Z Naturforsch B. 1967 Apr;22(4):413-7.

Protein-deficient ribosomes in chloramphenicol-treated Escherichia coli.氯霉素处理的大肠杆菌中蛋白质缺乏的核糖体。

Nature. 1970 Aug 8;227(5258):604-6. doi: 10.1038/227604a0.

Puromycin analogs. Studies on ribosomal binding with diastereomeric carbocyclic puromycin analogs.

J Med Chem. 1974 Jun;17(6):578-83. doi: 10.1021/jm00252a003.

Studies on the formation of transfer ribonucleic acid-ribosome complexes. 23. Chloramphenicol, aminoacyl-oligonucleotides, and Escherichia coli ribosomes.转移核糖核酸-核糖体复合物形成的研究。23. 氯霉素、氨酰寡核苷酸与大肠杆菌核糖体

J Biol Chem. 1972 Nov 10;247(21):6909-12.

Enhancement of the phenylalanyl-oligonucleotide binding to the peptidyl recognition center of ribosomal peptidyltransferase and inhibition of the chloramphenicol binding to ribosomes.苯丙氨酰-寡核苷酸与核糖体肽基转移酶的肽基识别中心结合增强，氯霉素与核糖体的结合受到抑制。

Biochim Biophys Acta. 1971 Dec 16;254(2):304-15. doi: 10.1016/0005-2787(71)90839-2.

The formation and stabilization of 30S and 50S ribosome couples in Escherichia coli.大肠杆菌中30S和50S核糖体偶联物的形成与稳定

Proc Natl Acad Sci U S A. 1967 Oct;58(4):1782-9. doi: 10.1073/pnas.58.4.1782.

Studies on the formation of transfer ribonucleic acid-ribosome complexes. IV. Effect of antibiotics on steps of bacterial protein synthesis: some new ribosomal inhibitors of translocation.转运核糖核酸-核糖体复合物形成的研究。IV. 抗生素对细菌蛋白质合成步骤的影响：一些新的转位核糖体抑制剂。

J Biol Chem. 1971 Dec 25;246(24):7715-22.

引用本文的文献

Amino acid esters of 9-(2',3'-dihydroxypropyl-1')-adenine are the specific inhibitors of protein synthesis on ribosomes.9-(2',3'-二羟丙基-1')-腺嘌呤的氨基酸酯是核糖体上蛋白质合成的特异性抑制剂。

Mol Biol Rep. 1973 Oct;1(3):173-8. doi: 10.1007/BF00357159.

Syntheses of carbocyclic aminonucleosides and (-)-epi-4'-carbocyclic puromycin: Application of palladium(0)/indium iodide-allylations and tethered aminohydroxylations.碳环氨基核苷和（-）-表-4'-碳环嘌呤霉素的合成：钯（0）/碘化铟烯丙基化反应及连接氨基羟基化反应的应用

Tetrahedron Lett. 2010 Jun 9;51(23):3053-3056. doi: 10.1016/j.tetlet.2010.04.006.

Effect of puromycin analogues and other agents on peptidyl-puromycin synthesis on polyribosomes.嘌呤霉素类似物及其他试剂对多核糖体上肽基嘌呤霉素合成的影响。

Antimicrob Agents Chemother. 1973 Jul;4(1):37-43. doi: 10.1128/AAC.4.1.37.

Chloramphenicol binding site with analogues of chloramphenicol and puromycin.氯霉素结合位点与氯霉素和嘌呤霉素类似物

Antimicrob Agents Chemother. 1975 Oct;8(4):439-43. doi: 10.1128/AAC.8.4.439.

Peptidyl transferase centre of bacterial ribosomes: substrate specificity and binding sites.细菌核糖体的肽基转移酶中心：底物特异性和结合位点

Nucleic Acids Res. 1975 Dec;2(12):2223-36. doi: 10.1093/nar/2.12.2223.

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