[对放线菌素A中吡咯甲酰胺基团在实现其与DNA AT碱基对结合特异性方面贡献的定量评估] - Suppr | 超能文献

[Quantitative assessment of the contribution of the pyrrolcarboxamide groups in distamycin A antibiotic in achieving its binding specificity with DNA AT-pairs].

作者信息

Krylov A S, Grokhovskiĭ S L, Zasedatelev A S, Zhuze A L, Gurskiĭ G V

出版信息

Dokl Akad Nauk SSSR. 1978;239(3):732-5.

Abstract

摘要

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[Quantitative assessment of the contribution of the pyrrolcarboxamide groups in distamycin A antibiotic in achieving its binding specificity with DNA AT-pairs].[对放线菌素A中吡咯甲酰胺基团在实现其与DNA AT碱基对结合特异性方面贡献的定量评估]

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Quantitative estimation of the contribution of pyrrolcarboxamide groups of the antibiotic distamycin A into specificity of its binding to DNA AT pairs.抗生素偏端霉素A的吡咯甲酰胺基团对其与DNA中AT碱基对结合特异性贡献的定量评估。

Nucleic Acids Res. 1979 Jan;6(1):289-304. doi: 10.1093/nar/6.1.289.

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[Formation kinetics of the AT-specific complex: DNA-distamycin A].

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Characterization of the binding of distamycin A to damaged DNA: a comparison with the DNA recognition of the human DDB protein.放线菌素A与受损DNA结合的特性：与人DDB蛋白的DNA识别的比较。

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Synthesis, DNA binding and antiviral activity of distamycin analogues containing different heterocyclic moieties.

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引用本文的文献

1

Equilibrium and kinetic aspects of protein-DNA recognition.蛋白质-DNA识别的平衡和动力学方面

Nucleic Acids Res. 1979;6(6):2217-36. doi: 10.1093/nar/6.6.2217.

2

Quantitative estimation of the contribution of pyrrolcarboxamide groups of the antibiotic distamycin A into specificity of its binding to DNA AT pairs.抗生素偏端霉素A的吡咯甲酰胺基团对其与DNA中AT碱基对结合特异性贡献的定量评估。

Nucleic Acids Res. 1979 Jan;6(1):289-304. doi: 10.1093/nar/6.1.289.