Sequence specificity of quinoxaline antibiotics. 1. Solution structure of a 1:1 complex between triostin A and [d(GACGTC)]2 and comparison with the solution structure of the [N-MeCys3,N-MeCys7]TANDEM-[d(GATATC)]2 complex-Reference-Cited by-同舟云学术

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Sequence specificity of quinoxaline antibiotics. 1. Solution structure of a 1:1 complex between triostin A and [d(GACGTC)]2 and comparison with the solution structure of the [N-MeCys3,N-MeCys7]TANDEM-[d(GATATC)]2 complex

Published:1994-10 Issue:41 Volume:33 Page:12386-12396
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Addess Kenneth J.,Feigon Juli

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi00207a005

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Conversion of a Disulfide Bond into a Thioacetal Group during Echinomycin Biosynthesis;Angewandte Chemie International Edition;2013-12-02

2. Conversion of a Disulfide Bond into a Thioacetal Group during Echinomycin Biosynthesis;Angewandte Chemie;2013-12-02

3. Orthogonal Chemistry for the Synthesis of Thiocoraline–Triostin Hybrids. Exploring their Structure–Activity Relationship;Journal of Medicinal Chemistry;2013-06-19

4. In Vitro Characterization of Echinomycin Biosynthesis: Formation and Hydroxylation of L-Tryptophanyl-S-Enzyme and Oxidation of (2S,3S) β-Hydroxytryptophan;PLoS ONE;2013-02-21

5. Triostin A derived hybrid for simultaneous DNA binding and metal coordination;Amino Acids;2010-10-22

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