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Side-chain to backbone interactions dictate the conformational preferences of a cyclopentane arginine analogue
The intrinsic conformational preferences of the non-proteinogenic amino acids constructed by incorporating the arginine side chain in the β position of 1-aminocyclopentane-1-carboxylic acid (either in a cis or a trans orientation relative to the amino group) have been investigated using computationa...
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| 主要な著者: | , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2682113/ https://ncbi.nlm.nih.gov/pubmed/19236034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo802704h |
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