期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 25, 页码 7822-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja8029398
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资金
- NCI NIH HHS [R01 CA127622, R01 CA044848, R37 CA044848, R01 CA127622-03, CA44848, CA127622] Funding Source: Medline
A new shunt in the phenylalanine biosynthetic pathway to the nonproteinogenic amino acid L-3-cyclohex-2'-enylalanine was exploited in the marine bacterium Salinispora tropica by mutagenesis to allow for the genetic engineering of unnatural derivatives of the potent proteasome inhibitor salinosporamide A (2) such as antiprotealide (1).
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