Selective catalytic hydrogenation of the N-acyl and uridyl double bonds in the tunicamycin family of protein N-glycosylation inhibitors
Selective catalytic hydrogenation of the N-acyl and uridyl double bonds in the tunicamycin family of protein N-glycosylation inhibitors
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蛋白质 N-糖基化抑制剂衣霉素家族中 N-酰基和尿苷双键的选择性催化氢化
DOI:
10.1038/ja.2017.141
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发表时间:
2017-11
期刊:
影响因子:
--
通讯作者:
Biao Yu
中科院分区:
文献类型:
--
作者:
Neil PJ Price;Michael A Jackson;Karl E Vermillion;Judith A Blackburn;Jiakun Li;Biao Yu
Tunicamycin is a Streptomyces-derived inhibitor of eukaryotic protein N-glycosylation and bacterial cell wall biosynthesis, and is a potent and general toxin by these biological mechanisms. The antibacterial activity is dependent in part upon a π-π stacki
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DOI:
10.1126/science.1236501
发表时间:
2013-08-30
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
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通讯作者:
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影响因子:
64.8
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Lee SY
DOI:
10.1038/ja.2016.49
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期刊:
The Journal of Antibiotics
影响因子:
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作者:
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通讯作者:
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影响因子:
3.2
作者:
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