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Taxodione and arenarone inhibit farnesyl diphosphate synthase by binding to the isopentenyl diphosphate site

We used in silico methods to screen a library of 1,013 compounds for possible binding to the allosteric site in farnesyl diphosphate synthase (FPPS). Two of the 50 predicted hits had activity against either human FPPS (HsFPPS) or Trypanosoma brucei FPPS (TbFPPS), the most active being the quinone me...

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Hlavní autoři: Liu, Yi-Liang, Lindert, Steffen, Zhu, Wei, Wang, Ke, McCammon, J. Andrew, Oldfield, Eric
Médium: Artigo
Jazyk:Inglês
Vydáno: National Academy of Sciences 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4078810/
https://ncbi.nlm.nih.gov/pubmed/24927548
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1409061111
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