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Communication between the active sites and dimer interface of a herpesvirus protease revealed by a transition-state inhibitor

Structurally diverse organophosphonate inhibitors targeting the active site of the enzyme were used to investigate the relationship of the active site and the dimer interface of wild-type protease in solution. Positional scanning synthetic combinatorial libraries revealed Kaposi's sarcoma-assoc...

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Autores principales: Marnett, Alan B., Nomura, Anson M., Shimba, Nobuhisa, de Montellano, Paul R. Ortiz, Craik, Charles S.
Formato: Artigo
Lenguaje:Inglês
Publicado: National Academy of Sciences 2004
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC406434/
https://ncbi.nlm.nih.gov/pubmed/15118083
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0401613101
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