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pubmed-article:11200286rdf:typepubmed:Citationlld:pubmed
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pubmed-article:11200286pubmed:issue10-12lld:pubmed
pubmed-article:11200286pubmed:dateCreated2001-1-25lld:pubmed
pubmed-article:11200286pubmed:abstractTextThis paper deals with the synthesis of a new type of N-labeled peptidyl AMP, which would be used as a good substrate for analysis of the peptidyl transfer reaction on ribosome and for co-crystallization with ribosome. 4-(Dimethylamino)azobenzene-4'-sulfonyl (Dabsyl) was selected as the labeling group. (N-Dabsylglycyl)-L-leucyl AMP was synthesized from glycyl-L-leucine via a three-step procedure.lld:pubmed
pubmed-article:11200286pubmed:languageenglld:pubmed
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pubmed-article:11200286pubmed:statusMEDLINElld:pubmed
pubmed-article:11200286pubmed:issn1525-7770lld:pubmed
pubmed-article:11200286pubmed:authorpubmed-author:SakamotoKKlld:pubmed
pubmed-article:11200286pubmed:authorpubmed-author:YokoyamaSSlld:pubmed
pubmed-article:11200286pubmed:authorpubmed-author:NaritaHHlld:pubmed
pubmed-article:11200286pubmed:authorpubmed-author:MoriguchiTTlld:pubmed
pubmed-article:11200286pubmed:authorpubmed-author:SekineMMlld:pubmed
pubmed-article:11200286pubmed:authorpubmed-author:SeilFFlld:pubmed
pubmed-article:11200286pubmed:authorpubmed-author:MiyaguchiHHlld:pubmed
pubmed-article:11200286pubmed:issnTypePrintlld:pubmed
pubmed-article:11200286pubmed:volume19lld:pubmed
pubmed-article:11200286pubmed:ownerNLMlld:pubmed
pubmed-article:11200286pubmed:authorsCompleteYlld:pubmed
pubmed-article:11200286pubmed:pagination1993-2003lld:pubmed
pubmed-article:11200286pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11200286pubmed:articleTitleSynthesis of N-labeled peptidyl AMP.lld:pubmed
pubmed-article:11200286pubmed:affiliationDepartment of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Japan.lld:pubmed
pubmed-article:11200286pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11200286pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed