rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
21
|
pubmed:dateCreated |
2009-10-19
|
pubmed:abstractText |
Bioorganic synthesis of N- and C-terminal end-capped peptides by two simultaneous S-cyanocysteine-mediated cleavages of recombinant proteins is described. This approach is demonstrated in the preparation of anti-HIV fusion inhibitory peptides.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
1464-3391
|
pubmed:author |
pubmed-author:FujiiNobutakaN,
pubmed-author:HataYojiY,
pubmed-author:IzumiKazukiK,
pubmed-author:KajiwaraKazumiK,
pubmed-author:KodamaEiichiE,
pubmed-author:MatsuokaMasaoM,
pubmed-author:OhnoHiroakiH,
pubmed-author:OishiShinyaS,
pubmed-author:TanakaMichinoriM,
pubmed-author:TokiwaReiR,
pubmed-author:TsutsumiHirokoH,
pubmed-author:WatanabeKentaroK
|
pubmed:issnType |
Electronic
|
pubmed:day |
1
|
pubmed:volume |
17
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
7487-92
|
pubmed:meshHeading |
|
pubmed:year |
2009
|
pubmed:articleTitle |
Bioorganic synthesis of end-capped anti-HIV peptides by simultaneous cyanocysteine-mediated cleavages of recombinant proteins.
|
pubmed:affiliation |
Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8501, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|