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1 ia is initiated with methionine and not with formylmethionine.
2 ferably binds peptides bearing an N-terminal formylmethionine.
3 ty can be measured by quantifying hydrolyzed formylmethionine.
4 chondria and chloroplasts, is initiated with formylmethionine.
5 e eukaryotic cytoplasm can be initiated with formylmethionine, and, if so, what the consequences are
6 eaves chemotactic peptide f-MLF to release N-formylmethionine (f-Met) and dipeptide leucylphenylalani
7  Escherichia coli initiator tRNAs that carry formylmethionine (fMet), formylglutamine (fGln), or form
8                The absence of the N-terminal formylmethionine (fMet), or conversion of the sulfur in
9 removes the formyl group from the N-terminal formylmethionine in a polypeptide, rescues the slow-grow
10               The second enzyme hydrolyzes N-formylmethionine into formate and methionine with a k(ca
11 nthesis and that initiation of proteins with formylmethionine leads to the slow-growth phenotype.
12 -stimulating factor, lipopolysaccharide, and formylmethionine-leucine-phenylalanine.
13  were extracted from cells with or without N-formylmethionine leucyl-phenylalanine (fMLP) stimulation
14 atic, aqueous-based, buffered reactions with formylmethionine-N-hydroxysuccinimide ester to model 11
15 eactivity to different bacterially derived N-formylmethionine peptides.
16 , including both alpha-N-acetyl- and alpha-N-formylmethionine that exhibit higher activity than alpha

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