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 k and H4 modulate the level of circulating N-formylmethionine (fMet), which initiates mitochondrial p

10 removes the formyl group from the N-terminal formylmethionine in a polypeptide, rescues the slow-grow

11               The second enzyme hydrolyzes N-formylmethionine into formate and methionine with a k(ca

12 nthesis and that initiation of proteins with formylmethionine leads to the slow-growth phenotype.

13 -stimulating factor, lipopolysaccharide, and formylmethionine-leucine-phenylalanine.

14  were extracted from cells with or without N-formylmethionine leucyl-phenylalanine (fMLP) stimulation

15 ptor (ALX), with only a modest response to N-formylmethionine-leucyl-phenylalanine (fMLP), we did rev

16  conditions (no stimulant, anti-IgE, fMLP (N-formylmethionine-leucyl-phenylalanine), and anti-Fcepsil

17 atic, aqueous-based, buffered reactions with formylmethionine-N-hydroxysuccinimide ester to model 11

18 phobic sequence, suggesting the retention of formylmethionine on a substantial fraction of the secret

19 eactivity to different bacterially derived N-formylmethionine peptides.

20 , including both alpha-N-acetyl- and alpha-N-formylmethionine that exhibit higher activity than alpha