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1 one of three Cys and two Ser residues of the prepeptide.
2 st-translational modification of the mutacin prepeptide.
3 tional modification during maturation of the prepeptide.
4 cause they lack the first exon, encoding the prepeptide, and follow a translation stop in the C6.1A g
5 lividans of both the wild-type berninamycin prepeptide (BerA) and also a T3A mutant generates macroc
8 ncing has revealed several other phosphatase-prepeptide gene pairs in B. subtilis, suggesting that th
10 verts the C-terminal 14 residues of a 52-mer prepeptide into a related set of eight variants of the t
12 al of an N-terminal leader sequence from the prepeptide LctA and export of the mature lantibiotic.
13 acticin 481 is synthesized on ribosomes as a prepeptide (LctA) and posttranslationally modified to it
15 The mRNA is predicted to be translated to a prepeptide of 138 amino acids in length and processed to
16 e producing microbes, the genes encoding the prepeptide open reading frames are flanked in biosynthet
17 translational modifications on 50-60-residue prepeptide precursors that trim away the N-terminal lead
18 ed in the dehydration and cyclization of the prepeptide, several putative transporter and regulatory
20 ter maturation and secretion) proteins whose prepeptide substrates share a conserved double-glycine t
21 i permitted identification of a thiostrepton prepeptide, TsrA, and involvement of TsrA in thiostrepto
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