ライフサイエンスコーパス: gramicidin S

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1 the membrane-active cyclopeptide antibiotic, gramicidin S.

2 the membrane-active cyclopeptide antibiotic, gramicidin S.

3 incorporated into the decapeptide antibiotic gramicidin S.

4 llowed by cyclization to form the antibiotic gramicidin S.

5 for the two charge states of the decapeptide Gramicidin S.

6 Particles containing the peptides gramicidin S and gramicidin D were analyzed both with an

7 obic moments for two antimicrobial peptides, gramicidin S and PGLa, under different conditions.

8 osynthesize the symmetric cyclic decapeptide gramicidin S and the cyclic lipoheptapeptide surfactin A

9 clization of a decapeptide thioester to form gramicidin S, and the TE domain from the surfactin NRPS

10 trated using model peptide ions (bradykinin, gramicidin S, and trpzip 1).

11 nd 14 zmol (approximately 8400 molecules) of gramicidin S are reported.

12 enzymatic synthesis of the cyclic antibiotic gramicidin S by gramicidin S synthetase.

13 generation of the D-Phe-S-enzyme that starts gramicidin S chain growth.

14 ale the membrane affinity of the decapeptide Gramicidin S cyclo(d-Phe-Pro-Val-Orn-Leu-)2 (GS).

15 ly protonated substance P, doubly protonated gramicidin S, doubly protonated neurotensin, and triply

16 previously, dications of the cyclic peptide Gramicidin S (GS) and the photoactive organonometallic c

17 Physisorption of a cyclic peptide, Gramicidin S (GS), was studied for 8 h during deposition

18 on also was observed with the cyclic peptide gramicidin S, indicating the generality of the mechanism

19 l synthesis of the cyclic peptide antibiotic gramicidin S is accomplished by two large multifunctiona

20 The detection of 14 zmol of gramicidin S is to the best of our knowledge a record in

21 mounts of model peptides HLGLAR (m/z 666.8), gramicidin S (m/z 1142.5), and bovine insulin b chain (m

22 cyclization activity: the TE domain from the gramicidin S NRPS catalyzes head-to-tail cyclization of

23 n, cephalosporins, streptomycin, fosfomycin, gramicidin S, rapamycin, indolmycin, microcin B17, fumag

24 tion of DPD with viral DNA or the antibiotic gramicidin S resulted in significant biochemical alterat

25 f the nonribosomal peptide synthetase enzyme gramicidin S synthetase A (GrsA-PheA) for a set of nonco

26 tion module PheATE (GrsA) of Bacillus brevis gramicidin S synthetase catalyzes the activation, thiola

27 n (ATE) initiation module of Bacillus brevis gramicidin S synthetase equilibrates the Calpha configur

28 The gramicidin S synthetase initiation module (PheATE) is a

29 sis of the cyclic antibiotic gramicidin S by gramicidin S synthetase.

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