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1 bsorbance properties compared with authentic indolicidin.
2 rinated analogs of the antibacterial peptide indolicidin.
3 al partitioning free energies of variants of indolicidin, a cationic proline-rich antimicrobial pepti
4  we designed synthetic peptides derived from indolicidin, a naturally occurring HDP, and tested their
5  issue by means of CD measurements of native indolicidin and several of its analogues.
6 ations are the principal structural motif of indolicidin and that these turns greatly enhance membran
7 ture of the cross-linked byproduct, termed X-indolicidin, by absorbance and fluorescence spectroscopy
8                                      Because indolicidin can also inhibit topoisomerase I, we believe
9                                              Indolicidin crosslinks single- or double-stranded DNAs a
10                    The unique composition of indolicidin distinguishes it from alpha-helical and beta
11 tryptophan, we synthesized indolicidin-L and indolicidin-F in which all five tryptophans were replace
12                  Falla et al. suggested that indolicidin forms a poly-L-proline II helix based upon t
13                     Solid phase synthesis of indolicidin gave rise to a minor byproduct that possesse
14 teps and was shown be identical to authentic indolicidin in its microbicidal activity against Staphyl
15                               For the native indolicidin in SDS micelles, temperature increases resul
16  helix formation in the CD spectra of native indolicidin in various solvents or when bound to micelle
17   Consistent with experimental observations, indolicidin induces membrane thinning, although the simu
18 etric footprinting approaches, we found that indolicidin interferes with formation of the catalytic i
19                                              Indolicidin is a 13-residue antimicrobial peptide-amide
20                                              Indolicidin is a 13-residue cationic, antimicrobial pept
21                                              Indolicidin is a host defense tridecapeptide that inhibi
22 s associated with tryptophan, we synthesized indolicidin-L and indolicidin-F in which all five trypto
23          This phenomenon, which is absent in indolicidin-L variants with single Leu-->Trp substitutio
24 w that the addition of several natural AMPs (indolicidin, LL-37, magainin II, and aurein 2.2) causes
25 m (CD) spectra of a closely related peptide (indolicidin methyl ester).
26 cluding melittin, fowlicidin-1, tritrpticin, indolicidin, puroindoline A peptide, magainin II F5W, la
27 tructured cationic peptides, because five of indolicidin's 13 residues are tryptophans: H-Ile-Leu-Pro
28 a 2-atomic mass unit reduction compared with indolicidin, suggesting the deprotonation of two indole
29 ergy of the 13-residue antimicrobial peptide indolicidin to a lipid bilayer.
30 dependent of the PWWP motif but involves the indolicidin unique lysine residue and the N- and C- term
31                 Compared with indolicidin, X-indolicidin was partially resistant to digestion with tr
32                        Molecular modeling of indolicidin with a -Trp(6)-cis-Pro(7)-Trp(8)- type VIa t
33                                Compared with indolicidin, X-indolicidin was partially resistant to di