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1 opyranoside and also bound equivalently to a dodecapeptide.
2 ng peptides synthesized on pins, overlapping dodecapeptides (170) were synthesized to cover the extra
3 fective mutant, and a synthetic N-acetylated dodecapeptide, Ac-Asn-Gly-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Gl
5 By targeting a pH-dependent membrane-lytic dodecapeptide and a disulfide-linked fluorophore to thes
6 3 A resolution, and of a complex between the dodecapeptide and a SurA fragment lacking the second PPI
7 demonstrate that a combinatorially-selected dodecapeptide and its variants self-assemble into peptid
8 inding activity in the absence of the gammaC-dodecapeptide and the alpha-chain RGD sequences suggests
9 ant (p < 0.01) differences between the all-L-dodecapeptide and the ones containing a d-serine or a D-
10 containing roughly 4.0+/-1.6% of the random dodecapeptides and 7.9+/-2.6% of the random constrained
12 f small molecules for the binding of a known dodecapeptide assembly inhibitor to the C-terminal domai
14 S-peptide-I is a synthetic tris-sulfotyrosyl dodecapeptide corresponding to the major site of insulin
16 l effects are also seen for the diprotonated dodecapeptide H2N-Leu-Val-Phe-Phe-Ala-Glu-Asp-Val-Gly-Se
18 ng a phage-epitope library expressing random dodecapeptides in the pIII coat protein of fd phage usin
19 ation of bacitracin components (i.e., cyclic dodecapeptides) in the aquatic environment was investiga
20 cules that includes a-factor, a farnesylated dodecapeptide, involved in the mating of Saccharomyces c
21 due fraction and also of synthetic deca- and dodecapeptide libraries, because peptides of this size s
22 of NK-1 and SP and (2) screening of a random dodecapeptide library for SP(1-4) interacting sites.
23 ositions within the inserted peptides of the dodecapeptide library, +1, +3 and +12 downstream from th
25 cein-labeled derivative of the COOH-terminal dodecapeptide of hirudin ([5F] Hir54-65) to exosite I wa
26 urther biochemical characterization define a dodecapeptide of NPAC (residues 214-225) as the minimal
27 of two effector genes, a tetramer of the SM1 dodecapeptide or the phospholipase A2 gene (PLA2) from h
28 he a-factor of Saccharomyces cerevisiae is a dodecapeptide pheromone (YIIKGVFWDPAC(Farnesyl)-OCH(3),
29 he a-factor of Saccharomyces cerevisiae is a dodecapeptide pheromone [YIIKGVFWDPAC(farnesyl)-OCH3] in
31 udy was to determine amino acids within this dodecapeptide region that are required for interaction w
34 ere a regular helix formed by the C-terminal dodecapeptide segment, alpha7, occupies the ligand-bindi
35 se data indicate that this tris-sulfotyrosyl dodecapeptide selectively enhances insulin signal transd
36 d alpha(E)C) but does not require the gammaC dodecapeptide sequence HHLGGAKQAGDV(400-411) for binding
37 phage display library covering 10(9) unique dodecapeptide sequences is incubated with nonassembling
38 ate at which PDK1 phosphorylated a synthetic dodecapeptide (T308tide), corresponding to the sequences
39 f the self-assembled protein cage displays a dodecapeptide that is capable of reducing silver ions to
40 minally isoprenylated and carboxylmethylated dodecapeptide that is initially synthesized as a larger
42 recombinant human PTP1B with phosphotyrosyl dodecapeptide TRDI(P)YETD(P)Y(P)YRK as the source of the
43 homologues of the six most active vertebrate dodecapeptides were now synthesized and tested as substr
44 Triply charged complexes of the protonated dodecapeptide with cobalt(II) ions undergo CAD at lower
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