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1 ied, maintaining the same hydrophobicity and amphipathicity.
2 whereas the N-terminal helices vary in their amphipathicity.
3 ctivity is due to lack of hydrophobicity and amphipathicity.
4 within a certain range of hydrophobicity and amphipathicity.
5 es as stimulants of CCK secretion, was their amphipathicity.
6 s, endowing this cyclotide with a pronounced amphipathicity.
7 gulation of bioactivities in the presence of amphipathicity.
8  retention in HILIC independently of peptide amphipathicity.
9  of Dyn A for BR recognition was identified: amphipathicity.
10 ometry and morphology but had reduced global amphipathicity.
11  the headgroups depends on their extents and amphipathicities.
12 finity for membranes based on hydrophobicity/amphipathicity analysis.
13 ts of peptide hydrophobicity/hydrophilicity, amphipathicity, and helicity (induced by single amino ac
14 ly correlated with high hydrophobicity, high amphipathicity, and high helicity.
15  possesses a coiled-coil propensity, but not amphipathicity, and is dispensable for membrane anchorin
16 f viral infection at the plasma membrane and amphipathicity-based mechanisms used for endosomal SARS-
17 es does not correlate exactly with helicity, amphipathicity, charge, the number of charges, the size
18 mpound, suggesting that overall topology and amphipathicity governed its antimicrobial activity.
19  histatin 5 to elucidate the role of peptide amphipathicity, hydrophobicity, and the propensity to ad
20               The importance of rigidity and amphipathicity imparted by the cyclic and cystine constr
21  Glu residues in the first 12 positions, and amphipathicity in the first 50 positions.
22 gh all defensin peptides are cationic, their amphipathicity is at least as important as their positiv
23 and calculations support the hypothesis that amphipathicity is the key motif for activity.
24  of the positive charge, hydrophobicity, and amphipathicity of an AMP and its potency to activate Pho
25 how differences in the histidine content and amphipathicity of peptides can elicit different directio
26 r structures were lost due to changes in the amphipathicity of the amino-terminal helix, suggesting t
27                                          The amphipathicity of the natively unstructured amyloid-beta
28 ackbones that correct for differences in the amphipathicity of their N- and C-ends, and their centers
29 trees and average hydropathy, similarity and amphipathicity plots for members of the four families ar
30                          While their extreme amphipathicity presents technical challenges, biological
31                     Because of its imperfect amphipathicity, protegrin binds weakly, at most, on the
32 , and analysis of the peptide hydrophobicity/amphipathicity relationship.
33 rs from that of PTH with respect to size and amphipathicity, suggesting an altered mode of binding fo
34 plesin I play a structural role in imparting amphipathicity to the peptide which has been shown to be
35                  We investigated the role of amphipathicity using an analogue of tachyplesin I (TP-I)
36 osylated beta-endorphin analogues of various amphipathicity were studied in vitro and in vivo in mice
37  entropy at the polar face but maintains its amphipathicity, whereas in clade B it accommodates hydro
38  correlation was attributed to the conserved amphipathicity within the TMDs as the interactions were