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. Author manuscript; available in PMC: 2012 Oct 1.
Published in final edited form as: Biochim Biophys Acta. 2011 Jul 6;1808(10):2403–2412. doi: 10.1016/j.bbamem.2011.06.018

Table 1.

Properties of the AS1- and AS2-containing peptides used in the study.

Receptora GIb Peptide Sequence Net Charge Hydrophobic moment (μH)c ΔGwif (kcal/mol)d
Af1503 (278-296) 1484730 AS1p-Af1503 STITRPIIELSNTADKIAE −1 6.28 −0.71
EnvZEc (180-198) 947272 AS1p-EnvZEc RIQNRPLVDLEHAALQVGK +1 3.84 −1.51
NarXEc (177-195) 945788 AS1p-NarXEc RLLQPWRQLLAMASAVSHR +3 6.19 −6.35
TarEc (214-232) 946399 AS1p-TarEc RMLLTPLAKIIAHIREIAG +2 5.79 −4.32
Af1503 (310-328) 1484730 AS2p-Af1503 DEIGILAKSIERLRRSLKV +2 5.42 −0.29
EnvZEc (211-229) 947272 AS2p-EnvZEc SEVRSVTRAFNHMAAGVKQ +2 3.46 −1.51
NarXEc (208-226) 945788 AS2p-NarXEc EMAMLGTALNNMSAELAES −3 5.57 −2.25
TarEc (246-263) 946399 AS2p-TarEc EMGDLAQSVSHMQRSLTD −2 4.81 −0.29
a

The receptor that served as the source of AS1- and AS2-containing peptides. The position of the residues within the primary structure is provided in parentheses.

b

The “GenInfo Identifier” sequence identification number.

c

The hydrophobic moment (μH) of the peptides according to Eisenberg [58].

d

The energy of interfacial partitioning (ΔGwif) calculated within MPEx [59]. Significantly different values are indicated in bold font.