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2 amide bond. Since backbone conformation and side chain disposition of cu-conformer of 32 was apparently different from the parent peptides 2 and 3, we assumed that the major trans-conformer could contribute to the bioactivities of 32, although contribution of the minor cis-conformer cannot be ruled out.
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2 amide bond. Since backbone conformation and side chain disposition of cu-conformer of 32 was apparently different from the parent peptides 2 and 3, we assumed that the major trans-conformer could contribute to the bioactivities of 32, although contribution of the minor cis-conformer cannot be ruled out.
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39
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33846432306
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Molecular anatomy of CCR5 engagement by physiologic and viral chemokines and HIV-1 envelope glycoproteins; Differences in primary structural requirements for RANTES. MIP-1α, and vMIP-II binding
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Navenot, J. M.; Wang, Z. X.; Trent, J. O.; Murray, J. L.; Hu, Q. X.; DeLeeuw, L.; Moore, P. S.; Chang, Y.; Peiper, S. C. Molecular anatomy of CCR5 engagement by physiologic and viral chemokines and HIV-1 envelope glycoproteins; Differences in primary structural requirements for RANTES. MIP-1α, and vMIP-II binding. J. Mol. Biol. 2001, 39, 380-393.
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(2001)
J. Mol. Biol
, vol.39
, pp. 380-393
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Navenot, J.M.1
Wang, Z.X.2
Trent, J.O.3
Murray, J.L.4
Hu, Q.X.5
DeLeeuw, L.6
Moore, P.S.7
Chang, Y.8
Peiper, S.C.9
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