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Design of peptides that bind in the minor groove of DNA at 5′-(A,T)G(A,T)C(A,T)-3′ sequences by a dimeric side-by-side motif
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Wade, W.S., Mrksich, M. & Dervan, P.B. (1992). Design of peptides that bind in the minor groove of DNA at 5′-(A,T)G(A,T)C(A,T)-3′ sequences by a dimeric side-by-side motif. J. Am. Chem. Soc. 114, 8783-8794.
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Antiparallel side-by-side motif for sequence-specific recognition in the minor groove of DNA by the designed peptide 1-methylimidazole-2-carboxamide netropsin
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Mrksich, M., Wade, W.S., Dwyer, T.J., Geierstanger, B.H., Wemmer, D.E. & Dervan, P.B (1992). Antiparallel side-by-side motif for sequence-specific recognition in the minor groove of DNA by the designed peptide 1-methylimidazole-2-carboxamide netropsin. Proc. Natl. Acad. Sci. USA 89, 7586-7590.
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3
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Binding affinities of synthetic peptides, pyridine-2-carboxamidenetropsin and 1-methylimidazole-2-carboxamidenetropsin, that form 2:1 complexes in the minor groove of double-helical DNA
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Wade, W.S., Mrksich, M. & Dervan, P.B. (1993). Binding affinities of synthetic peptides, pyridine-2-carboxamidenetropsin and 1-methylimidazole-2-carboxamidenetropsin, that form 2:1 complexes in the minor groove of double-helical DNA. Biochemistry 32, 11385-11389.
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Structural characterization of a 2-1 distamycin A·d(CGCAAATTTGGC) complex by two-dimensional NMR
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Mrksich, M. & Dervan, P.B. (1993). Antiparallel side-by-side heterodimer for sequence-specific recognition in the minor groove of DNA by a distamycin 1-methylimidazole-2-carboxamide pair. J. Am. Chem. Soc. 115, 2572-2576.
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Structural and dynamic characterization of the heterodimeric and homodimeric complexes of distamycin and 1-methylimidazole-2-carboxamide-netropsin bound to the minor-groove of DNA
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Geierstanger, B.H., Jacobsen, J-P., Mrksich, M., Dervan, P.B. & Wemmer, D.E. (1994). Structural and dynamic characterization of the heterodimeric and homodimeric complexes of distamycin and 1-methylimidazole-2-carboxamide-netropsin bound to the minor-groove of DNA. Biochemistry 33, 3055-3062.
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NMR characterization of a heterocomplex formed by distamycin and its analog 2-ImD with d(CGCAAGTTGGC)-d(GCC-AACTTGCG) - Preference for the 1/1/1 2-ImD-Dst-DNA complex over the 2/1 2-ImD-DNA and the 2/1 Dst-DNA complexes
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Geierstanger, B.H., Dwyer, T.J., Bathini, Y., Lown, J.W. & Wemmer, D.E. (1993). NMR characterization of a heterocomplex formed by distamycin and its analog 2-ImD with d(CGCAAGTTGGC)-d(GCC-AACTTGCG) - preference for the 1/1/1 2-ImD-Dst-DNA complex over the 2/1 2-ImD-DNA and the 2/1 Dst-DNA complexes. J. Am. Chem. Soc. 115, 4474-4482.
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Design of a G·C-specific minor groove-binding peptide
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Geierstanger, B.H., Mrksich, M., Dervan, P.B. & Wemmer, D.E. (1994). Design of a G·C-specific minor groove-binding peptide. Science 266, 646-650.
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Recognition in the minor-groove of DNA at 5′-(A,T)GCGC(A,T)-3′ by a four-ring tripeptide dimer - Reversal of the specificity of the natural product distamycin
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Mrksich, M. & Dervan, P.B. (1995). Recognition in the minor-groove of DNA at 5′-(A,T)GCGC(A,T)-3′ by a four-ring tripeptide dimer - reversal of the specificity of the natural product distamycin. J. Am. Chem. Soc. 117, 3325-3332.
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Design of a covalent peptide heterodimer for sequence-specific recognition in the minor-groove of double-helical DNA
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Mrksich, M. & Dervan, P.B. (1994). Design of a covalent peptide heterodimer for sequence-specific recognition in the minor-groove of double-helical DNA. J. Am. Chem. Soc. 116, 3663-3664.
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Hairpin peptide motif - A new class of oligopeptides for sequence-specific recognition in the minor-groove of double-helical DNA
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Mrksich, M., Parks, M.E. & Dervan, P.B. (1994). Hairpin peptide motif - a new class of oligopeptides for sequence-specific recognition in the minor-groove of double-helical DNA. J. Am. Chem. Soc. 116, 7983-7988.
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