The tripeptide ImPImP containing alternating imidazole and pyrrole carboxamides specifically binds the designated six base pair site 5’-d(A,T)GCGC(A,T)-3’ in the minor groove of DNA. Quantitative footprint titration experiments demonstrate that ImPImP binds the sites 5’-AGCGCT-3’ and 5’-TGCGCA-3’ with apparent first order binding affinities of 3.8 x 10(5) M(-1) and 3.6 x 10(5) M(-1), respectively (25 mM tris acetate, 10 mM NaCl, pH 7.0 and 22 degrees C). Affinity cleaving experiments with ImPImP-EDTA . Fe reveals equal cleavage on both sides of the 5’-(A,T)GCGC(A,T)-3’ site, consistent with a side-by-side antiparallel arrangement of the four ring peptides in the minor groove, This reversal of specificity of the natural product distamycin which prefers to bind pure A,T sequences underscores the utility of 2:1 peptide-DNA models for the design of ligands for sequence-specific recognition in the minor groove of DNA. By extending these peptides to four ring systems, a new lower limit of six base pair binding by 2:1 peptide-DNA complexes has been defined.