GC base sequence recognition by oligoimidazolecarboxamide and C-terminus-modified analogs of distamycin deduced from circular dichroism, proton nuclear magnetic resonance, and methidiumpropylethylenediaminetetraacetate-iron(II) footprinting studies

GC base sequence recognition by oligoimidazolecarboxamide and C-terminus-modified analogs of distamycin deduced from circular dichroism, proton nuclear magnetic resonance, and methidiumpropylethylenediaminetetraacetate-iron(II) footprinting studies

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Veröffentlicht in:Biochemistry (Easton) 1993-04, Vol.32 (16), p.4237-4245
Hauptverfasser: Lee, Moses, Rhodes, Andrea L, Wyatt, Michael D, Forrow, Stephen, Hartley, John A
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container_end_page 4245
container_issue 16
container_start_page 4237
container_title Biochemistry (Easton)
container_volume 32
creator Lee, Moses
Rhodes, Andrea L
Wyatt, Michael D
Forrow, Stephen
Hartley, John A
description
doi_str_mv 10.1021/bi00067a011
format Article
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title GC base sequence recognition by oligoimidazolecarboxamide and C-terminus-modified analogs of distamycin deduced from circular dichroism, proton nuclear magnetic resonance, and methidiumpropylethylenediaminetetraacetate-iron(II) footprinting studies
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