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Biochemistry ; 42(21): 6559-64, 2003 Jun 03.
Article in English | MEDLINE | ID: mdl-12767239

ABSTRACT

The identity of the axial ligand contributed by the drug in hydroperoxide-Co(III)-bleomycin and hydroperoxide-Co(III)-deglycobleomycin has been in doubt. With each structure, a combination of (1)H[(15)N] HSQC and HMBC and (1)H COSY and NOESY NMR spectroscopy was used to observe and completely assign the nonaromatic (15)N chemical shifts of natural abundance bleomycin in the two hydroperoxide-Co(III) structures. Together with the (15)N assignments from a published 1D (15)N spectrum, the results permitted the assignment of the primary amine nitrogen to an axial ligand position in both structures.


Subject(s)
Bleomycin/analogs & derivatives , Bleomycin/chemistry , Cobalt/chemistry , Ligands , Magnetic Resonance Spectroscopy , Models, Chemical , Nitrogen/chemistry , Peplomycin/chemistry , Protein Binding , Protons , Temperature
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