| Literature DB >> 12767239 |
Chaunwu Xia1, F Holger Försterling, David H Petering.
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.Entities:
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Year: 2003 PMID: 12767239 DOI: 10.1021/bi030016c
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162