BIROn - Birkbeck Institutional Research Online

    x-ray structures of two forms of the antibiotic oligomycin A: an inhibitor of ATP synthase

    Palmer, Rex A. and Ladd, M. and Howlin, B.J. and Lisgarten, D.R. (2013) x-ray structures of two forms of the antibiotic oligomycin A: an inhibitor of ATP synthase. Future Medicinal Chemistry 5 (8), pp. 881-893. ISSN 1756-8919.

    Full text not available from this repository.

    Abstract

    Background: Corrections to the chemical and x-ray structures of two forms of the antibiotic oligomycin A are presented: the original and best known, form (E), from Streptomyces diastatochromogenes, and a new form (C) from Streptomyces diastaticus. Method: The crystal structures are isomorphous, crystallizing in space group P212121, with Z = 4[C45H73O11.CH3OH] per unit cell. Oligomycin A(E) refined with R1 = 0.0734, using Cu Kα x-radiation; and for Oligomycin A(C) R1 = 0.0651 using Mo Kα x-radiation. Conclusion: Serious corrections to the previously published structure of oligomycin A(C) are discussed and implemented. As a supplementary study geometry optimization of side group R4 of oligomycin A(E) was undertaken and achieved by energy minimization. These additional results clearly confirm the delocalization in this region observed in both x-ray structures. This result is contrary to the generally accepted formulation. Knowledge of the correct structures is important to those involved in the study and applications of the pharmacological and biological properties of these materials.

    Metadata

    Item Type: Article
    School: Birkbeck Faculties and Schools > Faculty of Science > School of Natural Sciences
    Depositing User: Administrator
    Date Deposited: 22 May 2013 08:49
    Last Modified: 02 Aug 2023 17:04
    URI: https://eprints.bbk.ac.uk/id/eprint/6953

    Statistics

    Activity Overview
    6 month trend
    0Downloads
    6 month trend
    179Hits

    Additional statistics are available via IRStats2.

    Archive Staff Only (login required)

    Edit/View Item Edit/View Item