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Inhibitory effect of modified bafilomycins and concanamycins on P- and V-type adenosinetriphosphatases

Droese, Stefan, Bindseil, Kai U., Bowman, Emma J., Siebers, Annette, Zeeck, Axel, Altendorf, Karlheinz·1993·Biochemistry

Abstract

Various ATPases have been tested for their sensitivity to naturally occurring unusual macrolides and their chemically modified derivatives, which are structurally related to bafilomycin A1 (1), the first specific inhibitor of vacuolar ATPases. The structure-activity study showed that in general the concanamycins, 18-membered macrolides, are better and more specific inhibitors than the bafilomycins of this class of membrane-bound ATPases. The additional carbohydrate residue is not responsible for the improved activity. The importance of an intact hemiketal ring, which is part of an intramolecular hydrogen-bonding network, and the effects of the size of the macrolactone ring are discussed. The structurally related elaiophylin (13), a C2-symmetric macrodiolide antibiotic, proved to be inactive on vacuolar ATPases but still retained its inhibitory effect on P-type ATPases.

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Metadata

Authors
Droese, S., Bindseil, K. U., Bowman, E. J., Siebers, A., Zeeck, A., & Altendorf, K.
Venue
Biochemistry
Published
1993-04-20
Volume
32
Issue
15
Pages
3902-3906
ISSN
  • 0006-2960 (ISSN-L)
  • 1520-4995
OpenAlex
W2006176190
Cited by
416
References
0
FWCI
4.75
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Inhibitory effect of modified bafilomycins and concanamycins on P- and V-type adenosinetriphosphatases. https://app.cochat.ai/papers/10.1021/bi00066a008
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Droese, S., Bindseil, K. U., Bowman, E. J., Siebers, A., Zeeck, A., & Altendorf, K. (1993). Inhibitory effect of modified bafilomycins and concanamycins on P- and V-type adenosinetriphosphatases. Biochemistry. https://doi.org/10.1021/bi00066a008

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