Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Acinetobacter Baumannii (strain Atcc 17978 / Cip 53.77 / Lmg 1025 / Ncdc Kc755 / 5377)
TISSUE(S): Cell Culture
SUBMITTER:
Carter Brzezinski
LAB HEAD: Stephan Sieber
PROVIDER: PXD056737 | Pride | 2025-12-15
REPOSITORIES: Pride
| Action | DRS | |||
|---|---|---|---|---|
| 20240322_CB_AB-ABPP_1-4xC.raw | Raw | |||
| 20240322_CB_AB-ABPP_1-8xC.raw | Raw | |||
| 20240322_CB_AB-ABPP_1D.raw | Raw | |||
| 20240322_CB_AB-ABPP_1P-.raw | Raw | |||
| 20240322_CB_AB-ABPP_1P.raw | Raw |
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Colquhoun Jennifer M JM Brzezinski Carter U CU Ji Andrew A Marotta Julianna J Elsen Franziska A V FAV Bonomo Robert A RA May Kerrie L KL Sieber Stephan A SA Grabowicz Marcin M Wuest William M WM Rather Philip N PN
Proceedings of the National Academy of Sciences of the United States of America 20250610 24
The OXA β-lactamases in <i>Acinetobacter baumannii</i> represent a primary mechanism for resistance to the carbapenems, a class of antibiotics that represent a last line for treatment. In a screen of an U.S. Food and Drug Administration (FDA)-approved drug library, we identified fendiline, a calcium channel blocker, had significantly more antimicrobial activity against OXA-23 expressing cells. Genetic and proteomic studies revealed that fendiline inhibited the essential lipoprotein trafficking p ...[more]