نتایج جستجو برای: ژن pdr5

تعداد نتایج: 15881  

Journal: :The Journal of biological chemistry 2003
John Golin Suresh V Ambudkar Michael M Gottesman Asif Dominic Habib John Sczepanski William Ziccardi Leopold May

The yeast (Saccharomyces cerevisiae) multidrug transporter Pdr5p effluxes a broad range of substrates that are variable in structure and mode of action. Previous work suggested that molecular size and ionization could be important parameters. In this study, we compared the relative sensitivity of isogenic PDR5 and pdr5 strains toward putative substrates that are similar in chemical structure. T...

2014
Sanjoy Paul W. Scott Moye-Rowley

A critical risk to the continued success of antifungal chemotherapy is the acquisition of resistance; a risk exacerbated by the few classes of effective antifungal drugs. Predictably, as the use of these drugs increases in the clinic, more resistant organisms can be isolated from patients. A particularly problematic form of drug resistance that routinely emerges in the major fungal pathogens is...

Journal: :EMBO reports 2001
C A Jakob D Bodmer U Spirig P Battig A Marcil D Dignard J J Bergeron D Y Thomas M Aebi

Misfolded proteins are recognized in the endoplasmic reticulum (ER), transported back to the cytoplasm and degraded by the proteasome. Processing intermediates of N-linked oligosaccharides on incompletely folded glycoproteins have an important role in their folding/refolding, and also in their targeting to proteolytic degradation. In Saccharomyces cerevisiae, we have identified a gene coding fo...

2016
Tanvi Shekhar-Guturja G M Kamal B Gunaherath E M Kithsiri Wijeratne Jean-Philippe Lambert Anna F Averette Soo Chan Lee Taeyup Kim Yong-Sun Bahn Farida Tripodi Ron Ammar Katja Döhl Karolina Niewola-Staszkowska Lutz Schmitt Robbie J Loewith Frederick P Roth Dominique Sanglard David Andes Corey Nislow Paola Coccetti Anne-Claude Gingras Joseph Heitman A A Leslie Gunatilaka Leah E Cowen

There is an urgent need for new strategies to treat invasive fungal infections, which are a leading cause of human mortality. Here, we establish two activities of the natural product beauvericin, which potentiates the activity of the most widely deployed class of antifungal against the leading human fungal pathogens, blocks the emergence of drug resistance, and renders antifungal-resistant path...

2015
Tadahiro Suzuki Yumiko Iwahashi

Host plants excrete a glucosylation enzyme onto the plant surface that changes mycotoxins derived from fungal secondary metabolites to glucosylated products. Deoxynivalenol-3-glucoside (DON3G) is synthesized by grain uridine diphosphate-glucosyltransferase, and is found worldwide, although information on its toxicity is lacking. Here, we conducted growth tests and DNA microarray analysis to elu...

Journal: :Molecular pharmacology 2008
Alexander Stepanov Karin C Nitiss Geoffrey Neale John L Nitiss

Yeast is a powerful model system for studying the action of small-molecule therapeutics. An important limitation has been low efficacy of many small molecules in yeast due to limited intracellular accumulation. We used the DNA binding domain of the pleiotropic drug resistance regulator pleiotropic drug resistance 1 (Pdr1) fused in-frame to transcription repressors to repress Pdr1-regulated gene...

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