A structure-based mechanism for drug binding by multidrug transporters (Q33832047)

29 July 2017

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title

A structure-based mechanism for drug binding by multidrug transporters (English)

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29 July 2017

Zheleznova EE

1

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29 July 2017

Markham P

2

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29 July 2017

Edgar R

3

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29 July 2017

Bibi E

4

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29 July 2017

Neyfakh AA

5

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29 July 2017

Brennan RG

6

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29 July 2017

publication date

1 February 2000

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29 July 2017

number of pages

5

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Trends in Biochemical Sciences

inferred from page(s)

published in

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29 July 2017

volume

25

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29 July 2017

issue

2

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29 July 2017

page(s)

39-43

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The P-glycoprotein efflux pump: how does it transport drugs?

29 July 2017

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Is the multidrug transporter a flippase?

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The nitrogen of the acetamido group of colchicine modulates P-glycoprotein-mediated multidrug resistance.

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A single membrane-embedded negative charge is critical for recognizing positively charged drugs by the Escherichia coli multidrug resistance protein MdfA.

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Membrane vesicles from multidrug-resistant human cancer cells contain a specific 150- to 170-kDa protein detected by photoaffinity labeling

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7 January 2021

The pharmacological profile of the vesicular monoamine transporter resembles that of multidrug transporters

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7 January 2021

Use of fluorescence probes to monitor function of the subunit proteins of the MexA-MexB-oprM drug extrusion machinery in Pseudomonas aeruginosa

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7 January 2021

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7 January 2021

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7 January 2021

Multiple residues contribute independently to differences in ligand recognition between vesicular monoamine transporters 1 and 2.

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7 January 2021

Stimulation of P-glycoprotein-mediated drug transport by prazosin and progesterone. Evidence for a third drug-binding site.

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7 January 2021

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7 January 2021

Multidrug resistance protein (Mdr)-alkaline phosphatase hybrids in Escherichia coli suggest a major revision in the topology of the C-terminal half of Mdr.

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7 January 2021

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Identifiers

DOI

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29 July 2017

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