Identification of the major phosphorylation domain of murine mdr1b P-glycoprotein. Analysis of the protein kinase A and protein kinase C phosphorylation sites.-Reference-Cited by-同舟云学术

Identification of the major phosphorylation domain of murine mdr1b P-glycoprotein. Analysis of the protein kinase A and protein kinase C phosphorylation sites.

Published:1993-11 Issue:33 Volume:268 Page:25054-25062
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Orr G A,Han E K,Browne P C,Nieves E,O'Connor B M,Yang C P,Horwitz S B

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference50 articles.

1. The multidrug resistance (mdr1) gene product functions as an ATP channel.

2. [11] Phosphopeptide mapping and phosphoamino acid analysis by two-dimensional separation on thin-layer cellulose plates

3. Mechanisms regulating cell resistance to adriamycin evidence that drug accumulation in resistant cells is modulated by phosphorylation of a plasma membrane glycoprotein

4. Protein kinase C phosphorylates P-glycoprotein in multidrug resistant human KB carcinoma cells.

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