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1.
Mini Rev Med Chem ; 5(2): 165-72, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15720286

ABSTRACT

The aim of the present review is to summarize recent progress in identifying substrate binding domains of P-glycoprotein by photoaffinity labeling. Preferred substrate binding regions have been identified using a number of photoaffinity ligands, including anthracyclines, the quinazoline iodoarylazidoprazosine (IAAP), dihydropyridines, taxanes and propafenones. These studies allowed identification of protein regions, which are involved in ligand interaction.


Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/chemistry , Photoaffinity Labels/chemistry , ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Animals , Binding Sites , Humans , Ligands
2.
Mol Cell ; 9(3): 515-25, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11931760

ABSTRACT

The separation of sister chromatids in anaphase depends on the dissociation of cohesin from chromosomes. In vertebrates, some cohesin is removed from chromosomes at the onset of anaphase by proteolytic cleavage. In contrast, the bulk of cohesin is removed from chromosomes already in prophase and prometaphase by an unknown mechanism that does not involve cohesin cleavage. We show that Polo-like kinase is required for the cleavage-independent dissociation of cohesin from chromosomes in Xenopus. Cohesin phosphorylation depends on Polo-like kinase and reduces the ability of cohesin to bind to chromatin. These results suggest that Polo-like kinase regulates the dissociation of cohesin from chromosomes early in mitosis.


Subject(s)
Cell Cycle/physiology , Chromosomes/physiology , Nuclear Proteins/metabolism , Protein Kinases/metabolism , Animals , Aurora Kinases , Cell Cycle Proteins/metabolism , Cell Fractionation , Chromosomal Proteins, Non-Histone , DNA-Binding Proteins/metabolism , Fungal Proteins , HeLa Cells , Humans , Nuclear Proteins/chemistry , Nuclear Proteins/isolation & purification , Oocytes/physiology , Phosphorylation , Protein Serine-Threonine Kinases/metabolism , Proto-Oncogene Proteins , Tissue Extracts/chemistry , Tissue Extracts/metabolism , Xenopus Proteins , Xenopus laevis , Cohesins , Polo-Like Kinase 1
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