scholarly article | Q13442814 |
P2093 | author name string | A F Castro | |
C Wang | |||
D M Wilkes | |||
G A Altenberg | |||
P2860 | cites work | Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to glutathione-S-transferase. | Q54613850 |
Factor Xa cleavage of fusion proteins. Elimination of non-specific cleavage by reversible acylation. | Q54714779 | ||
Recombinant synthesis, purification, and nucleotide binding characteristics of the first nucleotide binding domain of the cystic fibrosis gene product | Q67895667 | ||
A method for the determination of inorganic phosphate in the presence of labile organic phosphate and high concentrations of protein: application to lens ATPases | Q69825502 | ||
Recombinant N-terminal nucleotide-binding domain from mouse P-glycoprotein. Overexpression, purification, and role of cysteine 430 | Q71142739 | ||
Pas de deux or more: the sulfonylurea receptor and K+ channels | Q72155505 | ||
Covalent inhibitors of P-glycoprotein ATPase activity | Q72671369 | ||
Protein kinase C-mediated phosphorylation of the human multidrug resistance P-glycoprotein regulates cell volume-activated chloride channels | Q28910230 | ||
The ATP-binding component of a prokaryotic traffic ATPase is exposed to the periplasmic (external) surface | Q36064136 | ||
A recombinant peptide model of the first nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator: comparison of wild-type and delta F508 mutant forms | Q36279470 | ||
Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein | Q36846356 | ||
Detection of P-glycoprotein isoforms by gene-specific monoclonal antibodies | Q37660701 | ||
Nucleotide binding to the hydrophilic C-terminal domain of the transporter associated with antigen processing (TAP). | Q38308202 | ||
The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein | Q38314343 | ||
Domain organization of murine mdr1b P-glycoprotein: the cytoplasmic linker region is a potential dimerization domain. | Q38349319 | ||
Overexpression of integral membrane proteins for structural studies | Q40370871 | ||
The Cystic Fibrosis Transmembrane Conductance Regulator | Q40486029 | ||
The nucleotide binding folds of the cystic fibrosis transmembrane conductance regulator are extracellularly accessible | Q41103955 | ||
Phosphorylation by cAMP-dependent protein kinase causes a conformational change in the R domain of the cystic fibrosis transmembrane conductance regulator | Q41661209 | ||
Multidrug transporters from bacteria to man: similarities in structure and function | Q41688649 | ||
Muscarinic stimulation of gallbladder epithelium. III. Antagonism of cAMP-mediated effects | Q42493563 | ||
Inhibition of drug transport by genistein in multidrug-resistant cells expressing P-glycoprotein | Q42804859 | ||
Expression and characterization of the NBD1-R domain region of CFTR: evidence for subunit-subunit interactions | Q46698059 | ||
Overexpression and purification of the carboxyl-terminal nucleotide-binding domain from mouse P-glycoprotein. Strategic location of a tryptophan residue. | Q50769282 | ||
A recombinant polypeptide model of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator functions as an active ATPase, GTPase and adenylate kinase. | Q53967795 | ||
Stimulation of CFTR activity by its phosphorylated R domain. | Q54558597 | ||
Cystic fibrosis transmembrane conductance regulator: the first nucleotide binding fold targets the membrane with retention of its ATP binding function. | Q54567502 | ||
Expression in Escherichia coli of cytoplasmic portions of the cystic fibrosis transmembrane conductance regulator: apparent bacterial toxicity of peptides containing R-domain sequences. | Q54593967 | ||
Cloning, overexpression, purification, and characterization of the carboxyl-terminal nucleotide binding domain of P-glycoprotein. | Q54610591 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | glutathione | Q116907 |
multiple drug resistance | Q643839 | ||
P304 | page(s) | 77-81 | |
P577 | publication date | 1999-02-01 | |
P1433 | published in | Biochemical Journal | Q864221 |
P1476 | title | Expression and purification of the first nucleotide-binding domain and linker region of human multidrug resistance gene product: comparison of fusions to glutathione S-transferase, thioredoxin and maltose-binding protein | |
P478 | volume | 338 ( Pt 1) |
Q34228979 | A critical review of the methods for cleavage of fusion proteins with thrombin and factor Xa. |
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Q44075217 | S-decyl-glutathione nonspecifically stimulates the ATPase activity of the nucleotide-binding domains of the human multidrug resistance-associated protein, MRP1 (ABCC1). |
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