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Structural modeling of an outer membrane electron conduit from a metal-reducing bacterium suggests electron transfer via periplasmic redox partners

The Journal of biological chemistry, 2018-05, Vol.293 (21), p.8103-8112

2018

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Human P-glycoprotein Contains a Greasy Ball-and-Socket Joint at the Second Transmission Interface

The Journal of biological chemistry, 2013-07, Vol.288 (28), p.20326-20333

2013

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Location of the Rhodamine-binding Site in the Human Multidrug Resistance P-glycoprotein

The Journal of biological chemistry, 2002-11, Vol.277 (46), p.44332-44338

2002

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Simultaneous Binding of Two Different Drugs in the Binding Pocket of the Human Multidrug Resistance P-glycoprotein

The Journal of biological chemistry, 2003-10, Vol.278 (41), p.39706-39710

2003

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The "LSGGQ" motif in each nucleotide-binding domain of human P-glycoprotein is adjacent to the opposing walker A sequence

The Journal of biological chemistry, 2002-11, Vol.277 (44), p.41303-41306

2002

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Determining the Dimensions of the Drug-binding Domain of Human P-glycoprotein Using Thiol Cross-linking Compounds as Molecular Rulers

The Journal of biological chemistry, 2001-10, Vol.276 (40), p.36877-36880

2001

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Defining the Drug-binding Site in the Human Multidrug Resistance P-glycoprotein Using a Methanethiosulfonate Analog of Verapamil, MTS-verapamil

The Journal of biological chemistry, 2001-05, Vol.276 (18), p.14972-14979

2001

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Methanethiosulfonate Derivatives of Rhodamine and Verapamil Activate Human P-glycoprotein at Different Sites

The Journal of biological chemistry, 2003-12, Vol.278 (50), p.50136-50141

2003

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Correction of Defective Protein Kinesis of Human P-glycoprotein Mutants by Substrates and Modulators

The Journal of biological chemistry, 1997-01, Vol.272 (2), p.709-712

1997

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Membrane Topology of a Cysteine-less Mutant of Human P-glycoprotein (∗)

The Journal of biological chemistry, 1995-01, Vol.270 (2), p.843-848

1995

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Cross-linking of Human Multidrug Resistance P-glycoprotein by the Substrate, Tris-(2-maleimidoethyl)amine, Is Altered by ATP Hydrolysis

The Journal of biological chemistry, 2001-08, Vol.276 (34), p.31800-31805

2001

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Covalent Modification of Human P-glycoprotein Mutants Containing a Single Cysteine in Either Nucleotide-binding Fold Abolishes Drug-stimulated ATPase Activity

The Journal of biological chemistry, 1995-09, Vol.270 (39), p.22957-22961

1995

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Yeast and Rat Coq3 and Escherichia coli UbiG Polypeptides Catalyze Both O-Methyltransferase Steps in Coenzyme Q Biosynthesis

The Journal of biological chemistry, 1999-07, Vol.274 (31), p.21665-21672

1999

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Reconstitution of drug-stimulated ATPase activity following co-expression of each half of human P-glycoprotein as separate polypeptides

The Journal of biological chemistry, 1994-03, Vol.269 (10), p.7750-7755

1994

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Drug-stimulated ATPase Activity of Human P-glycoprotein Is Blocked by Disulfide Cross-linking between the Nucleotide-binding Sites

The Journal of biological chemistry, 2000-06, Vol.275 (26), p.19435-19438

2000

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Inhibition of the G2 DNA Damage Checkpoint and of Protein Kinases Chk1 and Chk2 by the Marine Sponge Alkaloid Debromohymenialdisine

The Journal of biological chemistry, 2001-05, Vol.276 (21), p.17914-17919

2001

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Identification of the Extracellular Matrix Binding Sites for Insulin-like Growth Factor-binding Protein 5

The Journal of biological chemistry, 1996-06, Vol.271 (23), p.13523-13529

1996

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Substrate-induced Conformational Changes in the Transmembrane Segments of Human P-glycoprotein

The Journal of biological chemistry, 2003-04, Vol.278 (16), p.13603-13606

2003

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The short loop between epidermal growth factor-like domains 4 and 5 is critical for human thrombomodulin function

The Journal of biological chemistry, 1993-03, Vol.268 (9), p.6309-6315

1993

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Expression of a Functionally Active Human Renal Sodium-Calcium Exchanger Lacking a Signal Sequence

The Journal of biological chemistry, 1995-08, Vol.270 (33), p.19345-19350

1995

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Identification of Residues in the Drug-binding Domain of Human P-glycoprotein

The Journal of biological chemistry, 1999-12, Vol.274 (50), p.35388-35392

1999

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Structural modeling of an outer membrane electron conduit from a metal-reducing bacterium suggests electron transfer via periplasmic redox partners

Human P-glycoprotein Contains a Greasy Ball-and-Socket Joint at the Second Transmission Interface

Location of the Rhodamine-binding Site in the Human Multidrug Resistance P-glycoprotein

Simultaneous Binding of Two Different Drugs in the Binding Pocket of the Human Multidrug Resistance P-glycoprotein

The "LSGGQ" motif in each nucleotide-binding domain of human P-glycoprotein is adjacent to the opposing walker A sequence

Determining the Dimensions of the Drug-binding Domain of Human P-glycoprotein Using Thiol Cross-linking Compounds as Molecular Rulers

Defining the Drug-binding Site in the Human Multidrug Resistance P-glycoprotein Using a Methanethiosulfonate Analog of Verapamil, MTS-verapamil

Methanethiosulfonate Derivatives of Rhodamine and Verapamil Activate Human P-glycoprotein at Different Sites

Correction of Defective Protein Kinesis of Human P-glycoprotein Mutants by Substrates and Modulators

Membrane Topology of a Cysteine-less Mutant of Human P-glycoprotein (∗)

Cross-linking of Human Multidrug Resistance P-glycoprotein by the Substrate, Tris-(2-maleimidoethyl)amine, Is Altered by ATP Hydrolysis

Covalent Modification of Human P-glycoprotein Mutants Containing a Single Cysteine in Either Nucleotide-binding Fold Abolishes Drug-stimulated ATPase Activity

Yeast and Rat Coq3 and Escherichia coli UbiG Polypeptides Catalyze Both O-Methyltransferase Steps in Coenzyme Q Biosynthesis

Reconstitution of drug-stimulated ATPase activity following co-expression of each half of human P-glycoprotein as separate polypeptides

Drug-stimulated ATPase Activity of Human P-glycoprotein Is Blocked by Disulfide Cross-linking between the Nucleotide-binding Sites

Inhibition of the G2 DNA Damage Checkpoint and of Protein Kinases Chk1 and Chk2 by the Marine Sponge Alkaloid Debromohymenialdisine

Identification of the Extracellular Matrix Binding Sites for Insulin-like Growth Factor-binding Protein 5

Substrate-induced Conformational Changes in the Transmembrane Segments of Human P-glycoprotein

The short loop between epidermal growth factor-like domains 4 and 5 is critical for human thrombomodulin function

Expression of a Functionally Active Human Renal Sodium-Calcium Exchanger Lacking a Signal Sequence

Identification of Residues in the Drug-binding Domain of Human P-glycoprotein

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