-
1
-
-
0032900953
-
Biochemical, cellular, and pharmacological aspects of the multidrug transporter
-
Ambudkar, S. V., Dey, S., Hrycyna, C. A., Ramachandra, M., Pastan, I., and Gottesman, M. M. (1999) Biochemical, cellular, and pharmacological aspects of the multidrug transporter, Annu. Rev. Pharmacol. Toxicol. 39, 361-398.
-
(1999)
Annu. Rev. Pharmacol. Toxicol.
, vol.39
, pp. 361-398
-
-
Ambudkar, S.V.1
Dey, S.2
Hrycyna, C.A.3
Ramachandra, M.4
Pastan, I.5
Gottesman, M.M.6
-
2
-
-
0023447098
-
Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues
-
Thiebaut, F., Tsuruo, T., Hamada, H., Gottesman, M. M., Pastan, I., and Willingham, M. C. (1987) Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues, Proc. Natl. Acad. Sci. U.S.A. 84, 7735-7738.
-
(1987)
Proc. Natl. Acad. Sci. U.S.A.
, vol.84
, pp. 7735-7738
-
-
Thiebaut, F.1
Tsuruo, T.2
Hamada, H.3
Gottesman, M.M.4
Pastan, I.5
Willingham, M.C.6
-
3
-
-
0032601621
-
Molecular Dissection of the Human Multidrug Resistance P-glycoprotein
-
Loo, T. W., and Clarke, D. M. (1999) Molecular Dissection of the Human Multidrug Resistance P-glycoprotein, Blochem. Cell. Biol. 77, 11-23.
-
(1999)
Blochem. Cell. Biol.
, vol.77
, pp. 11-23
-
-
Loo, T.W.1
Clarke, D.M.2
-
4
-
-
0028229150
-
Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs
-
Schinkel, A. H., Smit, J. J., van Tellingen, O., Beijnen, J. H., Wagenaar, E., van Deemter, L., Mol, C. A., van der Valk, M. A., Robanus-Maandag, E. C., te Riele, H. P., Berns, A. J. M., and Borst, P. (1994) Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs, Cell 77, 491-502.
-
(1994)
Cell
, vol.77
, pp. 491-502
-
-
Schinkel, A.H.1
Smit, J.J.2
Van Tellingen, O.3
Beijnen, J.H.4
Wagenaar, E.5
Van Deemter, L.6
Mol, C.A.7
Van Der Valk, M.A.8
Robanus-Maandag, E.C.9
Te Riele, H.P.10
Berns, A.J.M.11
Borst, P.12
-
5
-
-
0032540001
-
HIV-1 protease inhibitors are substrates for the MDR1 multidrug transporter
-
Lee, C. G., Gottesman, M. M., Cardarelli, C. O., Ramachandra, M., Jeang, K. T., Ambudkar, S. V., Pastan, I., and Dey, S. (1998) HIV-1 protease inhibitors are substrates for the MDR1 multidrug transporter, Biochemistry 37, 3594-3601.
-
(1998)
Biochemistry
, vol.37
, pp. 3594-3601
-
-
Lee, C.G.1
Gottesman, M.M.2
Cardarelli, C.O.3
Ramachandra, M.4
Jeang, K.T.5
Ambudkar, S.V.6
Pastan, I.7
Dey, S.8
-
6
-
-
0034917716
-
The human ATP-binding cassette (ABC) transporter superfamily
-
Dean, M., Rzhetsky, A., and Allikmets, R. (2001) The human ATP-binding cassette (ABC) transporter superfamily, Genome Res. 11, 1156-1166.
-
(2001)
Genome Res.
, vol.11
, pp. 1156-1166
-
-
Dean, M.1
Rzhetsky, A.2
Allikmets, R.3
-
7
-
-
0022972654
-
Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cells
-
Chen, C. J., Chin, J. E., Ueda, K., Clark, D. P., Pastan, I., Gottesman, M. M., and Roninson, I. B. (1986) Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cells, Cell 47, 381-389.
-
(1986)
Cell
, vol.47
, pp. 381-389
-
-
Chen, C.J.1
Chin, J.E.2
Ueda, K.3
Clark, D.P.4
Pastan, I.5
Gottesman, M.M.6
Roninson, I.B.7
-
8
-
-
0028229881
-
Reconstitution of drug-stimulated ATPase activity following co- expression of each half of human P-glycoprotein as separate polypeptides
-
Loo, T. W., and Clarke, D. M. (1994) Reconstitution of drug-stimulated ATPase activity following co- expression of each half of human P-glycoprotein as separate polypeptides, J. Biol. Chem. 269, 7750-7755.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 7750-7755
-
-
Loo, T.W.1
Clarke, D.M.2
-
9
-
-
0028786395
-
Both P-glycoprotein nucleotide-binding sites are catalytically active
-
Urbatsch, I. L., Sankaran, B., Bhagat, S., and Senior, A. E. (1995) Both P-glycoprotein nucleotide-binding sites are catalytically active, J. Biol. Chem. 270, 26956-26961.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 26956-26961
-
-
Urbatsch, I.L.1
Sankaran, B.2
Bhagat, S.3
Senior, A.E.4
-
10
-
-
0024307162
-
Discrete mutations introduced in the predicted nucleotide-binding sites of the mdr1 gene abolish its ability to confer multidrug resistance
-
Azzaria, M., Schurr, E., and Gros, P. (1989) Discrete mutations introduced in the predicted nucleotide-binding sites of the mdr1 gene abolish its ability to confer multidrug resistance. Mol. Cell. Biol. 9, 5289-5297.
-
(1989)
Mol. Cell. Biol.
, vol.9
, pp. 5289-5297
-
-
Azzaria, M.1
Schurr, E.2
Gros, P.3
-
11
-
-
0029121417
-
Covalent modification of human P-glycoprotein mutants containing a single cysteine in either nucleotide-binding fold abolishes drug- stimulated ATPase activity
-
Loo, T. W., and Clarke, D. M. (1995) Covalent modification of human P-glycoprotein mutants containing a single cysteine in either nucleotide-binding fold abolishes drug- stimulated ATPase activity, J. Biol. Chem. 270, 22957-22961.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 22957-22961
-
-
Loo, T.W.1
Clarke, D.M.2
-
12
-
-
0031156388
-
ATP hydrolysis cycles and mechanism in P-glycoprotein and CFTR
-
Senior, A. E., and Gadsby, D. C. (1997) ATP hydrolysis cycles and mechanism in P-glycoprotein and CFTR, Semin. Cancer Biol. 8, 143-150.
-
(1997)
Semin. Cancer Biol.
, vol.8
, pp. 143-150
-
-
Senior, A.E.1
Gadsby, D.C.2
-
13
-
-
0034705293
-
Structural biology of Rad50 ATPase: ATP-driven conformational control in DNA double-strand break repair and the ABC-ATPase superfamily
-
Hopfner, K. P., Karcher, A., Shin, D. S., Craig, L., Arthur, L. M., Carney, J. P., and Tainer, J. A. (2000) Structural biology of Rad50 ATPase: ATP-driven conformational control in DNA double-strand break repair and the ABC-ATPase superfamily, Cell 101, 789-800.
-
(2000)
Cell
, vol.101
, pp. 789-800
-
-
Hopfner, K.P.1
Karcher, A.2
Shin, D.S.3
Craig, L.4
Arthur, L.M.5
Carney, J.P.6
Tainer, J.A.7
-
14
-
-
0036829647
-
The "LSGGQ" motif in each nucleotide-binding domain of human P-glycoprotein is adjacent to the opposing walker a sequence
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2002) The "LSGGQ" motif in each nucleotide-binding domain of human P-glycoprotein is adjacent to the opposing walker A sequence, J. Biol. Chem. 277, 41303-41306.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 41303-41306
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
15
-
-
0037162468
-
Vanadate-catalyzed photocleavage of the signature motif of an ATP-binding cassette (ABC) transporter
-
Fetsch, E. E., and Davidson, A. L. (2002) Vanadate-catalyzed photocleavage of the signature motif of an ATP-binding cassette (ABC) transporter, Proc. Natl. Acad. Sci. U.S.A. 99, 9685-9690.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 9685-9690
-
-
Fetsch, E.E.1
Davidson, A.L.2
-
16
-
-
0037449746
-
Drug binding in human P-glycoprotein causes conformational changes in both nucleotide-binding domains
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2003) Drug binding in human P-glycoprotein causes conformational changes in both nucleotide-binding domains, J. Biol. Chem. 278, 1575-1578.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 1575-1578
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
17
-
-
0034671916
-
Identification of residues within the drug-binding domain of the human multidrug resistance P-glycoprotein by cysteine-scanning mutagenesis and reaction with dibromobimane
-
Loo, T. W., and Clarke, D. M. (2000) Identification of residues within the drug-binding domain of the human multidrug resistance P-glycoprotein by cysteine-scanning mutagenesis and reaction with dibromobimane, J. Biol. Chem. 275, 39272-39278.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 39272-39278
-
-
Loo, T.W.1
Clarke, D.M.2
-
18
-
-
0035805573
-
Defining the drug-binding site in the human multidrug resistance P-glycoprotein using MTS-verapamil
-
Loo, T. W., and Clarke, D. M. (2001) Defining the drug-binding site in the human multidrug resistance P-glycoprotein using MTS-verapamil. J. Biol. Chem. 276, 14972-14979.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 14972-14979
-
-
Loo, T.W.1
Clarke, D.M.2
-
19
-
-
0035813143
-
Determining the dimensions of the drug-binding domain of human P-glycoprotein using thiol cross-linkers as molecular rulers
-
Loo, T. W., and Clarke, D. M. (2001) Determining the dimensions of the drug-binding domain of human P-glycoprotein using thiol cross-linkers as molecular rulers, J. Biol. Chem. 276, 36877-36880.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 36877-36880
-
-
Loo, T.W.1
Clarke, D.M.2
-
20
-
-
0037113961
-
Location of the rhodamine-binding site in the human multidrug resistance P-glycoprotein
-
Loo, T. W., and Clarke, D. M. (2002) Location of the rhodamine-binding site in the human multidrug resistance P-glycoprotein, J. Biol. Chem. 277, 44332-44338.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 44332-44338
-
-
Loo, T.W.1
Clarke, D.M.2
-
21
-
-
13444266621
-
P-glycoprotein substrate binding domains are located at the transmembrane domain/transmembrane domain interfaces: A combined photoaffinity labeling-protein homology modeling approach
-
Pleban, K., Kopp, S., Csaszar, E., Peer, M., Hrebicek, T., Rizzi, A., Ecker, G. F., and Chiba, P. (2005) P-glycoprotein substrate binding domains are located at the transmembrane domain/transmembrane domain interfaces: a combined photoaffinity labeling-protein homology modeling approach, Mol. Pharmacol. 67, 365-374.
-
(2005)
Mol. Pharmacol.
, vol.67
, pp. 365-374
-
-
Pleban, K.1
Kopp, S.2
Csaszar, E.3
Peer, M.4
Hrebicek, T.5
Rizzi, A.6
Ecker, G.F.7
Chiba, P.8
-
22
-
-
0033609856
-
The transmembrane domains of the human multidrug resistance P-glycoprotein are sufficient to mediate drug binding and trafficking to the cell surface
-
Loo, T. W., and Clarke, D. M. (1999) The transmembrane domains of the human multidrug resistance P-glycoprotein are sufficient to mediate drug binding and trafficking to the cell surface, J. Biol. Chem. 274, 24759-24765.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 24759-24765
-
-
Loo, T.W.1
Clarke, D.M.2
-
23
-
-
0030924052
-
Evidence for two nonidentical drug-interaction sites in the human P-glycoprotein
-
Dey, S., Ramachandra, M., Pastan, I., Gottesman, M. M., and Ambudkar, S. V. (1997) Evidence for two nonidentical drug-interaction sites in the human P-glycoprotein, Proc. Natl. Acad. Sci. U.S.A. 94, 10594-10599.
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 10594-10599
-
-
Dey, S.1
Ramachandra, M.2
Pastan, I.3
Gottesman, M.M.4
Ambudkar, S.V.5
-
24
-
-
0032528254
-
Multidrug resistance transporter P-glycoprotein has distinct but interacting binding sites for cytotoxic drugs and reversing agents
-
Pascaud, C., Garrigos, M., and Orlowski, S. (1998) Multidrug resistance transporter P-glycoprotein has distinct but interacting binding sites for cytotoxic drugs and reversing agents, Biochem. J. 333, 351-358.
-
(1998)
Biochem. J.
, vol.333
, pp. 351-358
-
-
Pascaud, C.1
Garrigos, M.2
Orlowski, S.3
-
25
-
-
0033083015
-
Stimulation of P-glycoprotein-mediated drug transport by prazosin and progesterone. Evidence for a third drug-binding site
-
Shapiro, A. B., Fox, K., Lam, P., and Ling, V. (1999) Stimulation of P-glycoprotein-mediated drug transport by prazosin and progesterone. Evidence for a third drug-binding site, Eur. J. Biochem. 259, 841-850.
-
(1999)
Eur. J. Biochem.
, vol.259
, pp. 841-850
-
-
Shapiro, A.B.1
Fox, K.2
Lam, P.3
Ling, V.4
-
26
-
-
0037687304
-
Substrate-induced Conformational Changes in the Transmembrane Segments of Human P-glycoprotein. DIRECT EVIDENCE for the SUBSTRATE-INDUCED FIT MECHANISM for DRUG BINDING
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2003) Substrate-induced Conformational Changes in the Transmembrane Segments of Human P-glycoprotein. DIRECT EVIDENCE FOR THE SUBSTRATE-INDUCED FIT MECHANISM FOR DRUG BINDING, J. Biol. Chem. 278, 13603-13606.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 13603-13606
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
27
-
-
0030779102
-
Drug-stimulated ATPase activity of human P-glycoprotein requires movement between transmembrane segments 6 and 12
-
Loo, T. W., and Clarke, D. M. (1997) Drug-stimulated ATPase activity of human P-glycoprotein requires movement between transmembrane segments 6 and 12, J. Biol. Chem. 272, 20986-20989.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 20986-20989
-
-
Loo, T.W.1
Clarke, D.M.2
-
28
-
-
0035943691
-
Cross-linking of human multidrug resistance P-glycoprotein by the substrate, Tris-(2-maleimidoethyl)amine, is altered by ATP hydrolysis: Evidence for rotation of a transmembrane helix
-
Loo, T. W., and Clarke, D. M. (2001) Cross-linking of human multidrug resistance P-glycoprotein by the substrate, Tris-(2-maleimidoethyl)amine, is altered by ATP hydrolysis: Evidence for rotation of a transmembrane helix, J. Biol. Chem. 276, 31800-31805.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 31800-31805
-
-
Loo, T.W.1
Clarke, D.M.2
-
29
-
-
4544284056
-
The topography of transmembrane segment six is altered during the catalytic cycle of P-glycoprotein
-
Rothnie, A., Storm, J., Campbell, J., Linton, K. J., Kerr, I. D., and Callaghan, R. (2004) The topography of transmembrane segment six is altered during the catalytic cycle of P-glycoprotein, J. Biol. Chem. 279, 34913-34921.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 34913-34921
-
-
Rothnie, A.1
Storm, J.2
Campbell, J.3
Linton, K.J.4
Kerr, I.D.5
Callaghan, R.6
-
30
-
-
0037133616
-
Vanadate trapping of nucleotide at the ATP-binding sites of human multidrug resistance P-glycoprotein exposes different residues to the drug-binding site
-
Loo, T. W., and Clarke, D. M. (2002) Vanadate trapping of nucleotide at the ATP-binding sites of human multidrug resistance P-glycoprotein exposes different residues to the drug-binding site, Proc. Natl. Acad. Sci. U.S.A. 99, 3511-3516.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 3511-3516
-
-
Loo, T.W.1
Clarke, D.M.2
-
31
-
-
0027215242
-
Functional analysis of P-glycoprotein mutants identifies predicted transmembrane domain 11 as a putative drug binding site
-
Kajiji, S., Talbot, F., Grizzuti, K., Van Dyke-Phillips, V., Agresti, M., Safa, A. R., and Gros, P. (1993) Functional analysis of P-glycoprotein mutants identifies predicted transmembrane domain 11 as a putative drug binding site, Biochemistry 32, 4185-4194.
-
(1993)
Biochemistry
, vol.32
, pp. 4185-4194
-
-
Kajiji, S.1
Talbot, F.2
Grizzuti, K.3
Van Dyke-Phillips, V.4
Agresti, M.5
Safa, A.R.6
Gros, P.7
-
32
-
-
0033544851
-
Identification of residues in the drug-binding domain of human P-glycoprotein: Analysis of transmembrane segment 11 by cysteine-scanning mutagenesis and inhibition by dibromobimane
-
Loo, T. W., and Clarke, D. M. (1999) Identification of residues in the drug-binding domain of human P-glycoprotein: Analysis of transmembrane segment 11 by cysteine-scanning mutagenesis and inhibition by dibromobimane, J. Biol. Chem. 274, 35388-35392.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 35388-35392
-
-
Loo, T.W.1
Clarke, D.M.2
-
33
-
-
14644425991
-
Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"?
-
Loo, T. W., and Clarke, D. M. (2005) Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"?, Biochem. Biophys. Res. Commun. 329, 419-422.
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.329
, pp. 419-422
-
-
Loo, T.W.1
Clarke, D.M.2
-
34
-
-
0027997698
-
Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoprotein
-
Loo, T. W., and Clarke, D. M. (1994) Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoprotein. Biochemistry 33, 14049-14057.
-
(1994)
Biochemistry
, vol.33
, pp. 14049-14057
-
-
Loo, T.W.1
Clarke, D.M.2
-
35
-
-
0028928984
-
Membrane topology of a cysteine-less mutant of human P-glycoprotein
-
Loo, T. W., and Clarke, D. M. (1995) Membrane topology of a cysteine-less mutant of human P-glycoprotein, J. Biol. Chem. 270, 843-848.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 843-848
-
-
Loo, T.W.1
Clarke, D.M.2
-
36
-
-
0029100095
-
Rapid purification of human P-glycoprotein mutants expressed transiently in HEK 293 cells by nickel-chelate chromatography and characterization of their drug-stimulated ATPase activities
-
Loo, T. W., and Clarke, D. M. (1995) Rapid purification of human P-glycoprotein mutants expressed transiently in HEK 293 cells by nickel-chelate chromatography and characterization of their drug-stimulated ATPase activities, J. Biol. Chem. 270, 21449-21452.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 21449-21452
-
-
Loo, T.W.1
Clarke, D.M.2
-
37
-
-
0028127183
-
Prolonged association of temperature-sensitive mutants of human P-glycoprotein with calnexin during biogenesis
-
Loo, T. W., and Clarke, D. M. (1994) Prolonged association of temperature-sensitive mutants of human P-glycoprotein with calnexin during biogenesis, J. Biol. Chem. 269, 28683-28689.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 28683-28689
-
-
Loo, T.W.1
Clarke, D.M.2
-
38
-
-
0028245416
-
Functional consequences of glycine mutations in the predicted cytoplasmic loops of P-glycoprotein
-
Loo, T. W., and Clarke, D. M. (1994) Functional consequences of glycine mutations in the predicted cytoplasmic loops of P-glycoprotein, J. Biol. Chem. 269, 7243-7248.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 7243-7248
-
-
Loo, T.W.1
Clarke, D.M.2
-
39
-
-
0029099301
-
P-glycoprotein. Associations between domains and between domains and molecular chaperones
-
Loo, T. W., and Clarke, D. M. (1995) P-glycoprotein. Associations between domains and between domains and molecular chaperones, J. Biol. Chem. 270, 21839-21844.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 21839-21844
-
-
Loo, T.W.1
Clarke, D.M.2
-
40
-
-
0029909604
-
Inhibition of oxidative cross-linking between engineered cysteine residues at positions 332 in predicted transmembrane segments (TM) 6 and 975 in predicted TM12 of human P-glycoprotein by drug substrates
-
Loo, T. W., and Clarke, D. M. (1996) Inhibition of oxidative cross-linking between engineered cysteine residues at positions 332 in predicted transmembrane segments (TM) 6 and 975 in predicted TM12 of human P-glycoprotein by drug substrates, J. Biol. Chem. 271, 27482-27487.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 27482-27487
-
-
Loo, T.W.1
Clarke, D.M.2
-
41
-
-
0020023988
-
Myosin active-site trapping with vanadate ion
-
Goodno, C. C. (1982) Myosin active-site trapping with vanadate ion, Methods Enzymol. 85, 116-123.
-
(1982)
Methods Enzymol.
, vol.85
, pp. 116-123
-
-
Goodno, C.C.1
-
42
-
-
0031021804
-
Correction of defective protein kinesis of human P-glycoprotein mutants by substrates and modulators
-
Loo, T. W., and Clarke, D. M. (1997) Correction of defective protein kinesis of human P-glycoprotein mutants by substrates and modulators, J. Biol. Chem. 272, 709-712.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 709-712
-
-
Loo, T.W.1
Clarke, D.M.2
-
43
-
-
0032510958
-
Superfolding of the partially unfolded core-glycosylated intermediate of human P-glycoprotein into the mature enzyme is promoted by substrate-induced transmembrane domain interactions
-
Loo, T. W., and Clarke, D. M. (1998) Superfolding of the Partially Unfolded Core-glycosylated Intermediate of Human P-glycoprotein into the Mature Enzyme Is Promoted by Substrate-induced Transmembrane Domain Interactions, J. Biol. Chem. 273, 14671-14674.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 14671-14674
-
-
Loo, T.W.1
Clarke, D.M.2
-
44
-
-
0037008685
-
Introduction of the most common cystic fibrosis mutation (Delta f508) into human P-glycoprotein disrupts packing of the transmembrane segments
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2002) Introduction of the Most Common Cystic Fibrosis Mutation (Delta F508) into Human P-glycoprotein Disrupts Packing of the Transmembrane Segments, J. Biol. Chem. 277, 27585-27588.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 27585-27588
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
45
-
-
0023874147
-
A method for the determination of inorganic phosphate in the presence of labile organic phosphate and high concentrations of protein: Application to lens ATPases
-
Chifflet, S., Torriglia, A., Chiesa, R., and Tolosa, S. (1988) A method for the determination of inorganic phosphate in the presence of labile organic phosphate and high concentrations of protein: application to lens ATPases, Anal. Biochem. 168, 1-4.
-
(1988)
Anal. Biochem.
, vol.168
, pp. 1-4
-
-
Chifflet, S.1
Torriglia, A.2
Chiesa, R.3
Tolosa, S.4
-
46
-
-
0034051662
-
The packing of the transmembrane segments of human multidrug resistance P-glycoprotein is revealed by disulfide cross-linking analysis
-
Loo, T. W., and Clarke, D. M. (2000) The packing of the transmembrane segments of human multidrug resistance P-glycoprotein is revealed by disulfide cross-linking analysis, J. Biol. Chem. 275, 5253-5256.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 5253-5256
-
-
Loo, T.W.1
Clarke, D.M.2
-
47
-
-
0031434236
-
Identification of residues in the drug-binding site of human P-glycoprotein using a thiol-reactive substrate
-
Loo, T. W., and Clarke, D. M. (1997) Identification of residues in the drug-binding site of human P-glycoprotein using a thiol-reactive substrate. J. Biol. Chem. 272, 31945-31948.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 31945-31948
-
-
Loo, T.W.1
Clarke, D.M.2
-
48
-
-
2442597224
-
Residues V133 and C137 in transmembrane segment 2 are close to residues A935 and G939 in transmembrane segment 11 of human P-glycoprotein
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2004) Residues V133 and C137 in transmembrane segment 2 are close to residues A935 and G939 in transmembrane segment 11 of human P-glycoprotein, J. Biol. Chem. 279, 18232-18238.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 18232-18238
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
49
-
-
0642272487
-
An atomic detail model for the human ATP binding cassette transporter P-glycoprotein derived from disulfide cross-linking and homology modeling
-
Stenham, D. R., Campbell, J. D., Sansom, M. S., Higgins, C. F., Kerr, I. D., and Linton, K. J. (2003) An atomic detail model for the human ATP binding cassette transporter P-glycoprotein derived from disulfide cross-linking and homology modeling, FASEB J. 17, 2287-2289.
-
(2003)
FASEB J.
, vol.17
, pp. 2287-2289
-
-
Stenham, D.R.1
Campbell, J.D.2
Sansom, M.S.3
Higgins, C.F.4
Kerr, I.D.5
Linton, K.J.6
-
50
-
-
0029124166
-
P-glycoprotein is stably inhibited by vanadate-induced trapping of nucleotide at a single catalytic site
-
Urbatsch, I. L., Sankaran, B., Weber, J., and Senior, A. E. (1995) P-glycoprotein is stably inhibited by vanadate-induced trapping of nucleotide at a single catalytic site, J. Biol. Chem. 270, 19383-19390.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 19383-19390
-
-
Urbatsch, I.L.1
Sankaran, B.2
Weber, J.3
Senior, A.E.4
-
51
-
-
0030868612
-
Relation between the turnover number for vinblastine transport and for vinblastine-stimulated ATP hydrolysis by human P-glycoprotein
-
Ambudkar, S. V., Cardarelli, C. O., Pashinsky, I., and Stein, W. D. (1997) Relation between the turnover number for vinblastine transport and for vinblastine-stimulated ATP hydrolysis by human P-glycoprotein, J. Biol. Chem. 272, 21160-21166.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 21160-21166
-
-
Ambudkar, S.V.1
Cardarelli, C.O.2
Pashinsky, I.3
Stein, W.D.4
-
52
-
-
0033862765
-
Communication between multiple drug binding sites on P-glycoprotein
-
Martin, C., Berridge, G., Higgins, C. F., Mistry, P., Charlton, P., and Callaghan, R. (2000) Communication between multiple drug binding sites on P-glycoprotein, Mol. Pharmacol. 58, 624-632.
-
(2000)
Mol. Pharmacol.
, vol.58
, pp. 624-632
-
-
Martin, C.1
Berridge, G.2
Higgins, C.F.3
Mistry, P.4
Charlton, P.5
Callaghan, R.6
-
53
-
-
4644265234
-
The drug-binding pocket of the human multidrug resistance P-glycoprotein is accessible to the aqueous medium
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2004) The drug-binding pocket of the human multidrug resistance P-glycoprotein is accessible to the aqueous medium, Biochemistry 43, 12081-12089.
-
(2004)
Biochemistry
, vol.43
, pp. 12081-12089
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
54
-
-
0033580854
-
Ligand-mediated tertiary structure changes of reconstituted P-glycoprotein. A tryptophan fluorescence quenching analysis
-
Sonveaux, N., Vigano, C., Shapiro, A. B., Ling, V., and Ruysschaert, J. M. (1999) Ligand-mediated tertiary structure changes of reconstituted P-glycoprotein. A tryptophan fluorescence quenching analysis, J. Biol. Chem. 274, 17649-17654.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 17649-17654
-
-
Sonveaux, N.1
Vigano, C.2
Shapiro, A.B.3
Ling, V.4
Ruysschaert, J.M.5
-
55
-
-
13244292479
-
Three-dimensional structure of P-glycoprotein: The transmembrane regions adopt an asymmetric configuration in the nucleotide-bound state
-
Rosenberg, M. F., Callaghan, R., Modok, S., Higgins, C. F., and Ford, R. C. (2005) Three-dimensional structure of P-glycoprotein: the transmembrane regions adopt an asymmetric configuration in the nucleotide-bound state, J. Biol. Chem. 280, 2857-2862.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 2857-2862
-
-
Rosenberg, M.F.1
Callaghan, R.2
Modok, S.3
Higgins, C.F.4
Ford, R.C.5
-
56
-
-
0346732289
-
Transition state analysis of the coupling of drug transport to ATP hydrolysis by P-glycoprotein
-
Al-Shawi, M. K., Polar, M. K., Omote, H., and Figler, R. A. (2003) Transition state analysis of the coupling of drug transport to ATP hydrolysis by P-glycoprotein, J. Biol. Chem. 278, 52629-52640.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 52629-52640
-
-
Al-Shawi, M.K.1
Polar, M.K.2
Omote, H.3
Figler, R.A.4
-
57
-
-
0038799725
-
Structure of MsbA from Vibrio cholera: A Multidrug Resistance ABC transporter Homolog in a Closed Conformation
-
Chang, G. (2003) Structure of MsbA from Vibrio cholera: A Multidrug Resistance ABC transporter Homolog in a Closed Conformation, J. Mol. Biol. 330, 419-430.
-
(2003)
J. Mol. Biol.
, vol.330
, pp. 419-430
-
-
Chang, G.1
-
58
-
-
18644363550
-
Structure of the ABC transporter MsbA in complex with ADP.vanadate and lipopolysaccharide
-
Reyes, C. L., and Chang, G. (2005) Structure of the ABC transporter MsbA in complex with ADP.vanadate and lipopolysaccharide, Science 308, 1028-1031.
-
(2005)
Science
, vol.308
, pp. 1028-1031
-
-
Reyes, C.L.1
Chang, G.2
|