-
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
-
-
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. et al. (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
-
3
-
-
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
-
4
-
-
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
-
5
-
-
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
-
6
-
-
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
-
7
-
-
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
-
8
-
-
0029910016
-
The minimum functional unit of human P-glycoprotein appears to be a monomer
-
Loo, T. W. and Clarke, D. M. (1996) The minimum functional unit of human P-glycoprotein appears to be a monomer. J. Biol. Chem. 271, 27488-27492
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 27488-27492
-
-
Loo, T.W.1
Clarke, D.M.2
-
9
-
-
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
-
10
-
-
0034733677
-
Drug-stimulated ATPase activity of human P-glycoprotein is blocked by disulfide cross-linking between the nucleotide-binding sites
-
Loo, T. W. and Clarke, D. M. (2000) Drug-stimulated ATPase activity of human P-glycoprotein is blocked by disulfide cross-linking between the nucleotide-binding sites. J. Biol. Chem. 275, 19435-19438
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 19435-19438
-
-
Loo, T.W.1
Clarke, D.M.2
-
11
-
-
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
-
12
-
-
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
-
13
-
-
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
-
14
-
-
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
-
15
-
-
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
-
16
-
-
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
-
17
-
-
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
-
18
-
-
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
-
19
-
-
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
-
20
-
-
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
-
21
-
-
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
-
22
-
-
12144262818
-
Interaction of LDS-751 with P-glycoprotein and mapping of the location of the R drug binding site
-
Lugo, M. R. and Sharom, F. J. (2005) Interaction of LDS-751 with P-glycoprotein and mapping of the location of the R drug binding site. Biochemistry 44, 643-655
-
(2005)
Biochemistry
, vol.44
, pp. 643-655
-
-
Lugo, M.R.1
Sharom, F.J.2
-
23
-
-
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
-
24
-
-
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
-
25
-
-
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
-
26
-
-
1542320036
-
Disulfide cross-linking analysis shows that transmembrane segments 5 and 8 of human P-glycoprotein are close together on the cytoplasmic side of the membrane
-
Loo, T. W., Bartlett, M. C. and Clarke, D. M. (2004) Disulfide cross-linking analysis shows that transmembrane segments 5 and 8 of human P-glycoprotein are close together on the cytoplasmic side of the membrane. J. Biol. Chem. 279, 7692-7697
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 7692-7697
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
27
-
-
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
-
28
-
-
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
-
29
-
-
0032483985
-
Quality control by proteases in the endoplasmic reticulum. Removal of a protease-sensitive site enhances expression of human P-glycoprotein
-
Loo, T. W. and Clarke, D. M. (1998) Quality control by proteases in the endoplasmic reticulum. Removal of a protease-sensitive site enhances expression of human P-glycoprotein. J. Biol. Chem. 273, 32373-32376
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 32373-32376
-
-
Loo, T.W.1
Clarke, D.M.2
-
30
-
-
23044503311
-
ATP hydrolysis promotes interactions between the extracellular ends of transmembrane segments 1 and 11 of human multidrug resistance P-glycoprotein
-
Loo, T. W., Bartlett, M. C. and Clarke, D. M. (2005) ATP hydrolysis promotes interactions between the extracellular ends of transmembrane segments 1 and 11 of human multidrug resistance P-glycoprotein. Biochemistry 44, 10250-10258
-
(2005)
Biochemistry
, vol.44
, pp. 10250-10258
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
31
-
-
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
-
32
-
-
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
-
33
-
-
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
-
34
-
-
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
-
35
-
-
27144481548
-
Rescue of ΔF508 and other misprocessed CFTR mutants by a novel quinazoline compound
-
Loo, T. W., Bartlett, M. C. and Clarke, D. M. (2005) Rescue of ΔF508 and other misprocessed CFTR mutants by a novel quinazoline compound. Mol. Pharmacol. 2, 407-413
-
(2005)
Mol. Pharmacol.
, vol.2
, pp. 407-413
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
36
-
-
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
-
37
-
-
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
-
38
-
-
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
-
39
-
-
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
-
40
-
-
0038419822
-
Permanent activation of the human P-glycoprotein by covalent modification of a residue in the drug-binding site
-
Loo, T. W., Bartlett, M. C. and Clarke, D. M. (2003) Permanent activation of the human P-glycoprotein by covalent modification of a residue in the drug-binding site. J. Biol. Chem. 278, 20449-20452
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20449-20452
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
41
-
-
0347379911
-
Methanethiosulfonate derivatives of rhodamine and verapamil activate human P-glycoprotein at different sites
-
Loo, T. W., Bartlett, M. C. and Clarke, D. M. (2003) Methanethiosulfonate derivatives of rhodamine and verapamil activate human P-glycoprotein at different sites. J. Biol. Chem. 278, 50136-50141
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 50136-50141
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
42
-
-
0024292717
-
An altered pattern of cross-resistance in multidrug-resistant human cells results from spontaneous mutations in the mdr1 (P-glycoprotein) gene
-
Choi, K. H., Chen, C. J., Kriegler, M. and Roninson, I. B. (1988) An altered pattern of cross-resistance in multidrug-resistant human cells results from spontaneous mutations in the mdr1 (P-glycoprotein) gene. Cell 53, 519-529
-
(1988)
Cell
, vol.53
, pp. 519-529
-
-
Choi, K.H.1
Chen, C.J.2
Kriegler, M.3
Roninson, I.B.4
-
43
-
-
0028831929
-
Effects of lipids on ATPase activity of purified Chinese hamster P-glycoprotein
-
Urbatsch, I. L. and Senior, A. E. (1995) Effects of lipids on ATPase activity of purified Chinese hamster P-glycoprotein. Arch. Biochem. Biophys. 316, 135-140
-
(1995)
Arch. Biochem. Biophys.
, vol.316
, pp. 135-140
-
-
Urbatsch, I.L.1
Senior, A.E.2
-
44
-
-
0030858837
-
Alteration of substrate specificity by mutations at the His61 position in predicted transmembrane domain 1 of human MDR1/P-glycoprotein
-
Taguchi, Y., Kino, K., Morishima, M., Komano, T., Kane, S. E. and Ueda, K. (1997) Alteration of substrate specificity by mutations at the His61 position in predicted transmembrane domain 1 of human MDR1/P-glycoprotein. Biochemistry 36, 8883-8889
-
(1997)
Biochemistry
, vol.36
, pp. 8883-8889
-
-
Taguchi, Y.1
Kino, K.2
Morishima, M.3
Komano, T.4
Kane, S.E.5
Ueda, K.6
-
45
-
-
0030796990
-
Amino acid substitutions in the first transmembrane domain (TM1) of P-glycoprotein that alter substrate specificity
-
Taguchi, Y., Morishima, M., Komano, T. and Ueda, K. (1997) Amino acid substitutions in the first transmembrane domain (TM1) of P-glycoprotein that alter substrate specificity. FEBS Lett. 413, 142-146
-
(1997)
FEBS Lett.
, vol.413
, pp. 142-146
-
-
Taguchi, Y.1
Morishima, M.2
Komano, T.3
Ueda, K.4
-
46
-
-
0025868103
-
Demonstration that CFTR is a chloride channel by alteration of its anion selectivity
-
Anderson, M. P., Gregory, R. J., Thompson, S., Souza, D. W., Paul, S., Mulligan, R. C., Smith, A. E. and Welsh, M. J. (1991) Demonstration that CFTR is a chloride channel by alteration of its anion selectivity. Science 253, 202-205
-
(1991)
Science
, vol.253
, pp. 202-205
-
-
Anderson, M.P.1
Gregory, R.J.2
Thompson, S.3
Souza, D.W.4
Paul, S.5
Mulligan, R.C.6
Smith, A.E.7
Welsh, M.J.8
-
47
-
-
0028264188
-
Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator
-
Akabas, M. H., Kaufmann, C., Cook, T. A. and Archdeacon, P. (1994) Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator. J. Biol. Chem. 269, 14865-14868
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 14865-14868
-
-
Akabas, M.H.1
Kaufmann, C.2
Cook, T.A.3
Archdeacon, P.4
-
48
-
-
11244339684
-
Direct comparison of the functional roles played by different transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore
-
Ge, N., Muise, C. N., Gong, X. and Linsdell, P. (2004) Direct comparison of the functional roles played by different transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore. J. Biol. Chem. 279, 55283-55289
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 55283-55289
-
-
Ge, N.1
Muise, C.N.2
Gong, X.3
Linsdell, P.4
-
49
-
-
0035933511
-
The human nuclear xenobiotic receptor PXR: Structural determinants of directed promiscuity
-
Watkins, R. E., Wisely, G. B., Moore, L. B., Collins, J. L., Lambert, M. H., Williams, S. P., Willson, T. M., Kliewer, S. A. and Redinbo, M. R. (2001) The human nuclear xenobiotic receptor PXR: structural determinants of directed promiscuity. Science 292, 2329-2333
-
(2001)
Science
, vol.292
, pp. 2329-2333
-
-
Watkins, R.E.1
Wisely, G.B.2
Moore, L.B.3
Collins, J.L.4
Lambert, M.H.5
Williams, S.P.6
Willson, T.M.7
Kliewer, S.A.8
Redinbo, M.R.9
-
50
-
-
0141994817
-
Simultaneous binding of two different drugs in the binding pocket of the human multidrug resistance P-glycoprotein
-
Loo, T. W., Bartlett, M. C. and Clarke, D. M. (2003) Simultaneous binding of two different drugs in the binding pocket of the human multidrug resistance P-glycoprotein. J. Biol. Chem. 278, 39706-39710
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 39706-39710
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
|