-
1
-
-
0000712439
-
Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood-brain barrier sites
-
Cordon-Cardo, C., O'Brien, J. P., Casals, D., Rittman-Grauer, L., Biedler, J. L., Melamed, M. R., and Bertino, J. R. (1989) Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood-brain barrier sites. Proc. Natl. Acad. Sci. U.S.A. 86, 695-698.
-
(1989)
Proc. Natl. Acad. Sci. U.S.A.
, vol.86
, pp. 695-698
-
-
Cordon-Cardo, C.1
O'Brien, J.P.2
Casals, D.3
Rittman-Grauer, L.4
Biedler, J.L.5
Melamed, M.R.6
Bertino, J.R.7
-
2
-
-
0027212626
-
Detection of P-glycoprotein with four monoclonal antibodies in normal and tumor tissues
-
Pavelic, Z. P., Reising, J., Pavelic, L., Kelley, D. J., Stambrook, P. J., and Gluckman, J. L. (1993) Detection of P-glycoprotein with four monoclonal antibodies in normal and tumor tissues. Arch. Otolaryngol., Head Neck Surg. 119, 753-757. (Pubitemid 23198694)
-
(1993)
Archives of Otolaryngology - Head and Neck Surgery
, vol.119
, Issue.7
, pp. 753-757
-
-
Pavelic, Z.P.1
Reising, J.2
Pavelic, L.3
Kelley, D.J.4
Stambrook, P.J.5
Gluckman, J.L.6
-
3
-
-
0028112934
-
Tissue distribution of the human MDR3 P-glycoprotein
-
Smit, J. J., Schinkel, A. H., Mol, C. A., Majoor, D., Mooi, W. J., Jongsma, A. P., Lincke, C. R., and Borst, P. (1994) Tissue distribution of the human MDR3 P-glycoprotein. Lab. Invest. 71, 638-649.
-
(1994)
Lab. Invest.
, vol.71
, pp. 638-649
-
-
Smit, J.J.1
Schinkel, A.H.2
Mol, C.A.3
Majoor, D.4
Mooi, W.J.5
Jongsma, A.P.6
Lincke, C.R.7
Borst, P.8
-
4
-
-
0025071180
-
Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues
-
Cordon-Cardo, C., O'Brien, J. P., Boccia, J., Casals, D., Bertino, J. R., and Melamed, M. R. (1990) Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues. J. Histochem. Cytochem. 38, 1277-1287.
-
(1990)
J. Histochem. Cytochem.
, vol.38
, pp. 1277-1287
-
-
Cordon-Cardo, C.1
O'Brien, J.P.2
Boccia, J.3
Casals, D.4
Bertino, J.R.5
Melamed, M.R.6
-
5
-
-
0036364467
-
Multidrug resistance in cancer: Role of ATP-dependent transporters
-
Gottesman, M. M., Fojo, T., and Bates, S. E. (2002) Multidrug resistance in cancer: Role of ATP-dependent transporters. Nat. Rev. Cancer 2, 48-58.
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 48-58
-
-
Gottesman, M.M.1
Fojo, T.2
Bates, S.E.3
-
6
-
-
33846419807
-
How can we best use structural information on P-glycoprotein to design inhibitors?
-
DOI 10.1016/j.pharmthera.2006.10.003, PII S0163725806001860
-
McDevitt, C. A., and Callaghan, R. (2007) How can we best use structural information on P-glycoprotein to design inhibitors? Pharmacol. Ther. 113 429-441. (Pubitemid 46149055)
-
(2007)
Pharmacology and Therapeutics
, vol.113
, Issue.2
, pp. 429-441
-
-
McDevitt, C.A.1
Callaghan, R.2
-
7
-
-
33745831231
-
Structure, function, expression, genomic organization, and single nucleotide polymorphisms of human ABCB1 (MDR1), ABCC (MRP), and ABCG2 (BCRP) efflux transporters
-
Choudhuri, S., and Klaassen, C. D. (2006) Structure, function, expression, genomic organization, and single nucleotide polymorphisms of human ABCB1 (MDR1), ABCC (MRP), and ABCG2 (BCRP) efflux transporters. Int. J. Toxicol. 25, 231-259.
-
(2006)
Int. J. Toxicol.
, vol.25
, pp. 231-259
-
-
Choudhuri, S.1
Klaassen, C.D.2
-
8
-
-
0030004763
-
Co-operative, competitive and non-competitive interactions between modulators of P-glycoprotein
-
Ayesh, S., Shao, Y. M., and Stein, W. D. (1996) Co-operative, competitive and non-competitive interactions between modulators of P-glycoprotein. Biochim. Biophys. Acta 1316, 8-18.
-
(1996)
Biochim. Biophys. Acta
, vol.1316
, pp. 8-18
-
-
Ayesh, S.1
Shao, Y.M.2
Stein, W.D.3
-
9
-
-
0026475310
-
P-Glycoprotein possesses a 1,4-dihydropyridine-selective drug acceptor site which is alloserically coupled to a vinca-alkaloid-selective binding site
-
Ferry, D. R., Russell, M. A., and Cullen, M. H. (1992) P-Glycoprotein possesses a 1,4-dihydropyridine-selective drug acceptor site which is alloserically coupled to a vinca-alkaloid-selective binding site. Biochem. Biophys. Res. Commun. 188, 440-445.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.188
, pp. 440-445
-
-
Ferry, D.R.1
Russell, M.A.2
Cullen, M.H.3
-
10
-
-
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 (part 2), 351-358. (Pubitemid 28379536)
-
(1998)
Biochemical Journal
, vol.333
, Issue.2
, pp. 351-358
-
-
Pascaud, C.1
Garrigos, M.2
Orlowski, S.3
-
11
-
-
0030782511
-
Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities
-
Shapiro, A. B., and Ling, V. (1997) Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities. Eur. J. Biochem. 250, 130-137.
-
(1997)
Eur. J. Biochem.
, vol.250
, pp. 130-137
-
-
Shapiro, A.B.1
Ling, V.2
-
12
-
-
33745008903
-
Transmembrane segment 1 of human P-glycoprotein contributes to the drug-binding pocket
-
DOI 10.1042/BJ20060012
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2006) Transmembrane segment 1 of human P-glycoprotein contributes to the drug-binding pocket. Biochem. J. 396, 537-545. (Pubitemid 44228168)
-
(2006)
Biochemical Journal
, vol.396
, Issue.3
, pp. 537-545
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
13
-
-
33749985062
-
Transmembrane segment 7 of human P-glycoprotein forms part of the drug-binding pocket
-
DOI 10.1042/BJ20060715
-
Loo, T. W., Bartlett, M. C., and Clarke, D. M. (2006) Transmembrane segment 7 of human P-glycoprotein forms part of the drug-binding pocket. Biochem. J. 399, 351-359. (Pubitemid 44570297)
-
(2006)
Biochemical Journal
, vol.399
, Issue.2
, pp. 351-359
-
-
Loo, T.W.1
Bartlett, M.C.2
Clarke, D.M.3
-
14
-
-
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
-
15
-
-
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
-
16
-
-
0037424343
-
Three-dimensional structures of the mammalian multidrug resistance P-glycoprotein demonstrate major conformational changes in the transmembrane domains upon nucleotide binding
-
Rosenberg, M. F., Kamis, A. B., Callaghan, R., Higgins, C. F., and Ford, R. C. (2003) Three-dimensional structures of the mammalian multidrug resistance P-glycoprotein demonstrate major conformational changes in the transmembrane domains upon nucleotide binding. J. Biol. Chem. 278, 8294-8299
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 8294-8299
-
-
Rosenberg, M.F.1
Kamis, A.B.2
Callaghan, R.3
Higgins, C.F.4
Ford, R.C.5
-
17
-
-
0030698855
-
P-Glycoprotein function involves conformational transitions detectable by differential immunoreactivity
-
Mechetner, E. B., Schott, B., Morse, B. S., Stein, W. D., Druley, T., Davis, K. A., Tsuruo, T., and Roninson, I. B. (1997) P-Glycoprotein function involves conformational transitions detectable by differential immunoreactivity. Proc. Natl. Acad. Sci. U.S.A. 94, 12908-12913
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 12908-12913
-
-
Mechetner, E.B.1
Schott, B.2
Morse, B.S.3
Stein, W.D.4
Druley, T.5
Davis, K.A.6
Tsuruo, T.7
Roninson, I.B.8
-
18
-
-
0035006827
-
P-Glycoprotein conformational changes detected by antibody competition
-
Nagy, H., Goda, K., Arceci, R., Cianfriglia, M., Mechetner, E., and Szabo, G. Jr. (2001) P-Glycoprotein conformational changes detected by antibody competition. Eur. J. Biochem. 268, 2416-2420
-
(2001)
Eur. J. Biochem.
, vol.268
, pp. 2416-2420
-
-
Nagy, H.1
Goda, K.2
Arceci, R.3
Cianfriglia, M.4
Mechetner, E.5
Szabo Jr., G.6
-
19
-
-
0034681959
-
Nucleotide-induced conformational changes in P-glycoprotein and in nucleotide binding site mutants monitored by trypsin sensitivity
-
DOI 10.1021/bi992744z
-
Julien, M., and Gros, P. (2000) Nucleotide-induced conformational changes in P-glycoprotein and in nucleotide binding site mutants monitored by trypsin sensitivity. Biochemistry 39, 4559-4568. (Pubitemid 30212673)
-
(2000)
Biochemistry
, vol.39
, Issue.15
, pp. 4559-4568
-
-
Julien, M.1
Gros, P.2
-
20
-
-
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
-
21
-
-
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
-
22
-
-
0032881342
-
The molecular interaction of the high affinity reversal agent XR9576 with P-glycoprotein
-
Martin, C., Berridge, G., Mistry, P., Higgins, C., Charlton, P., and Callaghan, R. (1999) The molecular interaction of the high affinity reversal agent XR9576 with P-glycoprotein. Br. J. Pharmacol. 128, 403-411.
-
(1999)
Br. J. Pharmacol.
, vol.128
, pp. 403-411
-
-
Martin, C.1
Berridge, G.2
Mistry, P.3
Higgins, C.4
Charlton, P.5
Callaghan, R.6
-
23
-
-
0035951073
-
The vinblastine binding site adopts high- And low-affinity conformations during a transport cycle of P-glycoprotein
-
DOI 10.1021/bi011211z
-
Martin, C., Higgins, C. F., and Callaghan, R. (2001) The vinblastine binding site adopts high- and low-affinity conformations during a transport cycle of P-glycoprotein. Biochemistry 40, 15733-15742. (Pubitemid 34015202)
-
(2001)
Biochemistry
, vol.40
, Issue.51
, pp. 15733-15742
-
-
Martin, C.1
Higgins, C.F.2
Callaghan, R.3
-
24
-
-
17944370228
-
Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycle
-
DOI 10.1093/emboj/20.20.5615
-
Rosenberg, M. F., Velarde, G., Ford, R. C., Martin, C., Berridge, G., Kerr, I. D., Callaghan, R., Schmidlin, A., Wooding, C., Linton, K. J., and Higgins, C. F. (2001) Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycle. EMBO J. 20, 5615-5625. (Pubitemid 33010039)
-
(2001)
EMBO Journal
, vol.20
, Issue.20
, pp. 5615-5625
-
-
Rosenberg, M.F.1
Velarde, G.2
Ford, R.C.3
Martin, C.4
Berridge, G.5
Kerr, I.D.6
Callaghan, R.7
Schmidlin, A.8
Wooding, C.9
Linton, K.J.10
Higgins, C.F.11
-
25
-
-
31844448665
-
The translocation mechanism of P-glycoprotein
-
Callaghan, R., Ford, R. C., and Kerr, I. D. (2006) The translocation mechanism of P-glycoprotein. FEBS Lett. 580, 1056-1063.
-
(2006)
FEBS Lett.
, vol.580
, pp. 1056-1063
-
-
Callaghan, R.1
Ford, R.C.2
Kerr, I.D.3
-
26
-
-
0031021530
-
Characterization of transport through the periplasmic histidine permease using proteoliposomes reconstituted by dialysis
-
Liu, C. E., and Ames, G. F. (1997) Characterization of transport through the periplasmic histidine permease using proteoliposomes reconstituted by dialysis. J. Biol. Chem. 272, 859-866.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 859-866
-
-
Liu, C.E.1
Ames, G.F.2
-
27
-
-
3843140625
-
Combined mutation of catalytic glutamate residues in the two nucleotide binding domains of P-glycoprotein generates a conformation that binds ATP and ADP tightly
-
Tombline, G., Bartholomew, L. A., Urbatsch, I. L., and Senior, A. E. (2004) Combined mutation of catalytic glutamate residues in the two nucleotide binding domains of P-glycoprotein generates a conformation that binds ATP and ADP tightly. J. Biol. Chem. 279, 31212-31220.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 31212-31220
-
-
Tombline, G.1
Bartholomew, L.A.2
Urbatsch, I.L.3
Senior, A.E.4
-
28
-
-
33748644877
-
Structure of a bacterial multidrug ABC transporter
-
DOI 10.1038/nature05155, PII NATURE05155
-
Dawson, R. J., and Locher, K. P. (2006) Structure of a bacterial multidrug ABC transporter. Nature 443, 180-185. (Pubitemid 44387602)
-
(2006)
Nature
, vol.443
, Issue.7108
, pp. 180-185
-
-
Dawson, R.J.P.1
Locher, K.P.2
-
29
-
-
0027260959
-
Functional consequences of phenylalanine mutations in the predicted transmembrane domain of P-glycoprotein
-
Loo, T. W., and Clarke, D. M. (1993) Functional consequences of phenylalanine mutations in the predicted transmembrane domain of P-glycoprotein. J. Biol. Chem. 268, 19965-19972.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 19965-19972
-
-
Loo, T.W.1
Clarke, D.M.2
-
30
-
-
0026556302
-
Amino acid substitutions in the sixth transmembrane domain of P-glycoprotein altermultidrug resistance
-
Devine, S. E., Ling, V., and Melera, P. W. (1992) Amino acid substitutions in the sixth transmembrane domain of P-glycoprotein altermultidrug resistance. Proc.Natl. Acad. Sci.U.S.A. 89, 4564-4568.
-
(1992)
Proc.Natl. Acad. Sci.U.S.A.
, vol.89
, pp. 4564-4568
-
-
Devine, S.E.1
Ling, V.2
Melera, P.W.3
-
31
-
-
0034765599
-
Further characterization of the sixth transmembrane domain of Pgp1 by site-directed mutagenesis
-
Song, J., and Melera, P. W. (2001) Further characterization of the sixth transmembrane domain of Pgp1 by site-directed mutagenesis. Cancer Chemother. Pharmacol. 48, 339-346.
-
(2001)
Cancer Chemother. Pharmacol.
, vol.48
, pp. 339-346
-
-
Song, J.1
Melera, P.W.2
-
32
-
-
0036176213
-
Identification of ligand-binding regions of P-glycoprotein by activated-pharmacophore photoaffinity labeling and matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry
-
Ecker, G. F., Csaszar, E., Kopp, S., Plagens, B., Holzer, W., Ernst, W., and Chiba, P. (2002) Identification of ligand-binding regions of P-glycoprotein by activated-pharmacophore photoaffinity labeling and matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry. Mol. Pharmacol. 61, 637-648.
-
(2002)
Mol. Pharmacol.
, vol.61
, pp. 637-648
-
-
Ecker, G.F.1
Csaszar, E.2
Kopp, S.3
Plagens, B.4
Holzer, W.5
Ernst, W.6
Chiba, P.7
-
33
-
-
0027216104
-
Major photoaffinity drug labeling sites for iodoaryl azidoprazosin in P-glycoprotein are within, or immediately C-terminal to, transmembrane domains 6 and 12
-
Greenberger, L. M. (1993) Major photoaffinity drug labeling sites for iodoaryl azidoprazosin in P-glycoprotein are within, or immediately C-terminal to, transmembrane domains 6 and 12. J. Biol. Chem. 268, 11417-11425.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 11417-11425
-
-
Greenberger, L.M.1
-
34
-
-
0027997698
-
Mutations to amino acids located in predicted transmembrane segment 6 (TM6) modulate the activity and substrate specificity of human P-glycoprotein
-
DOI 10.1021/bi00251a013
-
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 (Pubitemid 24382347)
-
(1994)
Biochemistry
, vol.33
, Issue.47
, pp. 14049-14057
-
-
Loo, T.W.1
Clarke, D.M.2
-
35
-
-
0035805573
-
Defining the Drug-binding Site in the Human Multidrug Resistance P-glycoprotein Using a Methanethiosulfonate Analog of Verapamil, MTS-verapamil
-
DOI 10.1074/jbc.M100407200
-
Loo, T. W., and Clarke, D. M. (2001) Defining the drug-binding site in the human multidrug resistance P-glycoprotein using a methanethiosulfonate analog of verapamil, MTS-verapamil. J. Biol. Chem. 276, 14972-14979 (Pubitemid 37373379)
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.18
, pp. 14972-14979
-
-
Loo, T.W.1
Clarke, D.M.2
-
36
-
-
0028901538
-
Functional evidence that transmembrane 12 and the loop between transmembrane 11 and 12 form part of the drug-binding domain in P-glycoprotein encoded by MDR1
-
Zhang, X., Collins, K. I., and Greenberger, L. M. (1995) Functional evidence that transmembrane 12 and the loop between transmembrane 11 and 12 form part of the drug-binding domain in P-glycoprotein encoded by MDR1. J. Biol. Chem. 270, 5441-5448
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 5441-5448
-
-
Zhang, X.1
Collins, K.I.2
Greenberger, L.M.3
-
37
-
-
41149140334
-
Cytosolic region ofTM6in P-glycoprotein: Topographical analysis and functional perturbation by site directed labeling
-
Storm, J., Modok, S., O'Mara, M. L., Tieleman, D. P., Kerr, I. D., and Callaghan, R. (2008) Cytosolic region ofTM6in P-glycoprotein: Topographical analysis and functional perturbation by site directed labeling. Biochemistry 47, 3615-3624.
-
(2008)
Biochemistry
, vol.47
, pp. 3615-3624
-
-
Storm, J.1
Modok, S.2
O'Mara, M.L.3
Tieleman, D.P.4
Kerr, I.D.5
Callaghan, R.6
-
38
-
-
34548507482
-
Residue G346 in transmembrane segment six is involved in inter-domain communication in P-glycoprotein
-
DOI 10.1021/bi700447p
-
Storm, J., O'Mara, M. L., Crowley, E. H., Peall, J., Tieleman, D. P., Kerr, I. D., and Callaghan, R. (2007) Residue G346 in transmembrane segment six is involved in inter-domain communication in P-glycoprotein. Biochemistry 46, 9899-9910. (Pubitemid 47378580)
-
(2007)
Biochemistry
, vol.46
, Issue.35
, pp. 9899-9910
-
-
Storm, J.1
O'Mara, M.L.2
Crowley, E.H.3
Peall, J.4
Tieleman, D.P.5
Kerr, I.D.6
Callaghan, R.7
-
39
-
-
0035674849
-
Detailed characterization of cysteine-less P-glycoprotein reveals subtle pharmacological differences in function from wildtype protein
-
Taylor, A. M., Storm, J., Soceneantu, L., Linton, K. J., Gabriel, M., Martin, C., Woodhouse, J., Blott, E., Higgins, C. F., and Callaghan, R. (2001) Detailed characterization of cysteine-less P-glycoprotein reveals subtle pharmacological differences in function from wildtype protein. Br. J. Pharmacol. 134, 1609-1618.
-
(2001)
Br. J. Pharmacol.
, vol.134
, pp. 1609-1618
-
-
Taylor, A.M.1
Storm, J.2
Soceneantu, L.3
Linton, K.J.4
Gabriel, M.5
Martin, C.6
Woodhouse, J.7
Blott, E.8
Higgins, C.F.9
Callaghan, R.10
-
40
-
-
0030669223
-
A single chain Fv fragment of P-glycoprotein-specific monoclonal antibody C219. Design, expression, and crystal structure at 2.4 a ° resolution
-
Hoedemaeker, F. J., Signorelli, T., Johns, K., Kuntz, D. A., and Rose, D. R. (1997) A single chain Fv fragment of P-glycoprotein-specific monoclonal antibody C219. Design, expression, and crystal structure at 2.4 A ° resolution. J. Biol. Chem. 272, 29784-29789.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 29784-29789
-
-
Hoedemaeker, F.J.1
Signorelli, T.2
Johns, K.3
Kuntz, D.A.4
Rose, D.R.5
-
41
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford, M. M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248-254.
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
42
-
-
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
-
43
-
-
0030697879
-
The multi-drug resistance reversal agent SR33557 and modulation of vinca alkaloid binding to P-glycoprotein by an allosteric interaction
-
Martin, C., Berridge, G., Higgins, C. F., and Callaghan, R. (1997) The multi-drug resistance reversal agent SR33557 and modulation of vinca alkaloid binding to P-glycoprotein by an allosteric interaction. Br. J. Pharmacol. 122, 765-771.
-
(1997)
Br. J. Pharmacol.
, vol.122
, pp. 765-771
-
-
Martin, C.1
Berridge, G.2
Higgins, C.F.3
Callaghan, R.4
-
44
-
-
34548133239
-
P-glycoprotein models of the apo and ATP-bound states based on homology with Sav1866 and MalK
-
DOI 10.1016/j.febslet.2007.07.069, PII S0014579307008393
-
O'Mara, M. L., and Tieleman, D. P. (2007) P-glycoprotein models of the apo andATP-bound states based on homology with Sav1866 and MalK. FEBS Lett. 581, 4217-4222. (Pubitemid 47301854)
-
(2007)
FEBS Letters
, vol.581
, Issue.22
, pp. 4217-4222
-
-
O'Mara, M.L.1
Tieleman, D.P.2
-
45
-
-
0031473847
-
SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling
-
DOI 10.1002/elps.1150181505
-
Guex, N., and Peitsch, M. C. (1997) SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling. Electrophoresis 18, 2714-2723. (Pubitemid 28059943)
-
(1997)
Electrophoresis
, vol.18
, Issue.15
, pp. 2714-2723
-
-
Guex, N.1
Peitsch, M.C.2
-
46
-
-
63449139456
-
Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding
-
Aller, S. G., Yu, J., Ward, A., Weng, Y., Chittaboina, S., Zhuo, R., Harrell, P. M., Trinh, Y. T., Zhang, Q., Urbatsch, I. L., and Chang, G. (2009) Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding. Science 323, 1718-1722.
-
(2009)
Science
, vol.323
, pp. 1718-1722
-
-
Aller, S.G.1
Yu, J.2
Ward, A.3
Weng, Y.4
Chittaboina, S.5
Zhuo, R.6
Harrell, P.M.7
Trinh, Y.T.8
Zhang, Q.9
Urbatsch, I.L.10
Chang, G.11
-
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
-
-
0037393965
-
The nucleotide-binding domains of P-glycoprotein. Functional symmetry in the isolated domain demonstrated by N-ethylmaleimide labelling
-
Berridge, G., Walker, J. A., Callaghan, R., and Kerr, I. D. (2003) The nucleotide-binding domains of P-glycoprotein. Functional symmetry in the isolated domain demonstrated by N-ethylmaleimide labelling. Eur. J. Biochem. 270, 1483-1492.
-
(2003)
Eur. J. Biochem.
, vol.270
, pp. 1483-1492
-
-
Berridge, G.1
Walker, J.A.2
Callaghan, R.3
Kerr, I.D.4
-
49
-
-
0025738363
-
Purification and characterization of the membrane-associated components of the maltose transport system from Escherichia coli
-
Davidson, A. L., and Nikaido, H. (1991) Purification and characterization of the membrane-associated components of the maltose transport system from Escherichia coli. J. Biol. Chem. 266, 8946-8951.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 8946-8951
-
-
Davidson, A.L.1
Nikaido, H.2
-
50
-
-
0029113976
-
The first nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator can function as an active ATPase
-
Ko, Y. H., and Pedersen, P. L. (1995) The first nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator can function as an active ATPase. J. Biol. Chem. 270, 22093-22096.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 22093-22096
-
-
Ko, Y.H.1
Pedersen, P.L.2
-
51
-
-
0030822352
-
Purification and characterization of HisP, the ATP-binding subunit of a traffic ATPase (ABC transporter), the histidine permease of Salmonella typhimurium. Solubility, dimerization, and ATPase activity
-
Nikaido, K., Liu, P. Q., and Ames, G. F. (1997) Purification and characterization of HisP, the ATP-binding subunit of a traffic ATPase (ABC transporter), the histidine permease of Salmonella typhimurium. Solubility, dimerization, and ATPase activity. J. Biol. Chem. 272, 27745-27752.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 27745-27752
-
-
Nikaido, K.1
Liu, P.Q.2
Ames, G.F.3
-
52
-
-
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
-
53
-
-
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
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