The ATP switch model for ABC transporters
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[1] H. Nikaido,et al. Mechanism of maltose transport in Escherichia coli: transmembrane signaling by periplasmic binding proteins. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[2] V. Ling,et al. Stoichiometry of coupling of rhodamine 123 transport to ATP hydrolysis by P-glycoprotein. , 1998, European journal of biochemistry.
[3] G. Ames,et al. Salmonella typhimurium histidine periplasmic permease mutations that allow transport in the absence of histidine-binding proteins , 1991, Journal of bacteriology.
[4] I. Pastan,et al. Mechanism of Action of Human P-glycoprotein ATPase Activity , 1998, The Journal of Biological Chemistry.
[5] C. B. Roth,et al. Structure of MsbA from E. coli: a homolog of the multidrug resistance ATP binding cassette (ABC) transporters. , 2001, Science.
[6] W. Davidson,et al. Apolipoprotein A-I Structural Modification and the Functionality of Reconstituted High Density Lipoprotein Particles in Cellular Cholesterol Efflux* , 1996, The Journal of Biological Chemistry.
[7] G. Ferro-Luzzi Ames,et al. Nonequivalence of the nucleotide-binding subunits of an ABC transporter, the histidine permease, and conformational changes in the membrane complex. , 2000, Biochemistry.
[8] B. Sankaran,et al. P-glycoprotein Is Stably Inhibited by Vanadate-induced Trapping of Nucleotide at a Single Catalytic Site (*) , 1995, The Journal of Biological Chemistry.
[9] S. Cole,et al. Comparison of the Functional Characteristics of the Nucleotide Binding Domains of Multidrug Resistance Protein 1* , 2000, The Journal of Biological Chemistry.
[10] R. Tampé,et al. Thermodynamics of peptide binding to the transporter associated with antigen processing (TAP). , 2002, Journal of molecular biology.
[11] D. Clarke,et al. Identification of Residues within the Drug-binding Domain of the Human Multidrug Resistance P-glycoprotein by Cysteine-scanning Mutagenesis and Reaction with Dibromobimane* , 2000, The Journal of Biological Chemistry.
[12] H. Shuman. Active transport of maltose in Escherichia coli K12. Role of the periplasmic maltose-binding protein and evidence for a substrate recognition site in the cytoplasmic membrane. , 1982, The Journal of biological chemistry.
[13] K. Nikaido,et al. Complete nucleotide sequence and identification of membrane components of the histidine transport operon of S. typhimurium , 1982, Nature.
[14] J. Schellens,et al. Evidence for Two Interacting Ligand Binding Sites in Human Multidrug Resistance Protein 2 (ATP Binding Cassette C2)* , 2003, Journal of Biological Chemistry.
[15] M. Welsh,et al. The Two Nucleotide-binding Domains of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Have Distinct Functions in Controlling Channel Activity (*) , 1995, The Journal of Biological Chemistry.
[16] F. Sharom,et al. Site-directed fluorescence labeling of P-glycoprotein on cysteine residues in the nucleotide binding domains. , 1996, Biochemistry.
[17] Karl Kuchler,et al. ABC proteins : from bacteria to man , 2003 .
[18] Z. Sauna,et al. Evidence for a requirement for ATP hydrolysis at two distinct steps during a single turnover of the catalytic cycle of human P-glycoprotein. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[19] K. Linton,et al. Repacking of the transmembrane domains of P‐glycoprotein during the transport ATPase cycle , 2001, The EMBO journal.
[20] S. Cole,et al. Role of Carboxylate Residues Adjacent to the Conserved Core Walker B Motifs in the Catalytic Cycle of Multidrug Resistance Protein 1 (ABCC1)* , 2003, Journal of Biological Chemistry.
[21] A. Davidson,et al. Vanadate-Induced Trapping of Nucleotides by Purified Maltose Transport Complex Requires ATP Hydrolysis , 2000, Journal of bacteriology.
[22] B. Sankaran,et al. Both P-glycoprotein Nucleotide-binding Sites Are Catalytically Active (*) , 1995, The Journal of Biological Chemistry.
[23] F. Quiocho,et al. A tweezers-like motion of the ATP-binding cassette dimer in an ABC transport cycle. , 2003, Molecular cell.
[24] John A. Tainer,et al. Structural Biology of Rad50 ATPase ATP-Driven Conformational Control in DNA Double-Strand Break Repair and the ABC-ATPase Superfamily , 2000, Cell.
[25] Z. Sauna,et al. Characterization of the Catalytic Cycle of ATP Hydrolysis by Human P-glycoprotein , 2001, The Journal of Biological Chemistry.
[26] B. Dijkstra,et al. Crystal structures of the ATPase subunit of the glucose ABC transporter from Sulfolobus solfataricus: nucleotide-free and nucleotide-bound conformations. , 2003, Journal of molecular biology.
[27] F. Sharom,et al. Fluorescence studies on the nucleotide binding domains of the P-glycoprotein multidrug transporter. , 1997, Biochemistry.
[28] K. Nikaido,et al. One Intact ATP-binding Subunit Is Sufficient to Support ATP Hydrolysis and Translocation in an ABC Transporter, the Histidine Permease* , 1999, The Journal of Biological Chemistry.
[29] S. Seino,et al. Cooperative binding of ATP and MgADP in the sulfonylurea receptor is modulated by glibenclamide. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[30] J A McCammon,et al. Hinge-bending in L-arabinose-binding protein. The "Venus's-flytrap" model. , 1982, The Journal of biological chemistry.
[31] C. Higgins,et al. Nucleotide binding by membrane components of bacterial periplasmic binding protein‐dependent transport systems. , 1985, The EMBO journal.
[32] C. Higgins,et al. Communication between multiple drug binding sites on P-glycoprotein. , 2000, Molecular pharmacology.
[33] A. Davidson,et al. Mutation of a single MalK subunit severely impairs maltose transport activity in Escherichia coli , 1997, Journal of bacteriology.
[34] F. Sharom,et al. Stoichiometry and affinity of nucleotide binding to P-glycoprotein during the catalytic cycle. , 2003, Biochemistry.
[35] M. Hofnung,et al. Subunit interactions in ABC transporters: a conserved sequence in hydrophobic membrane proteins of periplasmic permeases defines an important site of interaction with the ATPase subunits , 1997, The EMBO journal.
[36] I. J. Evans,et al. A family of related ATP-binding subunits coupled to many distinct biological processes in bacteria , 1986, Nature.
[37] P. Gros,et al. Analysis of catalytic carboxylate mutants E552Q and E1197Q suggests asymmetric ATP hydrolysis by the two nucleotide-binding domains of P-glycoprotein. , 2003, Biochemistry.
[38] A. E. Senior,et al. Combined Mutation of Catalytic Glutamate Residues in the Two Nucleotide Binding Domains of P-glycoprotein Generates a Conformation That Binds ATP and ADP Tightly* , 2004, Journal of Biological Chemistry.
[39] J. Riordan,et al. The non‐hydrolytic pathway of cystic fibrosis transmembrane conductance regulator ion channel gating , 2000, The Journal of physiology.
[40] PETER MITCHELL,et al. A General Theory of Membrane Transport From Studies of Bacteria , 1957, Nature.
[41] R. Fishel,et al. The Human Mismatch Recognition Complex hMSH2-hMSH6 Functions as a Novel Molecular Switch , 1997, Cell.
[42] P. Gros,et al. Mutations in either nucleotide-binding site of P-glycoprotein (Mdr3) prevent vanadate trapping of nucleotide at both sites. , 1998, Biochemistry.
[43] J. Riordan,et al. ATP Binding, Not Hydrolysis, at the First Nucleotide-binding Domain of Multidrug Resistance-associated Protein MRP1 Enhances ADP·Vi Trapping at the Second Domain* , 2003, The Journal of Biological Chemistry.
[44] D. Keppler,et al. 81 MRP4 (ABCC4) is localized to the basolateral hepatotcyte membrane and functions as a cotransporter of reduced glutathione with bile salts , 2003 .
[45] Robert Tampé,et al. The transporter associated with antigen processing: function and implications in human diseases. , 2002, Physiological reviews.
[46] D. Gadsby,et al. ATP hydrolysis cycles and mechanism in P-glycoprotein and CFTR. , 1997, Seminars in cancer biology.
[47] Wei Yang,et al. Crystal structures of mismatch repair protein MutS and its complex with a substrate DNA , 2000, Nature.
[48] J. Riordan,et al. Intermediate Structural States Involved in MRP1-mediated Drug Transport , 2003, The Journal of Biological Chemistry.
[49] K. Linton,et al. P-glycoprotein misfolds in Escherichia coli : evidence against alternating-topology models of the transport cycle , 2002, Molecular membrane biology.
[50] K. Held,et al. ROLE OF GLUTATHIONE , 1988 .
[51] A. Nairn,et al. Prolonged Nonhydrolytic Interaction of Nucleotide with CFTR's NH2-terminal Nucleotide Binding Domain and its Role in Channel Gating , 2003, The Journal of general physiology.
[52] F. Sharom,et al. FRET analysis indicates that the two ATPase active sites of the P-glycoprotein multidrug transporter are closely associated. , 2001, Biochemistry.
[53] A. E. Senior,et al. The catalytic cycle of P‐glycoprotein , 1995, FEBS letters.
[54] A. Davidson,et al. Demonstration of Conformational Changes Associated with Activation of the Maltose Transport Complex* , 2001, The Journal of Biological Chemistry.
[55] C. McArdle,et al. Asn102 of the Gonadotropin-releasing Hormone Receptor Is a Critical Determinant of Potency for Agonists Containing C-terminal Glycinamide* , 1996, The Journal of Biological Chemistry.
[56] J. Riordan,et al. ATP Binding to the First Nucleotide Binding Domain of Multidrug Resistance-associated Protein Plays a Regulatory Role at Low Nucleotide Concentration, whereas ATP Hydrolysis at the Second Plays a Dominant Role in ATP-dependent Leukotriene C4 Transport* , 2003, Journal of Biological Chemistry.
[57] I. Pastan,et al. Both ATP sites of human P-glycoprotein are essential but not symmetric. , 1999, Biochemistry.
[58] C. Higgins,et al. Three-dimensional Structures of the Mammalian Multidrug Resistance P-glycoprotein Demonstrate Major Conformational Changes in the Transmembrane Domains upon Nucleotide Binding* , 2003, The Journal of Biological Chemistry.
[59] Douglas C. Rees,et al. The E. coli BtuCD Structure: A Framework for ABC Transporter Architecture and Mechanism , 2002, Science.
[60] M. Lamers,et al. The alternating ATPase domains of MutS control DNA mismatch repair , 2003, The EMBO journal.
[61] S. Ambudkar,et al. Relation Between the Turnover Number for Vinblastine Transport and for Vinblastine-stimulated ATP Hydrolysis by Human P-glycoprotein* , 1997, The Journal of Biological Chemistry.
[62] K. Nikaido,et al. Phosphate-Containing Proteins of Salmonella typhimurium and Escherichia coii , 2005 .
[63] R. Tampé,et al. Peptides Induce ATP Hydrolysis at Both Subunits of the Transporter Associated with Antigen Processing* , 2003, Journal of Biological Chemistry.
[64] O. Kellermann,et al. Active transport of maltose in Escherichia coli K12. Involvement of a "periplasmic" maltose binding protein. , 1974, European journal of biochemistry.
[65] T. Amachi,et al. Nonequivalent Nucleotide Trapping in the Two Nucleotide Binding Folds of the Human Multidrug Resistance Protein MRP1* , 2000, The Journal of Biological Chemistry.
[66] A. E. Senior,et al. P-glycoprotein Catalytic Mechanism , 2003, Journal of Biological Chemistry.
[67] C. Vigano,et al. Secondary and Tertiary Structure Changes of Reconstituted LmrA Induced by Nucleotide Binding or Hydrolysis , 2000, The Journal of Biological Chemistry.
[68] V. Ling,et al. Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities. , 1997, European journal of biochemistry.
[69] T. Meyer,et al. Requirements for Peptide Binding to the Human Transporter Associated with Antigen Processing Revealed by Peptide Scans and Complex Peptide Libraries (*) , 1995, The Journal of Biological Chemistry.
[70] C. Higgins,et al. Drug binding sites on P-glycoprotein are altered by ATP binding prior to nucleotide hydrolysis. , 2000, Biochemistry.
[71] C. Higgins,et al. The multi‐drug resistance reversal agent SR33557 and modulation of vinca alkaloid binding to P‐glycoprotein by an allosteric interaction , 1997, British journal of pharmacology.
[72] C. Higgins,et al. The homodimeric ATP‐binding cassette transporter LmrA mediates multidrug transport by an alternating two‐site (two‐cylinder engine) mechanism , 2000, The EMBO journal.
[73] J. Griffith,et al. hMSH2-hMSH6 forms a hydrolysis-independent sliding clamp on mismatched DNA. , 1999, Molecular cell.
[74] John F Hunt,et al. ATP binding to the motor domain from an ABC transporter drives formation of a nucleotide sandwich dimer. , 2002, Molecular cell.
[75] R. Tampé,et al. The ATP Hydrolysis Cycle of the Nucleotide-binding Domain of the Mitochondrial ATP-binding Cassette Transporter Mdl1p* , 2003, Journal of Biological Chemistry.
[76] K. Nikaido,et al. Purification and Characterization of HisP, the ATP-binding Subunit of a Traffic ATPase (ABC Transporter), the Histidine Permease of Salmonella typhimurium , 1997, The Journal of Biological Chemistry.
[77] C. Higgins,et al. The vinblastine binding site adopts high- and low-affinity conformations during a transport cycle of P-glycoprotein. , 2001, Biochemistry.
[78] F. Quiocho,et al. Trapping the transition state of an ATP-binding cassette transporter: evidence for a concerted mechanism of maltose transport. , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[79] John A. Tainer,et al. Structural Biochemistry and Interaction Architecture of the DNA Double-Strand Break Repair Mre11 Nuclease and Rad50-ATPase , 2001, Cell.
[80] H. Omote,et al. Transition State Analysis of the Coupling of Drug Transport to ATP Hydrolysis by P-glycoprotein* , 2003, Journal of Biological Chemistry.
[81] A. Davidson,et al. The Maltose Transport System of Escherichia coli Displays Positive Cooperativity in ATP Hydrolysis (*) , 1996, The Journal of Biological Chemistry.
[82] D. Clarke,et al. Covalent Modification of Human P-glycoprotein Mutants Containing a Single Cysteine in Either Nucleotide-binding Fold Abolishes Drug-stimulated ATPase Activity (*) , 1995, The Journal of Biological Chemistry.
[83] K. Linton,et al. An atomic detail model for the human ATP binding cassette transporter P‐glycoprotein derived from disulphide cross‐ linking and homology modeling , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[84] H. Rosenberg,et al. Intronic Enhancer Activity of the Eosinophil-derived Neurotoxin (RNS2) and Eosinophil Cationic Protein (RNS3) Genes Is Mediated by an NFAT-1 Consensus Binding Sequence* , 1997, The Journal of Biological Chemistry.
[85] S. Cole,et al. Characterization of vincristine transport by the M(r) 190,000 multidrug resistance protein (MRP): evidence for cotransport with reduced glutathione. , 1998, Cancer research.
[86] E. Welker,et al. Drug-stimulated Nucleotide Trapping in the Human Multidrug Transporter MDR1 , 1998, The Journal of Biological Chemistry.
[87] B. Dijkstra,et al. Formation of the productive ATP-Mg2+-bound dimer of GlcV, an ABC-ATPase from Sulfolobus solfataricus. , 2003, Journal of molecular biology.
[88] M. P. Gallagher,et al. Energy coupling to periplasmic binding protein-dependent transport systems: stoichiometry of ATP hydrolysis during transport in vivo. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[89] Giovanna Ferro‐Luzzi Ames,et al. Characterization of the Adenosine Triphosphatase Activity of the Periplasmic Histidine Permease, a Traffic ATPase (ABC Transporter)* , 1997, The Journal of Biological Chemistry.
[90] G. Ames,et al. Binding protein-independent histidine permease mutants. Uncoupling of ATP hydrolysis from transmembrane signaling. , 1991, The Journal of biological chemistry.
[91] K. Gunderson,et al. Conformational states of CFTR associated with channel gating: The role of ATP binding and hydrolysis , 1995, Cell.
[92] H. V. van Veen,et al. Reversible Transport by the ATP-binding Cassette Multidrug Export Pump LmrA , 2004, Journal of Biological Chemistry.
[93] G. Ames,et al. ATP-binding sites in the membrane components of histidine permease, a periplasmic transport system. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[94] H. W. Veen,et al. An ABC transporter with a secondary-active multidrug translocator domain , 2003, Nature.
[95] G. Ames,et al. Reconstitution of a bacterial periplasmic permease in proteoliposomes and demonstration of ATP hydrolysis concomitant with transport. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[96] C. Vigano,et al. Ligand-mediated Tertiary Structure Changes of Reconstituted P-glycoprotein , 1999, The Journal of Biological Chemistry.
[97] F. Sharom,et al. Transition state P-glycoprotein binds drugs and modulators with unchanged affinity, suggesting a concerted transport mechanism. , 2003, Biochemistry.
[98] H. Omote,et al. A Novel Electron Paramagnetic Resonance Approach to Determine the Mechanism of Drug Transport by P-glycoprotein* , 2002, The Journal of Biological Chemistry.
[99] R. Boucher,et al. Expression of the human multidrug resistance cDNA in insect cells generates a high activity drug-stimulated membrane ATPase. , 1992, The Journal of biological chemistry.
[100] Z. Sauna,et al. Correlation between Steady-state ATP Hydrolysis and Vanadate-induced ADP Trapping in Human P-glycoprotein , 2001, The Journal of Biological Chemistry.
[101] On the Mechanism of MgATP-dependent Gating of CFTR Cl− Channels , 2003, The Journal of general physiology.
[102] D. Rees,et al. The structure of Escherichia coli BtuF and binding to its cognate ATP binding cassette transporter , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[103] S. Mowbray,et al. Mutations that affect chemotaxis and transport , 1992 .
[104] I. Pastan,et al. Human P-glycoprotein exhibits reduced affinity for substrates during a catalytic transition state. , 1998, Biochemistry.
[105] C. Higgins,et al. Structure of the Multidrug Resistance P-glycoprotein to 2.5 nm Resolution Determined by Electron Microscopy and Image Analysis* , 1997, The Journal of Biological Chemistry.
[106] F. Quiocho,et al. Crystallographic evidence of a large ligand-induced hinge-twist motion between the two domains of the maltodextrin binding protein involved in active transport and chemotaxis. , 1992, Biochemistry.
[107] L. Schmitt,et al. Crystal structure of the nucleotide-binding domain of the ABC-transporter haemolysin B: identification of a variable region within ABC helical domains. , 2003, Journal of molecular biology.