Functional importance of three basic residues clustered at the cytosolic interface of transmembrane helix 15 in the multidrug and organic anion transporter MRP1 (ABCC1). (Q40361067)

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scientific article published on 17 October 2005

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English	Functional importance of three basic residues clustered at the cytosolic interface of transmembrane helix 15 in the multidrug and organic anion transporter MRP1 (ABCC1).	scientific article published on 17 October 2005

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8 January 2020

Functional importance of three basic residues clustered at the cytosolic interface of transmembrane helix 15 in the multidrug and organic anion transporter MRP1 (ABCC1) (English)

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8 January 2020

transmembrane protein

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Susan P.C. Cole

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8 January 2020

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8 January 2020

Journal of Biological Chemistry

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8 January 2020

Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line

1 reference

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The MRP-related and BCRP/ABCG2 multidrug resistance proteins: biology, substrate specificity and regulation

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Polymorphisms of MRP1 (ABCC1) and related ATP-dependent drug transporters

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Mutation of a single conserved tryptophan in multidrug resistance protein 1 (MRP1/ABCC1) results in loss of drug resistance and selective loss of organic anion transport

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Molecular modeling correctly predicts the functional importance of Phe863 in transmembrane helix 11 of the multidrug resistance protein, MRP1 (ABCC1).

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Multiple membrane-associated tryptophan residues contribute to the transport activity and substrate specificity of the human multidrug resistance protein, MRP1.

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Identification of proline residues in the core cytoplasmic and transmembrane regions of multidrug resistance protein 1 (MRP1/ABCC1) important for transport function, substrate specificity, and nucleotide interactions.

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Mutational analysis of ionizable residues proximal to the cytoplasmic interface of membrane spanning domain 3 of the multidrug resistance protein, MRP1 (ABCC1): glutamate 1204 is important for both the expression and catalytic activity of the transp

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Identification of a nonconserved amino acid residue in multidrug resistance protein 1 important for determining substrate specificity: evidence for functional interaction between transmembrane helices 14 and 17.

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Determinants of the substrate specificity of multidrug resistance protein 1: role of amino acid residues with hydrogen bonding potential in predicted transmembrane helix 17.

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Functional importance of polar and charged amino acid residues in transmembrane helix 14 of multidrug resistance protein 1 (MRP1/ABCC1): identification of an aspartate residue critical for conversion from a high to low affinity substrate binding sta

1 reference

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21 January 2018

Identification of the structural and functional boundaries of the multidrug resistance protein 1 cytoplasmic loop 3.

1 reference

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21 January 2018

Functional and structural consequences of cysteine substitutions in the NH2 proximal region of the human multidrug resistance protein 1 (MRP1/ABCC1).

1 reference

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21 January 2018

Mutation of proline residues in the NH(2)-terminal region of the multidrug resistance protein, MRP1 (ABCC1): effects on protein expression, membrane localization, and transport function

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21 January 2018

A naturally occurring mutation in MRP1 results in a selective decrease in organic anion transport and in increased doxorubicin resistance

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21 January 2018

A positively charged amino acid proximal to the C-terminus of TM17 of MRP1 is indispensable for GSH-dependent binding of substrates and for transport of LTC4.

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21 January 2018

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21 January 2018

Limited modulation of the transport activity of the human multidrug resistance proteins MRP1, MRP2 and MRP3 by nicotine glucuronide metabolites

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21 January 2018

Comparison of the functional characteristics of the nucleotide binding domains of multidrug resistance protein 1.

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21 January 2018

Characterization of binding of leukotriene C4 by human multidrug resistance protein 1: evidence of differential interactions with NH2- and COOH-proximal halves of the protein.

1 reference

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21 January 2018

Role of carboxylate residues adjacent to the conserved core Walker B motifs in the catalytic cycle of multidrug resistance protein 1 (ABCC1).

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Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum

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8 January 2020

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