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Título

Domain interactions in the yeast ATP binding cassette transporter Ycf1p: Intragenic suppressor analysis of mutations in the nucleotide binding domains

AutorFalcón-Pérez, Juan M.; Martínez-Burgos, Mónica; Mazón, María J. ; Eraso, Pilar
Fecha de publicaciónago-2001
EditorAmerican Society for Microbiology
CitaciónJournal of Bacteriology 183(16): 4761-4770 (2001)
ResumenThe yeast cadmium factor (Ycf1p) is a vacuolar ATP binding cassette (ABC) transporter required for heavy metal and drug detoxification. Cluster analysis shows that Ycf1p is strongly related to the human multidrug-associated protein (MRP1) and cystic fibrosis transmembrane conductance regulator and therefore may serve as an excellent model for the study of eukaryotic ABC transporter structure and function. Identifying intramolecular interactions in these transporters may help to elucidate energy transfer mechanisms during transport. To identify regions in Ycf1p that may interact to couple ATPase activity to substrate binding and/or movement across the membrane, we sought intragenic suppressors of ycf1 mutations that affect highly conserved residues presumably involved in ATP binding and/or hydrolysis. Thirteen intragenic second-site suppressors were identified for the D777N mutation which affects the invariant Asp residue in the Walker B motif of the first nucleotide binding domain (NBD1). Two of the suppressor mutations (V543I and F565L) are located in the first transmembrane domain (TMD1), nine (A1003V, A1021T, A1021V, N1027D, Q1107R, G1207D, G1207S, S1212L, and W1225C) are found within TMD2, one (S674L) is in NBD1, and another one (R1415G) is in NBD2, indicating either physical proximity or functional interactions between NBD1 and the other three domains. The original D777N mutant protein exhibits a strong defect in the apparent affinity for ATP and V(max) of transport. The phenotypic characterization of the suppressor mutants shows that suppression does not result from restoring these alterations but rather from a change in substrate specificity. We discuss the possible involvement of Asp777 in coupling ATPase activity to substrate binding and/or transport across the membrane.
Descripción10 pages, 5 figures, 3 tables.
Versión del editorhttp://dx.doi.org/10.1128/JB.183.16.4761-4770.2001
URIhttp://hdl.handle.net/10261/24377
DOI10.1128/JB.183.16.4761-4770.2001
ISSN0021-9193
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