0000000001024652

AUTHOR

Robert C. Ford

0000-0002-0958-1505

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What monomeric nucleotide binding domains can teach us about dimeric ABC proteins

2020

The classic conceptualization of ATP binding cassette (ABC) transporter function is an ATP-dependent conformational change coupled to transport of a substrate across a biological membrane via the transmembrane domains (TMDs). The binding of two ATP molecules within the transporter's two nucleotide binding domains (NBDs) induces their dimerization. Despite retaining the ability to bind nucleotides, isolated NBDs frequently fail to dimerize. ABC proteins without a TMD, for example ABCE and ABCF, have NBDs tethered via elaborate linkers, further supporting that NBD dimerization does not readily occur for isolated NBDs. Intriguingly, even in full-length transporters, the NBD-dimerized, outward-…

Conformational changeBiophysicsContext (language use)ATP-binding cassette transporterBiochemistry03 medical and health sciencesAdenosine TriphosphateProtein DomainsStructural BiologyGeneticsAnimalsHumansNucleotideMolecular Biology030304 developmental biologychemistry.chemical_classification0303 health sciencesBinding Sites030302 biochemistry & molecular biologyTransporterBiological membraneCell BiologyTransmembrane domainchemistryCyclic nucleotide-binding domainBiophysicsATP-Binding Cassette Transporterslipids (amino acids peptides and proteins)Protein MultimerizationProtein BindingFEBS Letters
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