8BWR
Cryo-EM structure of nanodisc-reconstituted wildtype human MRP4 (in complex with prostaglandin E2)
Summary for 8BWR
| Entry DOI | 10.2210/pdb8bwr/pdb |
| Related | 8BJF 8BWO 8BWP 8BWQ |
| EMDB information | 16088 16292 16293 16294 16295 |
| Descriptor | ATP-binding cassette sub-family C member 4, (Z)-7-[(1R,2R,3R)-3-hydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxo-cyclopentyl]hept-5-enoic acid (2 entities in total) |
| Functional Keywords | abc transporter, abcc4, mrp4, pge2 bound abc transporter, translocase |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 1 |
| Total formula weight | 150046.39 |
| Authors | Raj, I.,Bloch, M.,Pape, T.H.,Taylor, N.M.I. (deposition date: 2022-12-07, release date: 2023-08-30, Last modification date: 2023-11-15) |
| Primary citation | Bloch, M.,Raj, I.,Pape, T.,Taylor, N.M.I. Structural and mechanistic basis of substrate transport by the multidrug transporter MRP4. Structure, 31:1407-1418.e6, 2023 Cited by PubMed Abstract: Multidrug resistance-associated protein 4 (MRP4) is an ATP-binding cassette (ABC) transporter expressed at multiple tissue barriers where it actively extrudes a wide variety of drug compounds. Overexpression of MRP4 provides resistance to clinically used antineoplastic agents, making it a highly attractive therapeutic target for countering multidrug resistance. Here, we report cryo-EM structures of multiple physiologically relevant states of lipid bilayer-embedded human MRP4, including complexes between MRP4 and two widely used chemotherapeutic agents and a complex between MRP4 and its native substrate. The structures display clear similarities and distinct differences in the coordination of these chemically diverse substrates and, in combination with functional and mutational analysis, reveal molecular details of the transport mechanism. Our study provides key insights into the unusually broad substrate specificity of MRP4 and constitutes an important contribution toward a general understanding of multidrug transporters. PubMed: 37683641DOI: 10.1016/j.str.2023.08.014 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (4 Å) |
Structure validation
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