6BPL
E. coli MsbA in complex with LPS and inhibitor G907
6BPL の概要
| エントリーDOI | 10.2210/pdb6bpl/pdb |
| 分子名称 | Lipid A export ATP-binding/permease protein MsbA, LAURIC ACID, DIPHOSPHATE, ... (11 entities in total) |
| 機能のキーワード | abc transporter, inhibitor, lps, msba, lipid transport |
| 由来する生物種 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 136482.65 |
| 構造登録者 | |
| 主引用文献 | Ho, H.,Miu, A.,Alexander, M.K.,Garcia, N.K.,Oh, A.,Zilberleyb, I.,Reichelt, M.,Austin, C.D.,Tam, C.,Shriver, S.,Hu, H.,Labadie, S.S.,Liang, J.,Wang, L.,Wang, J.,Lu, Y.,Purkey, H.E.,Quinn, J.,Franke, Y.,Clark, K.,Beresini, M.H.,Tan, M.W.,Sellers, B.D.,Maurer, T.,Koehler, M.F.T.,Wecksler, A.T.,Kiefer, J.R.,Verma, V.,Xu, Y.,Nishiyama, M.,Payandeh, J.,Koth, C.M. Structural basis for dual-mode inhibition of the ABC transporter MsbA. Nature, 557:196-201, 2018 Cited by PubMed Abstract: The movement of core-lipopolysaccharide across the inner membrane of Gram-negative bacteria is catalysed by an essential ATP-binding cassette transporter, MsbA. Recent structures of MsbA and related transporters have provided insights into the molecular basis of active lipid transport; however, structural information about their pharmacological modulation remains limited. Here we report the 2.9 Å resolution structure of MsbA in complex with G907, a selective small-molecule antagonist with bactericidal activity, revealing an unprecedented mechanism of ABC transporter inhibition. G907 traps MsbA in an inward-facing, lipopolysaccharide-bound conformation by wedging into an architecturally conserved transmembrane pocket. A second allosteric mechanism of antagonism occurs through structural and functional uncoupling of the nucleotide-binding domains. This study establishes a framework for the selective modulation of ABC transporters and provides rational avenues for the design of new antibiotics and other therapeutics targeting this protein family. PubMed: 29720648DOI: 10.1038/s41586-018-0083-5 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.908 Å) |
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