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Open data
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Basic information
| Entry | Database: PDB / ID: 9lgb | |||||||||||||||||||||||||||
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| Title | bovine ABCC1 bound to leukotriene C4 | |||||||||||||||||||||||||||
Components | Multidrug resistance-associated protein 1 | |||||||||||||||||||||||||||
Keywords | PROTEIN TRANSPORT / ABC transporter / inward-open ABCC1 / LTC4 | |||||||||||||||||||||||||||
| Function / homology | Function and homology informationSphingolipid de novo biosynthesis / Heme degradation / Synthesis of Leukotrienes (LT) and Eoxins (EX) / Transport of RCbl within the body / cyclic nucleotide transport / Paracetamol ADME / ABC-family protein mediated transport / glutathione transmembrane transport / leukotriene transport / Cytoprotection by HMOX1 ...Sphingolipid de novo biosynthesis / Heme degradation / Synthesis of Leukotrienes (LT) and Eoxins (EX) / Transport of RCbl within the body / cyclic nucleotide transport / Paracetamol ADME / ABC-family protein mediated transport / glutathione transmembrane transport / leukotriene transport / Cytoprotection by HMOX1 / glutathione transmembrane transporter activity / ABC-type glutathione-S-conjugate transporter / carboxylic acid transmembrane transporter activity / ABC-type glutathione S-conjugate transporter activity / ABC-type xenobiotic transporter / ABC-type xenobiotic transporter activity / lipid transport / xenobiotic transmembrane transporter activity / xenobiotic transport / ABC-type transporter activity / positive regulation of inflammatory response / basolateral plasma membrane / response to xenobiotic stimulus / ATP hydrolysis activity / ATP binding / plasma membrane Similarity search - Function | |||||||||||||||||||||||||||
| Biological species | ![]() | |||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.34 Å | |||||||||||||||||||||||||||
Authors | Sun, P.P. / Liu, K.X. / Gao, P. | |||||||||||||||||||||||||||
| Funding support | China, 1items
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Citation | Journal: Nat Commun / Year: 2025Title: Substrate recognition diversity and transport dynamics of ABCC1. Authors: Panpan Sun / Kexin Liu / Linnan Zhang / Qixiang Zhang / Yina Gao / Zhaolong Li / Yalan Zhu / Songqing Liu / Liguo Zhang / Ang Gao / Pu Gao / ![]() Abstract: ABCC1 is an ATP-binding cassette (ABC) transporter that exports diverse endogenous and exogenous substrates, conferring resistance to many anticancer drugs and mediating various physiological ...ABCC1 is an ATP-binding cassette (ABC) transporter that exports diverse endogenous and exogenous substrates, conferring resistance to many anticancer drugs and mediating various physiological functions. Here, we present ten cryo-EM structures of ABCC1 in different functional states, providing systematic insights into its substrate recognition diversity and transport dynamics. ABCC1 utilizes a plastic bipartite substrate-binding pocket and a substrate-induced conformational flexibility to accommodate molecules with diverse properties, including bimolecular glutathione (GSH)-substrate pairs, GSH conjugates, and GSH-independent cyclic dinucleotides. A herein characterized substrate-releasing intermediate state reveals ATP-mediated overall conformational transitions and detailed pocket reorganization during substrate loading, pre-release, and post-release. Unexpectedly, we identify a sequential nucleotide release mechanism where the hydrolysis product ADP, rather than unhydrolyzed ATP, releases first, priming the transporter for turnover and resetting. Complemented by mutagenesis and functional assays, these findings provide a complete framework for understanding ABCC1's molecular basis and offer a foundation for developing next-generation modulators. | |||||||||||||||||||||||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9lgb.cif.gz | 271.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9lgb.ent.gz | 212.7 KB | Display | PDB format |
| PDBx/mmJSON format | 9lgb.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/lg/9lgb ftp://data.pdbj.org/pub/pdb/validation_reports/lg/9lgb | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 63060MC ![]() 9lg6C ![]() 9lg7C ![]() 9lg8C ![]() 9lg9C ![]() 9lgaC ![]() 9lgcC ![]() 9lgdC ![]() 9lgeC ![]() 9lgfC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 175004.688 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() References: UniProt: Q8HXQ5, ABC-type xenobiotic transporter, ABC-type glutathione-S-conjugate transporter |
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| #2: Chemical | ChemComp-LTX / ( |
| Has ligand of interest | Y |
| Has protein modification | N |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: inward-open bABCC1 bound to LTC4 / Type: COMPLEX / Entity ID: #1 / Source: RECOMBINANT |
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| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 8 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TALOS ARCTICA |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2000 nm / Nominal defocus min: 1000 nm |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K2 QUANTUM (4k x 4k) |
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Processing
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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| 3D reconstruction | Resolution: 3.34 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 183842 / Symmetry type: POINT |
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FIELD EMISSION GUN