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Yorodumi- PDB-7vzb: Cryo-EM structure of C22:0-CoA bound human very long-chain fatty ... -
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Basic information
| Entry | Database: PDB / ID: 7vzb | ||||||
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| Title | Cryo-EM structure of C22:0-CoA bound human very long-chain fatty acid ABC transporter ABCD1 | ||||||
Components | Peroxisomal Membrane Protein related,ATP-binding cassette sub-family D member 1 | ||||||
Keywords | TRANSPORT PROTEIN / very long-chain fatty / Peroxisome / ABC transporter | ||||||
| Function / homology | Function and homology informationABC transporters in lipid homeostasis / Linoleic acid (LA) metabolism / alpha-linolenic acid (ALA) metabolism / Beta-oxidation of very long chain fatty acids / Class I peroxisomal membrane protein import / ABC-type fatty-acyl-CoA transporter activity / peroxisomal membrane transport / very long-chain fatty-acyl-CoA catabolic process / very long-chain fatty acyl-CoA hydrolase activity / positive regulation of unsaturated fatty acid biosynthetic process ...ABC transporters in lipid homeostasis / Linoleic acid (LA) metabolism / alpha-linolenic acid (ALA) metabolism / Beta-oxidation of very long chain fatty acids / Class I peroxisomal membrane protein import / ABC-type fatty-acyl-CoA transporter activity / peroxisomal membrane transport / very long-chain fatty-acyl-CoA catabolic process / very long-chain fatty acyl-CoA hydrolase activity / positive regulation of unsaturated fatty acid biosynthetic process / Linoleic acid (LA) metabolism / Defective ABCD1 causes ALD / long-chain fatty acid catabolic process / long-chain fatty acid import into peroxisome / very long-chain fatty acid catabolic process / alpha-linolenic acid (ALA) metabolism / regulation of fatty acid beta-oxidation / Beta-oxidation of very long chain fatty acids / fatty acid derivative biosynthetic process / alpha-linolenic acid metabolic process / very long-chain fatty acid metabolic process / sterol homeostasis / Class I peroxisomal membrane protein import / unsaturated fatty acid biosynthetic process / peroxisome organization / fatty acyl-CoA hydrolase activity / regulation of mitochondrial depolarization / ABC transporters in lipid homeostasis / myelin maintenance / regulation of oxidative phosphorylation / regulation of cellular response to oxidative stress / positive regulation of fatty acid beta-oxidation / linoleic acid metabolic process / Hydrolases; Acting on ester bonds; Thioester hydrolases / fatty acid elongation / Translocases; Catalysing the translocation of other compounds; Linked to the hydrolysis of a nucleoside triphosphate / peroxisomal membrane / long-chain fatty acid biosynthetic process / long-chain fatty acid transmembrane transporter activity / fatty acid beta-oxidation / ATPase-coupled transmembrane transporter activity / fatty acid homeostasis / ABC-type transporter activity / negative regulation of reactive oxygen species biosynthetic process / neuron projection maintenance / negative regulation of cytokine production involved in inflammatory response / ADP binding / mitochondrial membrane / peroxisome / lysosomal membrane / endoplasmic reticulum membrane / perinuclear region of cytoplasm / enzyme binding / protein homodimerization activity / ATP hydrolysis activity / ATP binding / identical protein binding / membrane / cytoplasm / cytosol Similarity search - Function | ||||||
| Biological species | ![]() Homo sapiens (human) | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.59 Å | ||||||
Authors | Chen, Z.P. / Xu, D. / Wang, L. / Mao, Y.X. / Yang, L. / Cheng, M.T. / Hou, W.T. / Chen, Y.X. / Zhou, C.Z. | ||||||
| Funding support | China, 1items
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Citation | Journal: Nat Commun / Year: 2022Title: Structural basis of substrate recognition and translocation by human very long-chain fatty acid transporter ABCD1. Authors: Zhi-Peng Chen / Da Xu / Liang Wang / Yao-Xu Mao / Yang Li / Meng-Ting Cheng / Cong-Zhao Zhou / Wen-Tao Hou / Yuxing Chen / ![]() Abstract: Human ABC transporter ABCD1 transports very long-chain fatty acids from cytosol to peroxisome for β-oxidation, dysfunction of which usually causes the X-linked adrenoleukodystrophy (X-ALD). Here, we ...Human ABC transporter ABCD1 transports very long-chain fatty acids from cytosol to peroxisome for β-oxidation, dysfunction of which usually causes the X-linked adrenoleukodystrophy (X-ALD). Here, we report three cryogenic electron microscopy structures of ABCD1: the apo-form, substrate- and ATP-bound forms. Distinct from what was seen in the previously reported ABC transporters, the two symmetric molecules of behenoyl coenzyme A (C22:0-CoA) cooperatively bind to the transmembrane domains (TMDs). For each C22:0-CoA, the hydrophilic 3'-phospho-ADP moiety of CoA portion inserts into one TMD, with the succeeding pantothenate and cysteamine moiety crossing the inter-domain cavity, whereas the hydrophobic fatty acyl chain extends to the opposite TMD. Structural analysis combined with biochemical assays illustrates snapshots of ABCD1-mediated substrate transport cycle. It advances our understanding on the selective oxidation of fatty acids and molecular pathology of X-ALD. | ||||||
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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 | 7vzb.cif.gz | 226.5 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7vzb.ent.gz | 177.8 KB | Display | PDB format |
| PDBx/mmJSON format | 7vzb.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7vzb_validation.pdf.gz | 1.1 MB | Display | wwPDB validaton report |
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| Full document | 7vzb_full_validation.pdf.gz | 1.1 MB | Display | |
| Data in XML | 7vzb_validation.xml.gz | 42.7 KB | Display | |
| Data in CIF | 7vzb_validation.cif.gz | 61.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/vz/7vzb ftp://data.pdbj.org/pub/pdb/validation_reports/vz/7vzb | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 32224MC ![]() 7vwcC ![]() 7vx8C 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: 87931.000 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human)Gene: pmp-4, CELE_T02D1.5, T02D1.5, ABCD1, ALD / Plasmid: pCAG / Cell line (production host): HEK293F / Production host: Homo sapiens (human)References: UniProt: O45730, UniProt: P33897, Hydrolases; Acting on ester bonds; Thioester hydrolases, Translocases; Catalysing the translocation of other compounds; Linked to the hydrolysis of a nucleoside triphosphate #2: Chemical | #3: Chemical | Has ligand of interest | Y | |
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-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: human peroxisomal ABCD1 / Type: ORGANELLE OR CELLULAR COMPONENT / Entity ID: #1 / Source: RECOMBINANT | ||||||||||||
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| Molecular weight | Value: 175.6 kDa/nm / Experimental value: NO | ||||||||||||
| Source (natural) |
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| Source (recombinant) | Organism: Homo sapiens (human) / Cell: HEK 293F / Plasmid: pCAG | ||||||||||||
| Buffer solution | pH: 7.5 | ||||||||||||
| Specimen | Conc.: 8 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||
| Specimen support | Grid type: Quantifoil R1.2/1.3 | ||||||||||||
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 8 K |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: OTHER |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: -2000 nm / Nominal defocus min: -1500 nm |
| Specimen holder | Cryogen: NITROGEN |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | |||||||||
| 3D reconstruction | Resolution: 3.59 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 336741 / Symmetry type: POINT | |||||||||
| Atomic model building | Protocol: AB INITIO MODEL / Space: REAL |
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About Yorodumi




Homo sapiens (human)
China, 1items
Citation




PDBj



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