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Open data
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Basic information
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Title | Cryo-EM structure of the apo yeast Ceramide Synthase | |||||||||
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![]() | Ceramide Synthase / MEMBRANE PROTEIN | |||||||||
Function / homology | ![]() very-long-chain ceramide synthase / acyl-CoA ceramide synthase complex / Sphingolipid de novo biosynthesis / sphingosine N-acyltransferase activity / ceramide biosynthetic process / nuclear periphery / nuclear envelope / endoplasmic reticulum membrane / endoplasmic reticulum Similarity search - Function | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.0 Å | |||||||||
![]() | Schaefer J / Clausmeyer L / Koerner C / Moeller A / Froehlich F | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Structure of the yeast ceramide synthase. Authors: Jan-Hannes Schäfer / Lena Clausmeyer / Carolin Körner / Bianca M Esch / Verena N Wolf / Jennifer Sapia / Yara Ahmed / Stefan Walter / Stefano Vanni / Dovile Januliene / Arne Moeller / Florian Fröhlich / ![]() ![]() Abstract: Ceramides are essential lipids involved in forming complex sphingolipids and acting as signaling molecules. They result from the N-acylation of a sphingoid base and a CoA-activated fatty acid, a ...Ceramides are essential lipids involved in forming complex sphingolipids and acting as signaling molecules. They result from the N-acylation of a sphingoid base and a CoA-activated fatty acid, a reaction catalyzed by the ceramide synthase (CerS) family of enzymes. Yet, the precise structural details and catalytic mechanisms of CerSs have remained elusive. Here we used cryo-electron microscopy single-particle analysis to unravel the structure of the yeast CerS complex in both an active and a fumonisin B1-inhibited state. Our results reveal the complex's architecture as a dimer of Lip1 subunits bound to the catalytic subunits Lag1 and Lac1. Each catalytic subunit forms a hydrophobic crevice connecting the cytosolic site with the intermembrane space. The active site, located centrally in the tunnel, was resolved in a substrate preloaded state, representing one intermediate in ceramide synthesis. Our data provide evidence for competitive binding of fumonisin B1 to the acyl-CoA-binding tunnel. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 328.3 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 25 KB 25 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 14.8 KB | Display | ![]() |
Images | ![]() | 125.7 KB | ||
Masks | ![]() | 347.6 MB | ![]() | |
Filedesc metadata | ![]() | 7.3 KB | ||
Others | ![]() ![]() | 322.7 MB 322.8 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 1.2 MB | Display | ![]() |
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Full document | ![]() | 1.2 MB | Display | |
Data in XML | ![]() | 24.2 KB | Display | |
Data in CIF | ![]() | 31.5 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8qtnMC ![]() 8qtrC M: atomic model generated by this map C: citing same article ( |
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Similar structure data | Similarity search - Function & homology ![]() |
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Links
EMDB pages | ![]() ![]() |
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Map
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.68 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Mask #1
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-Half map: #2
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Density Histograms |
-Half map: #1
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Density Histograms |
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Sample components
-Entire : Heterotetrameric complex of yeast ceramide synthase with Lag1, La...
Entire | Name: Heterotetrameric complex of yeast ceramide synthase with Lag1, Lac1 and Lip1 |
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Components |
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-Supramolecule #1: Heterotetrameric complex of yeast ceramide synthase with Lag1, La...
Supramolecule | Name: Heterotetrameric complex of yeast ceramide synthase with Lag1, Lac1 and Lip1 type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#3 |
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Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 140 KDa |
-Macromolecule #1: Ceramide synthase LAG1
Macromolecule | Name: Ceramide synthase LAG1 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 37.150789 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: YREMNYRHSW LTPFFILVCV YSAYFLSGNR TESNPLHMFV AISYQVDGTD SYAKGIKDLS FVFFYMIFFT FLREFLMDVV IRPFTVYLN VTSEHRQKRM LEQMYAIFYC GVSGPFGLYI MYHSDLWLFK TKPMYRTYPV ITNPFLFKIF YLGQAAFWAQ Q ACVLVLQL ...String: YREMNYRHSW LTPFFILVCV YSAYFLSGNR TESNPLHMFV AISYQVDGTD SYAKGIKDLS FVFFYMIFFT FLREFLMDVV IRPFTVYLN VTSEHRQKRM LEQMYAIFYC GVSGPFGLYI MYHSDLWLFK TKPMYRTYPV ITNPFLFKIF YLGQAAFWAQ Q ACVLVLQL EKPRKDYKEL VFHHIVTLLL IWSSYVFHFT KMGLAIYITM DVSDFFLSLS KTLNYLNSVF TPFVFGLFVF FW IYLRHVV NIRILWSVLT EFRHEGNYVL NFATQQYKCW ISLPIVFVLI AALQLVNLYW LFLILRILYR LI UniProtKB: Ceramide synthase LAG1 |
-Macromolecule #2: Ceramide synthase LAC1
Macromolecule | Name: Ceramide synthase LAC1 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 36.235555 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: FREISYRHAW IAPLMILIAV YSAYFTSGNT TKTNVLHRFV AVSYQIGDTN AYGKGINDLC FVFYYMIFFT FLREFLMDVV IRPFAIRLH VTSKHRIKRI MEQMYAIFYT GVSGPFGIYC MYHSDLWFFN TKAMYRTYPD FTNPFLFKVF YLGQAAFWAQ Q ACILVLQL ...String: FREISYRHAW IAPLMILIAV YSAYFTSGNT TKTNVLHRFV AVSYQIGDTN AYGKGINDLC FVFYYMIFFT FLREFLMDVV IRPFAIRLH VTSKHRIKRI MEQMYAIFYT GVSGPFGIYC MYHSDLWFFN TKAMYRTYPD FTNPFLFKVF YLGQAAFWAQ Q ACILVLQL EKPRKDHNEL TFHHIVTLLL IWSSYVFHFT KMGLPIYITM DVSDFLLSFS KTLNYLDSGL AFFSFAIFVV AW IYLRHYI NLKILWSVLT QFRTEGNYVL NFATQQYKCW ISLPIVFVLI GALQLVNLYW LFLIFRVL UniProtKB: Ceramide synthase LAC1 |
-Macromolecule #3: Ceramide synthase subunit LIP1
Macromolecule | Name: Ceramide synthase subunit LIP1 / type: protein_or_peptide / ID: 3 / Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 15.44453 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: PKIFNLFRVC FISLLLIAAV EYFKYGTRIN YEWFHCTPIK EPQSGSVIKL WARGGPSCDK RGEYKTIVKR ITRDYEPNDE HLSFCIIEN DNVPPVHYPI HEDKGEPGYV AYVGYDTDSE LVQELCADST IYHM UniProtKB: Ceramide synthase subunit LIP1 |
-Macromolecule #4: 1,2-Distearoyl-sn-glycerophosphoethanolamine
Macromolecule | Name: 1,2-Distearoyl-sn-glycerophosphoethanolamine / type: ligand / ID: 4 / Number of copies: 4 / Formula: 3PE |
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Molecular weight | Theoretical: 748.065 Da |
Chemical component information | ![]() ChemComp-3PE: |
-Macromolecule #5: hexacosanoic acid
Macromolecule | Name: hexacosanoic acid / type: ligand / ID: 5 / Number of copies: 2 / Formula: 7PO |
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Molecular weight | Theoretical: 396.69 Da |
Chemical component information | ![]() ChemComp-7PO: |
-Macromolecule #6: [(2S)-1-hexadecanoyloxy-3-[hydroxy-[(2S,3R,5S,6R)-2,3,4,5,6-penta...
Macromolecule | Name: [(2S)-1-hexadecanoyloxy-3-[hydroxy-[(2S,3R,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy-phosphoryl]oxy-propan-2-yl] heptadecanoate type: ligand / ID: 6 / Number of copies: 2 / Formula: PIJ |
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Molecular weight | Theoretical: 825.059 Da |
-Macromolecule #7: AMMONIUM ION
Macromolecule | Name: AMMONIUM ION / type: ligand / ID: 7 / Number of copies: 2 / Formula: NH4 |
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Molecular weight | Theoretical: 18.038 Da |
Chemical component information | ![]() ChemComp-NH4: |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 6.5 |
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Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | TFS GLACIOS |
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Specialist optics | Energy filter - Name: TFS Selectris |
Image recording | Film or detector model: TFS FALCON 4i (4k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.8 µm |