+
Open data
-
Basic information
| Entry | ![]() | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Title | Cholinephosphotransferase in complex with diacylglycerol | |||||||||
Map data | Primary Map | |||||||||
Sample |
| |||||||||
Keywords | lipid metabolism / phospholipid synthesis / membrane protein enzyme / choline metabolism / MEMBRANE PROTEIN | |||||||||
| Function / homology | Function and homology informationSynthesis of PC / Synthesis of PE / diacylglycerol cholinephosphotransferase / diacylglycerol cholinephosphotransferase activity / CDP-choline pathway / mitochondrial outer membrane / endoplasmic reticulum membrane / endoplasmic reticulum / Golgi apparatus / metal ion binding Similarity search - Function | |||||||||
| Biological species | ![]() ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.2 Å | |||||||||
Authors | Roberts JR / Maeda S / Ohi MD | |||||||||
| Funding support | 1 items
| |||||||||
Citation | Journal: Nat Commun / Year: 2025Title: Structural basis for catalysis and selectivity of phospholipid synthesis by eukaryotic choline-phosphotransferase. Authors: Jacquelyn R Roberts / Yasuhiro Horibata / Frank E Kwarcinski / Vinson Lam / Ashleigh M Raczkowski / Akane Hubbard / Betsy White / Hiroyuki Sugimoto / Gregory G Tall / Melanie D Ohi / Shoji Maeda / ![]() Abstract: Phospholipids are the most abundant component in lipid membranes and are essential for the structural and functional integrity of the cell. In eukaryotic cells, phospholipids are primarily ...Phospholipids are the most abundant component in lipid membranes and are essential for the structural and functional integrity of the cell. In eukaryotic cells, phospholipids are primarily synthesized de novo through the Kennedy pathway that involves multiple enzymatic processes. The terminal reaction is mediated by a group of cytidine-5'-diphosphate (CDP)-choline /CDP-ethanolamine-phosphotransferases (CPT/EPT) that use 1,2-diacylglycerol (DAG) and CDP-choline or CDP-ethanolamine to produce phosphatidylcholine (PC) or phosphatidylethanolamine (PE) that are the main phospholipids in eukaryotic cells. Here we present the structure of the yeast CPT1 in multiple substrate-bound states. Structural and functional analysis of these binding-sites reveal the critical residues for the DAG acyl-chain preference and the choline/ethanolamine selectivity. Additionally, we present the structure in complex with a potent inhibitor characterized in this study. The ensemble of structures allows us to propose the reaction mechanism for phospholipid biosynthesis by the family of CDP-alcohol phosphotransferases (CDP-APs). | |||||||||
| History |
|
-
Structure visualization
| Supplemental images |
|---|
-
Downloads & links
-EMDB archive
| Map data | emd_42357.map.gz | 59.7 MB | EMDB map data format | |
|---|---|---|---|---|
| Header (meta data) | emd-42357-v30.xml emd-42357.xml | 15.8 KB 15.8 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_42357_fsc.xml | 8.4 KB | Display | FSC data file |
| Images | emd_42357.png | 143.7 KB | ||
| Filedesc metadata | emd-42357.cif.gz | 6.3 KB | ||
| Others | emd_42357_half_map_1.map.gz emd_42357_half_map_2.map.gz | 59.2 MB 59.2 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-42357 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42357 | HTTPS FTP |
-Validation report
| Summary document | emd_42357_validation.pdf.gz | 741 KB | Display | EMDB validaton report |
|---|---|---|---|---|
| Full document | emd_42357_full_validation.pdf.gz | 740.5 KB | Display | |
| Data in XML | emd_42357_validation.xml.gz | 16.1 KB | Display | |
| Data in CIF | emd_42357_validation.cif.gz | 21.1 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42357 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42357 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 8ul9MC ![]() 8urpC ![]() 8urtC M: atomic model generated by this map C: citing same article ( |
|---|---|
| Similar structure data | Similarity search - Function & homology F&H Search |
-
Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
|---|
-
Map
| File | Download / File: emd_42357.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Annotation | Primary Map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.08 Å | ||||||||||||||||||||||||||||||||||||
| Density |
| ||||||||||||||||||||||||||||||||||||
| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
|
-Supplemental data
-Half map: Half map B
| File | emd_42357_half_map_1.map | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Annotation | Half map B | ||||||||||||
| Projections & Slices |
| ||||||||||||
| Density Histograms |
-Half map: Half map A
| File | emd_42357_half_map_2.map | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Annotation | Half map A | ||||||||||||
| Projections & Slices |
| ||||||||||||
| Density Histograms |
-
Sample components
-Entire : Saccharomyces cerevisiae CDP-choline phosphotransferase in comple...
| Entire | Name: Saccharomyces cerevisiae CDP-choline phosphotransferase in complex with diacyl-glycerol |
|---|---|
| Components |
|
-Supramolecule #1: Saccharomyces cerevisiae CDP-choline phosphotransferase in comple...
| Supramolecule | Name: Saccharomyces cerevisiae CDP-choline phosphotransferase in complex with diacyl-glycerol type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
|---|---|
| Source (natural) | Organism: ![]() |
-Supramolecule #2: nanobody24
| Supramolecule | Name: nanobody24 / type: complex / ID: 2 / Parent: 1 |
|---|---|
| Source (natural) | Organism: ![]() |
-Supramolecule #3: yCPT1
| Supramolecule | Name: yCPT1 / type: complex / ID: 3 / Parent: 1 / Macromolecule list: #1 |
|---|---|
| Source (natural) | Organism: ![]() |
-Macromolecule #1: Cholinephosphotransferase 1
| Macromolecule | Name: Cholinephosphotransferase 1 / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
|---|---|
| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 44.147277 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: (ACE)GFFIPQSSL GNLKLYKYQS DDRSFLSNHV LRPFWRKFAT IFPLWMAPNL VTLLGFCFII FNVLTTLYYD PYFDQE SPR WTYFSYAIGL FLYQTFDACD GMHARRTGQQ GPLGELFDHC IDSINTTLSM IPVCSMTGMG YTYMTIFSQF AILCSFY LS TWEEYHTHKL ...String: (ACE)GFFIPQSSL GNLKLYKYQS DDRSFLSNHV LRPFWRKFAT IFPLWMAPNL VTLLGFCFII FNVLTTLYYD PYFDQE SPR WTYFSYAIGL FLYQTFDACD GMHARRTGQQ GPLGELFDHC IDSINTTLSM IPVCSMTGMG YTYMTIFSQF AILCSFY LS TWEEYHTHKL YLAEFCGPVE GIIVLCISFI AVGIYGPQTI WHTKVAQFSW QDFVFDVETV HLMYAFCTGA LIFNIVTA H TNVVRYYESQ STKSATPSKT AENISKAVNG LLPFFAYFSS IFTLVLIQPS FISLALILSI GFSVAFVVGR MIIAHLTMQ PFPMVNFPFL IPTIQLVLYA FMVYVLDYQK GSIVSALVWM GLGLTLAIHG MFINDIIYDI TTFLDIYALS IK UniProtKB: Cholinephosphotransferase 1 |
-Macromolecule #2: MAGNESIUM ION
| Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 2 / Number of copies: 4 / Formula: MG |
|---|---|
| Molecular weight | Theoretical: 24.305 Da |
-Macromolecule #3: 1,2-DIOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE
| Macromolecule | Name: 1,2-DIOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE / type: ligand / ID: 3 / Number of copies: 6 / Formula: PCW |
|---|---|
| Molecular weight | Theoretical: 787.121 Da |
| Chemical component information | ![]() ChemComp-PCW: |
-Macromolecule #4: DIACYL GLYCEROL
| Macromolecule | Name: DIACYL GLYCEROL / type: ligand / ID: 4 / Number of copies: 2 / Formula: DGA |
|---|---|
| Molecular weight | Theoretical: 625.018 Da |
| Chemical component information | ![]() ChemComp-DGA: |
-Macromolecule #5: water
| Macromolecule | Name: water / type: ligand / ID: 5 / Number of copies: 1 / Formula: HOH |
|---|---|
| Molecular weight | Theoretical: 18.015 Da |
| Chemical component information | ![]() ChemComp-HOH: |
-Experimental details
-Structure determination
| Method | cryo EM |
|---|---|
Processing | single particle reconstruction |
| Aggregation state | particle |
-
Sample preparation
| Concentration | 2 mg/mL |
|---|---|
| Buffer | pH: 7.5 |
| Vitrification | Cryogen name: NITROGEN |
-
Electron microscopy
| Microscope | TFS KRIOS |
|---|---|
| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 60.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.4 µm / Nominal defocus min: 1.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
Movie
Controller
About Yorodumi




Keywords

Authors
Citation







Z (Sec.)
Y (Row.)
X (Col.)








































Processing
FIELD EMISSION GUN

