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Yorodumi- EMDB-23075: Structure of the S. cerevisiae phosphatidylcholine flippase Dnf1-... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-23075 | |||||||||
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Title | Structure of the S. cerevisiae phosphatidylcholine flippase Dnf1-Lem3 complex in the E2P state | |||||||||
Map data | Cryo-EM 3D map of the S. cerevisiae phosphatidylcholine flippase Dnf1-Lem3 complex in the E2P state | |||||||||
Sample |
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Keywords | P4 ATPase / Phosphatidylcholine Flippases / TRANSLOCASE | |||||||||
Function / homology | Function and homology information regulation of vacuole organization / glycosylceramide flippase activity / mating projection tip membrane / aminophospholipid translocation / Ion transport by P-type ATPases / phosphatidylcholine flippase activity / phosphatidylserine flippase activity / ceramide translocation / ATPase-coupled intramembrane lipid transporter activity / phospholipid-translocating ATPase complex ...regulation of vacuole organization / glycosylceramide flippase activity / mating projection tip membrane / aminophospholipid translocation / Ion transport by P-type ATPases / phosphatidylcholine flippase activity / phosphatidylserine flippase activity / ceramide translocation / ATPase-coupled intramembrane lipid transporter activity / phospholipid-translocating ATPase complex / phosphatidylserine floppase activity / phosphatidylethanolamine flippase activity / cell septum / phosphatidylcholine floppase activity / cellular bud neck / P-type phospholipid transporter / phospholipid translocation / establishment or maintenance of cell polarity / Neutrophil degranulation / cell periphery / intracellular protein transport / endocytosis / cell surface receptor signaling pathway / endosome membrane / Golgi apparatus / magnesium ion binding / endoplasmic reticulum / ATP hydrolysis activity / mitochondrion / ATP binding / identical protein binding / plasma membrane / cytoplasm Similarity search - Function | |||||||||
Biological species | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.8 Å | |||||||||
Authors | Bai L / You Q / Jain BK / Duan HD / Kovach A / Graham TR / Li H | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Elife / Year: 2020 Title: Transport mechanism of P4 ATPase phosphatidylcholine flippases. Authors: Lin Bai / Qinglong You / Bhawik K Jain / H Diessel Duan / Amanda Kovach / Todd R Graham / Huilin Li / Abstract: The P4 ATPases use ATP hydrolysis to transport large lipid substrates across lipid bilayers. The structures of the endosome- and Golgi-localized phosphatidylserine flippases-such as the yeast Drs2 ...The P4 ATPases use ATP hydrolysis to transport large lipid substrates across lipid bilayers. The structures of the endosome- and Golgi-localized phosphatidylserine flippases-such as the yeast Drs2 and human ATP8A1-have recently been reported. However, a substrate-binding site on the cytosolic side has not been found, and the transport mechanisms of P4 ATPases with other substrates are unknown. Here, we report structures of the Dnf1-Lem3 and Dnf2-Lem3 complexes. We captured substrate phosphatidylcholine molecules on both the exoplasmic and cytosolic sides and found that they have similar structures. Unexpectedly, Lem3 contributes to substrate binding. The conformational transitions of these phosphatidylcholine transporters match those of the phosphatidylserine transporters, suggesting a conserved mechanism among P4 ATPases. Dnf1/Dnf2 have a unique P domain helix-turn-helix insertion that is important for function. Therefore, P4 ATPases may have retained an overall transport mechanism while evolving distinct features for different lipid substrates. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_23075.map.gz | 10.9 MB | EMDB map data format | |
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Header (meta data) | emd-23075-v30.xml emd-23075.xml | 15.4 KB 15.4 KB | Display Display | EMDB header |
Images | emd_23075.png | 53.4 KB | ||
Filedesc metadata | emd-23075.cif.gz | 6.7 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-23075 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-23075 | HTTPS FTP |
-Validation report
Summary document | emd_23075_validation.pdf.gz | 401.1 KB | Display | EMDB validaton report |
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Full document | emd_23075_full_validation.pdf.gz | 400.7 KB | Display | |
Data in XML | emd_23075_validation.xml.gz | 6.3 KB | Display | |
Data in CIF | emd_23075_validation.cif.gz | 7.3 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-23075 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-23075 | HTTPS FTP |
-Related structure data
Related structure data | 7kycMC 7ky5C 7ky6C 7ky7C 7ky8C 7ky9C 7kyaC 7kybC C: citing same article (ref.) M: atomic model generated by this map |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_23075.map.gz / Format: CCP4 / Size: 83.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Cryo-EM 3D map of the S. cerevisiae phosphatidylcholine flippase Dnf1-Lem3 complex in the E2P state | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.826 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : S. cerevisiae phosphatidylcholine flippase Dnf1-Lem3 complex in t...
Entire | Name: S. cerevisiae phosphatidylcholine flippase Dnf1-Lem3 complex in the E2P state |
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Components |
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-Supramolecule #1: S. cerevisiae phosphatidylcholine flippase Dnf1-Lem3 complex in t...
Supramolecule | Name: S. cerevisiae phosphatidylcholine flippase Dnf1-Lem3 complex in the E2P state type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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Source (natural) | Organism: Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c |
-Macromolecule #1: Phospholipid-transporting ATPase DNF1
Macromolecule | Name: Phospholipid-transporting ATPase DNF1 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO / EC number: P-type phospholipid transporter |
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Source (natural) | Organism: Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c |
Molecular weight | Theoretical: 178.000172 KDa |
Recombinant expression | Organism: Saccharomyces cerevisiae S288C (yeast) |
Sequence | String: MSGTFHGDGH APMSPFEDTF QFEDNSSNED THIAPTHFDD GATSNKYSRP QVSFNDETPK NKREDAEEFT FNDDTEYDNH SFQPTPKLN NGSGTFDDVE LDNDSGEPHT NYDGMKRFRM GTKRNKKGNP IMGRSKTLKW ARKNIPNPFE DFTKDDIDPG A INRAQELR ...String: MSGTFHGDGH APMSPFEDTF QFEDNSSNED THIAPTHFDD GATSNKYSRP QVSFNDETPK NKREDAEEFT FNDDTEYDNH SFQPTPKLN NGSGTFDDVE LDNDSGEPHT NYDGMKRFRM GTKRNKKGNP IMGRSKTLKW ARKNIPNPFE DFTKDDIDPG A INRAQELR TVYYNMPLPK DMIDEEGNPI MQYPRNKIRT TKYTPLTFLP KNILFQFHNF ANVYFLVLII LGAFQIFGVT NP GLSAVPL VVIVIITAIK DAIEDSRRTV LDLEVNNTKT HILEGVENEN VSTDNISLWR RFKKANSRLL FKFIQYCKEH LTE EGKKKR MQRKRHELRV QKTVGTSGPR SSLDSIDSYR VSADYGRPSL DYDNLEQGAG EANIVDRSLP PRTDCKFAKN YWKG VKVGD IVRIHNNDEI PADIILLSTS DTDGACYVET KNLDGETNLK VRQSLKCTNT IRTSKDIART KFWIESEGPH SNLYT YQGN MKWRNLADGE IRNEPITINN VLLRGCTLRN TKWAMGVVMF TGGDTKIMLN SGITPTKKSR ISRELNFSVV INFVLL FIL CFVSGIANGV YYDKKGRSRF SYEFGTIAGS AATNGFVSFW VAVILYQSLV PISLYISVEI IKTAQAAFIY GDVLLYN AK LDYPCTPKSW NISDDLGQVE YIFSDKTGTL TQNVMEFKKC TINGVSYGRA YTEALAGLRK RQGIDVETEG RREKAEIA K DRDTMIDELR ALSGNSQFYP EEVTFVSKEF VRDLKGASGE VQQRCCEHFM LALALCHSVL VEANPDNPKK LDLKAQSPD EAALVATARD VGFSFVGKTK KGLIIEMQGI QKEFEILNIL EFNSSRKRMS CIVKIPGLNP GDEPRALLIC KGADSIIYSR LSRQSGSNS EAILEKTALH LEQYATEGLR TLCIAQRELS WSEYEKWNEK YDIAAASLAN REDELEVVAD SIERELILLG G TAIEDRLQ DGVPDCIELL AEAGIKLWVL TGDKVETAIN IGFSCNLLNN EMELLVIKTT GDDVKEFGSE PSEIVDALLS KY LKEYFNL TGSEEEIFEA KKDHEFPKGN YAIVIDGDAL KLALYGEDIR RKFLLLCKNC RAVLCCRVSP SQKAAVVKLV KDS LDVMTL AIGDGSNDVA MIQSADVGIG IAGEEGRQAV MCSDYAIGQF RYLARLVLVH GRWSYKRLAE MIPEFFYKNM IFAL ALFWY GIYNDFDGSY LYEYTYMMFY NLAFTSLPVI FLGILDQDVN DTISLVVPQL YRVGILRKEW NQRKFLWYML DGLYQ SIIC FFFPYLVYHK NMIVTSNGLG LDHRYFVGVY VTTIAVISCN TYVLLHQYRW DWFSGLFIAL SCLVVFAWTG IWSSAI ASR EFFKAAARIY GAPSFWAVFF VAVLFCLLPR FTYDSFQKFF YPTDVEIVRE MWQHGHFDHY PPGYDPTDPN RPKVTKA GQ HGEKIIEGIA LSDNLGGSNY SRDSVVTEEI PMTFMHGEDG SPSGYQKQET WMTSPKETQD LLQSPQFQQA QTFGRGPS T NVRSSLDRTR EQMIATNQLD NRYSVERART SLDLPGVTNA ASLIGTQQNN UniProtKB: Phospholipid-transporting ATPase DNF1 |
-Macromolecule #2: Alkylphosphocholine resistance protein LEM3
Macromolecule | Name: Alkylphosphocholine resistance protein LEM3 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (yeast) Strain: ATCC 204508 / S288c |
Molecular weight | Theoretical: 47.490395 KDa |
Recombinant expression | Organism: Saccharomyces cerevisiae S288C (yeast) |
Sequence | String: MVNFDLGQVG EVFRRKDKGA IVSGDNPEEE EDVDASEFEE DEVKPVRTKN RRPKEDAFTQ QRLAAINPVL TPRTVLPLYL LIAVVFVIV GGCILAQNSK VDEVTIYYQD CMTNATSSWS DIPSEHWQFV FHKYKTYNTA PQWRFVDDES DDFTKQRGTC Q IRFTTPSD ...String: MVNFDLGQVG EVFRRKDKGA IVSGDNPEEE EDVDASEFEE DEVKPVRTKN RRPKEDAFTQ QRLAAINPVL TPRTVLPLYL LIAVVFVIV GGCILAQNSK VDEVTIYYQD CMTNATSSWS DIPSEHWQFV FHKYKTYNTA PQWRFVDDES DDFTKQRGTC Q IRFTTPSD MKNNVYLNYV LEKFAANHRR YVLSFSEDQI RGEDASYETV HDATGINCKP LSKNADGKIY YPCGLIANSM FN DTFPLQL TNVGDTSNNY SLTNKGINWE SDKKRYKKTK YNYTQIAPPP YWEKMYPDGY NETNIPDIQD WEEFQNWMRP GAF DKITKL IRINKNDTLP AGEYQLDIGL HWPVLEFNGK KGIYLTHGSH LGGRNPFLGI VYLIGGCICA AMALILLTFW LFGG RKIAD ASSLSWNMK UniProtKB: Phospholipid-transporting ATPase accessory subunit LEM3 |
-Macromolecule #5: BERYLLIUM TRIFLUORIDE ION
Macromolecule | Name: BERYLLIUM TRIFLUORIDE ION / type: ligand / ID: 5 / Number of copies: 1 / Formula: BEF |
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Molecular weight | Theoretical: 66.007 Da |
Chemical component information | ChemComp-BEF: |
-Macromolecule #6: MAGNESIUM ION
Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 6 / Number of copies: 1 / Formula: MG |
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Molecular weight | Theoretical: 24.305 Da |
-Macromolecule #7: (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(tri...
Macromolecule | Name: (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate type: ligand / ID: 7 / Number of copies: 3 / Formula: POV |
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Molecular weight | Theoretical: 760.076 Da |
Chemical component information | ChemComp-POV: |
-Macromolecule #8: 2-acetamido-2-deoxy-beta-D-glucopyranose
Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 8 / Number of copies: 2 / Formula: NAG |
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Molecular weight | Theoretical: 221.208 Da |
Chemical component information | ChemComp-NAG: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 1.5 mg/mL |
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Buffer | pH: 7.4 |
Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 64.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: OTHER / Imaging mode: BRIGHT FIELD |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: PDB ENTRY |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 2.8 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 590043 |
Initial angle assignment | Type: NOT APPLICABLE |
Final angle assignment | Type: NOT APPLICABLE |