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Yorodumi- EMDB-76432: Constituent EM map: Focused refinement of inner membrane portions... -
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Open data
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Basic information
| Entry | ![]() | ||||||||||||
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| Title | Constituent EM map: Focused refinement of inner membrane portions of the E. coli lipopolysaccharide transport bridge LptBFGC in complex with ATP | ||||||||||||
Map data | Unsharpened map | ||||||||||||
Sample |
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Keywords | Complex / Lipopolysaccharide / ABC / ATP binding cassette / transporter / bridge / intermembrane / LIPID TRANSPORT | ||||||||||||
| Biological species | ![]() | ||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 7.4 Å | ||||||||||||
Authors | Taylor RJ / Pahil KS / Walsh Jr RM / Caruso A / Kahne DE | ||||||||||||
| Funding support | United States, 3 items
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Citation | Journal: To Be PublishedTitle: Structural basis for regulating lipopolysaccharide transmembrane transport Authors: Taylor RJ / Pahil KS / Walsh Jr RM / Kahne DE | ||||||||||||
| History |
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_76432.map.gz | 15.1 MB | EMDB map data format | |
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| Header (meta data) | emd-76432-v30.xml emd-76432.xml | 25.7 KB 25.7 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_76432_fsc.xml | 6.7 KB | Display | FSC data file |
| Images | emd_76432.png | 58.5 KB | ||
| Filedesc metadata | emd-76432.cif.gz | 6.2 KB | ||
| Others | emd_76432_additional_1.map.gz emd_76432_half_map_1.map.gz emd_76432_half_map_2.map.gz | 28.7 MB 28.4 MB 28.4 MB | ||
| Archive directory | https://data.pdbj.org/pub/emdb/structures/EMD-76432 ftp://data.pdbj.org/pub/emdb/structures/EMD-76432 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_76432.map.gz / Format: CCP4 / Size: 30.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Unsharpened map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.48 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Additional map: Sharpened map
| File | emd_76432_additional_1.map | ||||||||||||
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| Annotation | Sharpened map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Half map
| File | emd_76432_half_map_1.map | ||||||||||||
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| Annotation | Half map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Half map
| File | emd_76432_half_map_2.map | ||||||||||||
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| Annotation | Half map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : Intermembrane lipopolysaccharide transport bridge composed of Lpt...
| Entire | Name: Intermembrane lipopolysaccharide transport bridge composed of LptD, LptE, LptA, LptC, LptF, LptG, and two molecules of LptB |
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| Components |
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-Supramolecule #1: Intermembrane lipopolysaccharide transport bridge composed of Lpt...
| Supramolecule | Name: Intermembrane lipopolysaccharide transport bridge composed of LptD, LptE, LptA, LptC, LptF, LptG, and two molecules of LptB type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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| Source (natural) | Organism: ![]() |
-Supramolecule #2: Inner membrane portion of lipopolysaccharide transporter
| Supramolecule | Name: Inner membrane portion of lipopolysaccharide transporter type: complex / ID: 2 / Parent: 1 / Macromolecule list: all |
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| Source (natural) | Organism: ![]() |
-Supramolecule #3: Outer membrane portion of lipopolysaccharide transporter
| Supramolecule | Name: Outer membrane portion of lipopolysaccharide transporter type: complex / ID: 3 / Parent: 1 |
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| Source (natural) | Organism: ![]() |
-Macromolecule #1: Lipopolysaccharide export system ATP-binding protein LptB
| Macromolecule | Name: Lipopolysaccharide export system ATP-binding protein LptB type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MATLTAKNLA KAYKGRRVVE DVSLTVNSGE IVGLLGPNGA GKTTTFYMVV GIVPRDAGNI IIDDDDISLL PLHARARRGI GYLPQEASIF RRLSVYDNLM AVLQIRDDLS AEQREDRANE LMEEFHIEHL RDSMGQSLSG GERRRVEIAR ALAANPKFIL LDQPFAGVDP ...String: MATLTAKNLA KAYKGRRVVE DVSLTVNSGE IVGLLGPNGA GKTTTFYMVV GIVPRDAGNI IIDDDDISLL PLHARARRGI GYLPQEASIF RRLSVYDNLM AVLQIRDDLS AEQREDRANE LMEEFHIEHL RDSMGQSLSG GERRRVEIAR ALAANPKFIL LDQPFAGVDP ISVIDIKRII EHLRDSGLGV LITDHNVRET LAVCERAYIV SQGHLIAHGT PTEILQDEHV KRVYLGEDFR L |
-Macromolecule #2: Lipopolysaccharide export system protein LptC,Lipopolysaccharide ...
| Macromolecule | Name: Lipopolysaccharide export system protein LptC,Lipopolysaccharide export system protein LptA type: protein_or_peptide / ID: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MSKARRWVII VLSLAVLVMI GINMAEKDDT AQVVVNNNDP TYKSEHTDTL VYNPEGALSY RLIAQHVEYY SDQAVSWFTQ PVLTTFDKD KIPTWSVKAD KAKLTNDRML YLYGHVEVNA LVPDSQLRRI TTDNAQINLV TQDVTSEDLV TLYGTTFNSS G LKMRGNLR ...String: MSKARRWVII VLSLAVLVMI GINMAEKDDT AQVVVNNNDP TYKSEHTDTL VYNPEGALSY RLIAQHVEYY SDQAVSWFTQ PVLTTFDKD KIPTWSVKAD KAKLTNDRML YLYGHVEVNA LVPDSQLRRI TTDNAQINLV TQDVTSEDLV TLYGTTFNSS G LKMRGNLR SKNAELIEKV RTSYEIQNKQ TQPLVPGGSG GGGSGGGGSG GGGSVTGDTD QPIHIESDQQ SLDMQGNVVT FT GNVIVTQ GTIKINADKV VVTRPGGEQG KEVIDGYGKP ATFYQMQDNG KPVEGHASQM HYELAKDFVV LTGNAYLQQV DSN IKGDKI TYLVKEQKMQ AFSDKGKRVT TVLVPSQLQD KNNKGQTPAQ KKGNLVPRGS HHHHHHH |
-Macromolecule #3: Lipopolysaccharide export system permease protein LptF
| Macromolecule | Name: Lipopolysaccharide export system permease protein LptF type: protein_or_peptide / ID: 3 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MIIIRYLVRE TLKSQLAILF ILLLIFFCQK LVRILGAAVD GDIPANLVLS LLGLGVPEMA QLILPLSLFL GLLMTLGKLY TESEITVMH ACGLSKAVLV KAAMILAVFT AIVAAVNVMW AGPWSSRHQD EVLAEAKANP GMAALAQGQF QQATNGSSVL F IESVDGSD ...String: MIIIRYLVRE TLKSQLAILF ILLLIFFCQK LVRILGAAVD GDIPANLVLS LLGLGVPEMA QLILPLSLFL GLLMTLGKLY TESEITVMH ACGLSKAVLV KAAMILAVFT AIVAAVNVMW AGPWSSRHQD EVLAEAKANP GMAALAQGQF QQATNGSSVL F IESVDGSD FKDVFLAQIR PKGNARPSVV VADSGHLTQL RDGSQVVTLN QGTRFEGTAL LRDFRITDFQ DYQAIIGHQA VA LDPNDTD QMDMRTLWNT DTDRARAELN WRITLVFTVF MMALMVVPLS VVNPRQGRVL SMLPAMLLYL LFFLIQTSLK SNG GKGKLD PTLWMWTVNL IYLALAIVLN LWDTVPVRRL RASFSRKGAV |
-Macromolecule #4: Lipopolysaccharide export system permease protein LptG
| Macromolecule | Name: Lipopolysaccharide export system permease protein LptG type: protein_or_peptide / ID: 4 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MQPFGVLDRY IGKTIFTTIM MTLFMLVSLS GIIKFVDQLK KAGQGSYDAL GAGMYTLLSV PKDVQIFFPM AALLGALLGL GMLAQRSEL VVMQASGFTR MQVALSVMKT AIPLVLLTMA IGEWVAPQGE QMARNYRAQA MYGGSLLSTQ QGLWAKDGNN F VYIERVKG ...String: MQPFGVLDRY IGKTIFTTIM MTLFMLVSLS GIIKFVDQLK KAGQGSYDAL GAGMYTLLSV PKDVQIFFPM AALLGALLGL GMLAQRSEL VVMQASGFTR MQVALSVMKT AIPLVLLTMA IGEWVAPQGE QMARNYRAQA MYGGSLLSTQ QGLWAKDGNN F VYIERVKG DEELGGISIY AFNENRRLQS VRYAATAKFD PEHKVWRLSQ VDESDLTNPK QITGSQTVSG TWKTNLTPDK LG VVALDPD ALSISGLHNY VKYLKSSGQD AGRYQLNMWS KIFQPLSVAV MMLMALSFIF GPLRSVPMGV RVVTGISFGF VFY VLDQIF GPLTLVYGIP PIIGALLPSA SFFLISLWLL MRKS |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 8 Component:
Details: 20mM Tris HCl, 150mM NaCl, 1% glycerol, 1% DMSO, 1% ethylene glycol, 0.02% GDN, 5 mM ATP, 1 mM MgCl2 | |||||||||||||||||||||||||||
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| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV | |||||||||||||||||||||||||||
| Details | This sample was monodisperse as determined by SEC. |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 51.0 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: 3.0 µm / Nominal defocus min: 1.2 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Keywords
Authors
United States, 3 items
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Z (Sec.)
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Processing
FIELD EMISSION GUN

