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Yorodumi- EMDB-71294: Constituent EM map: Outer membrane and periplasmic portions of th... -
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Basic information
| Entry | ![]() | ||||||||||||
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| Title | Constituent EM map: Outer membrane and periplasmic portions of the lipopolysaccharide transport bridge from E coli | ||||||||||||
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: 3.39 Å | ||||||||||||
Authors | Taylor RJ / Pahil KS / Walsh Jr RM / 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_71294.map.gz | 410.5 MB | EMDB map data format | |
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| Header (meta data) | emd-71294-v30.xml emd-71294.xml | 22.8 KB 22.8 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_71294_fsc.xml | 20 KB | Display | FSC data file |
| Images | emd_71294.png | 59.1 KB | ||
| Filedesc metadata | emd-71294.cif.gz | 6.1 KB | ||
| Others | emd_71294_additional_1.map.gz emd_71294_half_map_1.map.gz emd_71294_half_map_2.map.gz | 778.4 MB 765.6 MB 765.6 MB | ||
| Archive directory | https://data.pdbj.org/pub/emdb/structures/EMD-71294 ftp://data.pdbj.org/pub/emdb/structures/EMD-71294 | 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_71294.map.gz / Format: CCP4 / Size: 824 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: 0.83 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_71294_additional_1.map | ||||||||||||
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| Annotation | Sharpened map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Half map
| File | emd_71294_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_71294_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 in complex with lipopolysaccharide |
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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 in complex with lipopolysaccharide type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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-Supramolecule #2: Outer membrane portion of lipopolysaccharide transporter with LptA
| Supramolecule | Name: Outer membrane portion of lipopolysaccharide transporter with LptA type: complex / ID: 2 / Parent: 1 / Macromolecule list: all |
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| Source (natural) | Organism: ![]() |
-Supramolecule #3: Inner membrane portion of lipopolysaccharide transporter
| Supramolecule | Name: Inner membrane portion of lipopolysaccharide transporter type: complex / ID: 3 / Parent: 1 |
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| Source (natural) | Organism: ![]() |
-Macromolecule #1: LptD
| Macromolecule | Name: LptD / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MKKRIPTLLA TMIATALYS Q QGLAADLA SQ CMLGVPS YDR PLVQGD TNDL PVTIN ADHAK GDYP DDAVFT GSV DIMQGNS RL QADEVQLH Q KEAPGQPEP VRTVDALGNV HYDDNQVIL K GPKGWANL NT KDTNVWE GDY QMVGRQ GRGK ADLMK ...String: MKKRIPTLLA TMIATALYS Q QGLAADLA SQ CMLGVPS YDR PLVQGD TNDL PVTIN ADHAK GDYP DDAVFT GSV DIMQGNS RL QADEVQLH Q KEAPGQPEP VRTVDALGNV HYDDNQVIL K GPKGWANL NT KDTNVWE GDY QMVGRQ GRGK ADLMK QRGEN RYTI LDNGSF TSC LPGSDTW SV VGSEIIHD R EEQVAEIWN ARFKVGPVPI FYSPYLQLP V GDKRRSGF LI PNAKYTT TNY FEFYLP YYWN IAPNM DATIT PHYM HRRGNI MWE NEFRYLS QA GAGLMELD Y LPSDKVYED EHPNDDSSRR WLFYWNHSG V MDQVWRFN VD YTKVSDP SYF NDFDNK YGSS TDGYA TQKFS VGYA VQNFNA TVS TKQFQVF SE QNTSSYSA E PQLDVNYYQ NDVGPFDTRI YGQAVHFVN T RDDMPEAT RV HLEPTIN LPL SNNWGS INTE AKLLA THYQQ TNLD WYNSRN TTK LDESVNR VM PQFKVDGK M VFERDMEML APGYTQTLEP RAQYLYVPY R DQSDIYNY DS SLLQSDY SGL FRDRTY GGLD RIASA NQVTT GVTS RIYDDA AVE RFNISVG QI YYFTESRT G DDNITWEND DKTGSLVWAG DTYWRISER W GLRGGIQY DT RLDNVAT SNS SIEYRR DEDR LVQLN YRYAS PEYI QATLPK YYS TAEQYKN GI SQVGAVAS W PIADRWSIV GAYYYDTNAN KQADSMLGV Q YSSCCYAI RV GYERKLN GWD NDKQHA VYDN AIGFN IELRG LSSN YGLGTQ EML RSNILPY QN TL |
-Macromolecule #2: LptE
| Macromolecule | Name: LptE / type: protein_or_peptide / ID: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MRYLATLLLS LAVLITAGC G WHLRDTTQ VP STMKVMI LDS GDPNGP LSRA VRNQL RLNGV ELLD KETTRK DVP SLRLGKV SI AKDTASVF R NGQTAEYQM IMTVNATVLI PGRDIYPIS A KVFRSFFD NP QMALAKD NEQ DMIVKE MYDR AAEQL ...String: MRYLATLLLS LAVLITAGC G WHLRDTTQ VP STMKVMI LDS GDPNGP LSRA VRNQL RLNGV ELLD KETTRK DVP SLRLGKV SI AKDTASVF R NGQTAEYQM IMTVNATVLI PGRDIYPIS A KVFRSFFD NP QMALAKD NEQ DMIVKE MYDR AAEQL IRKLP SIRA ADIRSD EEQ TSTTTDT PA TPARVSTT L GN |
-Macromolecule #3: LptA
| Macromolecule | Name: LptA / type: protein_or_peptide / ID: 3 / Details: LptA expressed as a fusion with LptC / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Recombinant expression | Organism: ![]() |
| Sequence | String: VTGDTDQPIH IESDQQSLDM QGNVVTFTGN VIVTQGTIKI NADKVVVTRP GGEQGKEVID GYGKPATFYQ MQDNGKPVEG HASQMHYELA KDFVVLTGNA YLQQVDSNIK GDKITYLVKE QKMQAFSDKG KRVTTVLVPS QLQDKNNKGQ TPAQKKGNLV PRGSHHHHHH H |
-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 | |||||||||||||||||||||
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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: GATAN K3 BIOCONTINUUM (6k x 4k) / Average electron dose: 50.0 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: 2.2 µm / Nominal defocus min: 1.1 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Authors
United States, 3 items
Citation


















Z (Sec.)
Y (Row.)
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Processing
FIELD EMISSION GUN

