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Yorodumi- EMDB-49901: Cryo-EM structure of a bacterial prototype ATP-binding cassette t... -
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Basic information
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| Title | Cryo-EM structure of a bacterial prototype ATP-binding cassette transporter MalFGK2. | |||||||||
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Keywords | bacterial prototype ATP-binding cassette transporter / TRANSPORT PROTEIN | |||||||||
| Function / homology | Function and homology informationABC-type maltose transporter / ABC-type maltose transporter activity / maltose transport complex / maltodextrin transmembrane transport / ATP-binding cassette (ABC) transporter complex, substrate-binding subunit-containing / ATP hydrolysis activity / ATP binding / plasma membrane Similarity search - Function | |||||||||
| Biological species | ![]() ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.51 Å | |||||||||
Authors | Qian R / Jing W / Vinay I / Shanwen Z / Jeehae S / William GL / Luis MRH / Jong HS / Young AG / IIya L ...Qian R / Jing W / Vinay I / Shanwen Z / Jeehae S / William GL / Luis MRH / Jong HS / Young AG / IIya L / Kirill M / Baron C / Huan B | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Nat Commun / Year: 2025Title: DeFrND: detergent-free reconstitution into native nanodiscs with designer membrane scaffold peptides. Authors: Qian Ren / Jing Wang / Vinay Idikuda / Shanwen Zhang / Jeehae Shin / W Grant Ludlam / Luis M Real Hernandez / Sara Zdancewicz / Alex J B Kreutzberger / Hucheng Chang / Volker Kiessling / ...Authors: Qian Ren / Jing Wang / Vinay Idikuda / Shanwen Zhang / Jeehae Shin / W Grant Ludlam / Luis M Real Hernandez / Sara Zdancewicz / Alex J B Kreutzberger / Hucheng Chang / Volker Kiessling / Lukas K Tamm / Ahmad Jomaa / Ilya Levental / Kirill Martemyanov / Baron Chanda / Huan Bao / ![]() Abstract: Membrane scaffold protein-based nanodiscs have facilitated unprecedented structural and biophysical analysis of membrane proteins in a near-native lipid environment. However, successful ...Membrane scaffold protein-based nanodiscs have facilitated unprecedented structural and biophysical analysis of membrane proteins in a near-native lipid environment. However, successful reconstitution of membrane proteins in nanodiscs requires prior solubilization and purification in detergents, which may impact their physiological structure and function. Furthermore, the detergent-mediated reconstitution of nanodiscs is unlikely to recapitulate the precise composition or asymmetry of native membranes. To circumvent this fundamental limitation of traditional nanodisc technology, we herein describe the development of membrane-solubilizing peptides to directly extract membrane proteins from native cell membranes into nanoscale discoids. By systematically protein engineering and screening, we create a class of chemically modified Apolipoprotein-A1 mimetic peptides to enable the formation of detergent-free nanodiscs with high efficiency. Nanodiscs generated with these engineered membrane scaffold peptides are suitable for obtaining high-resolution structures using single-particle cryo-EM with native lipids. To further highlight the versatility of our approach, we directly extract a sampling of membrane signaling proteins with their surrounding native membranes for biochemical and biophysical interrogations. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_49901.map.gz | 107.1 MB | EMDB map data format | |
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| Header (meta data) | emd-49901-v30.xml emd-49901.xml | 20.3 KB 20.3 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_49901_fsc.xml | 10.6 KB | Display | FSC data file |
| Images | emd_49901.png | 34.2 KB | ||
| Filedesc metadata | emd-49901.cif.gz | 6.6 KB | ||
| Others | emd_49901_half_map_1.map.gz emd_49901_half_map_2.map.gz | 116.2 MB 116.2 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-49901 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-49901 | HTTPS FTP |
-Validation report
| Summary document | emd_49901_validation.pdf.gz | 949.5 KB | Display | EMDB validaton report |
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| Full document | emd_49901_full_validation.pdf.gz | 949.1 KB | Display | |
| Data in XML | emd_49901_validation.xml.gz | 19.2 KB | Display | |
| Data in CIF | emd_49901_validation.cif.gz | 24.8 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-49901 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-49901 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9nxcMC ![]() 9bcrC ![]() 9nqjC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_49901.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| 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:
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-Supplemental data
-Half map: #1
| File | emd_49901_half_map_1.map | ||||||||||||
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-Half map: #2
| File | emd_49901_half_map_2.map | ||||||||||||
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Sample components
-Entire : ATP-binding cassette transporter MalFGK2
| Entire | Name: ATP-binding cassette transporter MalFGK2 |
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| Components |
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-Supramolecule #1: ATP-binding cassette transporter MalFGK2
| Supramolecule | Name: ATP-binding cassette transporter MalFGK2 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 250 KDa |
-Macromolecule #1: Maltose/maltodextrin transport system permease protein MalF
| Macromolecule | Name: Maltose/maltodextrin transport system permease protein MalF type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 57.679711 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MRKNPMDVIK KKHWWQSDAL KWSVLGLLGL LVGYLVVLMY AQGEYLFAIT TLILSSAGLY IFANRKAYAW RYVYPGMAGM GLFVLFPLV CTIAIAFTNY SSTNQLTFER AQEVLLDRSW QAGKIYNFGL YPAGDEWQLA LSDGETGKNY LSDAFKFGGE Q KLQLKESA ...String: MRKNPMDVIK KKHWWQSDAL KWSVLGLLGL LVGYLVVLMY AQGEYLFAIT TLILSSAGLY IFANRKAYAW RYVYPGMAGM GLFVLFPLV CTIAIAFTNY SSTNQLTFER AQEVLLDRSW QAGKIYNFGL YPAGDEWQLA LSDGETGKNY LSDAFKFGGE Q KLQLKESA TQPEGERANL RVITQNRQAL SDITAILPDG NKVMMSSLRQ FSGTQPLYTL DGDGTLTNNQ SGVKYRPNNQ IG FYQSITA DGNWGDEKLS PGYTVTTGWK NFTRVFTDEG IQKPFLAIFV WTVVFSLITV FLTVAVGMVL ACLVQWEALR GKA VYRVLL ILPYAVPSFI SILIFKGLFN QSFGEINMML SALFGVKPAW FSDPTTARTM LIIVNTWLGY PYMMILCMGL LKAI PDDLY EASAMDGAGP FQNFFKITLP LLIKPLTPLM IASFAFNFNN FVLIQLLTNG GPDRLGTTTP AGYTDLLVNY TYRIA FEGG GGQDFGLAAA IATLIFLLVG ALAIVNLKAT RMKFD UniProtKB: Maltose/maltodextrin transport system permease protein MalF |
-Macromolecule #2: Maltose/maltodextrin transport system permease protein MalG
| Macromolecule | Name: Maltose/maltodextrin transport system permease protein MalG type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 31.53134 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: AMVQPKSQKA RLFITHLLLL LFIAAIMFPL LMVVAISLRQ GNFATGSLWP EQISWDHWKL ALGFSVEQAD GRIWPPPFPV LLWLWNSVK VAGISAIGIV ALSTTCAYAF ARMRFPGKAT LLKGMLIFQM FPAVLSLVAL YALFDRLGEY IPFIGLNTHG G VIFAYLGG ...String: AMVQPKSQKA RLFITHLLLL LFIAAIMFPL LMVVAISLRQ GNFATGSLWP EQISWDHWKL ALGFSVEQAD GRIWPPPFPV LLWLWNSVK VAGISAIGIV ALSTTCAYAF ARMRFPGKAT LLKGMLIFQM FPAVLSLVAL YALFDRLGEY IPFIGLNTHG G VIFAYLGG IALHVWTIKG YFETIDSSLE EAAALDGATP WQAFRLVLLP LSVPILAVVF ILSFIAAITE VPVASLLLRD VN SYTLAVG MQQYLNPQNY LWGDFAAAAV MSALPITIVF LLAQRWLVN UniProtKB: Maltose/maltodextrin transport system permease protein MalG |
-Macromolecule #3: Maltose/maltodextrin import ATP-binding protein MalK
| Macromolecule | Name: Maltose/maltodextrin import ATP-binding protein MalK / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO / EC number: ABC-type maltose transporter |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 40.979234 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: ASVQLQNVTK AWGEVVVSKD INLDIHEGEF VVFVGPSGCG KSTLLRMIAG LETITSGDLF IGEKRMNDTP PAERGVGMVF QSYALYPHL SVAENMSFGL KLAGAKKEVI NQRVNQVAEV LQLAHLLDRK PKALSGGQRQ RVAIGRTLVA EPSVFLLDEP L SNLDAALR ...String: ASVQLQNVTK AWGEVVVSKD INLDIHEGEF VVFVGPSGCG KSTLLRMIAG LETITSGDLF IGEKRMNDTP PAERGVGMVF QSYALYPHL SVAENMSFGL KLAGAKKEVI NQRVNQVAEV LQLAHLLDRK PKALSGGQRQ RVAIGRTLVA EPSVFLLDEP L SNLDAALR VQMRIEISRL HKRLGRTMIY VTHDQVEAMT LADKIVVLDA GRVAQVGKPL ELYHYPADRF VAGFIGSPKM NF LPVKVTA TAIDQVQVEL PMPNRQQVWL PVESRDVQVG ANMSLGIRPE HLLPSDIADV ILEGEVQVVE QLGNETQIHI QIP SIRQNL VYRQNDVVLV EEGATFAIGL PPERCHLFRE DGTACRRLHK EPGVA UniProtKB: Maltose/maltodextrin import ATP-binding protein MalK |
-Macromolecule #4: Maltose/maltodextrin import ATP-binding protein MalK
| Macromolecule | Name: Maltose/maltodextrin import ATP-binding protein MalK / type: protein_or_peptide / ID: 4 / Number of copies: 1 / Enantiomer: LEVO / EC number: ABC-type maltose transporter |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 41.255527 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: ASVQLQNVTK AWGEVVVSKD INLDIHEGEF VVFVGPSGCG KSTLLRMIAG LETITSGDLF IGEKRMNDTP PAERGVGMVF QSYALYPHL SVAENMSFGL KLAGAKKEVI NQRVNQVAEV LQLAHLLDRK PKALSGGQRQ RVAIGRTLVA EPSVFLLDEP L SNLDAALR ...String: ASVQLQNVTK AWGEVVVSKD INLDIHEGEF VVFVGPSGCG KSTLLRMIAG LETITSGDLF IGEKRMNDTP PAERGVGMVF QSYALYPHL SVAENMSFGL KLAGAKKEVI NQRVNQVAEV LQLAHLLDRK PKALSGGQRQ RVAIGRTLVA EPSVFLLDEP L SNLDAALR VQMRIEISRL HKRLGRTMIY VTHDQVEAMT LADKIVVLDA GRVAQVGKPL ELYHYPADRF VAGFIGSPKM NF LPVKVTA TAIDQVQVEL PMPNRQQVWL PVESRDVQVG ANMSLGIRPE HLLPSDIADV ILEGEVQVVE QLGNETQIHI QIP SIRQNL VYRQNDVVLV EEGATFAIGL PPERCHLFRE DGTACRRLHK EPGVAHH UniProtKB: Maltose/maltodextrin import ATP-binding protein MalK |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 2 mg/mL |
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| Buffer | pH: 8 |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 283.15 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 1.116 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: 2.7 µm / Nominal defocus min: 0.3 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Keywords
Authors
United States, 1 items
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Processing
FIELD EMISSION GUN


