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Yorodumi- EMDB-49373: CryoEM Structure of De Novo Antibody Fragment scFv 6 with C. diff... -
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Open data
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Basic information
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| Title | CryoEM Structure of De Novo Antibody Fragment scFv 6 with C. difficile Toxin B (TcdB) | ||||||||||||||||||||||||||||||||||||
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Keywords | TcdB / De Novo / scFv 6 / De Novo Antibody / DE NOVO PROTEIN | ||||||||||||||||||||||||||||||||||||
| Function / homology | Function and homology informationsymbiont-mediated perturbation of host actin cytoskeleton via filamentous actin depolymerization / glucosyltransferase activity / Transferases; Glycosyltransferases; Hexosyltransferases / host cell cytosol / cysteine-type peptidase activity / host cell endosome membrane / toxin activity / Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases / lipid binding / host cell plasma membrane ...symbiont-mediated perturbation of host actin cytoskeleton via filamentous actin depolymerization / glucosyltransferase activity / Transferases; Glycosyltransferases; Hexosyltransferases / host cell cytosol / cysteine-type peptidase activity / host cell endosome membrane / toxin activity / Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases / lipid binding / host cell plasma membrane / proteolysis / extracellular region / metal ion binding / membrane Similarity search - Function | ||||||||||||||||||||||||||||||||||||
| Biological species | synthetic construct (others) / Clostridioides difficile (bacteria) | ||||||||||||||||||||||||||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.6 Å | ||||||||||||||||||||||||||||||||||||
Authors | Weidle C / Borst AJ | ||||||||||||||||||||||||||||||||||||
| Funding support | United States, European Union, United Kingdom, 11 items
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Citation | Journal: Nature / Year: 2025Title: Atomically accurate de novo design of antibodies with RFdiffusion Authors: Bennett NR / Watson JL / Ragotte RJ / Borst AJ / See DL / Weidle C / Biswas R / Yu Y / Shrock EL / Ault R / Leung PJY / Huang B / Goreshnik I / Tam J / Carr KD / Singer B / Criswell C / ...Authors: Bennett NR / Watson JL / Ragotte RJ / Borst AJ / See DL / Weidle C / Biswas R / Yu Y / Shrock EL / Ault R / Leung PJY / Huang B / Goreshnik I / Tam J / Carr KD / Singer B / Criswell C / Wicky BIM / Vafeados D / Sanchez MG / Kim HM / Torres ST / Chan S / Sun SM / Spear T / Sun Y / O'Reilly K / Maris JM / Sgourakis NG / Melnyk RA / Liu CC / Baker D | ||||||||||||||||||||||||||||||||||||
| History |
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_49373.map.gz | 351 MB | EMDB map data format | |
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| Header (meta data) | emd-49373-v30.xml emd-49373.xml | 28.4 KB 28.4 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_49373_fsc.xml | 15.2 KB | Display | FSC data file |
| Images | emd_49373.png | 86 KB | ||
| Filedesc metadata | emd-49373.cif.gz | 9.1 KB | ||
| Others | emd_49373_additional_1.map.gz emd_49373_half_map_1.map.gz emd_49373_half_map_2.map.gz | 185.2 MB 344.9 MB 344.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-49373 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-49373 | HTTPS FTP |
-Validation report
| Summary document | emd_49373_validation.pdf.gz | 1.1 MB | Display | EMDB validaton report |
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| Full document | emd_49373_full_validation.pdf.gz | 1.1 MB | Display | |
| Data in XML | emd_49373_validation.xml.gz | 24.4 KB | Display | |
| Data in CIF | emd_49373_validation.cif.gz | 31.9 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-49373 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-49373 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9nfuMC ![]() 9nh7C 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_49373.map.gz / Format: CCP4 / Size: 371.3 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: 0.885 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Additional map: #1
| File | emd_49373_additional_1.map | ||||||||||||
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-Half map: #2
| File | emd_49373_half_map_1.map | ||||||||||||
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-Half map: #1
| File | emd_49373_half_map_2.map | ||||||||||||
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Sample components
-Entire : Toxin B in complex with scFv 6
| Entire | Name: Toxin B in complex with scFv 6 |
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| Components |
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-Supramolecule #1: Toxin B in complex with scFv 6
| Supramolecule | Name: Toxin B in complex with scFv 6 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 Details: Toxin B was expressed and purified. scFv 6 was expressed and purified. scFv 6 was mixed with Toxin B at a 3:1 molar ratio. |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 271.17119 KDa |
-Macromolecule #1: Toxin B
| Macromolecule | Name: Toxin B / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO EC number: Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases |
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| Source (natural) | Organism: Clostridioides difficile (bacteria) |
| Molecular weight | Theoretical: 241.229938 KDa |
| Recombinant expression | Organism: Priestia megaterium NBRC 15308 = ATCC 14581 (bacteria) |
| Sequence | String: MYMSLVNRKQ LEKMANVRFR TQEDEYVAIL DALEEYHNMS ENTVVEKYLK LKDINSLTDI YIDTYKKSGR NKALKKFKEY LVTEVLELK NNNLTPVEKN LHFVAIGGQI NDTAINYINQ WKDVNSDYNV NVFYDSNAFL INTLKKTVVE SAINDTLESF R ENLNDPRF ...String: MYMSLVNRKQ LEKMANVRFR TQEDEYVAIL DALEEYHNMS ENTVVEKYLK LKDINSLTDI YIDTYKKSGR NKALKKFKEY LVTEVLELK NNNLTPVEKN LHFVAIGGQI NDTAINYINQ WKDVNSDYNV NVFYDSNAFL INTLKKTVVE SAINDTLESF R ENLNDPRF DYNKFFRKRM EIIYDKQKNF INYYKAQREE NPELIIDDIV KTYLSNEYSK EIDELNTYIE ESLNKITQNS GN DVRNFEE FKNGESFNLY EQELVERWNL AAASDILRIS ALKEIGGMYL NVNMLPGIQP DLFESIEKPS SVTVDFWEMT KLE AIMKYK EYIPEYTSEH FDMLDEEVQS SFESVLASKS DKSEIFSSLG DMEASPLEVK IAFNSKGIIN QGLISVKDSY CSNL IVKQI ENRYKILNNS LNPAISEDND FNTTTNTFID SIMAEANADN GRFMMELGKY LRVGFFPDVK TTINLSGPEA YAAAY QDLL MFKEGSMNIH LIEADLRNFE ISKTNISQST EQEMASLWSF DDARAKAQFE EYKRNYFEGS AGEDDNLDFS QNIVVD KEY LLEKISSLAR SSERGYIHYI VQLQGDKISY EAACNLFAKT PYDSVLFQKN IEDSEIAYYY NPGDGEIQEI DKYKIPS II SDRPKIKLTF IGHGKDEFNT DIFAGFDVDS LSTEIEAAID LAKEDISPKS IEINLLGCNM FSYSINVEET YPGKLLLK V KDKISELMPS ISQDSIIVSA NQYEVRINSE GRRELLDHSG EWINKEESII KDISSKEYIS FNPKENKITV KSKNLPELS TLLQEIRNNS NSSDIELEEK VMLTECEINV ISNIDTQIVE ERIEEAKNLT SDSINYIKDE FKLIESISDA LCDLKQQNEL EDSHFISFE DISETDEGFS IRFINKETGE SIFVETEKTI FSEYANHITE EISKIKGTIF DTVNGKLVKK VNLDTTHEVN T LNAAFFIQ SLIEYNSSKE SLSNLSVAMK VQVYAQLFST GLNTITDAAK VVELVSTALD ETIDLLPTLS EGLPIIATII DG VSLGAAI KELSETSDPL LRQEIEAKIG IMAVNLTTAT TAIITSSLGI ASGFSILLVP LAGISAGIPS LVNNELVLRD KAT KVVDYF KHVSLVETEG VFTLLDDKIM MPQDDLVISE IDFNNNSIVL GKCEIWRMEG GSGHTVTDDI DHFFSAPSIT YREP HLSIY DVLEVQKEEL DLSKDLMVLP NAPNRVFAWE TGWTPGLRSL ENDGTKLLDR IRDNYEGEFY WRYFAFIADA LITTL KPRY EDTNIRINLD SNTRSFIVPI ITTEYIREKL SYSFYGSGGT YALSLSQYNM GINIELSESD VWIIDVDNVV RDVTIE SDK IKKGDLIEGI LSTLSIEENK IILNSHEINF SGEVNGSNGF VSLTFSILEG INAIIEVDLL SKSYKLLISG ELKILML NS NHIQQKIDYI GFNSELQKNI PYSFVDSEGK ENGFINGSTK EGLFVSELPD VVLISKVYMD DSKPSFGYYS NNLKDVKV I TKDNVNILTG YYLKDDIKIS LSLTLQDEKT IKLNSVHLDE SGVAEILKFM NRKGNTNTSD SLMSFLESMN IKSIFVNFL QSNIKFILDA NFIISGTTSI GQFEFICDEN DNIQPYFIKF NTLETNYTLY VGNRQNMIVE PNYDLDDSGD ISSTVINFSQ KYLYGIDSC VNKVVISPNI YTDEINITPV YETNNTYPEV IVLDANYINE KINVNINDLS IRYVWSNDGN DFILMSTSEE N KVSQVKIR FVNVFKDKTL ANKLSFNFSD KQDVPVSEII LSFTPSYYED GLIGYDLGLV SLYNEKFYIN NFGMMVSGLI YI NDSLYYF KPPVNNLITG FVTVGDDKYY FNPINGGAAS IGETIIDDKN YYFNQSGVLQ TGVFSTEDGF KYFAPANTLD ENL EGEAID FTGKLIIDEN IYYFDDNYRG AVEWKELDGE MHYFSPETGK AFKGLNQIGD YKYYFNSDGV MQKGFVSIND NKHY FDDSG VMKVGYTEID GKHFYFAENG EMQIGVFNTE DGFKYFAHHN EDLGNEEGEE ISYSGILNFN NKIYYFDDSF TAVVG WKDL EDGSKYYFDE DTAEAYIGGY RPHAGLRGSH HHHHH UniProtKB: Toxin B |
-Macromolecule #2: scFv 6 Heavy Chain, scFv 6 Light Chain
| Macromolecule | Name: scFv 6 Heavy Chain, scFv 6 Light Chain / type: protein_or_peptide / ID: 2 / Details: Heavy Chain with Linker to Light Chain / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 30.211605 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MGWSCIILFL VATATGVHSE VQLVESGGGL VQPGGSLRLS CAASGFSIKN TYIHWVRQAP GKGLEWVARI WPANGKTRYA DSVKGRFTI SADTSKNTAY LQMNSLRAED TAVYYCSRQL DPYNLYGNDV WGQGTLVTVS SPNSASHSGS APQTSSAPGS D IQMTQSPS ...String: MGWSCIILFL VATATGVHSE VQLVESGGGL VQPGGSLRLS CAASGFSIKN TYIHWVRQAP GKGLEWVARI WPANGKTRYA DSVKGRFTI SADTSKNTAY LQMNSLRAED TAVYYCSRQL DPYNLYGNDV WGQGTLVTVS SPNSASHSGS APQTSSAPGS D IQMTQSPS SLSASVGDRV TITCKTSSSY VNWYQQKPGK APKLLIYRNS FRAPGVPSRF SGSRSGTDFT LTISSLQPED FA TYYCSTM NNDGNLVFGQ GTKVEIKENL YFQGSHHHHH 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
| Concentration | 0.81 mg/mL | |||||||||
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| Buffer | pH: 7.5 Component:
Details: 150 mM NaCl, 40 mM Tris/ HCl pH 7.5 | |||||||||
| Grid | Model: C-flat-2/2 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY / Support film - Film thickness: 40 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 25 sec. / Pretreatment - Atmosphere: AIR / Pretreatment - Pressure: 39.0 kPa / Details: 15 mA current | |||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295.15 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS GLACIOS |
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| Specialist optics | Energy filter - Name: GIF Bioquantum |
| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Number grids imaged: 1 / Number real images: 10897 / Average exposure time: 5.0 sec. / Average electron dose: 44.0 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 1.8 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 45000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
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Image processing
-Atomic model buiding 1
| Initial model |
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| Details | TcdB was built using the published 3.87 Angstrom crystal structure as a starting model (PDB: 6OQ5). The three bound VHH domains in the crystal structure were removed in PyMOL, and the structure was docked into density using Chimera. The initial model was refined in Coot before alignment with the design model in PyMOL, the scFv docked well in density. The entire model was refined with iterative rounds in Coot, Interactive Structure Optimization by Local Direct Exploration (ISOLDE) were performed at a simulated 25 Kelvin, and Phenix real-space refinement. The final model quality was analyzed using Molprobity. | |||||||||
| Refinement | Space: REAL / Protocol: FLEXIBLE FIT | |||||||||
| Output model | ![]() PDB-9nfu: |
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About Yorodumi



Keywords
Clostridioides difficile (bacteria)
Authors
United States, European Union,
United Kingdom, 11 items
Citation





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FIELD EMISSION GUN

