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Yorodumi- EMDB-63435: Bacteriophage Mycofy1 proximal head-to-tail interface (C6 symmetry) -
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Open data
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Basic information
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| Title | Bacteriophage Mycofy1 proximal head-to-tail interface (C6 symmetry) | |||||||||
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Keywords | Mycobacterium / bacteriophage / prolate head / head-to-tail connector / portal protein / adaptor protein / VIRUS / VIRAL PROTEIN | |||||||||
| Function / homology | Bacteriophage/Gene transfer agent portal protein / Phage portal protein / viral capsid / Portal protein Function and homology information | |||||||||
| Biological species | Mycolicibacterium phage Mycofy1 (virus) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.46 Å | |||||||||
Authors | Li X / Shao Q / Li L / Xie L / Ruan Z / Fang Q | |||||||||
| Funding support | China, 2 items
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Citation | Journal: J Mol Biol / Year: 2025Title: Cryo-EM Reveals Structural Diversity in Prolate-headed Mycobacteriophage Mycofy1. Authors: Xiangyun Li / Qianqian Shao / Lin Li / Linlin Xie / Zhiyang Ruan / Qianglin Fang / ![]() Abstract: Mycobacteriophages show promise in treating antibiotic-resistant mycobacterial infections. Here, we isolated Mycofy1, a mycobacteriophage, using M. smegmatis as a host. Cryo-EM analysis revealed that ...Mycobacteriophages show promise in treating antibiotic-resistant mycobacterial infections. Here, we isolated Mycofy1, a mycobacteriophage, using M. smegmatis as a host. Cryo-EM analysis revealed that Mycofy1 possesses a prolate head and a long non-contractile tail. We determined structures of its head, head-to-tail interface, terminator, and tail tube to resolutions of ∼3.5 Å. Unexpectedly, we identified two distinct types of prolate head structures, exhibiting a 36° relative rotation in the top cap region. Additionally, the head-to-tail interface demonstrated flexibility. Our structures provide high-resolution cryo-EM data of a mycobacteriophage with a prolate head, as well as detailed structural information of the head-to-tail interface and head-proximal tail region in this phage group. These findings advance our understanding of assembly mechanisms in tailed bacteriophages. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_63435.map.gz | 49.2 MB | EMDB map data format | |
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| Header (meta data) | emd-63435-v30.xml emd-63435.xml | 18.3 KB 18.3 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_63435_fsc.xml | 8.5 KB | Display | FSC data file |
| Images | emd_63435.png | 106.3 KB | ||
| Masks | emd_63435_msk_1.map | 52.7 MB | Mask map | |
| Filedesc metadata | emd-63435.cif.gz | 6.2 KB | ||
| Others | emd_63435_half_map_1.map.gz emd_63435_half_map_2.map.gz | 39.7 MB 39.7 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-63435 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-63435 | HTTPS FTP |
-Validation report
| Summary document | emd_63435_validation.pdf.gz | 1.1 MB | Display | EMDB validaton report |
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| Full document | emd_63435_full_validation.pdf.gz | 1.1 MB | Display | |
| Data in XML | emd_63435_validation.xml.gz | 14.1 KB | Display | |
| Data in CIF | emd_63435_validation.cif.gz | 19.9 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-63435 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-63435 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9lw9MC ![]() 9lw6C ![]() 9lw7C ![]() 9lw8C ![]() 9lwaC 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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Map
| File | Download / File: emd_63435.map.gz / Format: CCP4 / Size: 52.7 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: 1.372 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_63435_msk_1.map | ||||||||||||
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-Half map: #2
| File | emd_63435_half_map_1.map | ||||||||||||
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-Half map: #1
| File | emd_63435_half_map_2.map | ||||||||||||
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Sample components
-Entire : Mycolicibacterium phage Mycofy1
| Entire | Name: Mycolicibacterium phage Mycofy1 (virus) |
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| Components |
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-Supramolecule #1: Mycolicibacterium phage Mycofy1
| Supramolecule | Name: Mycolicibacterium phage Mycofy1 / type: virus / ID: 1 / Parent: 0 / Macromolecule list: #2, #1 / NCBI-ID: 3349809 / Sci species name: Mycolicibacterium phage Mycofy1 / Virus type: VIRION / Virus isolate: STRAIN / Virus enveloped: No / Virus empty: No |
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| Host (natural) | Organism: Mycolicibacterium smegmatis MC2 155 (bacteria) |
-Macromolecule #1: Portal protein
| Macromolecule | Name: Portal protein / type: protein_or_peptide / ID: 1 Details: Sequence reference for Mycolicibacterium phage Mycofy1 is not available at the time of biocuration. Current sequence reference is from UniProt id A0A0A7RVH8. Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Mycolicibacterium phage Mycofy1 (virus) |
| Molecular weight | Theoretical: 50.525547 KDa |
| Sequence | String: MRLIDRLLST RGAAQRMSID DYAHMLNEFA FNGIGYGFGG GVPRIQQTLA GPSTELAPDT FVGLATQAYQ ANGPVFACML VRQLVFSSV RFRWQRLRDG KPSDTFGSGD LQILETPWKG GTTQDMLSRM IQDADLAGNS YWTIVDGEFV RMRPDWVDVV V EERMVRGG ...String: MRLIDRLLST RGAAQRMSID DYAHMLNEFA FNGIGYGFGG GVPRIQQTLA GPSTELAPDT FVGLATQAYQ ANGPVFACML VRQLVFSSV RFRWQRLRDG KPSDTFGSGD LQILETPWKG GTTQDMLSRM IQDADLAGNS YWTIVDGEFV RMRPDWVDVV V EERMVRGG RGERGGGQLG WRKVGYLYTE GGRQSGNEPV GFLAEDVVHF APIPDPLASY RGMSWLTPIL REIRADQAMS KH QAKFFDN GATVNLVIKH NPMADPAAVK KWADEVNSKH AGVDNAWKNL NLYPGADAEV VGSNLQEIDF KNVRGGGETR IAA AAGVPP VIVGLSEGLA AATYSNYGQA RRRLADGTAH PLWQNLSGCI GHVMPDMGPD VRLWYDADDV PFLREDEKDA ADIQ KVRAE TINTLITAGY EPDSVVAAVN SGDLRLLKHT GLTSVQLLPP GVSASAPSDT PTSGGADDNG N UniProtKB: Portal protein |
-Macromolecule #2: Adaptor protein gp8
| Macromolecule | Name: Adaptor protein gp8 / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Mycolicibacterium phage Mycofy1 (virus) |
| Molecular weight | Theoretical: 19.875471 KDa |
| Sequence | String: MAELKPDDLP AKVRGQFADN TEAQAAIDAV LAAARRWCGW HVSPVIVDDV MELDGPGGRV LSLPTLNLVS VSSVVELGHA LDVSTLDRS RRKGTLTKPY GRWTARDGAI VVTATHGFTE AEAADWRRAV VQLVGQRAQT SRPSADLKRK KIDDVEYEWF E TAVSVDAE LSAVFSPFRI LPSP |
-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: 7.5 |
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| Grid | Model: Quantifoil R2/1 / Material: COPPER / Support film - Material: CARBON / Support film - topology: CONTINUOUS / Pretreatment - Type: GLOW DISCHARGE |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Software | Name: EPU |
| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average exposure time: 5.09 sec. / Average electron dose: 25.7 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 70.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.0 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 59000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Mycolicibacterium phage Mycofy1 (virus)
Keywords
Authors
China, 2 items
Citation








Z (Sec.)
Y (Row.)
X (Col.)












































Mycolicibacterium smegmatis MC2 155 (bacteria)
Processing
FIELD EMISSION GUN

