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Yorodumi- EMDB-60895: Cryo-EM structure of the large serine recombinase Bxb1 in complex... -
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Basic information
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| Title | Cryo-EM structure of the large serine recombinase Bxb1 in complex with attP and attB (GT/TT CDN) in the pre-strand exchange state (attB-L) | |||||||||
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Keywords | large serine recombinase / DNA BINDING PROTEIN | |||||||||
| Function / homology | Function and homology information | |||||||||
| Biological species | Mycolicibacterium smegmatis (bacteria) / Mycobacterium phage Bxb1 (virus) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.78 Å | |||||||||
Authors | Soma T / Hiraizumi M / Yamashita K / Nishimasu H | |||||||||
| Funding support | Japan, 2 items
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Citation | Journal: Mol Cell / Year: 2026Title: Structure and engineering of the large serine recombinase Bxb1 for gene integration. Authors: Teppei Soma / Masahiro Hiraizumi / Christopher W Fell / Dario Tagliaferri / Jason Lequyer / Sae Okazaki / Yukari Isayama / Kazuki Kato / Sworaj Sapkota / Harsh Ramani / Benjamin Arya / Cian ...Authors: Teppei Soma / Masahiro Hiraizumi / Christopher W Fell / Dario Tagliaferri / Jason Lequyer / Sae Okazaki / Yukari Isayama / Kazuki Kato / Sworaj Sapkota / Harsh Ramani / Benjamin Arya / Cian Schmitt-Ulms / Keitaro Yamashita / Jonathan S Gootenberg / Omar O Abudayyeh / Hiroshi Nishimasu / ![]() Abstract: The large serine recombinase Bxb1 catalyzes recombination between DNA molecules containing compatible attP and attB sequences, offering broad applications in genome engineering and gene therapies. ...The large serine recombinase Bxb1 catalyzes recombination between DNA molecules containing compatible attP and attB sequences, offering broad applications in genome engineering and gene therapies. Here, we present cryo-electron microscopy structures of the Bxb1-attP-attB synaptic complex in four distinct functional states during its recombination cycle. Notably, the Bxb1 complex structures in the pre-, mid-, and post-strand-exchange states explain how the attP- and attB-bound Bxb1 dimers are assembled into a tetrameric synaptic complex and how an approximately 180° rotation occurs between the left and right dimers after DNA cleavage, thereby enabling DNA strand exchange and religation. Furthermore, we engineered Bxb1 variants with altered DNA preferences and enhanced recombination activity, which improved programmable gene integration in human cells. Overall, our findings advance the mechanistic understanding of large serine recombinases and provide a structural framework for future engineering of Bxb1-mediated genome integration technologies. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_60895.map.gz | 49.7 MB | EMDB map data format | |
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| Header (meta data) | emd-60895-v30.xml emd-60895.xml | 23 KB 23 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_60895_fsc.xml | 7.9 KB | Display | FSC data file |
| Images | emd_60895.png | 51.2 KB | ||
| Masks | emd_60895_msk_1.map | 52.7 MB | Mask map | |
| Filedesc metadata | emd-60895.cif.gz | 6.6 KB | ||
| Others | emd_60895_half_map_1.map.gz emd_60895_half_map_2.map.gz | 48.9 MB 48.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-60895 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-60895 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9iuaMC ![]() 9iu2C ![]() 9iu3C ![]() 9iu4C ![]() 9iu5C ![]() 9iu6C ![]() 9iu7C ![]() 9iu8C ![]() 9iu9C ![]() 9iubC 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_60895.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: 1.17583 Å | ||||||||||||||||||||||||||||||||||||
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_60895_msk_1.map | ||||||||||||
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-Half map: #2
| File | emd_60895_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_60895_half_map_2.map | ||||||||||||
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Sample components
-Entire : The large serine recombinase Bxb1 in complex with attP and attB (...
| Entire | Name: The large serine recombinase Bxb1 in complex with attP and attB (GT/TT CDN) in the pre-strand exchange state (attB-L) |
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| Components |
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-Supramolecule #1: The large serine recombinase Bxb1 in complex with attP and attB (...
| Supramolecule | Name: The large serine recombinase Bxb1 in complex with attP and attB (GT/TT CDN) in the pre-strand exchange state (attB-L) type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#3 |
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-Supramolecule #2: attB-L
| Supramolecule | Name: attB-L / type: complex / ID: 2 / Parent: 1 / Macromolecule list: #1-#2 |
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| Source (natural) | Organism: Mycolicibacterium smegmatis (bacteria) / Synthetically produced: Yes |
-Supramolecule #3: large serine recombinase
| Supramolecule | Name: large serine recombinase / type: complex / ID: 3 / Parent: 1 / Macromolecule list: #3 |
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| Source (natural) | Organism: Mycobacterium phage Bxb1 (virus) |
-Macromolecule #1: attB-L
| Macromolecule | Name: attB-L / type: dna / ID: 1 / Number of copies: 1 / Classification: DNA |
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| Source (natural) | Organism: Mycolicibacterium smegmatis (bacteria) |
| Molecular weight | Theoretical: 7.443764 KDa |
| Sequence | String: (DG)(DG)(DC)(DC)(DG)(DG)(DC)(DT)(DT)(DG) (DT)(DC)(DG)(DA)(DC)(DG)(DA)(DC)(DG)(DG) (DC)(DG)(DG)(DT) GENBANK: GENBANK: LN831039.1 |
-Macromolecule #2: attB-L
| Macromolecule | Name: attB-L / type: dna / ID: 2 / Number of copies: 1 / Classification: DNA |
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| Source (natural) | Organism: Mycolicibacterium smegmatis (bacteria) |
| Molecular weight | Theoretical: 6.699307 KDa |
| Sequence | String: (DC)(DG)(DC)(DC)(DG)(DT)(DC)(DG)(DT)(DC) (DG)(DA)(DC)(DA)(DA)(DG)(DC)(DC)(DG)(DG) (DC)(DC) GENBANK: GENBANK: LN831039.1 |
-Macromolecule #3: Integrase
| Macromolecule | Name: Integrase / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: Mycobacterium phage Bxb1 (virus) |
| Molecular weight | Theoretical: 56.439949 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MRALVVIRLS RVTDATTSPE RQLESCQQLC AQRGWDVVGV AEDLDVSGAV DPFDRKRRPN LARWLAFEEQ PFDVIVAYRV DRLTRSIRH LQQLVHWAED HKKLVVSATE AHFDTTTPFA AVVIALMGTV AQMELEAIKE RNRSAAHFNI RAGKYRGSLP P WGYLPTRV ...String: MRALVVIRLS RVTDATTSPE RQLESCQQLC AQRGWDVVGV AEDLDVSGAV DPFDRKRRPN LARWLAFEEQ PFDVIVAYRV DRLTRSIRH LQQLVHWAED HKKLVVSATE AHFDTTTPFA AVVIALMGTV AQMELEAIKE RNRSAAHFNI RAGKYRGSLP P WGYLPTRV DGEWRLVPDP VQRERILEVY HRVVDNHEPL HLVAHDLNRR GVLSPKDYFA QLQGREPQGR EWSATALKRS MI SEAMLGY ATLNGKTVRD DDGAPLVRAE PILTREQLEA LRAELVKTSR AKPAVSTPSL LLRVLFCAVC GEPAYKFAGG GRK HPRYRC RSMGFPKHCG NGTVAMAEWD AFCEEQVLDL LGDAERLEKV WVAGSDSAVE LAEVNAELVD LTSLIGSPAY RAGS PQREA LDARIAALAA RQEELEGLEA RPSGWEWRET GQRFGDWWRE QDTAAKNTWL RSMNVRLTFD VRGGLTRTID FGDLQ EYEQ HLRLGSVVER LHTGMS UniProtKB: Integrase |
-Macromolecule #4: ZINC ION
| Macromolecule | Name: ZINC ION / type: ligand / ID: 4 / Number of copies: 1 / Formula: ZN |
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| Molecular weight | Theoretical: 65.409 Da |
-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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| Vitrification | Cryogen name: ETHANE |
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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: 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: 2.0 µm / Nominal defocus min: 0.8 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Mycolicibacterium smegmatis (bacteria)
Mycobacterium phage Bxb1 (virus)
Authors
Japan, 2 items
Citation



















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Processing
FIELD EMISSION GUN

