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- EMDB-61435: Structure of LaTranC complex bound to 6nt complementary DNA substrate -

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Basic information

Entry
Database: EMDB / ID: EMD-61435
TitleStructure of LaTranC complex bound to 6nt complementary DNA substrate
Map dataLaTranC complex (6-nt matched)
Sample
  • Complex: LaTranC
    • DNA: DNA (37-MER)
    • DNA: DNA (37-MER)
    • RNA: RNA (195-MER)
    • Protein or peptide: LaTranC
KeywordsLaTranC complexes / IMMUNE SYSTEM/DNA/RNA / IMMUNE SYSTEM-DNA-RNA complex
Biological speciesLawsonibacter sp. (bacteria)
Methodsingle particle reconstruction / cryo EM / Resolution: 2.96 Å
AuthorsZhang S / Liu J
Funding support China, 4 items
OrganizationGrant numberCountry
National Natural Science Foundation of China (NSFC)32201224 China
National Natural Science Foundation of China (NSFC)32250012 China
National Natural Science Foundation of China (NSFC)32230088 China
National Natural Science Foundation of China (NSFC)32201224 China
CitationJournal: Cell / Year: 2025
Title: Functional RNA splitting drove the evolutionary emergence of type V CRISPR-Cas systems from transposons.
Authors: Shuai Jin / Zixu Zhu / Yunjia Li / Shouyue Zhang / Yijing Liu / Danyuan Li / Yuanqing Li / Yingfeng Luo / Zhiheng Cheng / Kevin Tianmeng Zhao / Qiang Gao / Guanglei Yang / Hongchao Li / ...Authors: Shuai Jin / Zixu Zhu / Yunjia Li / Shouyue Zhang / Yijing Liu / Danyuan Li / Yuanqing Li / Yingfeng Luo / Zhiheng Cheng / Kevin Tianmeng Zhao / Qiang Gao / Guanglei Yang / Hongchao Li / Ronghong Liang / Rui Zhang / Jin-Long Qiu / Yong E Zhang / Jun-Jie Gogo Liu / Caixia Gao /
Abstract: Transposon-encoded TnpB nucleases gave rise to type V CRISPR-Cas12 effectors through multiple independent domestication events. These systems use different RNA molecules as guides for DNA targeting: ...Transposon-encoded TnpB nucleases gave rise to type V CRISPR-Cas12 effectors through multiple independent domestication events. These systems use different RNA molecules as guides for DNA targeting: transposon-derived right-end RNAs (reRNAs or omega RNAs) for TnpB and CRISPR RNAs for type V CRISPR-Cas systems. However, the molecular mechanisms bridging transposon activity and CRISPR immunity remain unclear. We identify TranCs (transposon-CRISPR intermediates) derived from distinct IS605- or IS607-TnpB lineages. TranCs utilize both CRISPR RNAs and reRNAs to direct DNA cleavage. The cryoelectron microscopy (cryo-EM) structure of LaTranC from Lawsonibacter sp. closely resembles that of the ISDra2 TnpB complex; however, unlike a single-molecule reRNA, the LaTranC guide RNA is functionally split into a tracrRNA and crRNA. An engineered RNA split of ISDra2 TnpB enabled activity with a CRISPR array. These findings indicate that functional RNA splitting was the primary molecular event driving the emergence of diverse type V CRISPR-Cas systems from transposons.
History
DepositionSep 5, 2024-
Header (metadata) releaseOct 8, 2025-
Map releaseOct 8, 2025-
UpdateNov 26, 2025-
Current statusNov 26, 2025Processing site: PDBc / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_61435.map.gz / Format: CCP4 / Size: 103 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
AnnotationLaTranC complex (6-nt matched)
Projections & slices

Image control

Size
Brightness
Contrast
Others
AxesZ (Sec.)Y (Row.)X (Col.)
0.84 Å/pix.
x 300 pix.
= 252.99 Å
0.84 Å/pix.
x 300 pix.
= 252.99 Å
0.84 Å/pix.
x 300 pix.
= 252.99 Å

Surface

Projections

Slices (1/3)

Slices (1/2)

Slices (2/3)

Images are generated by Spider.

Voxel sizeX=Y=Z: 0.8433 Å
Density
Contour LevelBy AUTHOR: 0.218
Minimum - Maximum-3.1846378 - 4.8914995
Average (Standard dev.)-0.0007533296 (±0.060594257)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions300300300
Spacing300300300
CellA=B=C: 252.98999 Å
α=β=γ: 90.0 °

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Supplemental data

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Half map: LaTranC complex (6-nt matched)

Fileemd_61435_half_map_1.map
AnnotationLaTranC complex (6-nt matched)
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Half map: LaTranC complex (6-nt matched)

Fileemd_61435_half_map_2.map
AnnotationLaTranC complex (6-nt matched)
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Sample components

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Entire : LaTranC

EntireName: LaTranC
Components
  • Complex: LaTranC
    • DNA: DNA (37-MER)
    • DNA: DNA (37-MER)
    • RNA: RNA (195-MER)
    • Protein or peptide: LaTranC

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Supramolecule #1: LaTranC

SupramoleculeName: LaTranC / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all
Source (natural)Organism: Lawsonibacter sp. (bacteria)

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Macromolecule #1: DNA (37-MER)

MacromoleculeName: DNA (37-MER) / type: dna / ID: 1 / Number of copies: 1 / Classification: DNA
Source (natural)Organism: Lawsonibacter sp. (bacteria)
Molecular weightTheoretical: 11.404304 KDa
SequenceString:
(DT)(DC)(DG)(DG)(DT)(DA)(DC)(DG)(DG)(DA) (DC)(DT)(DT)(DT)(DC)(DG)(DG)(DC)(DG)(DT) (DC)(DG)(DT)(DG)(DT)(DT)(DT)(DG)(DA) (DA)(DA)(DA)(DT)(DC)(DC)(DC)(DG)

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Macromolecule #2: DNA (37-MER)

MacromoleculeName: DNA (37-MER) / type: dna / ID: 2 / Number of copies: 1 / Classification: DNA
Source (natural)Organism: Lawsonibacter sp. (bacteria)
Molecular weightTheoretical: 11.383297 KDa
SequenceString:
(DC)(DG)(DG)(DG)(DA)(DT)(DT)(DT)(DT)(DC) (DC)(DT)(DC)(DG)(DT)(DG)(DG)(DA)(DC)(DG) (DC)(DC)(DG)(DA)(DA)(DA)(DG)(DT)(DC) (DC)(DG)(DT)(DA)(DC)(DC)(DG)(DA)

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Macromolecule #3: RNA (195-MER)

MacromoleculeName: RNA (195-MER) / type: rna / ID: 3 / Number of copies: 1
Source (natural)Organism: Lawsonibacter sp. (bacteria)
Molecular weightTheoretical: 62.94843 KDa
SequenceString: GGUGGGAGGU CUGUCCCCAC CAUGGGGUGC GAACCUUGUG UGCUCAUCAU UGCCGUGAGC GUUCGCACGU CCAAACGACC AUAUCAUCG UUGCCCUGCG ACCAUUCAGC GGCAAUCAAG ACGCAGGCAU GAUAUGUAAC CAUGCAUUGG AAAGUGCAUG G AGCAGAAG ...String:
GGUGGGAGGU CUGUCCCCAC CAUGGGGUGC GAACCUUGUG UGCUCAUCAU UGCCGUGAGC GUUCGCACGU CCAAACGACC AUAUCAUCG UUGCCCUGCG ACCAUUCAGC GGCAAUCAAG ACGCAGGCAU GAUAUGUAAC CAUGCAUUGG AAAGUGCAUG G AGCAGAAG AAACACAGUA GGAGGGACUU ACGUUAG

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Macromolecule #4: LaTranC

MacromoleculeName: LaTranC / type: protein_or_peptide / ID: 4 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Lawsonibacter sp. (bacteria)
Molecular weightTheoretical: 53.94609 KDa
Recombinant expressionOrganism: Escherichia coli-Pichia pastoris shuttle vector pPpARG4 (others)
SequenceString: SLNAKKIRLE NYAMKMRLYP SPTQAEQMDK MFLALRLAYN MTFHEVFQQN PAVCGDPDED GNVWPSYKKM ANKTWRKALI DQNPAIAEA PAAAITTNNG LFLSNGQKAW KTGMHNLPAN KADRKDFRFY SLSKPRRSFA VQIPPDCIIP SDTNQKVARI K LPKIDGAI ...String:
SLNAKKIRLE NYAMKMRLYP SPTQAEQMDK MFLALRLAYN MTFHEVFQQN PAVCGDPDED GNVWPSYKKM ANKTWRKALI DQNPAIAEA PAAAITTNNG LFLSNGQKAW KTGMHNLPAN KADRKDFRFY SLSKPRRSFA VQIPPDCIIP SDTNQKVARI K LPKIDGAI KARGFNRKIW FGPDGKHTYE EALAAHELSN NLTVRVSKDT CGDYFICITF SQGKVKGDKP TWEFYQEVRV SP IPEPIGL DVGIKDIAIL NTGTKYENKQ FKRDRAATLK KMSRQLSRRW GPANSAFRDY NKNIRAENRA LEKAQQDPGS SGV GPEAPV LKSVAQPSRR YLTIQKNRAK LERKIARRRD TYYHQVTAEV AGKSSLLAVE TLRVKNMLQN HRLAFALSDA AMSD FISKL KYKARRIQVP LVAIGTFQPS SQTCSVCGSI NPAVKNLSIR VWTCPNCGTR HNRDINAAKN ILAIAQNMLE KKV

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Experimental details

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Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation stateparticle

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Sample preparation

BufferpH: 7.5
VitrificationCryogen name: ETHANE

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Electron microscopy

MicroscopeTFS KRIOS
Image recordingFilm or detector model: GATAN K3 (6k x 4k) / Average electron dose: 50.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.5 µm
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

CTF correctionType: PHASE FLIPPING AND AMPLITUDE CORRECTION
Startup modelType of model: NONE
Final reconstructionResolution.type: BY AUTHOR / Resolution: 2.96 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 3229410
Initial angle assignmentType: ANGULAR RECONSTITUTION
Final angle assignmentType: ANGULAR RECONSTITUTION

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