+
Open data
-
Basic information
Entry | Database: EMDB / ID: EMD-8478 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | CRISPR RNA-guided surveillance complex | |||||||||
![]() | 3.3 angstrom EM map of Type 1-E Cascade in the full R-loop state from Thermobifida fusca | |||||||||
![]() |
| |||||||||
![]() | CRISPR-Cas / Cascacde / surveillance / IMMUNE SYSTEM | |||||||||
Function / homology | ![]() maintenance of CRISPR repeat elements / defense response to virus / RNA binding / identical protein binding Similarity search - Function | |||||||||
Biological species | ![]() ![]() ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.3 Å | |||||||||
![]() | Xiao Y / Luo M | |||||||||
![]() | ![]() Title: Structure Basis for Directional R-loop Formation and Substrate Handover Mechanisms in Type I CRISPR-Cas System. Authors: Yibei Xiao / Min Luo / Robert P Hayes / Jonathan Kim / Sherwin Ng / Fang Ding / Maofu Liao / Ailong Ke / ![]() Abstract: Type I CRISPR systems feature a sequential dsDNA target searching and degradation process, by crRNA-displaying Cascade and nuclease-helicase fusion enzyme Cas3, respectively. Here we present two cryo- ...Type I CRISPR systems feature a sequential dsDNA target searching and degradation process, by crRNA-displaying Cascade and nuclease-helicase fusion enzyme Cas3, respectively. Here we present two cryo-EM snapshots of the Thermobifida fusca type I-E Cascade: (1) unwinding 11 bp of dsDNA at the seed-sequence region to scout for sequence complementarity, and (2) further unwinding of the entire protospacer to form a full R-loop. These structures provide the much-needed temporal and spatial resolution to resolve key mechanistic steps leading to Cas3 recruitment. In the early steps, PAM recognition causes severe DNA bending, leading to spontaneous DNA unwinding to form a seed-bubble. The full R-loop formation triggers conformational changes in Cascade, licensing Cas3 to bind. The same process also generates a bulge in the non-target DNA strand, enabling its handover to Cas3 for cleavage. The combination of both negative and positive checkpoints ensures stringent yet efficient target degradation in type I CRISPR-Cas systems. | |||||||||
History |
|
-
Structure visualization
Movie |
![]() |
---|---|
Structure viewer | EM map: ![]() ![]() ![]() |
Supplemental images |
-
Downloads & links
-EMDB archive
Map data | ![]() | 59.7 MB | ![]() | |
---|---|---|---|---|
Header (meta data) | ![]() ![]() | 20.3 KB 20.3 KB | Display Display | ![]() |
Images | ![]() | 112.4 KB | ||
Filedesc metadata | ![]() | 7.1 KB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 5u0aMC ![]() 8477C ![]() 5u07C C: citing same article ( M: atomic model generated by this map |
---|---|
Similar structure data |
-
Links
EMDB pages | ![]() ![]() |
---|---|
Related items in Molecule of the Month |
-
Map
File | ![]() | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | 3.3 angstrom EM map of Type 1-E Cascade in the full R-loop state from Thermobifida fusca | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.23 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
|
-Supplemental data
-
Sample components
-Entire : CRISPR RNA-guided surveillance complex
Entire | Name: CRISPR RNA-guided surveillance complex |
---|---|
Components |
|
-Supramolecule #1: CRISPR RNA-guided surveillance complex
Supramolecule | Name: CRISPR RNA-guided surveillance complex / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#8 |
---|---|
Source (natural) | Organism: ![]() ![]() |
-Macromolecule #1: CRISPR-associated protein, Cse3 family
Macromolecule | Name: CRISPR-associated protein, Cse3 family / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 26.327938 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MTWLTKIVPD LRYRQTRADF RTAGNLHRKL IRLSSDLGEE RIANPRQQSG LLFRIEETRN ELYLLVQSHS PLRVDRLGPG YHGVQMRNL DPFLARLDKG SRVRYRIVAS PTKRLGRSEN NTQRLGLKEP PKKPREYTWA LRGAAAEEWW HSRAAANGLE L LSTYAQTL ...String: MTWLTKIVPD LRYRQTRADF RTAGNLHRKL IRLSSDLGEE RIANPRQQSG LLFRIEETRN ELYLLVQSHS PLRVDRLGPG YHGVQMRNL DPFLARLDKG SRVRYRIVAS PTKRLGRSEN NTQRLGLKEP PKKPREYTWA LRGAAAEEWW HSRAAANGLE L LSTYAQTL DDVRDPGTAD RSRKIRHPAV RFDGEAVISD VDAVRHAVLN GIGRGKSYGC GLLSLALIEE GEHG UniProtKB: CRISPR-associated protein, Cse3 family |
-Macromolecule #2: CRISPR-associated protein, Cse1 family
Macromolecule | Name: CRISPR-associated protein, Cse1 family / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 61.433297 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MLSVALCFLV GGAIPSPPSF DVTIAPWLIA RSRDVLAAPE MLGLRDVLIR SHELSDVEIP LPPGAAVLWR ILALITARIT GLDQPPNKN PKRKWQARRS QILSKGRLDP EAVDAYFADY SERFDLFHPE RPWLQDPRLR EECPKTSGVN KLAWGRTAGE N QVWLGGHH ...String: MLSVALCFLV GGAIPSPPSF DVTIAPWLIA RSRDVLAAPE MLGLRDVLIR SHELSDVEIP LPPGAAVLWR ILALITARIT GLDQPPNKN PKRKWQARRS QILSKGRLDP EAVDAYFADY SERFDLFHPE RPWLQDPRLR EECPKTSGVN KLAWGRTAGE N QVWLGGHH HDLDPHPLDS AEAVWHLLAT LGYGPSGMCT ARVVRGRSER NVTAGPLRGT VSYHPLGRTL FESLILNIPY PG TGAADLA FWEQPELNDP LGLPEESAGL AGILRLDHFR HAVLLHPSPD GSHVVDAWVT WAWRERNISP ELDPYLIYQT SKE GRVYPR PAEAERAIWR DLDALLHYGE DGNYRPTILD NCTPLAQVPQ EVLDSLRLRA FGFDQDGQAR DKQWFTATTP AVLR WLADR ETDDNENARI VRRITLARKA AEALGRRLEK ACKEAWKESN SPSSTSSGTN AKTETGVGPW VQHGMSRYWA KAEPV FWNI VYDRPAQGYT PGMAGPGNAF NLVALAAYDE VTGPYCERPR VAKVVERHRS TLFSNWTPKQ DKEAA UniProtKB: CRISPR-associated protein, Cse1 family |
-Macromolecule #3: CRISPR-associated protein, Cse4 family
Macromolecule | Name: CRISPR-associated protein, Cse4 family / type: protein_or_peptide / ID: 3 / Number of copies: 6 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 41.043043 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MTFVDIHAIQ TLPYSNINRD DLGSPKTVVY GGKERTRVSS QSWKRAVRHE VEARLGDKAV RTRRIISEIA KRLRERGWDA DLADAGARQ VVLSVGKKSG IKLEKEKDSE APATSVLFYL PVPAIDELAA IADEHRDAVA KEAAKKTPKG ILPADRITEV L KSRNVSVN ...String: MTFVDIHAIQ TLPYSNINRD DLGSPKTVVY GGKERTRVSS QSWKRAVRHE VEARLGDKAV RTRRIISEIA KRLRERGWDA DLADAGARQ VVLSVGKKSG IKLEKEKDSE APATSVLFYL PVPAIDELAA IADEHRDAVA KEAAKKTPKG ILPADRITEV L KSRNVSVN LFGRMLAELP STEVDGAVQF AHAFTVHGTT VEVDFFTAVD DIPKENDHGS GHMNAGQFSA GTFYRYANVN LD RLVENTG DAQTARTAVA EFLRAFLSTV PSGKQNATAA MTLPDLVHIA VRFDRPISFA PAFETALYGS DGYTLRACQE LNN YAERLR EVWPDDAIRG YATVENKTDL AALGERYDSY PALIDAMVAA AFEGERE UniProtKB: CRISPR-associated protein, Cse4 family |
-Macromolecule #4: Cse2
Macromolecule | Name: Cse2 / type: protein_or_peptide / ID: 4 / Number of copies: 2 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 27.446613 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MNSDYILQHA DALVKRVSKL IVNEPAARAA LRRGVGLAPE DPRMLAAHRV VAPYVPVPTD YDVDRRRAAS LWDVHAVERA FYAVAAIMA AQPRSARDQE AEATEEQTGE PQDSEALTEP TPAEESSATK DGKPDRRPNL GVSLAQAVFD KGLNADSTEQ R LHLIARQN ...String: MNSDYILQHA DALVKRVSKL IVNEPAARAA LRRGVGLAPE DPRMLAAHRV VAPYVPVPTD YDVDRRRAAS LWDVHAVERA FYAVAAIMA AQPRSARDQE AEATEEQTGE PQDSEALTEP TPAEESSATK DGKPDRRPNL GVSLAQAVFD KGLNADSTEQ R LHLIARQN LDGVHRHLPR LVLYLRSDQV HIDWGILIRD LARWGHTPRH VAREWVQDYH RTLETLTRQA EQKNKNNTTD EE AEAA UniProtKB: CRISPR-associated protein, Cse2 family |
-Macromolecule #7: CRISPR-associated protein, Cas5e family
Macromolecule | Name: CRISPR-associated protein, Cas5e family / type: protein_or_peptide / ID: 7 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 28.27926 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MSGFLLRLAG PMQSWGEHSM FGERDTLPYP SRSGLIGMFA AAQGVRRGDP LDRYKELKFT VRVDRPGVRL VDFHTIGGGL PKERTVPTA AGERRDPKKA TIVTSRSYLA DAVFTVAVTG PEADTIADAL AAPYWQPYLG RRAFVPDPLL VLRRRVADPV R ELVEAVPL ...String: MSGFLLRLAG PMQSWGEHSM FGERDTLPYP SRSGLIGMFA AAQGVRRGDP LDRYKELKFT VRVDRPGVRL VDFHTIGGGL PKERTVPTA AGERRDPKKA TIVTSRSYLA DAVFTVAVTG PEADTIADAL AAPYWQPYLG RRAFVPDPLL VLRRRVADPV R ELVEAVPL PHRRVEEDAA TVLVDLIYEE GEYPDTRTLT VLNDVPLSFD SKSRRYSTRQ IRVVPTEVPA TLVAGPGRDY QN KLFTYVK QCAEEAA UniProtKB: CRISPR-associated protein, Cas5e family |
-Macromolecule #5: crRNA
Macromolecule | Name: crRNA / type: rna / ID: 5 / Number of copies: 1 |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 19.790793 KDa |
Sequence | String: AUGGACCGCC AGUGAUAAGU GGAAUGCCAU GUGGGCUGUC GUGAGCCCCA CGCACGUGGG G |
-Macromolecule #6: Target Strand
Macromolecule | Name: Target Strand / type: dna / ID: 6 / Number of copies: 1 / Classification: DNA |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 15.251741 KDa |
Sequence | String: (DG)(DC)(DC)(DT)(DG)(DG)(DC)(DG)(DA)(DC) (DA)(DG)(DC)(DC)(DC)(DA)(DC)(DA)(DT)(DG) (DG)(DC)(DA)(DT)(DT)(DC)(DC)(DA)(DC) (DT)(DT)(DA)(DT)(DC)(DA)(DC)(DT)(DG)(DG) (DC) (DT)(DT)(DC)(DG)(DT)(DC)(DC)(DG) (DC)(DG) |
-Macromolecule #8: Nontarget Strand
Macromolecule | Name: Nontarget Strand / type: dna / ID: 8 / Number of copies: 1 / Classification: DNA |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 12.076723 KDa |
Sequence | String: (DC)(DG)(DC)(DG)(DG)(DA)(DC)(DG)(DA)(DA) (DG)(DC)(DC)(DA)(DG)(DT)(DG)(DA)(DC)(DC) (DA)(DT)(DG)(DT)(DG)(DG)(DG)(DC)(DT) (DG)(DT)(DC)(DG)(DC)(DC)(DA)(DG)(DG)(DC) |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
![]() | single particle reconstruction |
Aggregation state | particle |
-
Sample preparation
Concentration | 0.8 mg/mL |
---|---|
Buffer | pH: 7.5 / Details: 10 mM HEPES pH 7.5, 150 mM NaCl, 5 mM DTT |
Grid | Model: 400 mesh Quantifoil holey carbon grid / Material: COPPER / Pretreatment - Type: GLOW DISCHARGE |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 85 % / Instrument: GATAN CRYOPLUNGE 3 |
-
Electron microscopy
Microscope | FEI POLARA 300 |
---|---|
Temperature | Min: 80.0 K / Max: 105.0 K |
Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Number real images: 1072 / Average electron dose: 8.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Calibrated defocus max: 21.0 µm / Calibrated defocus min: 1.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.0 mm / Nominal magnification: 31000 |
Sample stage | Specimen holder model: GATAN LIQUID NITROGEN / Cooling holder cryogen: NITROGEN |
Experimental equipment | ![]() Model: Tecnai Polara / Image courtesy: FEI Company |
+
Image processing
-Atomic model buiding 1
Refinement | Protocol: OTHER |
---|---|
Output model | ![]() PDB-5u0a: |