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- PDB-9lis: CryoEM Structures Uncover the Unexpected Hinges of IscB for Enhan... -

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Basic information

Entry
Database: PDB / ID: 9lis
TitleCryoEM Structures Uncover the Unexpected Hinges of IscB for Enhanced Gene Editing
Components
  • DNA (5'-D(P*CP*TP*AP*GP*GP*TP*GP*GP*TP*TP*GP*TP*CP*GP*GP*CP*C)-3')
  • DNA (5'-D(P*CP*TP*CP*AP*AP*CP*CP*AP*CP*CP*TP*AP*C)-3')
  • Iscb
  • RNA (190-MER)
KeywordsRNA BINDING PROTEIN / Iscb / HNH
Function / homologyDNA / DNA (> 10) / RNA / RNA (> 10) / RNA (> 100)
Function and homology information
Biological speciessynthetic construct (others)
MethodELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.39 Å
AuthorsHu, C.Y. / Wang, F.Z. / Ma, S.S. / Zhang, S.F.
Funding support Singapore, 1items
OrganizationGrant numberCountry
Ministry of Education (MoE, Singapore) Singapore
CitationJournal: To Be Published
Title: CryoEM Structures Uncover the Unexpected Hinges of IscB for Enhanced Gene Editing
Authors: Hu, C.Y. / Wang, F.Z. / Ma, S.S. / Zhang, S.F.
History
DepositionJan 14, 2025Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0Jan 21, 2026Provider: repository / Type: Initial release
Revision 1.0Jan 21, 2026Data content type: EM metadata / Data content type: EM metadata / Provider: repository / Type: Initial release
Revision 1.0Jan 21, 2026Data content type: Half map / Part number: 1 / Data content type: Half map / Provider: repository / Type: Initial release
Revision 1.0Jan 21, 2026Data content type: Half map / Part number: 2 / Data content type: Half map / Provider: repository / Type: Initial release
Revision 1.0Jan 21, 2026Data content type: Image / Data content type: Image / Provider: repository / Type: Initial release
Revision 1.0Jan 21, 2026Data content type: Primary map / Data content type: Primary map / Provider: repository / Type: Initial release

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Iscb
B: RNA (190-MER)
C: DNA (5'-D(P*CP*TP*CP*AP*AP*CP*CP*AP*CP*CP*TP*AP*C)-3')
D: DNA (5'-D(P*CP*TP*AP*GP*GP*TP*GP*GP*TP*TP*GP*TP*CP*GP*GP*CP*C)-3')
hetero molecules


Theoretical massNumber of molelcules
Total (without water)132,7198
Polymers132,5804
Non-polymers1384
Water00
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: electron microscopy, not applicable
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1

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Components

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DNA chain , 2 types, 2 molecules CD

#3: DNA chain DNA (5'-D(P*CP*TP*CP*AP*AP*CP*CP*AP*CP*CP*TP*AP*C)-3')


Mass: 3840.528 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) synthetic construct (others) / Production host: synthetic construct (others)
#4: DNA chain DNA (5'-D(P*CP*TP*AP*GP*GP*TP*GP*GP*TP*TP*GP*TP*CP*GP*GP*CP*C)-3')


Mass: 5250.381 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) synthetic construct (others) / Production host: Escherichia coli (E. coli)

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Protein / RNA chain , 2 types, 2 molecules AB

#1: Protein Iscb


Mass: 62165.832 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) synthetic construct (others) / Production host: Escherichia coli (E. coli)
#2: RNA chain RNA (190-MER)


Mass: 61323.492 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) synthetic construct (others) / Production host: Escherichia coli (E. coli)

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Non-polymers , 2 types, 4 molecules

#5: Chemical ChemComp-ZN / ZINC ION


Mass: 65.409 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Zn / Feature type: SUBJECT OF INVESTIGATION
#6: Chemical ChemComp-MG / MAGNESIUM ION


Mass: 24.305 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: Mg / Feature type: SUBJECT OF INVESTIGATION

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Details

Has ligand of interestY
Has protein modificationN

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Experimental details

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Experiment

ExperimentMethod: ELECTRON MICROSCOPY
EM experimentAggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction

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Sample preparation

ComponentName: The binary complex of ISCB and wRNA / Type: COMPLEX / Entity ID: #1-#4 / Source: RECOMBINANT
Source (natural)Organism: synthetic construct (others)
Source (recombinant)Organism: Escherichia coli (E. coli)
Buffer solutionpH: 7.5
SpecimenEmbedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES
VitrificationCryogen name: ETHANE / Humidity: 100 %

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Electron microscopy imaging

Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company
MicroscopyModel: TFS KRIOS
Electron gunElectron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM
Electron lensMode: DIFFRACTION / Nominal defocus max: 1500 nm / Nominal defocus min: 800 nm
Image recordingElectron dose: 48.84 e/Å2 / Film or detector model: GATAN K3 (6k x 4k)

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Processing

EM software
IDNameVersionCategory
1cryoSPARCparticle selection
2PHENIX1.20.1_4487model refinement
13cryoSPARC3D reconstruction
CTF correctionType: PHASE FLIPPING AND AMPLITUDE CORRECTION
3D reconstructionResolution: 3.39 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 318267 / Symmetry type: POINT
RefinementHighest resolution: 3.39 Å
Stereochemistry target values: REAL-SPACE (WEIGHTED MAP SUM AT ATOM CENTERS)
Refine LS restraints
Refine-IDTypeDev idealNumber
ELECTRON MICROSCOPYf_bond_d0.0049289
ELECTRON MICROSCOPYf_angle_d0.69113586
ELECTRON MICROSCOPYf_dihedral_angle_d24.4483662
ELECTRON MICROSCOPYf_chiral_restr0.0361649
ELECTRON MICROSCOPYf_plane_restr0.005928

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