[English] 日本語
Yorodumi
- PDB-8j12: Cryo-EM structure of the AsCas12f-sgRNA-target DNA ternary complex -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 8j12
TitleCryo-EM structure of the AsCas12f-sgRNA-target DNA ternary complex
Components
  • (DNA (38-MER)) x 2
  • RNA (247-MER)
  • Transposase IS605 OrfB C-terminal domain-containing protein
KeywordsRNA BINDING PROTEIN/DNA/RNA / CRISPR-Cas / RNA BINDING PROTEIN-DNA COMPLEX / RNA BINDING PROTEIN / RNA BINDING PROTEIN-DNA-RNA complex
Function / homology
Function and homology information


endonuclease activity / Hydrolases; Acting on ester bonds / DNA binding / RNA binding / metal ion binding
Similarity search - Function
Transposase IS605, OrfB, C-terminal / Putative transposase DNA-binding domain
Similarity search - Domain/homology
DNA / DNA (> 10) / RNA / RNA (> 10) / RNA (> 100) / CRISPR-associated endodeoxyribonuclease Cas12f1
Similarity search - Component
Biological speciesAcidibacillus sulfuroxidans (bacteria)
Acidibacillus sulfooxidans (bacteria)
MethodELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.08 Å
AuthorsHino, T. / Omura, N.S. / Nakagawa, R. / Togashi, T. / Takeda, N.S. / Hiramoto, T. / Tasaka, S. / Hirano, H. / Tokuyama, T. / Uosaki, H. ...Hino, T. / Omura, N.S. / Nakagawa, R. / Togashi, T. / Takeda, N.S. / Hiramoto, T. / Tasaka, S. / Hirano, H. / Tokuyama, T. / Uosaki, H. / Ishiguro, H. / Yamano, H. / Ozaki, Y. / Motooka, D. / Mori, H. / Kirita, Y. / Kise, Y. / Itoh, Y. / Matoba, S. / Aburatani, H. / Yachie, N. / Siksnys, V. / Ohmori, T. / Hoshino, A. / Nureki, O.
Funding support Japan, 1items
OrganizationGrant numberCountry
Japan Agency for Medical Research and Development (AMED) Japan
CitationJournal: To Be Published
Title: Minimal and most efficient genome editing Cas enzyme
Authors: Hino, T. / Omura, N.S. / Nakagawa, R. / Togashi, T. / Takeda, N.S. / Hiramoto, T. / Tasaka, S. / Hirano, H. / Tokuyama, T. / Uosaki, H. / Ishiguro, H. / Yamano, H. / Ozaki, Y. / Motooka, D. ...Authors: Hino, T. / Omura, N.S. / Nakagawa, R. / Togashi, T. / Takeda, N.S. / Hiramoto, T. / Tasaka, S. / Hirano, H. / Tokuyama, T. / Uosaki, H. / Ishiguro, H. / Yamano, H. / Ozaki, Y. / Motooka, D. / Mori, H. / Kirita, Y. / Kise, Y. / Itoh, Y. / Matoba, S. / Aburatani, H. / Yachie, N. / Siksnys, V. / Ohmori, T. / Hoshino, A. / Nureki, O.
History
DepositionApr 12, 2023Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0Sep 27, 2023Provider: repository / Type: Initial release

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Transposase IS605 OrfB C-terminal domain-containing protein
B: Transposase IS605 OrfB C-terminal domain-containing protein
D: DNA (38-MER)
E: DNA (38-MER)
C: RNA (247-MER)
hetero molecules


Theoretical massNumber of molelcules
Total (without water)195,86514
Polymers195,5645
Non-polymers3019
Water0
1


  • Idetical with deposited unit
  • defined by author
  • Evidence: gel filtration
TypeNameSymmetry operationNumber
identity operation1_5551

-
Components

-
DNA chain , 2 types, 2 molecules DE

#2: DNA chain DNA (38-MER)


Mass: 11694.576 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Acidibacillus sulfooxidans (bacteria) / Production host: Escherichia coli (E. coli)
#3: DNA chain DNA (38-MER)


Mass: 11689.535 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Acidibacillus sulfooxidans (bacteria) / Production host: Escherichia coli (E. coli)

-
Protein / RNA chain , 2 types, 3 molecules ABC

#1: Protein Transposase IS605 OrfB C-terminal domain-containing protein / AsCas12f protein


Mass: 49925.008 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Acidibacillus sulfuroxidans (bacteria) / Gene: BM613_13600 / Production host: Escherichia coli (E. coli) / References: UniProt: A0A2U3D0N8
#4: RNA chain RNA (247-MER)


Mass: 72329.883 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Acidibacillus sulfooxidans (bacteria) / Production host: Escherichia coli (E. coli)

-
Non-polymers , 2 types, 9 molecules

#5: Chemical
ChemComp-MG / MAGNESIUM ION


Mass: 24.305 Da / Num. of mol.: 7 / Source method: obtained synthetically / Formula: Mg
#6: Chemical ChemComp-ZN / ZINC ION


Mass: 65.409 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: Zn

-
Details

Has ligand of interestN

-
Experimental details

-
Experiment

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

-
Sample preparation

ComponentName: AsCas12f-sgRNA-target DNA / Type: COMPLEX / Entity ID: #1-#4 / Source: RECOMBINANT
Molecular weightExperimental value: NO
Source (natural)Organism: Mycolicibacterium mucogenicum (bacteria)
Source (recombinant)Organism: Escherichia coli (E. coli)
Buffer solutionpH: 7.6
SpecimenEmbedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES
VitrificationCryogen name: ETHANE

-
Electron microscopy imaging

Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company
MicroscopyModel: FEI TITAN KRIOS
Electron gunElectron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: OTHER
Electron lensMode: BRIGHT FIELDBright-field microscopy / Nominal defocus max: 1600 nm / Nominal defocus min: 800 nm
Image recordingElectron dose: 50 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k)

-
Processing

CTF correctionType: PHASE FLIPPING AND AMPLITUDE CORRECTION
3D reconstructionResolution: 3.08 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 79011 / Symmetry type: POINT
Refine LS restraints
Refine-IDTypeDev idealNumber
ELECTRON MICROSCOPYf_bond_d0.00311302
ELECTRON MICROSCOPYf_angle_d0.43916162
ELECTRON MICROSCOPYf_dihedral_angle_d15.6563150
ELECTRON MICROSCOPYf_chiral_restr0.0361894
ELECTRON MICROSCOPYf_plane_restr0.0031352

+
About Yorodumi

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242):Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi

Thousand views of thousand structures

  • Yorodumi is a browser for structure data from EMDB, PDB, SASBDB, etc.
  • This page is also the successor to EM Navigator detail page, and also detail information page/front-end page for Omokage search.
  • The word "yorodu" (or yorozu) is an old Japanese word meaning "ten thousand". "mi" (miru) is to see.

Related info.:EMDB / PDB / SASBDB / Comparison of 3 databanks / Yorodumi Search / Aug 31, 2016. New EM Navigator & Yorodumi / Yorodumi Papers / Jmol/JSmol / Function and homology information / Changes in new EM Navigator and Yorodumi

Read more