+Open data
-Basic information
Entry | Database: PDB / ID: 7t8t | ||||||
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Title | CryoEM structure of PLCg1 | ||||||
Components | 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma | ||||||
Keywords | HYDROLASE / 1-phosphatidylinositol 4 / 5-bisphosphate phosphodiesterase gamma-1 cryo EM | ||||||
Function / homology | Function and homology information phosphoinositide phospholipase C / phospholipid catabolic process / phosphatidylinositol phospholipase C activity / intracellular signal transduction / calcium ion binding Similarity search - Function | ||||||
Biological species | Rattus norvegicus (Norway rat) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.68 Å | ||||||
Authors | Endo-Streeter, S. / Sondek, J. | ||||||
Funding support | United States, 1items
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Citation | Journal: To Be Published Title: CryoEM structure of PLCg1 Authors: Endo-Streeter, S. / Sondek, J. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 7t8t.cif.gz | 381.9 KB | Display | PDBx/mmCIF format |
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PDB format | pdb7t8t.ent.gz | 301.5 KB | Display | PDB format |
PDBx/mmJSON format | 7t8t.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 7t8t_validation.pdf.gz | 818 KB | Display | wwPDB validaton report |
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Full document | 7t8t_full_validation.pdf.gz | 822.8 KB | Display | |
Data in XML | 7t8t_validation.xml.gz | 32.7 KB | Display | |
Data in CIF | 7t8t_validation.cif.gz | 49.5 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/t8/7t8t ftp://data.pdbj.org/pub/pdb/validation_reports/t8/7t8t | HTTPS FTP |
-Related structure data
Related structure data | 25745MC M: map data used to model this data C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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-Components
#1: Protein | Mass: 138185.391 Da / Num. of mol.: 1 / Mutation: H335A Source method: isolated from a genetically manipulated source Source: (gene. exp.) Rattus norvegicus (Norway rat) / Gene: Plcg1, rCG_32419 / Production host: Trichoplusia ni (cabbage looper) References: UniProt: G3V845, phosphoinositide phospholipase C |
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#2: Chemical | ChemComp-CA / |
Has ligand of interest | Y |
-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
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EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-Sample preparation
Component | Name: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 Type: COMPLEX / Entity ID: #1 / Source: RECOMBINANT | ||||||||||||||||||||||||||||||
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Molecular weight | Experimental value: NO | ||||||||||||||||||||||||||||||
Source (natural) | Organism: Rattus norvegicus (Norway rat) | ||||||||||||||||||||||||||||||
Source (recombinant) | Organism: Trichoplusia ni (cabbage looper) | ||||||||||||||||||||||||||||||
Buffer solution | pH: 7.4 | ||||||||||||||||||||||||||||||
Buffer component |
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Specimen | Conc.: 10 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||||||||||||||||||||
Specimen support | Grid material: COPPER / Grid mesh size: 300 divisions/in. / Grid type: C-flat-1.2/1.3 | ||||||||||||||||||||||||||||||
Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE-PROPANE / Humidity: 95 % / Chamber temperature: 295 K |
-Electron microscopy imaging
Experimental equipment | Model: Talos Arctica / Image courtesy: FEI Company |
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Microscopy | Model: FEI TALOS ARCTICA |
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Cs: 2.7 mm |
Specimen holder | Cryogen: NITROGEN |
Image recording | Electron dose: 55 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Num. of grids imaged: 1 / Num. of real images: 4450 |
Image scans | Width: 5760 / Height: 4092 |
-Processing
Software |
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EM software |
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CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | |||||||||||||||||||||||||
Symmetry | Point symmetry: C1 (asymmetric) | |||||||||||||||||||||||||
3D reconstruction | Resolution: 3.68 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 238458 / Num. of class averages: 13 / Symmetry type: POINT | |||||||||||||||||||||||||
Atomic model building | B value: 135.93 / Protocol: FLEXIBLE FIT / Space: REAL / Target criteria: CC fit and model metrics | |||||||||||||||||||||||||
Atomic model building | PDB-ID: 6PBC Pdb chain-ID: A / Accession code: 6PBC / Pdb chain residue range: 21-1215 / Source name: PDB / Type: experimental model | |||||||||||||||||||||||||
Refinement | Cross valid method: NONE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2 | |||||||||||||||||||||||||
Displacement parameters | Biso mean: 135.93 Å2 | |||||||||||||||||||||||||
Refine LS restraints |
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