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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | GNATD focused acetyltransferase | |||||||||
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![]() | Acetyltransferase / TRANSFERASE | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.43 Å | |||||||||
![]() | Park JB / Rho SH | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Structural basis of the catalytic and allosteric mechanism of bacterial acetyltransferase PatZ. Authors: Park JB / Lee G / Han YY / Kim D / Heo K / Kim J / Park J / Yun H / Lee CW / Cho HS / Kim JS / Steinegger M / Seok YJ / Roh SH #1: Journal: mBio / Year: 2018 Title: Identification of Novel Protein Lysine Acetyltransferases in Escherichia coli. Authors: Christensen DG / Meyer JG / Baumgartner JT / D'Souza AK / Nelson WC / Payne SH / Kuhn ML / Schilling B / Wolfe AJ | |||||||||
History |
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Structure visualization
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Downloads & links
-EMDB archive
Map data | ![]() | 324 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 15 KB 15 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 14.7 KB | Display | ![]() |
Images | ![]() | 46.1 KB | ||
Filedesc metadata | ![]() | 4.2 KB | ||
Others | ![]() ![]() | 318.6 MB 318.6 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 894 KB | Display | ![]() |
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Full document | ![]() | 893.5 KB | Display | |
Data in XML | ![]() | 23.2 KB | Display | |
Data in CIF | ![]() | 30.5 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
File | ![]() | ||||||||||||||||||||
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Voxel size | X=Y=Z: 0.723 Å | ||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
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Sample components
-Entire : Acetyltransferase
Entire | Name: Acetyltransferase |
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Components |
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-Supramolecule #1: Acetyltransferase
Supramolecule | Name: Acetyltransferase / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: ![]() ![]() |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.4 |
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Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: DARK FIELD / Nominal defocus max: 8.0 µm / Nominal defocus min: 1.5 µm |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |