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- PDB-6zeu: Crystal structure of proteinase K lamella by electron diffraction... -

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Basic information

Entry
Database: PDB / ID: 6zeu
TitleCrystal structure of proteinase K lamella by electron diffraction with a 50 micrometre C2 condenser aperture
ComponentsProteinase K
KeywordsHYDROLASE / Protease / Serine protease
Function / homology
Function and homology information


peptidase K / serine-type endopeptidase activity / proteolysis / extracellular region / metal ion binding
Similarity search - Function
Proteinase K-like catalytic domain / Peptidase S8 propeptide/proteinase inhibitor I9 / Peptidase inhibitor I9 / Peptidase S8 propeptide/proteinase inhibitor I9 superfamily / Peptidase S8, subtilisin, His-active site / : / Serine proteases, subtilase family, histidine active site. / Serine proteases, subtilase family, aspartic acid active site. / Peptidase S8, subtilisin, Asp-active site / Serine proteases, subtilase family, serine active site. ...Proteinase K-like catalytic domain / Peptidase S8 propeptide/proteinase inhibitor I9 / Peptidase inhibitor I9 / Peptidase S8 propeptide/proteinase inhibitor I9 superfamily / Peptidase S8, subtilisin, His-active site / : / Serine proteases, subtilase family, histidine active site. / Serine proteases, subtilase family, aspartic acid active site. / Peptidase S8, subtilisin, Asp-active site / Serine proteases, subtilase family, serine active site. / Peptidase S8, subtilisin, Ser-active site / Peptidase S8, subtilisin-related / Serine proteases, subtilase domain profile. / Peptidase S8/S53 domain superfamily / Subtilase family / Peptidase S8/S53 domain
Similarity search - Domain/homology
Biological speciesParengyodontium album (fungus)
MethodELECTRON CRYSTALLOGRAPHY / electron crystallography / MOLECULAR REPLACEMENT / cryo EM / Resolution: 2.004 Å
AuthorsEvans, G. / Zhang, P. / Beale, E.V. / Waterman, D.G.
Funding support United Kingdom, 3items
OrganizationGrant numberCountry
Wellcome Trust206422/Z/17/Z United Kingdom
Biotechnology and Biological Sciences Research Council (BBSRC)BB/S003339/1 United Kingdom
Wellcome Trust202933/Z/16/Z United Kingdom
CitationJournal: Front Mol Biosci / Year: 2020
Title: A Workflow for Protein Structure Determination From Thin Crystal Lamella by Micro-Electron Diffraction.
Authors: Emma V Beale / David G Waterman / Corey Hecksel / Jason van Rooyen / James B Gilchrist / James M Parkhurst / Felix de Haas / Bart Buijsse / Gwyndaf Evans / Peijun Zhang /
Abstract: MicroED has recently emerged as a powerful method for the analysis of biological structures at atomic resolution. This technique has been largely limited to protein nanocrystals which grow either as ...MicroED has recently emerged as a powerful method for the analysis of biological structures at atomic resolution. This technique has been largely limited to protein nanocrystals which grow either as needles or plates measuring only a few hundred nanometers in thickness. Furthermore, traditional microED data processing uses established X-ray crystallography software that is not optimized for handling compound effects that are unique to electron diffraction data. Here, we present an integrated workflow for microED, from sample preparation by cryo-focused ion beam milling, through data collection with a standard Ceta-D detector, to data processing using the DIALS software suite, thus enabling routine atomic structure determination of protein crystals of any size and shape using microED. We demonstrate the effectiveness of the workflow by determining the structure of proteinase K to 2.0 Å resolution and show the advantage of using protein crystal lamellae over nanocrystals.
History
DepositionJun 16, 2020Deposition site: PDBE / Processing site: PDBE
Revision 1.0Oct 14, 2020Provider: repository / Type: Initial release
Revision 1.1Nov 25, 2020Group: Structure summary / Category: em_entity_assembly
Revision 1.2Feb 10, 2021Group: Database references / Category: pdbx_related_exp_data_set
Revision 1.3Sep 13, 2023Group: Data collection / Database references / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession
Revision 1.4Feb 14, 2024Group: Refinement description / Category: em_3d_fitting_list
Item: _em_3d_fitting_list.accession_code / _em_3d_fitting_list.initial_refinement_model_id ..._em_3d_fitting_list.accession_code / _em_3d_fitting_list.initial_refinement_model_id / _em_3d_fitting_list.source_name / _em_3d_fitting_list.type
Revision 1.5Nov 6, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature / Item: _pdbx_entry_details.has_protein_modification

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Structure visualization

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Structure viewerMolecule:
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Assembly

Deposited unit
AAA: Proteinase K
hetero molecules


Theoretical massNumber of molelcules
Total (without water)28,9992
Polymers28,9591
Non-polymers401
Water46826
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area90 Å2
ΔGint-12 kcal/mol
Surface area10020 Å2
MethodPISA
Unit cell
Length a, b, c (Å)67.331, 67.331, 106.878
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number96
Space group name H-MP43212

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Components

#1: Protein Proteinase K / Endopeptidase K / Tritirachium alkaline proteinase


Mass: 28958.791 Da / Num. of mol.: 1 / Source method: obtained synthetically / Details: Sigma-Aldrich, P2308 / Source: (synth.) Parengyodontium album (fungus) / References: UniProt: P06873, peptidase K
#2: Chemical ChemComp-CA / CALCIUM ION


Mass: 40.078 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Ca
#3: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 26 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestN
Has protein modificationY

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Experimental details

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Experiment

ExperimentMethod: ELECTRON CRYSTALLOGRAPHY
EM experimentAggregation state: 3D ARRAY / 3D reconstruction method: electron crystallography

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Sample preparation

ComponentName: proteinase K / Type: COMPLEX / Source: MULTIPLE SOURCES
Buffer solutionpH: 7.5
Buffer componentConc.: 25 mM / Name: Tris
SpecimenConc.: 50 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES
Specimen supportGrid type: Quantifoil R1.2/1.3
VitrificationCryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 293.15 K
Details: Excess liquid was removed by blotting for 4-6s with a Vitrobot

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Data collection

Experimental equipment
Model: Talos Arctica / Image courtesy: FEI Company
MicroscopyModel: FEI TALOS ARCTICA / Date: Apr 20, 2018
Electron gunElectron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM
Electron lensMode: DIFFRACTION / C2 aperture diameter: 50 µm
Image recording

Imaging-ID: 1 / Average exposure time: 0.85 sec. / Electron dose: 0.034 e/Å2 / Film or detector model: OTHER / Num. of grids imaged: 1 / Details: The images were recorded using a Ceta-D detector operated in rolling-shutter mode with 2x2 binning.

IDNum. of diffraction images
1122
278
Image scansSampling size: 28 µm / Width: 2048 / Height: 2048
EM diffractionCamera length: 1350 mm
EM diffraction statsFourier space coverage: 93 % / High resolution: 2 Å / Num. of intensities measured: 139242 / Num. of structure factors: 15787 / Phase error: 0 ° / Phase residual: 0.1 ° / Phase error rejection criteria: none / Rmerge: 0.303 / Rsym: 0.303
Reflection shellResolution: 2→2.06 Å / Redundancy: 9.1 % / Rmerge(I) obs: 1.3 / Mean I/σ(I) obs: 1.8 / Num. measured obs: 10323 / Num. unique obs: 1139 / CC1/2: 0.611 / Rpim(I) all: 0.627 / Rrim(I) all: 1.45 / Χ2: 1.07 / % possible all: 92.4

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Processing

Software
NameVersionClassification
REFMAC5.8.0258refinement
DIALS1.1data reduction
Aimless0.7.1data scaling
PHASER2.8.2phasing
EM software
IDNameVersionCategory
8REFMAC5.8.0258model refinement
9Phaser2.8.2molecular replacement
11POINTLESS1.11.12symmetry determination
12AIMLESS0.7.1crystallography merging
EM 3D crystal entity∠α: 90 ° / ∠β: 90 ° / ∠γ: 90 ° / A: 67.3308 Å / B: 67.3308 Å / C: 106.878 Å / Space group name: P43212 / Space group num: 96
CTF correctionType: NONE
3D reconstructionResolution method: DIFFRACTION PATTERN/LAYERLINES / Symmetry type: 3D CRYSTAL
Atomic model buildingSpace: RECIPROCAL
Atomic model buildingPDB-ID: 2ID8

2id8


Accession code: 2ID8 / Source name: PDB / Type: experimental model
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 2ID8

2id8


Resolution: 2.004→57.034 Å / Cor.coef. Fo:Fc: 0.941 / Cor.coef. Fo:Fc free: 0.914 / WRfactor Rfree: 0.209 / WRfactor Rwork: 0.18 / Average fsc free: 0.8925 / Average fsc work: 0.915 / Cross valid method: FREE R-VALUE / ESU R: 0.234 / ESU R Free: 0.183
Details: Hydrogens have been added in their riding positions
RfactorNum. reflection% reflectionSelection details
Rfree0.2343 793 5.032 %Random selection
Rwork0.1991 14966 --
all0.201 ---
obs-15759 91.825 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK BULK SOLVENT
Displacement parametersBiso mean: 16.43 Å2
Baniso -1Baniso -2Baniso -3
1--0.418 Å20 Å20 Å2
2---0.418 Å20 Å2
3---0.836 Å2
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
ELECTRON CRYSTALLOGRAPHYr_bond_refined_d0.0430.0122105
ELECTRON CRYSTALLOGRAPHYr_angle_refined_deg1.5091.6312869
ELECTRON CRYSTALLOGRAPHYr_dihedral_angle_1_deg5.0495286
ELECTRON CRYSTALLOGRAPHYr_dihedral_angle_2_deg34.27121.93998
ELECTRON CRYSTALLOGRAPHYr_dihedral_angle_3_deg13.96715305
ELECTRON CRYSTALLOGRAPHYr_dihedral_angle_4_deg16.7181512
ELECTRON CRYSTALLOGRAPHYr_chiral_restr0.0540.2283
ELECTRON CRYSTALLOGRAPHYr_gen_planes_refined0.0030.021645
ELECTRON CRYSTALLOGRAPHYr_nbd_refined0.2060.21144
ELECTRON CRYSTALLOGRAPHYr_nbtor_refined0.3160.21486
ELECTRON CRYSTALLOGRAPHYr_xyhbond_nbd_refined0.1420.2112
ELECTRON CRYSTALLOGRAPHYr_symmetry_nbd_refined0.2010.240
ELECTRON CRYSTALLOGRAPHYr_symmetry_xyhbond_nbd_refined0.2770.26
ELECTRON CRYSTALLOGRAPHYr_mcbond_it2.6461.4241123
ELECTRON CRYSTALLOGRAPHYr_mcangle_it3.1242.141404
ELECTRON CRYSTALLOGRAPHYr_scbond_it4.7141.823982
ELECTRON CRYSTALLOGRAPHYr_scangle_it5.5292.5621461
ELECTRON CRYSTALLOGRAPHYr_lrange_it5.67721.0383443
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.004-2.0560.255560.2461084ELECTRON CRYSTALLOGRAPHY91.7136
2.056-2.1130.275590.2371052ELECTRON CRYSTALLOGRAPHY92.6606
2.113-2.1740.356520.2391043ELECTRON CRYSTALLOGRAPHY92.0168
2.174-2.2410.28510.221980ELECTRON CRYSTALLOGRAPHY91.8077
2.241-2.3140.28560.241980ELECTRON CRYSTALLOGRAPHY92.1708
2.314-2.3950.28510.234938ELECTRON CRYSTALLOGRAPHY92.1715
2.395-2.4860.375480.223901ELECTRON CRYSTALLOGRAPHY91.6908
2.486-2.5870.32540.235872ELECTRON CRYSTALLOGRAPHY92.5075
2.587-2.7020.234470.229846ELECTRON CRYSTALLOGRAPHY91.778
2.702-2.8340.268430.212803ELECTRON CRYSTALLOGRAPHY92.0566
2.834-2.9870.289390.21770ELECTRON CRYSTALLOGRAPHY91.6195
2.987-3.1680.274320.196746ELECTRON CRYSTALLOGRAPHY92.071
3.168-3.3870.235430.184685ELECTRON CRYSTALLOGRAPHY91.9192
3.387-3.6580.164350.16646ELECTRON CRYSTALLOGRAPHY91.9028
3.658-4.0060.165340.159598ELECTRON CRYSTALLOGRAPHY91.5942
4.006-4.4790.123350.149550ELECTRON CRYSTALLOGRAPHY91.6928
4.479-5.170.119130.138499ELECTRON CRYSTALLOGRAPHY91.7563
5.17-6.3280.153200.187423ELECTRON CRYSTALLOGRAPHY90.9651
6.328-8.9340.188120.169344ELECTRON CRYSTALLOGRAPHY90.8163
8.934-57.0340.316130.258206ELECTRON CRYSTALLOGRAPHY89.7541

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