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- PDB-8b3v: Hen Egg White Lysozyme 8s in situ crystallization -

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Basic information

Entry
Database: PDB / ID: 8b3v
TitleHen Egg White Lysozyme 8s in situ crystallization
ComponentsLysozyme
KeywordsHYDROLASE
Function / homology
Function and homology information


Lactose synthesis / Antimicrobial peptides / Neutrophil degranulation / beta-N-acetylglucosaminidase activity / cell wall macromolecule catabolic process / lysozyme / lysozyme activity / defense response to Gram-negative bacterium / killing of cells of another organism / defense response to Gram-positive bacterium ...Lactose synthesis / Antimicrobial peptides / Neutrophil degranulation / beta-N-acetylglucosaminidase activity / cell wall macromolecule catabolic process / lysozyme / lysozyme activity / defense response to Gram-negative bacterium / killing of cells of another organism / defense response to Gram-positive bacterium / defense response to bacterium / endoplasmic reticulum / extracellular space / identical protein binding / cytoplasm
Similarity search - Function
Lysozyme - #10 / Glycoside hydrolase, family 22, lysozyme / Glycoside hydrolase family 22 domain / Glycosyl hydrolases family 22 (GH22) domain signature. / Glycoside hydrolase, family 22 / C-type lysozyme/alpha-lactalbumin family / Glycosyl hydrolases family 22 (GH22) domain profile. / Alpha-lactalbumin / lysozyme C / Lysozyme / Lysozyme-like domain superfamily ...Lysozyme - #10 / Glycoside hydrolase, family 22, lysozyme / Glycoside hydrolase family 22 domain / Glycosyl hydrolases family 22 (GH22) domain signature. / Glycoside hydrolase, family 22 / C-type lysozyme/alpha-lactalbumin family / Glycosyl hydrolases family 22 (GH22) domain profile. / Alpha-lactalbumin / lysozyme C / Lysozyme / Lysozyme-like domain superfamily / Orthogonal Bundle / Mainly Alpha
Similarity search - Domain/homology
ACETATE ION / Lysozyme C
Similarity search - Component
Biological speciesGallus gallus (chicken)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.74 Å
AuthorsHenkel, A. / Galchenkova, M. / Yefanov, O. / Hakanpaeae, J. / Chapman, H.N. / Oberthuer, D.
Funding support1items
OrganizationGrant numberCountry
Not funded
Citation
Journal: Iucrj / Year: 2023
Title: JINXED: just in time crystallization for easy structure determination of biological macromolecules.
Authors: Henkel, A. / Galchenkova, M. / Maracke, J. / Yefanov, O. / Klopprogge, B. / Hakanpaa, J. / Mesters, J.R. / Chapman, H.N. / Oberthuer, D.
#1: Journal: Biorxiv / Year: 2022
Title: JINXED: Just in time crystallization for easy structure determination of biological macromolecules
Authors: Henkel, A. / Galchenkova, M. / Maracke, J. / Yefanov, O. / Hakanpaa, J. / Mesters, J.R. / Chapman, H.N. / Oberthur, D.
History
DepositionSep 16, 2022Deposition site: PDBE / Processing site: PDBE
Revision 1.0Nov 30, 2022Provider: repository / Type: Initial release
Revision 1.1Mar 22, 2023Group: Database references / Category: citation / citation_author
Revision 1.2May 17, 2023Group: Database references / Category: citation / citation_author
Item: _citation.journal_volume / _citation.page_first ..._citation.journal_volume / _citation.page_first / _citation.page_last / _citation_author.identifier_ORCID
Revision 1.3Feb 7, 2024Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model
Revision 1.4Oct 23, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature / Item: _pdbx_entry_details.has_protein_modification

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Lysozyme
hetero molecules


Theoretical massNumber of molelcules
Total (without water)14,7329
Polymers14,3311
Non-polymers4018
Water1,22568
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area1300 Å2
ΔGint-23 kcal/mol
Surface area6530 Å2
MethodPISA
Unit cell
Length a, b, c (Å)79.200, 79.200, 37.800
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number96
Space group name H-MP43212
Space group name HallP4nw2abw
Symmetry operation#1: x,y,z
#2: -y+1/2,x+1/2,z+3/4
#3: y+1/2,-x+1/2,z+1/4
#4: x+1/2,-y+1/2,-z+1/4
#5: -x+1/2,y+1/2,-z+3/4
#6: -x,-y,z+1/2
#7: y,x,-z
#8: -y,-x,-z+1/2
Components on special symmetry positions
IDModelComponents
11A-335-

HOH

21A-345-

HOH

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Components

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Protein , 1 types, 1 molecules A

#1: Protein Lysozyme


Mass: 14331.160 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Gallus gallus (chicken) / Production host: Gallus gallus (chicken) / References: UniProt: P00698

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Non-polymers , 5 types, 76 molecules

#2: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: Cl
#3: Chemical ChemComp-NA / SODIUM ION


Mass: 22.990 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Na
#4: Chemical ChemComp-ACT / ACETATE ION


Mass: 59.044 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C2H3O2
#5: Chemical
ChemComp-EDO / 1,2-ETHANEDIOL / ETHYLENE GLYCOL


Mass: 62.068 Da / Num. of mol.: 4 / Source method: obtained synthetically / Formula: C2H6O2
#6: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 68 / Source method: isolated from a natural source / Formula: H2O

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Details

Has ligand of interestN
Has protein modificationY

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Experimental details

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Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

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Sample preparation

CrystalDensity Matthews: 2.07 Å3/Da / Density % sol: 40.53 %
Crystal growTemperature: 293 K / Method: microfluidic
Details: 0.1 M sodium acetate, pH 4.6, 2.7 M NaCl, 15 % PEG4000, 6 % ethylene glycol

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Data collection

DiffractionMean temperature: 293 K / Serial crystal experiment: Y
Diffraction sourceSource: SYNCHROTRON / Site: PETRA III, DESY / Beamline: P11 / Wavelength: 1.033 Å
DetectorType: DECTRIS EIGER2 X 16M / Detector: PIXEL / Date: Sep 19, 2021
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.033 Å / Relative weight: 1
ReflectionResolution: 1.74→39.6 Å / Num. obs: 12939 / % possible obs: 100 % / Redundancy: 469.92 % / Biso Wilson estimate: 23.47 Å2 / CC1/2: 0.992 / CC star: 0.998 / R split: 0.09 / Net I/σ(I): 11.93
Reflection shellResolution: 1.74→1.77 Å / Redundancy: 57.8 % / Num. unique obs: 620 / CC1/2: 0.289 / CC star: 0.67 / R split: 1.15 / % possible all: 100
Serial crystallography sample deliveryDescription: CFEL TapeDrive 2.0 / Method: injection

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Processing

Software
NameVersionClassification
PHENIX1.19.2_4158refinement
CrystFELdata reduction
CrystFELdata scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 6FTR

6ftr


Resolution: 1.74→39.6 Å / SU ML: 0.237 / Cross valid method: FREE R-VALUE / σ(F): 1.33 / Phase error: 18.2141
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.1849 1277 10.02 %
Rwork0.1658 11471 -
obs0.1677 12748 99.27 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 29.66 Å2
Refinement stepCycle: LAST / Resolution: 1.74→39.6 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1001 0 23 68 1092
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00531188
X-RAY DIFFRACTIONf_angle_d0.70951613
X-RAY DIFFRACTIONf_chiral_restr0.0448160
X-RAY DIFFRACTIONf_plane_restr0.0067222
X-RAY DIFFRACTIONf_dihedral_angle_d5.7823181
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.74-1.810.38841310.33671171X-RAY DIFFRACTION93.4
1.81-1.890.32971400.29411256X-RAY DIFFRACTION100
1.89-1.990.2261410.21781266X-RAY DIFFRACTION99.93
1.99-2.120.1921390.17861244X-RAY DIFFRACTION100
2.12-2.280.16821390.1541266X-RAY DIFFRACTION100
2.28-2.510.16231440.14061286X-RAY DIFFRACTION100
2.51-2.870.18781420.15341279X-RAY DIFFRACTION100
2.87-3.620.15931450.14911313X-RAY DIFFRACTION100
3.62-39.60.16471560.14631390X-RAY DIFFRACTION99.94
Refinement TLS params.Method: refined / Origin x: 0.752299791292 Å / Origin y: 99.8974890638 Å / Origin z: 9.10882951896 Å
111213212223313233
T0.158566207332 Å20.00881899692788 Å2-0.000157659718468 Å2-0.171816081519 Å20.024199233923 Å2--0.172395667331 Å2
L2.69979027102 °21.41786285586 °20.124537936442 °2-3.52924219983 °20.316044220426 °2--1.9099852815 °2
S-0.019155632961 Å °0.0302273652374 Å °-0.083455615194 Å °-0.0575313240403 Å °0.03771764704 Å °-0.158778922857 Å °0.0793344104303 Å °0.0707283116072 Å °-0.00259988912034 Å °
Refinement TLS groupSelection details: all

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