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- PDB-4h8x: Radiation damage study of lysozyme - 0.07 MGy -

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Basic information

Entry
Database: PDB / ID: 4h8x
TitleRadiation damage study of lysozyme - 0.07 MGy
ComponentsLysozyme C
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
Biological speciesGallus gallus (chicken)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / molecular replacement / Resolution: 1.1998 Å
AuthorsSutton, K.A. / Snell, E.H.
CitationJournal: Acta Crystallogr.,Sect.D / Year: 2013
Title: Insights into the mechanism of X-ray-induced disulfide-bond cleavage in lysozyme crystals based on EPR, optical absorption and X-ray diffraction studies.
Authors: Sutton, K.A. / Black, P.J. / Mercer, K.R. / Garman, E.F. / Owen, R.L. / Snell, E.H. / Bernhard, W.A.
History
DepositionSep 24, 2012Deposition site: RCSB / Processing site: RCSB
Revision 1.0May 15, 2013Provider: repository / Type: Initial release
Revision 1.1Dec 11, 2013Group: Database references
Revision 1.2Jan 1, 2014Group: Database references
Revision 1.3Sep 20, 2023Group: Data collection / Database references ...Data collection / Database references / Derived calculations / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id
Revision 1.4Nov 27, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Lysozyme C
hetero molecules


Theoretical massNumber of molelcules
Total (without water)14,5005
Polymers14,3311
Non-polymers1684
Water2,054114
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)78.767, 78.767, 36.866
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number96
Space group name H-MP43212
Components on special symmetry positions
IDModelComponents
11A-340-

HOH

21A-389-

HOH

31A-414-

HOH

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Components

#1: Protein Lysozyme C / 1 / 4-beta-N-acetylmuramidase C / Allergen Gal d IV


Mass: 14331.160 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Gallus gallus (chicken) / References: UniProt: P00698, lysozyme
#2: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: Cl
#3: Chemical ChemComp-EDO / 1,2-ETHANEDIOL / ETHYLENE GLYCOL


Mass: 62.068 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C2H6O2
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 114 / Source method: isolated from a natural source / Formula: H2O
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: 1.99 Å3/Da / Density % sol: 38.35 %
Crystal growTemperature: 298 K / Method: vapor diffusion, hanging drop / pH: 4.8
Details: 7.5% sodium chloride, 100 mM sodium acetate buffer and 25% ethylene glycol, pH 4.8, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: SSRL / Beamline: BL9-2 / Wavelength: 1.0332 Å
DetectorType: MARMOSAIC 325 mm CCD / Detector: CCD / Date: Feb 12, 2011 / Details: Mirrors
RadiationMonochromator: Double crystal monochromator / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.0332 Å / Relative weight: 1
ReflectionResolution: 1.1998→50 Å / Num. all: 36858 / Num. obs: 36858 / % possible obs: 99.3 % / Observed criterion σ(I): 5.2 / Redundancy: 4.5 % / Biso Wilson estimate: 10.67 Å2 / Rmerge(I) obs: 0.032 / Rsym value: 0.028 / Χ2: 1.144 / Net I/σ(I): 45.1
Reflection shell
Resolution (Å)Redundancy (%)Rmerge(I) obsNum. unique allΧ2Diffraction-ID% possible all
1.1998-1.224.30.318051.121100
1.22-1.244.40.25918221.0761100
1.24-1.274.40.24918151.1351100
1.27-1.294.40.20618051.1451100
1.29-1.324.40.18618181.0941100
1.32-1.354.40.1618041.1421100
1.35-1.394.40.14418361.2171100
1.39-1.424.50.12718101.2231100
1.42-1.464.50.10318201.2561100
1.46-1.514.50.09118141.3481100
1.51-1.574.50.07918431.316199.9
1.57-1.634.50.06218231.138199.9
1.63-1.74.50.05418331.032199.8
1.7-1.794.50.04918371.04199.8
1.79-1.94.60.04718391.2199.7
1.9-2.054.50.0418491.171199
2.05-2.264.60.03118581.037199.4
2.26-2.594.60.02518491.091198.7
2.59-3.264.60.02118630.986197.5
3.26-504.40.01819061.126193

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Phasing

PhasingMethod: molecular replacement

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Processing

Software
NameVersionClassificationNB
SCALEPACKdata scaling
MOLREPphasing
PHENIX1.7.2_862refinement
PDB_EXTRACT3.11data extraction
Blu-Icedata collection
HKL-2000data reduction
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: PDB entry 6LYZ

6lyz


Resolution: 1.1998→26.914 Å / Occupancy max: 1 / Occupancy min: 0.4 / FOM work R set: 0.8747 / SU ML: 0.27 / σ(F): 1.35 / Phase error: 19.05 / Stereochemistry target values: ML
RfactorNum. reflection% reflectionSelection details
Rfree0.1997 1831 5 %Random
Rwork0.1909 ---
all0.194 36858 --
obs0.1913 36613 99.35 %-
Solvent computationShrinkage radii: 0.86 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL / Bsol: 49.508 Å2 / ksol: 0.424 e/Å3
Displacement parametersBiso max: 41.95 Å2 / Biso mean: 13.4194 Å2 / Biso min: 6.44 Å2
Baniso -1Baniso -2Baniso -3
1-0.392 Å20 Å2-0 Å2
2--0.392 Å20 Å2
3----0.7839 Å2
Refine analyzeLuzzati coordinate error obs: 0.138 Å
Refinement stepCycle: LAST / Resolution: 1.1998→26.914 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1001 0 7 114 1122
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0071061
X-RAY DIFFRACTIONf_angle_d1.1091431
X-RAY DIFFRACTIONf_chiral_restr0.084147
X-RAY DIFFRACTIONf_plane_restr0.005190
X-RAY DIFFRACTIONf_dihedral_angle_d12.048384
LS refinement shell

Refine-ID: X-RAY DIFFRACTION / Total num. of bins used: 13

Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkNum. reflection all% reflection obs (%)
1.1998-1.23220.28751360.250126542790100
1.2322-1.26850.23291460.234426482794100
1.2685-1.30940.2231270.217326422769100
1.3094-1.35620.25871100.218926792789100
1.3562-1.41050.26391310.209326632794100
1.4105-1.47470.19061640.187926572821100
1.4747-1.55240.20551370.185226632800100
1.5524-1.64970.20081590.172826472806100
1.6497-1.7770.17791420.183126802822100
1.777-1.95580.19891380.1792689282799
1.9558-2.23870.21041440.18172696284099
2.2387-2.820.2091470.1872711285898
2.82-26.9210.17081500.19042753290395

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