[English] 日本語
Yorodumi
- PDB-8rus: Hen egg-white lysozyme (HEWL) structure from EuXFEL FXE, multi-hi... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 8rus
TitleHen egg-white lysozyme (HEWL) structure from EuXFEL FXE, multi-hit Droplet-on-Demand (DoD) injection, 9.3 keV photon energy, space group P432121
ComponentsLysozyme C
KeywordsHYDROLASE / XFEL / Lysozyme / HEWL / EuXFEL / European XFEL / Droplet on Demand / Droplet-on-Demand / DoD / multihit / multi-hit / kilohertz / SFX / Serial
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
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-like domain superfamily
Similarity search - Domain/homology
ACETATE ION / DI(HYDROXYETHYL)ETHER / Lysozyme C
Similarity search - Component
Biological speciesGallus gallus (chicken)
MethodX-RAY DIFFRACTION / FREE ELECTRON LASER / MOLECULAR REPLACEMENT / Resolution: 1.38 Å
AuthorsPerrett, S. / van Thor, J.J.
Funding supportEuropean Union, 1items
OrganizationGrant numberCountry
European Research Council (ERC)European Union
CitationJournal: Struct Dyn. / Year: 2024
Title: Kilohertz droplet-on-demand serial femtosecond crystallography at the European XFEL station FXE.
Authors: Perrett, S. / Fadini, A. / Hutchison, C.D.M. / Bhattacharya, S. / Morrison, C. / Turkot, O. / Jakobsen, M.B. / Grossler, M. / Licon-Salaiz, J. / Griese, F. / Flewett, S. / Valerio, J. / ...Authors: Perrett, S. / Fadini, A. / Hutchison, C.D.M. / Bhattacharya, S. / Morrison, C. / Turkot, O. / Jakobsen, M.B. / Grossler, M. / Licon-Salaiz, J. / Griese, F. / Flewett, S. / Valerio, J. / Schulz, J. / Biednov, M. / Jiang, Y. / Han, H. / Yousef, H. / Khakhulin, D. / Milne, C. / Barty, A. / van Thor, J.J.
History
DepositionJan 31, 2024Deposition site: PDBE / Processing site: PDBE
Revision 1.0Jul 24, 2024Provider: repository / Type: Initial release
Revision 1.1Oct 9, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature / Item: _pdbx_entry_details.has_protein_modification

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Lysozyme C
hetero molecules


Theoretical massNumber of molelcules
Total (without water)14,8389
Polymers14,3311
Non-polymers5078
Water1,40578
1


  • Idetical with deposited unit
  • defined by author
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)79.470, 79.470, 38.320
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number96
Space group name H-MP43212
Components on special symmetry positions
IDModelComponents
11A-329-

HOH

-
Components

-
Protein , 1 types, 1 molecules A

#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 genetically manipulated source
Source: (gene. exp.) Gallus gallus (chicken) / Gene: LYZ / Production host: Canavalia ensiformis (jack bean) / References: UniProt: P00698, lysozyme

-
Non-polymers , 5 types, 86 molecules

#2: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 3 / 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-PEG / DI(HYDROXYETHYL)ETHER


Mass: 106.120 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: C4H10O3
#6: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 78 / Source method: isolated from a natural source / Formula: H2O

-
Details

Has ligand of interestN
Has protein modificationY

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.11 Å3/Da / Density % sol: 41.73 %
Crystal growTemperature: 298 K / Method: batch mode / pH: 3.5
Details: 1:2 lysozyme (100 mg mL-1 in 50 mM NaOAc (pH 3.5)) and crystallization solution (0.1 M NaOAc (pH 3.5), 5% PEG6000 (v/v), 3.2 M NaCl) at 298K.

-
Data collection

DiffractionMean temperature: 298 K / Serial crystal experiment: Y
Diffraction sourceSource: FREE ELECTRON LASER / Site: European XFEL / Beamline: FXE / Wavelength: 1.333 Å
DetectorType: STFC Large Pixel Detector / Detector: PIXEL / Date: Nov 2, 2022
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.333 Å / Relative weight: 1
ReflectionResolution: 1.38→18.73 Å / Num. obs: 12383860 / % possible obs: 100 % / Redundancy: 479 % / Biso Wilson estimate: 35.6 Å2 / CC1/2: 0.99 / CC star: 0.997 / R split: 0.0836 / Net I/σ(I): 6.77
Reflection shellResolution: 1.38→1.4 Å / Redundancy: 43 % / Mean I/σ(I) obs: 0.9 / Num. unique obs: 107809 / CC1/2: 0.01 / CC star: 0.134 / R split: 0.5488 / % possible all: 100
Serial crystallography measurementFocal spot size: 10 µm2 / Pulse duration: 50 fsec. / Pulse photon energy: 9290 keV / XFEL pulse repetition rate: 47000 Hz
Serial crystallography sample deliveryDescription: Droplet on Demand / Method: injection
Serial crystallography sample delivery injectionCarrier solvent: PEG / Crystal conc.: 20000000 / Description: Droplet on Demand Multi Hit / Filter size: 20 µm / Injector diameter: 80 µm / Injector temperature: 298 K / Power by: piezoelectric
Serial crystallography data reductionFrames indexed: 74048 / Frames total: 255000 / XFEL run numbers: 3

-
Processing

Software
NameVersionClassification
PHENIX(1.20.1_4487: ???)refinement
CrystFELdata reduction
CrystFELdata scaling
PHENIXphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.38→18.73 Å / SU ML: 0.34 / Cross valid method: FREE R-VALUE / σ(F): 1.33 / Phase error: 30.89 / Stereochemistry target values: ML
RfactorNum. reflection% reflection
Rfree0.1998 2639 10.24 %
Rwork0.1484 --
obs0.1535 25781 99.96 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL
Refinement stepCycle: LAST / Resolution: 1.38→18.73 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms996 0 29 78 1103
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.009
X-RAY DIFFRACTIONf_angle_d0.948
X-RAY DIFFRACTIONf_dihedral_angle_d9.206160
X-RAY DIFFRACTIONf_chiral_restr0.078151
X-RAY DIFFRACTIONf_plane_restr0.009191
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.38-1.410.39351440.39551169X-RAY DIFFRACTION100
1.41-1.430.43071460.39841189X-RAY DIFFRACTION100
1.43-1.460.40111290.42111192X-RAY DIFFRACTION100
1.46-1.490.46071660.42711167X-RAY DIFFRACTION100
1.49-1.530.41591370.39851208X-RAY DIFFRACTION100
1.53-1.570.41261310.34871184X-RAY DIFFRACTION100
1.57-1.610.34181370.32051227X-RAY DIFFRACTION100
1.61-1.660.36061540.27561173X-RAY DIFFRACTION100
1.66-1.710.32951270.23591206X-RAY DIFFRACTION100
1.71-1.770.24841170.1871229X-RAY DIFFRACTION100
1.77-1.840.25281380.15551231X-RAY DIFFRACTION100
1.84-1.920.2561350.15171199X-RAY DIFFRACTION100
1.92-2.030.16651520.12051196X-RAY DIFFRACTION100
2.03-2.150.17791460.10011231X-RAY DIFFRACTION100
2.15-2.320.18381210.11421223X-RAY DIFFRACTION100
2.32-2.550.18111470.12621241X-RAY DIFFRACTION100
2.55-2.920.21451290.14151255X-RAY DIFFRACTION100
2.92-3.670.18711350.13291272X-RAY DIFFRACTION100
3.67-18.730.15421480.12531350X-RAY DIFFRACTION100

+
About Yorodumi

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242):Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi

Thousand views of thousand structures

  • Yorodumi is a browser for structure data from EMDB, PDB, SASBDB, etc.
  • This page is also the successor to EM Navigator detail page, and also detail information page/front-end page for Omokage search.
  • The word "yorodu" (or yorozu) is an old Japanese word meaning "ten thousand". "mi" (miru) is to see.

Related info.:EMDB / PDB / SASBDB / Comparison of 3 databanks / Yorodumi Search / Aug 31, 2016. New EM Navigator & Yorodumi / Yorodumi Papers / Jmol/JSmol / Function and homology information / Changes in new EM Navigator and Yorodumi

Read more