[English] 日本語
Yorodumi
- PDB-9i6n: Hen egg-white lysozyme structure collected at EuXFEL SPB/SFX with... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 9i6n
TitleHen egg-white lysozyme structure collected at EuXFEL SPB/SFX with HVE injection method
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
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
Biological speciesGallus gallus (chicken)
MethodX-RAY DIFFRACTION / FREE ELECTRON LASER / MOLECULAR REPLACEMENT / Resolution: 1.7 Å
AuthorsZabelskii, D. / Round, E. / Han, H. / von Stetten, D. / Melo, D. / de Wijn, R. / Bean, R. / Round, A.
Funding support1items
OrganizationGrant numberCountry
Not funded
CitationJournal: To Be Published
Title: Viscoelastic characterization of the lipid cubic phase provides insights into high-viscosity extrusion injection for XFEL experiments.
Authors: Zabelskii, D. / Round, E. / Han, H. / von Stetten, D. / Letrun, R. / Kim, C. / Sato, T. / Melo, D. / de Wijn, R. / Kharitonov, K. / Smyth, P. / Doerner, K. / Kloos, M. / Dietze, T. / Lopez, ...Authors: Zabelskii, D. / Round, E. / Han, H. / von Stetten, D. / Letrun, R. / Kim, C. / Sato, T. / Melo, D. / de Wijn, R. / Kharitonov, K. / Smyth, P. / Doerner, K. / Kloos, M. / Dietze, T. / Lopez, L. / Bean, R. / Round, A.
History
DepositionJan 30, 2025Deposition site: PDBE / Processing site: PDBE
Revision 1.0Jul 16, 2025Provider: repository / Type: Initial release

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Lysozyme C
hetero molecules


Theoretical massNumber of molelcules
Total (without water)14,5857
Polymers14,3311
Non-polymers2536
Water2,702150
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area820 Å2
ΔGint-37 kcal/mol
Surface area6570 Å2
MethodPISA
Unit cell
Length a, b, c (Å)79.300, 79.300, 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-1162-

HOH

21A-1168-

HOH

31A-1249-

HOH

41A-1250-

HOH

-
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-NA / SODIUM ION


Mass: 22.990 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Na
#3: Chemical ChemComp-CL / CHLORIDE ION


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


Mass: 62.068 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C2H6O2
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 150 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestN
Has protein modificationY

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.07 Å3/Da / Density % sol: 40.67 %
Crystal growTemperature: 297 K / Method: small tubes / pH: 3 / Details: 20% NaCl, 6% PEG 6000, 0.1M sodium acetate pH 3.0 / Temp details: Room temperature

-
Data collection

DiffractionMean temperature: 297 K / Ambient temp details: Room temperature / Serial crystal experiment: Y
Diffraction sourceSource: FREE ELECTRON LASER / Site: European XFEL / Beamline: SPB/SFX / Wavelength: 0.97 Å
DetectorType: PSI JUNGFRAU 4M / Detector: PIXEL / Date: Aug 22, 2024
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.97 Å / Relative weight: 1
ReflectionResolution: 1.7→22.65 Å / Num. obs: 13812 / % possible obs: 100 % / Redundancy: 267.1 % / Biso Wilson estimate: 24.4 Å2 / CC1/2: 0.956 / CC star: 0.989 / R split: 0.1543 / Net I/σ(I): 6.85
Reflection shellResolution: 1.7→1.76 Å / Redundancy: 195.8 % / Num. unique obs: 1348 / CC1/2: 0.88 / CC star: 0.97 / R split: 0.2734 / % possible all: 100
Serial crystallography sample deliveryDescription: HVE injection / Method: injection
Serial crystallography sample delivery injectionDescription: ASU injector / Injector diameter: 100 µm
Serial crystallography data reductionFrames indexed: 20484

-
Processing

Software
NameVersionClassification
PHENIX1.20.1_4487refinement
CrystFEL0.10.1data reduction
CrystFEL0.10.1data scaling
PHASERphasing
Cootmodel building
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.7→19.82 Å / SU ML: 0.2125 / Cross valid method: FREE R-VALUE / σ(F): 1.36 / Phase error: 18.1101
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.1988 1377 10 %
Rwork0.1618 12394 -
obs0.1654 13771 100 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 26.7 Å2
Refinement stepCycle: LAST / Resolution: 1.7→19.82 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1001 0 12 150 1163
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.01581141
X-RAY DIFFRACTIONf_angle_d1.38621555
X-RAY DIFFRACTIONf_chiral_restr0.0928158
X-RAY DIFFRACTIONf_plane_restr0.0109211
X-RAY DIFFRACTIONf_dihedral_angle_d13.7916433
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.7-1.760.33351340.30731213X-RAY DIFFRACTION100
1.76-1.830.25241360.23371214X-RAY DIFFRACTION100
1.83-1.910.21691340.18021207X-RAY DIFFRACTION100
1.91-2.020.19051350.15261216X-RAY DIFFRACTION100
2.02-2.140.18721370.16611229X-RAY DIFFRACTION100
2.14-2.310.19541350.1611222X-RAY DIFFRACTION100
2.31-2.540.20091370.16611234X-RAY DIFFRACTION100
2.54-2.90.20111390.16591247X-RAY DIFFRACTION100
2.91-3.650.19591410.15021263X-RAY DIFFRACTION100
3.66-19.820.18441490.14521349X-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