[English] 日本語
Yorodumi
- PDB-2otu: Crystal structure of Fv polyglutamine complex -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 2otu
TitleCrystal structure of Fv polyglutamine complex
Components
  • Fv heavy chain variable domain
  • Fv light chain variable domain
  • peptide antigen
KeywordsIMMUNE SYSTEM / Antibody Fv polyglutamine complex
Function / homology
Function and homology information


IgG immunoglobulin complex / immunoglobulin mediated immune response / antigen binding / blood microparticle
Similarity search - Function
: / Immunoglobulin V-Type / Immunoglobulin V-set domain / Immunoglobulin V-set domain / Immunoglobulin subtype / Immunoglobulin / Ig-like domain profile. / Immunoglobulin-like domain / Immunoglobulin-like domain superfamily / Immunoglobulins ...: / Immunoglobulin V-Type / Immunoglobulin V-set domain / Immunoglobulin V-set domain / Immunoglobulin subtype / Immunoglobulin / Ig-like domain profile. / Immunoglobulin-like domain / Immunoglobulin-like domain superfamily / Immunoglobulins / Immunoglobulin-like fold / Immunoglobulin-like / Sandwich / Mainly Beta
Similarity search - Domain/homology
Biological speciesMus musculus (house mouse)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.68 Å
AuthorsLi, P.
CitationJournal: To be Published
Title: Implications of the structure of a poly-Gln/anti-poly-Gln complex for disease progression and therapy
Authors: Li, P.
History
DepositionFeb 9, 2007Deposition site: RCSB / Processing site: RCSB
Revision 1.0Apr 24, 2007Provider: repository / Type: Initial release
Revision 1.1May 1, 2008Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3Aug 30, 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

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: Fv light chain variable domain
B: Fv heavy chain variable domain
C: Fv light chain variable domain
D: Fv heavy chain variable domain
E: Fv light chain variable domain
F: Fv heavy chain variable domain
G: Fv light chain variable domain
H: Fv heavy chain variable domain
P: peptide antigen
Q: peptide antigen
R: peptide antigen
S: peptide antigen


Theoretical massNumber of molelcules
Total (without water)108,59312
Polymers108,59312
Non-polymers00
Water16,718928
1
A: Fv light chain variable domain
B: Fv heavy chain variable domain
P: peptide antigen


Theoretical massNumber of molelcules
Total (without water)27,1483
Polymers27,1483
Non-polymers00
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
C: Fv light chain variable domain
D: Fv heavy chain variable domain
Q: peptide antigen


Theoretical massNumber of molelcules
Total (without water)27,1483
Polymers27,1483
Non-polymers00
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area3510 Å2
ΔGint-12 kcal/mol
Surface area11040 Å2
MethodPISA
3
E: Fv light chain variable domain
F: Fv heavy chain variable domain
R: peptide antigen


Theoretical massNumber of molelcules
Total (without water)27,1483
Polymers27,1483
Non-polymers00
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
4
G: Fv light chain variable domain
H: Fv heavy chain variable domain
S: peptide antigen


Theoretical massNumber of molelcules
Total (without water)27,1483
Polymers27,1483
Non-polymers00
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area3430 Å2
ΔGint-13 kcal/mol
Surface area11120 Å2
MethodPISA
Unit cell
Length a, b, c (Å)50.128, 142.681, 75.306
Angle α, β, γ (deg.)90.00, 92.66, 90.00
Int Tables number4
Space group name H-MP1211

-
Components

#1: Antibody
Fv light chain variable domain


Mass: 12460.883 Da / Num. of mol.: 4
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Gene: VL / Plasmid: pET22b(+) / Species (production host): Escherichia coli / Production host: Escherichia coli BL21(DE3) (bacteria) / Strain (production host): BL21(DE3)
#2: Antibody
Fv heavy chain variable domain


Mass: 13330.936 Da / Num. of mol.: 4
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Gene: VH / Plasmid: pET22b(+) / Production host: Spodoptera frugiperda (fall armyworm) / Strain (production host): BL21 (DE3) / References: UniProt: A2NN81
#3: Protein/peptide
peptide antigen


Mass: 1356.355 Da / Num. of mol.: 4 / Source method: obtained synthetically / Details: synthetic peptide
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 928 / Source method: isolated from a natural source / Formula: H2O

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.48 Å3/Da / Density % sol: 50.33 %
Crystal growTemperature: 298 K / Method: evaporation / pH: 6
Details: 0.1 M sodium citrate, 0.2 M NH4Ac, 27.5% PEG 4000, pH 6.0, EVAPORATION, temperature 298K

-
Data collection

DiffractionMean temperature: 173 K
Diffraction sourceSource: SYNCHROTRON / Site: ALS / Beamline: 8.2.2 / Wavelength: 1
DetectorType: ADSC QUANTUM 315 / Detector: CCD / Date: Jan 1, 2006 / Details: Si(111)
RadiationMonochromator: Si (111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 1.68→41 Å / Num. all: 119617 / Num. obs: 116627 / % possible obs: 97.5 % / Redundancy: 4.4 % / Rmerge(I) obs: 0.046 / Rsym value: 4.3 / Net I/σ(I): 34.3
Reflection shellResolution: 1.68→1.74 Å / Redundancy: 3.5 % / Rmerge(I) obs: 0.258 / Mean I/σ(I) obs: 3.4 / Num. unique all: 10848 / Rsym value: 25.8 / % possible all: 91.1

-
Processing

Software
NameVersionClassification
HKL-2000data collection
MOLREPphasing
CNS1.1refinement
HKL-2000data reduction
HKL-2000data scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: PDB entry 2GSG
Resolution: 1.68→41 Å / Isotropic thermal model: isotropic / Cross valid method: THROUGHOUT / σ(F): 0 / σ(I): 0 / Stereochemistry target values: Engh & Huber
RfactorNum. reflection% reflectionSelection details
Rfree0.214 5765 -random
Rwork0.2 ---
all0.2 119819 --
obs0.2 114322 95.4 %-
Refinement stepCycle: LAST / Resolution: 1.68→41 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms7640 0 0 928 8568
Refine LS restraints
Refine-IDTypeDev ideal
X-RAY DIFFRACTIONc_angle_d1.36
X-RAY DIFFRACTIONc_bond_d0.007
LS refinement shellHighest resolution: 1.68 Å
RfactorNum. reflection
Rfree0.214 5765
Rwork0.2 -
obs-114322

+
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