[English] 日本語
Yorodumi
- PDB-1f11: F124 FAB FRAGMENT FROM A MONOCLONAL ANTI-PRES2 ANTIBODY -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 1f11
TitleF124 FAB FRAGMENT FROM A MONOCLONAL ANTI-PRES2 ANTIBODY
Components
  • F124 IMMUNOGLOBULIN (IGG1 HEAVY CHAIN)
  • F124 IMMUNOGLOBULIN (KAPPA LIGHT CHAIN)
KeywordsIMMUNE SYSTEM / immunoglobulin / antibody / fab / hepatitis B / preS2
Function / homology
Function and homology information


Initial triggering of complement / Classical antibody-mediated complement activation / FCGR activation / Role of phospholipids in phagocytosis / Regulation of Complement cascade / Regulation of actin dynamics for phagocytic cup formation / phagocytosis, recognition / humoral immune response mediated by circulating immunoglobulin / positive regulation of type IIa hypersensitivity / positive regulation of type I hypersensitivity ...Initial triggering of complement / Classical antibody-mediated complement activation / FCGR activation / Role of phospholipids in phagocytosis / Regulation of Complement cascade / Regulation of actin dynamics for phagocytic cup formation / phagocytosis, recognition / humoral immune response mediated by circulating immunoglobulin / positive regulation of type IIa hypersensitivity / positive regulation of type I hypersensitivity / antibody-dependent cellular cytotoxicity / phagocytosis, engulfment / immunoglobulin complex, circulating / immunoglobulin receptor binding / immunoglobulin complex / immunoglobulin mediated immune response / complement activation, classical pathway / positive regulation of phagocytosis / antigen binding / B cell differentiation / positive regulation of immune response / antibacterial humoral response / blood microparticle / adaptive immune response / defense response to bacterium / immune response / external side of plasma membrane / extracellular space / extracellular exosome / extracellular region / metal ion binding / plasma membrane / cytoplasm
Similarity search - Function
: / : / : / Immunoglobulin V-Type / Immunoglobulin V-set domain / Immunoglobulin V-set domain / : / Immunoglobulin subtype / Immunoglobulin / Immunoglobulin/major histocompatibility complex, conserved site ...: / : / : / Immunoglobulin V-Type / Immunoglobulin V-set domain / Immunoglobulin V-set domain / : / Immunoglobulin subtype / Immunoglobulin / Immunoglobulin/major histocompatibility complex, conserved site / Immunoglobulins and major histocompatibility complex proteins signature. / Immunoglobulin C-Type / Immunoglobulin C1-set / Immunoglobulin C1-set domain / Ig-like domain profile. / Immunoglobulin-like domain / Immunoglobulin-like domain superfamily / Immunoglobulins / Immunoglobulin-like fold / Immunoglobulin-like / Sandwich / Mainly Beta
Similarity search - Domain/homology
Ig kappa chain V-III region PC 7043 / Immunoglobulin kappa constant / Ig gamma-1 chain C region, membrane-bound form / Ab 126.33 heavy chain variable and joining regions / Ig-like domain-containing protein
Similarity search - Component
Biological speciesMus musculus (house mouse)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 3 Å
AuthorsSaul, F.A. / Vulliez-Le Normand, B. / Passafiume, M. / Riottot, M.M. / Bentley, G.A.
Citation
Journal: Acta Crystallogr.,Sect.D / Year: 2000
Title: Structure of the Fab fragment from F124, a monoclonal antibody specific for hepatitis B surface antigen.
Authors: Saul, F.A. / Vulliez-Le Normand, B. / Passafiume, M. / Riottot, M.M. / Bentley, G.A.
#1: Journal: FEBS Lett. / Year: 1998
Title: Sequence Analysis of a Monoclonal Antibody Specific for the preS2 Region of Hepatitis B Surface Antigen, and the Cloning, Expression and Characterisation of its Single-chain Fv Construction
Authors: Passafiume, M. / Vulliez-le Normand, B. / Riottot, M.M. / Bentley, G.A.
History
DepositionMay 18, 2000Deposition site: RCSB / Processing site: RCSB
Revision 1.0Aug 30, 2000Provider: repository / Type: Initial release
Revision 1.1Apr 27, 2008Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3Jun 21, 2017Group: Database references / Source and taxonomy / Structure summary
Category: entity / entity_src_nat ...entity / entity_src_nat / struct_ref / struct_ref_seq / struct_ref_seq_dif
Item: _entity.pdbx_fragment / _struct_ref.db_code ..._entity.pdbx_fragment / _struct_ref.db_code / _struct_ref.db_name / _struct_ref.pdbx_align_begin / _struct_ref.pdbx_db_accession / _struct_ref.pdbx_seq_one_letter_code / _struct_ref_seq.db_align_beg / _struct_ref_seq.db_align_end / _struct_ref_seq.pdbx_auth_seq_align_beg / _struct_ref_seq.pdbx_auth_seq_align_end / _struct_ref_seq.pdbx_db_accession / _struct_ref_seq.seq_align_beg / _struct_ref_seq.seq_align_end
Revision 1.4Aug 9, 2023Group: Advisory / Data collection ...Advisory / 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 / pdbx_unobs_or_zero_occ_atoms / pdbx_unobs_or_zero_occ_residues
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: F124 IMMUNOGLOBULIN (KAPPA LIGHT CHAIN)
B: F124 IMMUNOGLOBULIN (IGG1 HEAVY CHAIN)
C: F124 IMMUNOGLOBULIN (KAPPA LIGHT CHAIN)
D: F124 IMMUNOGLOBULIN (IGG1 HEAVY CHAIN)


Theoretical massNumber of molelcules
Total (without water)95,1594
Polymers95,1594
Non-polymers00
Water00
1
A: F124 IMMUNOGLOBULIN (KAPPA LIGHT CHAIN)
B: F124 IMMUNOGLOBULIN (IGG1 HEAVY CHAIN)


Theoretical massNumber of molelcules
Total (without water)47,5802
Polymers47,5802
Non-polymers00
Water0
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area3150 Å2
ΔGint-20 kcal/mol
Surface area19250 Å2
MethodPISA
2
C: F124 IMMUNOGLOBULIN (KAPPA LIGHT CHAIN)
D: F124 IMMUNOGLOBULIN (IGG1 HEAVY CHAIN)


Theoretical massNumber of molelcules
Total (without water)47,5802
Polymers47,5802
Non-polymers00
Water0
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area3230 Å2
ΔGint-20 kcal/mol
Surface area19100 Å2
MethodPISA
Unit cell
Length a, b, c (Å)135.7, 54.0, 120.0
Angle α, β, γ (deg.)90.0, 101.0, 90.0
Int Tables number5
Space group name H-MC121

-
Components

#1: Antibody F124 IMMUNOGLOBULIN (KAPPA LIGHT CHAIN)


Mass: 23985.342 Da / Num. of mol.: 2
Fragment: FAB FRAGMENT (UNP P01665 residues 1-111, P01837 residues 1-106)
Source method: isolated from a natural source / Source: (natural) Mus musculus (house mouse) / References: UniProt: P01665, UniProt: P01837
#2: Antibody F124 IMMUNOGLOBULIN (IGG1 HEAVY CHAIN)


Mass: 23594.383 Da / Num. of mol.: 2
Fragment: FAB FRAGMENT (UNP Q65ZR6 residues 18-134, P01869 residues 2-102)
Source method: isolated from a natural source / Source: (natural) Mus musculus (house mouse)
References: UniProt: Q65ZR6, UniProt: P01869, UniProt: Q9D8L4*PLUS
Compound detailsantibody F124 (isotype IgG1, kappa light chain) recognizes an epitope in the segment 120-132 of the ...antibody F124 (isotype IgG1, kappa light chain) recognizes an epitope in the segment 120-132 of the preS2 region of the hepatitis B surface antigen.

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.3 Å3/Da / Density % sol: 45.73 %
Crystal growTemperature: 290 K / Method: vapor diffusion, hanging drop / pH: 4.6
Details: PEG 400, sodium acetate, ammonium sulfate, pH 4.6, VAPOR DIFFUSION, HANGING DROP, temperature 290K
Crystal grow
*PLUS
Method: vapor diffusion
Components of the solutions
*PLUS
IDConc.Common nameCrystal-IDSol-ID
12 Mammonium sulfate1reservoir
20.1 Msodium acetate1reservoir
35 %PEG4001reservoir
42.4 mg/mlprotein1drop
50.57 Mammonium sulfate1drop
60.028 Msodium acetate1drop
71.4 %PEG4001drop

-
Data collection

DiffractionMean temperature: 298 K
Diffraction sourceSource: SYNCHROTRON / Site: LURE / Beamline: DW32 / Wavelength: 0.96
DetectorType: MARRESEARCH / Detector: IMAGE PLATE / Date: Apr 1, 1999
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.96 Å / Relative weight: 1
ReflectionResolution: 3→30 Å / Num. all: 17261 / Num. obs: 17261 / % possible obs: 99.2 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / Redundancy: 1.9 % / Biso Wilson estimate: 30.6 Å2 / Rmerge(I) obs: 0.131 / Net I/σ(I): 6.7
Reflection shellResolution: 3→3.11 Å / Redundancy: 1.9 % / Rmerge(I) obs: 0.479 / Mean I/σ(I) obs: 1.8 / Num. unique all: 1665 / % possible all: 97.5
Reflection
*PLUS
Reflection shell
*PLUS
% possible obs: 97.5 % / Num. unique obs: 1665

-
Processing

Software
NameVersionClassification
DENZOdata reduction
SCALEPACKdata scaling
AMoREphasing
X-PLOR3.851refinement
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 1IGI
Resolution: 3→30 Å / σ(F): 0 / σ(I): 0 / Stereochemistry target values: Engh & Huber
Details: A bulk solvent model was used. Non-crystallographic symmetry restraints were applied. NCS GROUP 1: chains A,C (1 to 109). NCS GROUP 2: chains A,C (114 to 198, 203 to 212). NCS GROUP 3: ...Details: A bulk solvent model was used. Non-crystallographic symmetry restraints were applied. NCS GROUP 1: chains A,C (1 to 109). NCS GROUP 2: chains A,C (114 to 198, 203 to 212). NCS GROUP 3: chains B,D (1 to 40, 43 to 112). NCS GROUP 4: chains B,D (115 to 127, 137 to 227).
RfactorNum. reflection% reflectionSelection details
Rfree0.271 878 5 %RANDOM
Rwork0.184 ---
all0.191 17261 --
obs0.191 17261 99.2 %-
Refinement stepCycle: LAST / Resolution: 3→30 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms6598 0 0 0 6598
Refine LS restraints
Refine-IDTypeDev idealDev ideal target
X-RAY DIFFRACTIONx_bond_d0.008
X-RAY DIFFRACTIONx_angle_deg1.4
X-RAY DIFFRACTIONx_dihedral_angle_d29.7
X-RAY DIFFRACTIONx_improper_angle_d0.68
X-RAY DIFFRACTIONx_mcbond_it2
X-RAY DIFFRACTIONx_mcangle_it2.5
X-RAY DIFFRACTIONx_scbond_it2
X-RAY DIFFRACTIONx_scangle_it2.5
Refine LS restraints NCSNCS model details: RESTRAINED
LS refinement shellResolution: 3→3.14 Å / Total num. of bins used: 8
RfactorNum. reflection% reflection
Rfree0.35 124 5 %
Rwork0.25 1991 -
obs--98 %
Xplor fileSerial no: 1 / Param file: PARHCSDX.PRO / Topol file: TOPHCSDX.PRO
Software
*PLUS
Name: X-PLOR / Version: 3.851 / Classification: refinement
Refinement
*PLUS
Highest resolution: 3 Å / Lowest resolution: 30 Å / σ(F): 0 / % reflection Rfree: 5 % / Rfactor obs: 0.184
Solvent computation
*PLUS
Displacement parameters
*PLUS
Biso mean: 23.2 Å2
Refine LS restraints
*PLUS
Refine-IDTypeDev idealDev ideal target
X-RAY DIFFRACTIONx_angle_deg1.4
X-RAY DIFFRACTIONx_dihedral_angle_d
X-RAY DIFFRACTIONx_dihedral_angle_deg29.7
X-RAY DIFFRACTIONx_improper_angle_d
X-RAY DIFFRACTIONx_improper_angle_deg0.68
X-RAY DIFFRACTIONx_mcbond_it2
X-RAY DIFFRACTIONx_scbond_it2
X-RAY DIFFRACTIONx_mcangle_it2.5
X-RAY DIFFRACTIONx_scangle_it2.5
LS refinement shell
*PLUS
Rfactor Rfree: 0.35 / % reflection Rfree: 5 % / Rfactor Rwork: 0.25 / Rfactor obs: 0.271

+
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