[English] 日本語
Yorodumi
- PDB-4h1l: TCR interaction with peptide mimics of nickel offers structural i... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 4h1l
TitleTCR interaction with peptide mimics of nickel offers structural insights in nickel contact allergy
Components
  • Ani2.3 TCR A chain
  • Ani2.3 TCR B chain
  • HLA class II histocompatibility antigen, DR alpha chain
  • MHC class II antigen
  • mimotope peptide
KeywordsIMMUNE SYSTEM / PROTEIN-PROTEIN COMPLEX / immunoglobin fold / TCR recogniton of MHC / MHC II / glycosidation / membrane
Function / homology
Function and homology information


myeloid dendritic cell antigen processing and presentation / antigen processing and presentation of endogenous peptide antigen via MHC class II / autolysosome membrane / regulation of T-helper cell differentiation / positive regulation of CD4-positive, CD25-positive, alpha-beta regulatory T cell differentiation / MHC class II receptor activity / positive regulation of T cell mediated immune response to tumor cell / positive regulation of CD4-positive, alpha-beta T cell activation / antigen processing and presentation of peptide or polysaccharide antigen via MHC class II / positive regulation of memory T cell differentiation ...myeloid dendritic cell antigen processing and presentation / antigen processing and presentation of endogenous peptide antigen via MHC class II / autolysosome membrane / regulation of T-helper cell differentiation / positive regulation of CD4-positive, CD25-positive, alpha-beta regulatory T cell differentiation / MHC class II receptor activity / positive regulation of T cell mediated immune response to tumor cell / positive regulation of CD4-positive, alpha-beta T cell activation / antigen processing and presentation of peptide or polysaccharide antigen via MHC class II / positive regulation of memory T cell differentiation / polysaccharide binding / transport vesicle membrane / Translocation of ZAP-70 to Immunological synapse / Phosphorylation of CD3 and TCR zeta chains / Generation of second messenger molecules / immunological synapse / PD-1 signaling / T cell receptor binding / MHC class II antigen presentation / trans-Golgi network membrane / lumenal side of endoplasmic reticulum membrane / clathrin-coated endocytic vesicle membrane / ER to Golgi transport vesicle membrane / cognition / peptide antigen assembly with MHC class II protein complex / MHC class II protein complex / positive regulation of T cell mediated cytotoxicity / peptide antigen binding / antigen processing and presentation of exogenous peptide antigen via MHC class II / positive regulation of immune response / Interferon gamma signaling / endocytic vesicle membrane / positive regulation of T cell activation / Downstream TCR signaling / MHC class II protein complex binding / late endosome membrane / T cell receptor signaling pathway / early endosome membrane / adaptive immune response / lysosome / cell surface receptor signaling pathway / endosome membrane / immune response / lysosomal membrane / Golgi membrane / cell surface / signal transduction / extracellular exosome / membrane / plasma membrane
Similarity search - Function
: / : / Class II Histocompatibility Antigen, M Beta Chain; Chain B, domain 1 / Class II Histocompatibility Antigen, M Beta Chain; Chain B, domain 1 / MHC class II, beta chain, N-terminal / Class II histocompatibility antigen, beta domain / Class II histocompatibility antigen, beta domain / MHC class II, alpha chain, N-terminal / Class II histocompatibility antigen, alpha domain / Class II histocompatibility antigen, alpha domain ...: / : / Class II Histocompatibility Antigen, M Beta Chain; Chain B, domain 1 / Class II Histocompatibility Antigen, M Beta Chain; Chain B, domain 1 / MHC class II, beta chain, N-terminal / Class II histocompatibility antigen, beta domain / Class II histocompatibility antigen, beta domain / MHC class II, alpha chain, N-terminal / Class II histocompatibility antigen, alpha domain / Class II histocompatibility antigen, alpha domain / MHC class II, alpha/beta chain, N-terminal / Immunoglobulin V-Type / Immunoglobulin V-set domain / MHC classes I/II-like antigen recognition protein / 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 / Roll / Immunoglobulin-like fold / Immunoglobulin-like / Sandwich / Mainly Beta / Alpha Beta
Similarity search - Domain/homology
MHC class II antigen / Ani2.3 TCR A chain / Ani2.3 TCR B chain / HLA class II histocompatibility antigen, DR alpha chain / HLA class II histocompatibility antigen, DR beta 3 chain
Similarity search - Component
Biological speciesHomo sapiens (human)
Escherichia coli (E. coli)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 3.3 Å
AuthorsKappler, J.W. / Yin, L. / Dai, S. / Marrack, P.
CitationJournal: Proc.Natl.Acad.Sci.USA / Year: 2012
Title: T-cell receptor (TCR) interaction with peptides that mimic nickel offers insight into nickel contact allergy.
Authors: Yin, L. / Crawford, F. / Marrack, P. / Kappler, J.W. / Dai, S.
History
DepositionSep 10, 2012Deposition site: RCSB / Processing site: RCSB
Revision 1.0Nov 14, 2012Provider: repository / Type: Initial release
Revision 1.1Sep 4, 2013Group: Database references

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: HLA class II histocompatibility antigen, DR alpha chain
B: MHC class II antigen
C: mimotope peptide
D: HLA class II histocompatibility antigen, DR alpha chain
E: MHC class II antigen
F: mimotope peptide
G: Ani2.3 TCR A chain
H: Ani2.3 TCR B chain
I: Ani2.3 TCR A chain
J: Ani2.3 TCR B chain


Theoretical massNumber of molelcules
Total (without water)138,35310
Polymers138,35310
Non-polymers00
Water00
1
A: HLA class II histocompatibility antigen, DR alpha chain
B: MHC class II antigen
C: mimotope peptide
I: Ani2.3 TCR A chain
J: Ani2.3 TCR B chain


Theoretical massNumber of molelcules
Total (without water)69,1775
Polymers69,1775
Non-polymers00
Water0
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
D: HLA class II histocompatibility antigen, DR alpha chain
E: MHC class II antigen
F: mimotope peptide
G: Ani2.3 TCR A chain
H: Ani2.3 TCR B chain


Theoretical massNumber of molelcules
Total (without water)69,1775
Polymers69,1775
Non-polymers00
Water0
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)186.722, 186.722, 166.702
Angle α, β, γ (deg.)90.00, 90.00, 120.00
Int Tables number173
Space group name H-MP63
Noncrystallographic symmetry (NCS)NCS domain:
IDEns-ID
11
21
12
22
13
23
14
24
15
25

NCS domain segments:
Dom-IDComponent-IDEns-IDSelection details
111chain B and (resseq 4:105 or resseq 114:190 )
211chain E and (resseq 4:105 or resseq 114:190 )
112chain A and (resseq 3:180 )
212chain D and (resseq 3:180 )
113chain G and (resseq 1:113 )
213chain I and (resseq 1:113 )
114chain H and (resseq 1:111 )
214chain J and (resseq 1:111 )
115chain C and (resseq -1:11 )
215chain F and (resseq -1:11 )

NCS ensembles :
ID
1
2
3
4
5

-
Components

#1: Protein HLA class II histocompatibility antigen, DR alpha chain / MHC class II antigen DRA


Mass: 20727.402 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-DRA, HLA-DRA1 / Plasmid: baculovirus / Production host: HOMO SAPIENS (human) / References: UniProt: P01903
#2: Protein MHC class II antigen


Mass: 21848.451 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-DRB3 / Plasmid: baculovirus / Production host: HOMO SAPIENS (human) / References: UniProt: D0AB36, UniProt: P79483*PLUS
#3: Protein/peptide mimotope peptide


Mass: 1539.848 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Escherichia coli (E. coli) / Production host: Escherichia coli (E. coli)
#4: Antibody Ani2.3 TCR A chain


Mass: 12426.917 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Escherichia coli (E. coli) / Production host: Escherichia coli (E. coli) / References: UniProt: L7MTK9*PLUS
#5: Protein Ani2.3 TCR B chain


Mass: 12634.044 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Escherichia coli (E. coli) / Production host: Escherichia coli (E. coli) / References: UniProt: L7MTL0*PLUS
Sequence detailsTHESE MISMATCHES ARE CONSEQUENCE OF A GENE RARE ALLELE OF HUMAN DR GENE (DR52C)

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 6.15 Å3/Da / Density % sol: 80 %
Crystal growTemperature: 298 K / Method: vapor diffusion, hanging drop / pH: 7
Details: 0.1M Ammonium tartrate dibasic, 12% PEG 3350 , pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 298K

-
Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: ALS / Beamline: 8.2.2 / Wavelength: 1 Å
DetectorType: ADSC QUANTUM 315 / Detector: CCD
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 3.3→20 Å / Num. all: 50237 / Num. obs: 46186 / % possible obs: 91.9 % / Observed criterion σ(F): 2 / Observed criterion σ(I): 2

-
Processing

Software
NameVersionClassification
HKL-2000data collection
PHASESphasing
PHENIX(phenix.refine: 1.7_629)refinement
HKL-2000data reduction
HKL-2000data scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 3.3→19.826 Å / SU ML: 0.48 / σ(F): 0 / Phase error: 30.15 / Stereochemistry target values: ML
RfactorNum. reflection% reflectionSelection details
Rfree0.2846 2346 4.37 %RANDOM
Rwork0.2633 ---
obs0.2643 44267 87.93 %-
all-50343 --
Solvent computationShrinkage radii: 0.83 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL / Bsol: 15.192 Å2 / ksol: 0.241 e/Å3
Displacement parameters
Baniso -1Baniso -2Baniso -3
1-12.0564 Å2-0 Å2-0 Å2
2--12.0564 Å20 Å2
3----24.1129 Å2
Refinement stepCycle: LAST / Resolution: 3.3→19.826 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms9630 0 0 0 9630
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0139894
X-RAY DIFFRACTIONf_angle_d1.50213408
X-RAY DIFFRACTIONf_dihedral_angle_d20.0123602
X-RAY DIFFRACTIONf_chiral_restr0.0921426
X-RAY DIFFRACTIONf_plane_restr0.0061750
Refine LS restraints NCS
Ens-IDDom-IDAuth asym-IDNumberRefine-IDTypeRms dev position (Å)
11B1475X-RAY DIFFRACTIONPOSITIONAL
12E1475X-RAY DIFFRACTIONPOSITIONAL0.045
21A1465X-RAY DIFFRACTIONPOSITIONAL
22D1465X-RAY DIFFRACTIONPOSITIONAL0.069
31G878X-RAY DIFFRACTIONPOSITIONAL
32I878X-RAY DIFFRACTIONPOSITIONAL0.085
41H890X-RAY DIFFRACTIONPOSITIONAL
42J890X-RAY DIFFRACTIONPOSITIONAL0.075
51C107X-RAY DIFFRACTIONPOSITIONAL
52F107X-RAY DIFFRACTIONPOSITIONAL0.058
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
3.2791-3.36070.4314740.44071629X-RAY DIFFRACTION48
3.3607-3.45110.4281970.42982113X-RAY DIFFRACTION62
3.4511-3.55210.39171210.41442566X-RAY DIFFRACTION75
3.5521-3.66610.41381460.39172977X-RAY DIFFRACTION87
3.6661-3.79620.3751400.35733096X-RAY DIFFRACTION90
3.7962-3.94710.34631410.33373126X-RAY DIFFRACTION92
3.9471-4.12520.31881410.28453154X-RAY DIFFRACTION92
4.1252-4.34050.23821470.25593283X-RAY DIFFRACTION95
4.3405-4.60930.2631480.22743308X-RAY DIFFRACTION96
4.6093-4.960.23761540.20723334X-RAY DIFFRACTION98
4.96-5.44970.22171560.21053401X-RAY DIFFRACTION98
5.4497-6.21690.23181530.21363415X-RAY DIFFRACTION99
6.2169-7.7540.25231590.21033438X-RAY DIFFRACTION99
7.754-19.82640.24631570.213493X-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