[English] 日本語
Yorodumi
- PDB-8slr: Crystal Structure of mouse TRAIL -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 8slr
TitleCrystal Structure of mouse TRAIL
ComponentsTumor necrosis factor ligand superfamily member 10
KeywordsCYTOKINE / TRAIL / APOPTOSIS / PRO-APOPTOTIC / TNF SUPERFAMILY
Function / homology
Function and homology information


TRAIL signaling / Regulation by c-FLIP / CASP8 activity is inhibited / Dimerization of procaspase-8 / TRAIL binding / tumor necrosis factor receptor superfamily binding / tumor necrosis factor receptor binding / positive regulation of extrinsic apoptotic signaling pathway / positive regulation of release of cytochrome c from mitochondria / cytokine activity ...TRAIL signaling / Regulation by c-FLIP / CASP8 activity is inhibited / Dimerization of procaspase-8 / TRAIL binding / tumor necrosis factor receptor superfamily binding / tumor necrosis factor receptor binding / positive regulation of extrinsic apoptotic signaling pathway / positive regulation of release of cytochrome c from mitochondria / cytokine activity / response to insulin / male gonad development / positive regulation of canonical NF-kappaB signal transduction / immune response / positive regulation of apoptotic process / apoptotic process / extracellular space / zinc ion binding / identical protein binding / plasma membrane
Similarity search - Function
Tumour necrosis factor ligand 10/11 / Tumour necrosis factor, conserved site / Tumor necrosis factor (TNF) homology domain (THD) signature. / Tumour necrosis factor family. / TNF(Tumour Necrosis Factor) family / Tumour necrosis factor domain / Tumor necrosis factor (TNF) homology domain (THD) profile. / Tumour necrosis factor-like domain superfamily
Similarity search - Domain/homology
DI(HYDROXYETHYL)ETHER / Tumor necrosis factor ligand superfamily member 10
Similarity search - Component
Biological speciesMus musculus (house mouse)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.4 Å
AuthorsPedersen, L.C. / Xu, D.
Funding support United States, 2items
OrganizationGrant numberCountry
National Institutes of Health/National Institute of Environmental Health Sciences (NIH/NIEHS)ZIC-ES102645 United States
National Institutes of Health/National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIH/NIAMS)AR070179 United States
CitationJournal: Elife / Year: 2024
Title: Heparan sulfate promotes TRAIL-induced tumor cell apoptosis.
Authors: Luo, Y. / Hao, H. / Wang, Z. / Ong, C.Y. / Dutcher, R. / Xu, Y. / Liu, J. / Pedersen, L.C. / Xu, D.
History
DepositionApr 24, 2023Deposition site: RCSB / Processing site: RCSB
Revision 1.0Apr 3, 2024Provider: repository / Type: Initial release

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
D: Tumor necrosis factor ligand superfamily member 10
hetero molecules


Theoretical massNumber of molelcules
Total (without water)20,5647
Polymers20,2241
Non-polymers3406
Water1,856103
1
D: Tumor necrosis factor ligand superfamily member 10
hetero molecules

D: Tumor necrosis factor ligand superfamily member 10
hetero molecules

D: Tumor necrosis factor ligand superfamily member 10
hetero molecules


Theoretical massNumber of molelcules
Total (without water)61,69221
Polymers60,6723
Non-polymers1,02018
Water543
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
crystal symmetry operation5_555z,x,y1
crystal symmetry operation9_555y,z,x1
Buried area15660 Å2
ΔGint-186 kcal/mol
Surface area17020 Å2
MethodPISA
Unit cell
Length a, b, c (Å)147.350, 147.350, 147.350
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number213
Space group name H-MP4132
Space group name HallP4bd2ab3
Symmetry operation#1: x,y,z
#2: x+1/4,-z+1/4,y+3/4
#3: x+3/4,z+1/4,-y+1/4
#4: z+3/4,y+1/4,-x+1/4
#5: -z+1/4,y+3/4,x+1/4
#6: -y+1/4,x+3/4,z+1/4
#7: y+1/4,-x+1/4,z+3/4
#8: z,x,y
#9: y,z,x
#10: -y+1/2,-z,x+1/2
#11: z+1/2,-x+1/2,-y
#12: -y,z+1/2,-x+1/2
#13: -z+1/2,-x,y+1/2
#14: -z,x+1/2,-y+1/2
#15: y+1/2,-z+1/2,-x
#16: x+1/2,-y+1/2,-z
#17: -x,y+1/2,-z+1/2
#18: -x+1/2,-y,z+1/2
#19: y+3/4,x+1/4,-z+1/4
#20: -y+3/4,-x+3/4,-z+3/4
#21: z+1/4,-y+1/4,x+3/4
#22: -z+3/4,-y+3/4,-x+3/4
#23: -x+1/4,z+3/4,y+1/4
#24: -x+3/4,-z+3/4,-y+3/4
Components on special symmetry positions
IDModelComponents
11D-301-

ZN

21D-302-

CL

31D-467-

HOH

41D-482-

HOH

51D-503-

HOH

-
Components

-
Protein , 1 types, 1 molecules D

#1: Protein Tumor necrosis factor ligand superfamily member 10 / TNF-related apoptosis-inducing ligand / Protein TRAIL


Mass: 20223.967 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Gene: Tnfsf10, Trail / Production host: Escherichia coli (E. coli) / Strain (production host): Origami-B / References: UniProt: P50592

-
Non-polymers , 5 types, 109 molecules

#2: Chemical ChemComp-ZN / ZINC ION


Mass: 65.409 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Zn
#3: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: Cl
#4: Chemical ChemComp-PEG / DI(HYDROXYETHYL)ETHER


Mass: 106.120 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C4H10O3
#5: Chemical ChemComp-EDO / 1,2-ETHANEDIOL / ETHYLENE GLYCOL


Mass: 62.068 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C2H6O2
#6: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 103 / Source method: isolated from a natural source / Formula: H2O

-
Details

Has ligand of interestN

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 6.59 Å3/Da / Density % sol: 81.34 %
Crystal growTemperature: 277 K / Method: vapor diffusion, sitting drop
Details: Protein: 4.4mg/ml Trail+ 1mM 12merNS2S6S in 25mM HEPES pH 7.1, 150mM NaCl Reservoir: 0.085M HEPES pH 7.5, 8.5% PEG 8000, 8.5%EG

-
Data collection

DiffractionMean temperature: 173 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: APS / Beamline: 22-ID / Wavelength: 1 Å
DetectorType: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Feb 12, 2022
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 2.4→50 Å / Num. obs: 22033 / % possible obs: 99.9 % / Redundancy: 9.4 % / Biso Wilson estimate: 40.51 Å2 / CC1/2: 0.994 / CC star: 0.998 / Net I/σ(I): 4.6
Reflection shellResolution: 2.4→2.44 Å / Redundancy: 9.9 % / Mean I/σ(I) obs: 1.8 / Num. unique obs: 1097 / CC1/2: 0.784 / CC star: 0.937 / % possible all: 100

-
Processing

Software
NameVersionClassification
PHENIX1.20.1_4487refinement
HKL-2000data reduction
HKL-2000data scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 1DU3
Resolution: 2.4→44.43 Å / SU ML: 0.1919 / Cross valid method: FREE R-VALUE / σ(F): 1.38 / Phase error: 15.955
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.1825 1089 4.99 %
Rwork0.1598 20722 -
obs0.1609 21811 99.1 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 47.57 Å2
Refinement stepCycle: LAST / Resolution: 2.4→44.43 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1250 0 15 103 1368
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00611358
X-RAY DIFFRACTIONf_angle_d0.81631837
X-RAY DIFFRACTIONf_chiral_restr0.0566193
X-RAY DIFFRACTIONf_plane_restr0.0076238
X-RAY DIFFRACTIONf_dihedral_angle_d14.6437498
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.4-2.510.24391330.23232518X-RAY DIFFRACTION98.29
2.51-2.640.21661300.19592512X-RAY DIFFRACTION98.51
2.64-2.810.18421350.18222523X-RAY DIFFRACTION98.85
2.81-3.020.18661360.18752564X-RAY DIFFRACTION99.08
3.02-3.330.17711330.15952557X-RAY DIFFRACTION99.23
3.33-3.810.17251360.15172606X-RAY DIFFRACTION99.89
3.81-4.80.1421400.11872645X-RAY DIFFRACTION99.79
4.8-44.430.21491460.16852797X-RAY DIFFRACTION99.16
Refinement TLS params.

Method: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
12.9442262318-0.6871754126583.339231247556.11383842557-0.1852308598689.512437393760.4174989487650.4810514303030.4946642289930.346924602259-0.182524253870.106241619497-0.1012917604120.4315298686190.2358288513470.366303736758-0.002230616586770.09469322302280.222672210856-0.003872452828450.312735755422.068208839428.35568000939.89880976035
24.20355470658-2.24105252099-1.011593104091.44048963713-0.5260941113855.081864577580.236875290587-1.228740140270.9461399143490.132560137770.04656605677250.7106414502191.715722576320.374651550784-0.3621931255481.214165993780.00292525279885-0.2896358250660.860926026234-0.06372943126781.039711382753.7703353977625.2241858302-2.39792374384
36.29672848999-5.31994742245.608029388145.05717971713-3.916664541516.248412472570.3806704576750.564137754099-0.322795043547-1.23627788476-0.193670352642-0.3823665723630.1944713076690.435903399515-0.3367590750680.5480008357480.08762145325890.02136064593630.444707425755-0.0447898062590.392360468895-4.1680670381929.34989711936.2758051582
48.77034532274-2.916594306265.235024483023.54518173771-1.693609617633.1579173432-0.46521179815-0.780775595058-0.5937336874130.613816094970.5975993186760.584396153617-0.454566479569-0.576567501151-0.2528127382310.3747793836180.05465866552080.07656464677960.5111353396710.06831775181250.4118904157630.48376637375519.8218475227.3812567607
51.719661700490.174804945108-0.2599067010892.281310305760.9114266202651.485161771770.0174717998697-0.2234091418010.03935559680370.170690380103-0.004641205881940.0678626138191-0.112530613776-0.0528455660027-0.01564970941810.2818524069380.0366392239664-0.03126862688970.353194653360.0264844902480.249872106337.1691122640323.069231451923.4409096637
61.435671748480.154442275671-0.06833164175354.973071347231.246173601872.487916611620.02193797006450.222140780278-0.116466074766-0.1666734866240.009213601789190.05982423179960.135408355576-0.133801732114-0.02402460405320.3138184541690.0319452868982-0.01544944721630.386591726233-0.003389032606880.3137686379062.31415579822.73683934158.88408942754
71.29769626573-0.3395164077060.3414979301381.922295714420.7292537917381.76484042575-0.003913520205760.0871955401213-0.247854456808-0.2161030949160.03035386195330.2367476029230.152179104583-0.26731274963-0.1298911955240.342839412054-0.00782470681322-0.02144317728640.385067265245-0.00551298509780.3612937441583.7232802379910.92936436099.55595479507
86.462523467244.174128695744.077646251413.831683921544.098322053844.89587512580.027482309317-0.02852326318380.06738979079560.02075002216280.07228419089150.0364604098705-0.104843867087-0.0194245868841-0.07690750409060.2473004649420.04560871825430.0006827770420620.2704027575850.01034101931330.1980825435994.5593832364731.197957734119.0438617394
97.382020767991.127250405994.716265199391.716612988280.04144755870423.357847683510.124261989051-0.865080233403-0.1586125533670.129975974598-0.04894184865880.03760994859750.10349238253-1.07641826488-0.123412872450.331147286129-0.01990938997650.00499150079780.4765601032960.02917597435080.47017510807-2.4054596261712.305767809218.7122942154
103.090068559680.233518070869-1.392044628712.240399229-0.5826925103146.834118304710.346454662809-0.3674407090590.1060408902980.371593619678-0.1851432114-0.430221783997-0.1021640031420.685808077274-0.20931753860.2810831849870.0563206393365-0.04394633482440.301703399267-0.05159283818570.2995980509814.578948943423.806079466622.6194302851
Refinement TLS group

Refine-ID: X-RAY DIFFRACTION / Auth asym-ID: D / Label asym-ID: A

IDRefine TLS-IDSelection detailsAuth seq-IDLabel seq-ID
11chain 'D' and (resid 124 through 133 )124 - 1331 - 10
22chain 'D' and (resid 134 through 143 )134 - 14311 - 20
33chain 'D' and (resid 144 through 153 )144 - 15321 - 30
44chain 'D' and (resid 154 through 163 )154 - 16331 - 40
55chain 'D' and (resid 164 through 197 )164 - 19741 - 74
66chain 'D' and (resid 198 through 232 )198 - 23275 - 102
77chain 'D' and (resid 233 through 254 )233 - 254103 - 124
88chain 'D' and (resid 255 through 264 )255 - 264125 - 134
99chain 'D' and (resid 265 through 277 )265 - 277135 - 147
1010chain 'D' and (resid 278 through 285 )278 - 285148 - 155

+
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://pdbjlvh1.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