[English] 日本語
Yorodumi
- PDB-3mxm: TREX1 3' Exonuclease V201D Aicardi-Goutieres Syndrome Mutant -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 3mxm
TitleTREX1 3' Exonuclease V201D Aicardi-Goutieres Syndrome Mutant
Components
  • DNA (5'-D(*GP*AP*CP*G)-3')
  • Three prime repair exonuclease 1
KeywordsHYDROLASE/DNA / RNase H-like fold / Polyproline type II helix / HYDROLASE-DNA complex
Function / homology
Function and homology information


immune response in brain or nervous system / adenyl deoxyribonucleotide binding / CD86 biosynthetic process / immune complex formation / cellular response to type I interferon / organ or tissue specific immune response / activation of immune response / DNA synthesis involved in UV-damage excision repair / atrial cardiac muscle tissue development / MutSalpha complex binding ...immune response in brain or nervous system / adenyl deoxyribonucleotide binding / CD86 biosynthetic process / immune complex formation / cellular response to type I interferon / organ or tissue specific immune response / activation of immune response / DNA synthesis involved in UV-damage excision repair / atrial cardiac muscle tissue development / MutSalpha complex binding / T cell antigen processing and presentation / retrotransposition / oligosaccharyltransferase complex / regulation of lysosome organization / regulation of lipid biosynthetic process / DNA modification / regulation of fatty acid metabolic process / heart process / regulation of protein complex stability / MutLalpha complex binding / cellular response to hydroxyurea / lymphoid progenitor cell differentiation / regulation of type I interferon production / exodeoxyribonuclease III / double-stranded DNA 3'-5' DNA exonuclease activity / regulation of immunoglobulin production / 3'-5'-DNA exonuclease activity / macrophage activation involved in immune response / regulation of tumor necrosis factor production / regulation of T cell activation / DNA catabolic process / regulation of cellular respiration / negative regulation of cGAS/STING signaling pathway / inflammatory response to antigenic stimulus / apoptotic cell clearance / regulation of glycolytic process / DNA binding, bending / DNA metabolic process / DNA duplex unwinding / negative regulation of type I interferon-mediated signaling pathway / WW domain binding / type I interferon-mediated signaling pathway / regulation of innate immune response / blood vessel development / nuclear replication fork / cellular response to interferon-beta / heart morphogenesis / mitotic G1 DNA damage checkpoint signaling / response to UV / negative regulation of innate immune response / 3'-5' exonuclease activity / kidney development / DNA damage checkpoint signaling / protein-DNA complex / determination of adult lifespan / generation of precursor metabolites and energy / establishment of protein localization / cellular response to gamma radiation / cellular response to reactive oxygen species / cellular response to UV / single-stranded DNA binding / cellular response to oxidative stress / regulation of inflammatory response / double-stranded DNA binding / regulation of gene expression / defense response to virus / adaptive immune response / DNA replication / protein stabilization / inflammatory response / immune response / innate immune response / DNA damage response / magnesium ion binding / endoplasmic reticulum / protein homodimerization activity / DNA binding / identical protein binding / nucleus / cytosol / cytoplasm
Similarity search - Function
Three-prime repair exonuclease 1/2 / Exonuclease, RNase T/DNA polymerase III / EXOIII / Ribonuclease H-like superfamily/Ribonuclease H / Nucleotidyltransferase; domain 5 / Ribonuclease H superfamily / Ribonuclease H-like superfamily / 2-Layer Sandwich / Alpha Beta
Similarity search - Domain/homology
IODIDE ION / DNA / Three-prime repair exonuclease 1
Similarity search - Component
Biological speciesMus musculus (house mouse)
MethodX-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 1.75 Å
AuthorsBailey, S.L. / Hollis, T.
CitationJournal: To be Published
Title: X-ray Crystal Structures of TREX1 3' Exonuclease Autoimmune Disease Mutants
Authors: Bailey, S.L. / Harvey, S. / Perrino, F.W. / Hollis, T.
History
DepositionMay 7, 2010Deposition site: RCSB / Processing site: RCSB
Revision 1.0May 18, 2011Provider: repository / Type: Initial release
Revision 1.1Jul 13, 2011Group: Version format compliance
Revision 1.2Feb 21, 2024Group: Data collection / Database references / Derived calculations
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_struct_conn_angle / struct_conn / struct_ref_seq_dif / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _pdbx_struct_conn_angle.ptnr1_auth_asym_id / _pdbx_struct_conn_angle.ptnr1_auth_comp_id / _pdbx_struct_conn_angle.ptnr1_auth_seq_id / _pdbx_struct_conn_angle.ptnr1_label_asym_id / _pdbx_struct_conn_angle.ptnr1_label_atom_id / _pdbx_struct_conn_angle.ptnr1_label_comp_id / _pdbx_struct_conn_angle.ptnr1_label_seq_id / _pdbx_struct_conn_angle.ptnr2_auth_asym_id / _pdbx_struct_conn_angle.ptnr2_auth_seq_id / _pdbx_struct_conn_angle.ptnr2_label_asym_id / _pdbx_struct_conn_angle.ptnr3_auth_asym_id / _pdbx_struct_conn_angle.ptnr3_auth_comp_id / _pdbx_struct_conn_angle.ptnr3_auth_seq_id / _pdbx_struct_conn_angle.ptnr3_label_asym_id / _pdbx_struct_conn_angle.ptnr3_label_atom_id / _pdbx_struct_conn_angle.ptnr3_label_comp_id / _pdbx_struct_conn_angle.ptnr3_label_seq_id / _pdbx_struct_conn_angle.value / _struct_conn.pdbx_dist_value / _struct_conn.ptnr1_auth_asym_id / _struct_conn.ptnr1_auth_comp_id / _struct_conn.ptnr1_auth_seq_id / _struct_conn.ptnr1_label_asym_id / _struct_conn.ptnr1_label_atom_id / _struct_conn.ptnr1_label_comp_id / _struct_conn.ptnr1_label_seq_id / _struct_conn.ptnr2_auth_asym_id / _struct_conn.ptnr2_auth_comp_id / _struct_conn.ptnr2_auth_seq_id / _struct_conn.ptnr2_label_asym_id / _struct_conn.ptnr2_label_atom_id / _struct_conn.ptnr2_label_comp_id / _struct_conn.ptnr2_label_seq_id / _struct_ref_seq_dif.details / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
B: Three prime repair exonuclease 1
A: Three prime repair exonuclease 1
C: DNA (5'-D(*GP*AP*CP*G)-3')
D: DNA (5'-D(*GP*AP*CP*G)-3')
hetero molecules


Theoretical massNumber of molelcules
Total (without water)56,79520
Polymers55,1124
Non-polymers1,68316
Water9,710539
1


  • Idetical with deposited unit
  • defined by author
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
A: Three prime repair exonuclease 1
C: DNA (5'-D(*GP*AP*CP*G)-3')
hetero molecules

B: Three prime repair exonuclease 1
D: DNA (5'-D(*GP*AP*CP*G)-3')
hetero molecules


Theoretical massNumber of molelcules
Total (without water)56,79520
Polymers55,1124
Non-polymers1,68316
Water724
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
crystal symmetry operation2_555-x+1/2,-y,z+1/21
Buried area5320 Å2
ΔGint-63 kcal/mol
Surface area20790 Å2
MethodPISA
Unit cell
Length a, b, c (Å)70.468, 86.026, 92.790
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number19
Space group name H-MP212121

-
Components

#1: Protein Three prime repair exonuclease 1 / 3'-5' exonuclease TREX1


Mass: 26339.918 Da / Num. of mol.: 2 / Fragment: N-terminal fragment, residues 1-242 / Mutation: V201D
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Gene: Trex1 / Production host: Escherichia coli (E. coli) / References: UniProt: Q91XB0, exodeoxyribonuclease III
#2: DNA chain DNA (5'-D(*GP*AP*CP*G)-3')


Mass: 1215.843 Da / Num. of mol.: 2 / Source method: obtained synthetically
#3: Chemical
ChemComp-CA / CALCIUM ION


Mass: 40.078 Da / Num. of mol.: 4 / Source method: obtained synthetically / Formula: Ca
#4: Chemical
ChemComp-IOD / IODIDE ION


Mass: 126.904 Da / Num. of mol.: 12 / Source method: obtained synthetically / Formula: I
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 539 / 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: 2.55 Å3/Da / Density % sol: 51.8 %
Crystal growTemperature: 303 K / Method: vapor diffusion, sitting drop
Details: 16% PEG 3350 0.1 M NaI 5% 1,4-butanediol, VAPOR DIFFUSION, SITTING DROP, temperature 303K

-
Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: ROTATING ANODE / Type: RIGAKU MICROMAX-007 / Wavelength: 1.54 Å
DetectorType: RIGAKU / Detector: IMAGE PLATE
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.54 Å / Relative weight: 1
ReflectionResolution: 1.75→47 Å / Num. obs: 57078 / % possible obs: 99 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / Redundancy: 5.67 % / Biso Wilson estimate: 17.58 Å2 / Rmerge(I) obs: 0.068 / Net I/σ(I): 11.9
Reflection shellResolution: 1.75→1.81 Å / Redundancy: 2.62 % / Rmerge(I) obs: 0.24 / Mean I/σ(I) obs: 3.4 / % possible all: 91.2

-
Processing

Software
NameVersionClassification
CrystalCleardata collection
PHASERphasing
PHENIX(phenix.refine: 1.4_113)refinement
d*TREKdata reduction
d*TREKdata scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.75→18.706 Å / SU ML: 0.2 / σ(F): 1.34 / Stereochemistry target values: ML
RfactorNum. reflection% reflectionSelection details
Rfree0.2033 2870 5.08 %Random
Rwork0.1715 ---
obs0.1731 56543 98.33 %-
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL / Bsol: 49.851 Å2 / ksol: 0.392 e/Å3
Displacement parameters
Baniso -1Baniso -2Baniso -3
1-0.0014 Å20 Å2-0 Å2
2--0.6829 Å20 Å2
3----0.6843 Å2
Refinement stepCycle: LAST / Resolution: 1.75→18.706 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms3467 162 16 539 4184
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0063735
X-RAY DIFFRACTIONf_angle_d1.1125123
X-RAY DIFFRACTIONf_dihedral_angle_d18.1951393
X-RAY DIFFRACTIONf_chiral_restr0.076580
X-RAY DIFFRACTIONf_plane_restr0.005642
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.75-1.81250.24042660.19694875X-RAY DIFFRACTION91
1.8125-1.8850.21352750.18225339X-RAY DIFFRACTION99
1.885-1.97070.23482800.18145361X-RAY DIFFRACTION99
1.9707-2.07450.21673100.17435337X-RAY DIFFRACTION99
2.0745-2.20430.20582970.16275398X-RAY DIFFRACTION100
2.2043-2.37420.20412820.15865391X-RAY DIFFRACTION99
2.3742-2.61250.19973050.16235401X-RAY DIFFRACTION99
2.6125-2.98920.20042800.16545457X-RAY DIFFRACTION100
2.9892-3.76110.16692930.16085509X-RAY DIFFRACTION100
3.7611-18.70750.18352820.16145605X-RAY DIFFRACTION98
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)
10.7714-0.1550.04451.0386-0.25380.0315-0.059-0.01340.1310.11070.0535-0.0614-0.0376-0.00950.01990.0791-0.0011-0.01870.0810.00360.086417.499320.9162-4.7849
20.5288-0.68990.42421.0002-0.57550.33170.53730.43350.2488-0.352-0.26960.2533-0.36310.0775-0.21810.29550.19650.01560.46660.0840.183717.28122.7741-26.8404
31.45620.54060.06251.01640.70850.57650.34380.5845-0.0962-0.2502-0.00620.112-0.01970.3559-0.26230.19330.104-0.01660.26170.00310.12225.980621.4646-26.7752
40.1987-0.3552-0.08340.66710.16520.632-0.0036-0.0103-0.00460.0220.05010.06990.0173-0.045-0.03420.08040.0061-0.00280.10880.00470.078510.333110.699-1.5123
50.2979-0.3551-0.38410.73130.24160.5807-0.1076-0.00780.00180.09730.1103-0.16980.08920.0206-0.01920.0960.0065-0.02670.0981-0.01120.099722.28419.39690.2995
60.4364-0.06650.02320.2567-0.05771.0448-0.0423-0.03810.16740.050.0366-0.1017-0.04570.06850.00710.08790.0102-0.01720.0798-0.01870.13318.138925.4557-2.6406
79.52881.1349-5.59368.42660.46863.4935-0.0147-0.24510.7584-0.1441-0.48031.0908-0.0012-0.31110.42020.22410.04740.00410.2416-0.05940.46151.679738.8239-15.7752
80.646-0.13530.2970.2070.17491.1820.05940.02040.0943-0.0079-0.03880.03640.1088-0.0913-0.01940.09190.0113-0.00890.11640.01670.11491.843424.1381-15.436
90.6158-0.11870.03180.9759-0.62790.6520.07010.03730.15040.0591-0.00380.159-0.0483-0.0177-0.05210.08470.0164-0.00520.09350.00970.1111.029421.1977-14.8593
100.8243-0.45-0.04020.39050.08740.3155-0.0076-0.0110.31330.05020.0253-0.1090.04050.0488-0.01160.1017-0.0165-0.02320.0751-0.00130.179320.621730.3732-3.549
110.58680.09980.28580.45620.38710.67660.03950.0365-0.1050.01550.0056-0.04390.16430.1198-0.05040.11830.0245-0.00770.0997-0.00610.100122.258-5.3159-11.456
120.96270.6037-0.43060.4858-0.59561.1005-0.17970.34870.0329-0.02230.14610.10880.422-0.82730.07510.3351-0.24760.07430.683-0.1980.30561.7691-7.9583-5.9751
130.42830.21140.64790.3340.51481.143-0.0948-0.78250.59080.1452-0.11930.1672-0.0999-0.42020.20620.1249-0.0173-0.02550.2543-0.14130.2453-1.5458-6.1673-15.9183
140.4162-0.08180.26570.4450.1010.20640.00860.1860.0258-0.1663-0.009-0.01510.03560.12220.0040.1265-0.00130.00290.155-0.01020.076523.4034.8932-19.9446
150.2220.01760.52891.1931-0.32221.60070.09330.22290.04360.07380.0884-0.1721-0.21640.1511-0.1210.09050.00940.02650.1496-0.00120.163732.21649.3335-14.4236
160.4471-0.1534-0.00970.17070.07190.73040.0542-0.0129-0.18330.10720.0316-0.07290.24680.0893-0.06850.15240.0113-0.00980.1006-0.01460.130522.5491-4.5277-4.8991
170.52620.3494-0.08250.8380.28010.2443-0.04830.1768-0.124-0.05890.128-0.10510.12910.1109-0.0270.15930.03920.00650.1425-0.03440.126531.7723-6.4728-15.6723
180.7197-0.416-0.06770.59650.28551.0695-0.00760.1542-0.4051-0.06360.0639-0.0780.23030.1092-0.09020.1870.0012-0.02570.0788-0.03240.163619.5216-13.4234-12.715
190.71680.45830.14470.32240.18810.2931-0.01370.09690.0965-0.13990.04710.11280.10720.0014-0.01390.1394-0.0078-0.03210.1107-0.03840.12759.5502-5.2669-19.7296
201.64920.102-0.40020.1270.24961.3886-0.0265-0.0317-0.36380.0339-0.0121-0.1150.46160.030.03710.23470.0368-0.02230.0976-0.01480.202522.501-14.4755-9.0011
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1(chain A and resid 6:41)
2X-RAY DIFFRACTION2(chain A and resid 42:51)
3X-RAY DIFFRACTION3(chain A and resid 52:59)
4X-RAY DIFFRACTION4(chain A and resid 60:90)
5X-RAY DIFFRACTION5(chain A and resid 91:117)
6X-RAY DIFFRACTION6(chain A and resid 118:165)
7X-RAY DIFFRACTION7(chain A and resid 166:174)
8X-RAY DIFFRACTION8(chain A and resid 175:193)
9X-RAY DIFFRACTION9(chain A and resid 194:215)
10X-RAY DIFFRACTION10(chain A and resid 216:234)
11X-RAY DIFFRACTION11(chain B and resid 6:42)
12X-RAY DIFFRACTION12(chain B and resid 43:51)
13X-RAY DIFFRACTION13(chain B and resid 52:59)
14X-RAY DIFFRACTION14(chain B and resid 60:90)
15X-RAY DIFFRACTION15(chain B and resid 91:108)
16X-RAY DIFFRACTION16(chain B and resid 109:127)
17X-RAY DIFFRACTION17(chain B and resid 128:140)
18X-RAY DIFFRACTION18(chain B and resid 141:177)
19X-RAY DIFFRACTION19(chain B and resid 178:211)
20X-RAY DIFFRACTION20(chain B and resid 212:234)

+
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