[English] 日本語
Yorodumi
- PDB-6dka: Yeast Ddi2 Cyanamide Hydratase -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 6dka
TitleYeast Ddi2 Cyanamide Hydratase
ComponentsDNA damage-inducible protein
KeywordsLYASE / Zn-metalloprotein / HD-domain / hydratase / cyanamide / METAL BINDING PROTEIN
Function / homologyCyanamide hydratase / HD domain profile. / HD domain / HD domain / Metal dependent phosphohydrolases with conserved 'HD' motif. / HD/PDEase domain / metal ion binding / CYANAMIDE / DNA damage-inducible protein
Function and homology information
Biological speciesSaccharomyces cerevisiae (brewer's yeast)
MethodX-RAY DIFFRACTION / SYNCHROTRON / FOURIER SYNTHESIS / Resolution: 2.901 Å
AuthorsMoore, S.A. / Xiao, W. / Li, J.
Funding support Canada, 3items
OrganizationGrant numberCountry
Natural Sciences and Engineering Research Council (NSERC, Canada)RGPIN-2014-04580 Canada
Natural Sciences and Engineering Research Council (NSERC, Canada)RGPIN-2011-262138 Canada
Canadian Institutes of Health Research (CIHR)MOP-126155 Canada
CitationJournal: J.Biol.Chem. / Year: 2019
Title: Structure of Ddi2, a highly inducible detoxifying metalloenzyme fromSaccharomyces cerevisiae.
Authors: Li, J. / Jia, Y. / Lin, A. / Hanna, M. / Chelico, L. / Xiao, W. / Moore, S.A.
History
DepositionMay 29, 2018Deposition site: RCSB / Processing site: RCSB
Revision 1.0May 8, 2019Provider: repository / Type: Initial release
Revision 1.1Nov 27, 2019Group: Database references / Category: citation / citation_author
Item: _citation.country / _citation.journal_abbrev ..._citation.country / _citation.journal_abbrev / _citation.journal_id_ASTM / _citation.journal_id_CSD / _citation.journal_id_ISSN / _citation.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_DOI / _citation.pdbx_database_id_PubMed / _citation.title / _citation.year
Revision 1.2Jan 8, 2020Group: Author supporting evidence / Category: pdbx_audit_support / Item: _pdbx_audit_support.funding_organization
Revision 1.3Oct 11, 2023Group: Data collection / Database references ...Data collection / Database references / Derived calculations / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model / struct_conn
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _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

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: DNA damage-inducible protein
B: DNA damage-inducible protein
C: DNA damage-inducible protein
D: DNA damage-inducible protein
E: DNA damage-inducible protein
F: DNA damage-inducible protein
G: DNA damage-inducible protein
H: DNA damage-inducible protein
I: DNA damage-inducible protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)238,07851
Polymers234,6979
Non-polymers3,38142
Water4,774265
1
A: DNA damage-inducible protein
hetero molecules

A: DNA damage-inducible protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)52,94612
Polymers52,1552
Non-polymers79110
Water362
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
crystal symmetry operation4_557y,x,-z+21
Buried area4510 Å2
ΔGint-186 kcal/mol
Surface area17830 Å2
MethodPISA
2
B: DNA damage-inducible protein
C: DNA damage-inducible protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)53,23415
Polymers52,1552
Non-polymers1,07913
Water362
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area5000 Å2
ΔGint-230 kcal/mol
Surface area17750 Å2
MethodPISA
3
D: DNA damage-inducible protein
E: DNA damage-inducible protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)53,13814
Polymers52,1552
Non-polymers98312
Water362
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area4880 Å2
ΔGint-214 kcal/mol
Surface area18100 Å2
MethodPISA
4
F: DNA damage-inducible protein
G: DNA damage-inducible protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)52,85011
Polymers52,1552
Non-polymers6959
Water362
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area4050 Å2
ΔGint-157 kcal/mol
Surface area18070 Å2
MethodPISA
5
H: DNA damage-inducible protein
I: DNA damage-inducible protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)52,3825
Polymers52,1552
Non-polymers2273
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area3160 Å2
ΔGint-101 kcal/mol
Surface area17930 Å2
MethodPISA
Unit cell
Length a, b, c (Å)263.430, 263.430, 119.214
Angle α, β, γ (deg.)90.00, 90.00, 120.00
Int Tables number150
Space group name H-MP321

-
Components

#1: Protein
DNA damage-inducible protein


Mass: 26077.482 Da / Num. of mol.: 9 / Mutation: T157V
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Saccharomyces cerevisiae (strain YJM789) (yeast)
Strain: YJM789 / Gene: SCY_1694 / Plasmid: PGEX-6P1 / Details (production host): GST-fusion protein / Production host: Escherichia coli BL21(DE3) (bacteria) / Strain (production host): BL21(DE3) / References: UniProt: A7A1Y4
#2: Chemical
ChemComp-ZN / ZINC ION


Mass: 65.409 Da / Num. of mol.: 9 / Source method: obtained synthetically / Formula: Zn / Feature type: SUBJECT OF INVESTIGATION
#3: Chemical
ChemComp-CNN / CYANAMIDE


Mass: 42.040 Da / Num. of mol.: 7 / Source method: obtained synthetically / Formula: CH2N2 / Feature type: SUBJECT OF INVESTIGATION
#4: Chemical...
ChemComp-SO4 / SULFATE ION


Mass: 96.063 Da / Num. of mol.: 26 / Source method: obtained synthetically / Formula: SO4
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 265 / 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: 5.09 Å3/Da / Density % sol: 76 % / Description: flattened discs
Crystal growTemperature: 298 K / Method: vapor diffusion, hanging drop / pH: 5.8
Details: 1.1-1.3 M Ammonium Sulfate 0.2 M Arginine 0.1 M N-morpholino ethane sulfonate pH 5.8
PH range: 5.2-6.0

-
Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: CLSI / Beamline: 08B1-1 / Wavelength: 1.0246 Å
DetectorType: RAYONIX MX300HE / Detector: CCD / Date: Feb 20, 2016 / Details: Toroidal Focusing Mirrors
RadiationMonochromator: double crystal / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.0246 Å / Relative weight: 1
ReflectionResolution: 2.9→39.3 Å / Num. obs: 101420 / % possible obs: 96.8 % / Redundancy: 6.6 % / Biso Wilson estimate: 55.6 Å2 / Rmerge(I) obs: 0.114 / Net I/σ(I): 16.1
Reflection shellResolution: 2.9→2.95 Å / Redundancy: 6.5 % / Rmerge(I) obs: 0.63 / Mean I/σ(I) obs: 2.2 / Num. unique obs: 5107 / % possible all: 98.4

-
Processing

Software
NameVersionClassification
PHENIX(1.13_2998)refinement
HKL-2000data reduction
HKL-2000data scaling
PHENIXphasing
RefinementMethod to determine structure: FOURIER SYNTHESIS
Starting model: 6DK9

6dk9


Resolution: 2.901→29.966 Å / SU ML: 0.3 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 23.19
Details: Iterative maximum lilelihood refinement in PHENIX and model building with Coot. The authors state that although Chains H and I are included in the model structure, in general these chains ...Details: Iterative maximum lilelihood refinement in PHENIX and model building with Coot. The authors state that although Chains H and I are included in the model structure, in general these chains are considered unreliable due to high B-factors and poor electron density. These chains should not be used for any structural analysis.
RfactorNum. reflection% reflection
Rfree0.2296 2569 2.53 %
Rwork0.1978 --
obs0.1986 101380 96.66 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å
Refinement stepCycle: LAST / Resolution: 2.901→29.966 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms16158 0 160 265 16583
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00616677
X-RAY DIFFRACTIONf_angle_d0.84522788
X-RAY DIFFRACTIONf_dihedral_angle_d11.4869838
X-RAY DIFFRACTIONf_chiral_restr0.052625
X-RAY DIFFRACTIONf_plane_restr0.0062925
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.9011-2.95680.30281400.27235432X-RAY DIFFRACTION97
2.9568-3.01710.26351380.25795552X-RAY DIFFRACTION98
3.0171-3.08270.30161540.25145529X-RAY DIFFRACTION98
3.0827-3.15430.29021360.24735482X-RAY DIFFRACTION98
3.1543-3.23310.26731290.23355559X-RAY DIFFRACTION98
3.2331-3.32040.26461590.23375497X-RAY DIFFRACTION98
3.3204-3.4180.24911440.22335507X-RAY DIFFRACTION97
3.418-3.52820.21871280.20995489X-RAY DIFFRACTION97
3.5282-3.6540.18451130.19075509X-RAY DIFFRACTION97
3.654-3.80010.20871120.18655482X-RAY DIFFRACTION97
3.8001-3.97270.21991490.1835464X-RAY DIFFRACTION96
3.9727-4.18160.22411460.16985467X-RAY DIFFRACTION96
4.1816-4.44280.18571480.15725468X-RAY DIFFRACTION96
4.4428-4.78450.191520.15595456X-RAY DIFFRACTION96
4.7845-5.26370.22881640.1695466X-RAY DIFFRACTION96
5.2637-6.020.20221640.19885482X-RAY DIFFRACTION96
6.02-7.56430.22911560.21135471X-RAY DIFFRACTION95
7.5643-29.96790.26051370.20175499X-RAY DIFFRACTION93
Refinement TLS params.

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

IDL11 (°2)L12 (°2)L13 (°2)L22 (°2)L23 (°2)L33 (°2)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T11 (Å2)T12 (Å2)T13 (Å2)T22 (Å2)T23 (Å2)T33 (Å2)Origin x (Å)Origin y (Å)Origin z (Å)
10.9309-0.0880.34441.3988-0.20982.768-0.0646-0.12080.08620.00860.03780.0952-0.1725-0.50920.04230.3450.2367-0.01510.70610.01220.352234.792885.1313127.5125
21.1117-0.2176-0.09981.9883-0.14511.7103-0.0332-0.11130.04010.20850.09380.1724-0.304-0.3737-0.04840.35790.24420.00540.64290.06160.41220.7334104.679895.6517
31.3834-0.3076-0.08961.5627-0.36312.6524-0.0156-0.0062-0.0378-0.03080.00180.04340.10840.05990.00620.23760.1377-0.02630.4530.01490.333939.060388.28878.476
40.8551-0.0688-0.05021.78040.13981.7782-0.0361-0.08130.0450.12990.06230.0656-0.2097-0.1647-0.00380.36020.193-0.00820.4190.04850.42419.767133.539167.8588
51.148-0.44350.10571.60940.01972.01540.0114-0.0626-0.0093-0.041-0.0179-0.0214-0.06140.0561-0.00620.26250.1255-0.01270.38470.0530.348133.7106114.683148.969
61.50760.1806-0.36372.1010.20181.7498-0.0855-0.03860.1181-0.1269-0.04070.013-0.22380.15760.13230.58990.0158-0.10810.28690.01990.460132.539164.832846.7364
71.5031-0.1140.32753.1230.29861.9087-0.13220.2473-0.0017-0.840.0432-0.188-0.14980.26870.09410.73040.01080.06960.41730.0420.374241.4088145.934625.0721
81.85870.6057-0.51721.3354-0.15311.4814-0.22450.16170.8532-0.76260.1280.1334-0.63770.36150.07061.2237-0.2765-0.15070.66180.2171.084657.252192.579833.8741
90.2103-0.0170.38190.98680.88420.9845-0.62690.78230.4007-1.41410.5153-0.5018-0.35620.51620.06331.7378-0.53530.30571.40940.2881.060661.5988176.88638.8054
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1chain 'A' and (resid -3 through 225)
2X-RAY DIFFRACTION2chain 'B' and (resid -3 through 225)
3X-RAY DIFFRACTION3chain 'C' and (resid -3 through 225)
4X-RAY DIFFRACTION4chain 'D' and (resid -3 through 225)
5X-RAY DIFFRACTION5chain 'E' and (resid -3 through 225)
6X-RAY DIFFRACTION6chain 'F' and (resid -4 through 225)
7X-RAY DIFFRACTION7chain 'G' and (resid -3 through 225)
8X-RAY DIFFRACTION8chain 'H' and (resid 0 through 225)
9X-RAY DIFFRACTION9chain 'I' and (resid 1 through 225)

+
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