[English] 日本語
Yorodumi
- PDB-9ebk: Piperazate synthase (PipS) in complex with haem -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 9ebk
TitlePiperazate synthase (PipS) in complex with haem
ComponentsPiperazate synthase
KeywordsBIOSYNTHETIC PROTEIN / N-N bond / natural product biosynthesis / heme / piperazate / piperazic acid
Function / homologyPROTOPORPHYRIN IX CONTAINING FE
Function and homology information
Biological speciesStreptomyces griseus subsp. griseus (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.08006722536 Å
AuthorsHiggins, M.A. / Ryan, K.S.
Funding support Canada, 1items
OrganizationGrant numberCountry
Natural Sciences and Engineering Research Council (NSERC, Canada)RPGIN-2021-02626 Canada
CitationJournal: Nat Catal / Year: 2025
Title: Structure and mechanism of haem-dependent nitrogen-nitrogen bond formation in piperazate synthase
Authors: Higgins, M.A. / Shi, X. / Soler, J. / Harland, J.B. / Parkkila, T. / Lehnert, N. / Garcia-Borras, M. / Du, Y.L. / Ryan, K.S.
History
DepositionNov 12, 2024Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jan 22, 2025Provider: repository / Type: Initial release
Revision 1.1Feb 26, 2025Group: Database references / Category: citation / citation_author
Item: _citation.country / _citation.journal_abbrev ..._citation.country / _citation.journal_abbrev / _citation.journal_id_CSD / _citation.journal_id_ISSN / _citation.pdbx_database_id_DOI / _citation.year / _citation_author.identifier_ORCID

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
B: Piperazate synthase
A: Piperazate synthase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)51,6295
Polymers50,3042
Non-polymers1,3253
Water3,009167
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: gel filtration
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area7630 Å2
ΔGint-86 kcal/mol
Surface area16840 Å2
MethodPISA
Unit cell
Length a, b, c (Å)66.510, 66.510, 478.694
Angle α, β, γ (deg.)90.000, 90.000, 120.000
Int Tables number178
Space group name H-MP6122
Space group name HallP612(x,y,z+5/12)
Symmetry operation#1: x,y,z
#2: x-y,x,z+1/6
#3: y,-x+y,z+5/6
#4: -y,x-y,z+1/3
#5: -x+y,-x,z+2/3
#6: x-y,-y,-z
#7: -x,-x+y,-z+2/3
#8: -x,-y,z+1/2
#9: y,x,-z+1/3
#10: -y,-x,-z+5/6
#11: -x+y,y,-z+1/2
#12: x,x-y,-z+1/6
Components on special symmetry positions
IDModelComponents
11B-640-

HOH

21B-658-

HOH

31B-677-

HOH

Noncrystallographic symmetry (NCS)NCS domain:
IDEns-ID
11
21

NCS domain segments:

Ens-ID: 1

Dom-IDComponent-IDBeg auth comp-IDBeg label comp-IDEnd auth comp-IDEnd label comp-IDSelection detailsAuth asym-IDLabel asym-IDAuth seq-IDLabel seq-ID
11METMETILEILE(chain 'A' and (resid 1 through 19 or resid 21...AB1 - 191 - 19
12GLYGLYPROPRO(chain 'A' and (resid 1 through 19 or resid 21...AB21 - 21421 - 214
13HISHISHISHIS(chain 'A' and (resid 1 through 19 or resid 21...AB221 - 223221 - 223
24METMETILEILE(chain 'B' and (resid 1 through 19 or resid 21...BA1 - 191 - 19
25GLYGLYPROPRO(chain 'B' and (resid 1 through 19 or resid 21...BA21 - 21421 - 214
26HISHISHISHIS(chain 'B' and (resid 1 through 19 or resid 21...BA222 - 224222 - 224

-
Components

#1: Protein Piperazate synthase


Mass: 25152.146 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Streptomyces griseus subsp. griseus (bacteria)
Strain: NRRL F-5144 / Production host: Escherichia coli BL21(DE3) (bacteria)
#2: Chemical ChemComp-HEM / PROTOPORPHYRIN IX CONTAINING FE / HEME


Mass: 616.487 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C34H32FeN4O4 / Feature type: SUBJECT OF INVESTIGATION
#3: Chemical ChemComp-GOL / GLYCEROL / GLYCERIN / PROPANE-1,2,3-TRIOL


Mass: 92.094 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C3H8O3
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 167 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestY
Has protein modificationN

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 3.04 Å3/Da / Density % sol: 59.51 %
Crystal growTemperature: 293 K / Method: vapor diffusion, hanging drop
Details: 0.76 M sodium citrate tribasic dihydrate, 0.1 M sodium cacodylate, pH 6.5

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: CLSI / Beamline: 08ID-1 / Wavelength: 0.97949 Å
DetectorType: DECTRIS PILATUS3 S 6M / Detector: PIXEL / Date: Jun 7, 2017
RadiationProtocol: LAUE / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.97949 Å / Relative weight: 1
ReflectionResolution: 2.08→79.78 Å / Num. obs: 39715 / % possible obs: 100 % / Redundancy: 33.7 % / Biso Wilson estimate: 34.570676426 Å2 / CC1/2: 0.999 / Rpim(I) all: 0.044 / Net I/σ(I): 15.3
Reflection shellResolution: 2.08→2.14 Å / Num. unique obs: 2987 / CC1/2: 0.882 / Rpim(I) all: 0.476

-
Processing

Software
NameVersionClassification
PHENIX1.11.1_2575refinement
MOSFLMdata reduction
Aimlessdata scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.08006722536→79.78 Å / SU ML: 0.231386837288 / Cross valid method: FREE R-VALUE / σ(F): 1.33571543112 / Phase error: 22.7598007899
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.227741031055 1982 5.01594371615 %
Rwork0.188418974756 37532 -
obs0.190428077865 39514 99.9645820684 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 49.39028751 Å2
Refinement stepCycle: LAST / Resolution: 2.08006722536→79.78 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms3368 0 92 167 3627
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.008569452277693584
X-RAY DIFFRACTIONf_angle_d1.1719104814914
X-RAY DIFFRACTIONf_chiral_restr0.0595601690564511
X-RAY DIFFRACTIONf_plane_restr0.00665384220437637
X-RAY DIFFRACTIONf_dihedral_angle_d13.28272678962434
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.0801-2.13210.351895581471380.2830410980142586X-RAY DIFFRACTION99.9633027523
2.1321-2.18970.3149171058811340.2523925140122568X-RAY DIFFRACTION99.9630040696
2.1897-2.25420.2991504742421360.255969608542623X-RAY DIFFRACTION99.8552298227
2.2542-2.32690.310794161461440.2457215979892606X-RAY DIFFRACTION99.963649582
2.3269-2.41010.2980900643251400.2390338241362634X-RAY DIFFRACTION99.9279538905
2.4101-2.50660.2564066035051390.2258530388432608X-RAY DIFFRACTION99.9636098981
2.5066-2.62070.3022932679471210.213388066992660X-RAY DIFFRACTION100
2.6207-2.75890.2439199245951350.2144918522672676X-RAY DIFFRACTION99.9644381223
2.7589-2.93170.232467470391380.2084872213072642X-RAY DIFFRACTION100
2.9317-3.15810.2503865212921340.2091131363732694X-RAY DIFFRACTION100
3.1581-3.47590.2299922913381400.1810491900982706X-RAY DIFFRACTION99.9648753073
3.4759-3.97890.1951868174571490.154169253892715X-RAY DIFFRACTION100
3.9789-5.01290.1755926702591640.1333581686792781X-RAY DIFFRACTION100
5.0129-79.780.2006781641691700.1796899860473033X-RAY DIFFRACTION99.9375975039
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)
12.13855627133-1.437299488621.361689090872.41190068756-1.544190341886.214032494160.1419596747770.101413618836-0.0141265156707-0.0293690587576-0.0644191200819-0.03298239317030.04143567681160.240438675059-0.0726929749430.118917772171-0.03009277510940.04755596764890.288657051668-0.06263310100340.248626193528-15.271803502615.6653469883-9.9612133995
27.20595371471-0.4025911910244.034079376525.3996538812-0.899772937963.0394713414-0.100064829580.614035325606-1.29132609371-0.131725586674-1.246312832260.6777849945721.021522721330.005636798700791.1514673880.4676862117110.1582823885590.01707464658971.09981348158-0.2950085082140.91103356189-8.579270191964.42900133762-17.0439068357
32.933432831190.05597700109750.1692262217931.948730278570.2790631653734.993644918870.1443338451110.453306232837-0.307115156693-0.28902611668-0.0266525068947-0.01927469030470.1096500614210.29050129093-0.0734164732710.2059637167430.06848218727320.004955952199630.307606725428-0.100698733720.294930008951-19.327759630913.148118538-17.6906755464
45.647421707221.83639582394-1.328250006514.84705448609-1.02251646359.52585870215-0.121323035558-1.33431591048-0.8483148199390.9134926700930.05900991961560.2866510953970.355170115569-0.439087435114-0.06237390297390.4885420929720.002745742076120.09381249127290.5765576294150.09929240249240.433814199809-23.13868510328.259161730811.7849443055
58.50425737541-3.320908554041.403709608167.687063198042.480164472546.662289553550.0291473148368-1.01486507166-0.2825726286890.659813287470.3422160685290.2123814517750.190874786239-0.380561001334-0.4571841868260.493541353582-0.09363327682580.1101107226070.4411441377820.09114461332410.378254612843-22.32920015719.257108473475.3155896649
65.22069570526-3.45905506198-4.202374724985.095513414161.808422818137.563377056340.3510904826560.256822857110.134485115197-0.658771792675-0.6062828313060.77172087111-0.689385236387-0.5842379900350.2969931829920.3467752378270.039368971643-0.07258938104480.422536352854-0.07037811943520.320587380324-34.555974507824.9747671471-20.8053148784
70.553353869378-0.6175043547481.168825490212.940597506250.1633219634033.121495242270.0275596124175-0.1402688432870.018137696726-0.029223985332-0.0608921173374-0.150781046278-0.08322786127040.09222976256640.04203995188710.180875015096-0.06390553013020.04439410201250.30449743192-0.07050600796010.246742906208-22.970657768426.20881135-6.8952438327
87.55666347631-2.924842137651.777254593716.17841456951-0.9260297746127.13938450246-0.452287289701-1.233071411110.717036191525-0.239207646281-0.2305002261730.07402392007-0.671971252825-1.171971138090.6414652002370.2893928573220.0595260551857-0.01707697857070.557825946708-0.1109311146770.392444144773-34.880038889937.9808063652-3.72249190797
92.08844580760.008773599221141.246988355371.326910430780.8801974800593.675383803340.002022793931390.2376895645540.166860903121-0.1208677018510.10994540808-0.00937097062797-0.09995379634170.147355987403-0.1221548699240.157186071669-0.01478654698380.05576604384730.302360795885-0.05113877007960.27561192467-23.765581716823.9692686657-9.65283954218
106.670787759943.19155841876-1.721360190448.5706174698-0.996585939725.221920419320.102694250195-0.7176461305040.5831936371520.829312137525-0.04464575134570.768690431518-0.263828849017-0.821288086631-0.1705041441230.3393543709160.1013640585590.06303719910220.742166709105-0.1371717078230.357409725547-28.398172366427.860778910910.974383461
112.22922019119-0.3420509758590.5095788538023.209924115211.039702257242.91384659628-0.148763855644-0.7337745491110.3910321914850.3897171051550.0165951457328-0.147187617829-0.391149634042-0.2537790849970.05658514971430.186750529336-0.0009761415436730.04240853209880.458630939188-0.1630442534980.362507031411-23.764596928230.03367199324.53663532853
126.880329390612.915279428112.566987693817.334687833781.462692413766.976022161980.3020727866740.505126910425-0.4738738539190.0607020438168-0.4290779374411.396808777370.69329581591-0.9731964552470.1054635998530.319791373653-0.0616815809621-0.003316181311370.584397158033-0.2106816439070.592514781322-41.96967220739.4721670133-19.8638094509
137.43561081832-5.150134516530.2020916092878.060320390193.50855315063.595357101690.4762998713010.377225163326-0.413487339528-0.988773288705-0.299482485880.4240681917950.559208852052-0.387823451977-0.1396614323010.454334591337-0.1711897703280.05266721810990.535027079472-0.131355387820.396259419515-38.810650137312.8155891622-14.4160878195
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1chain 'B' and (resid 1 through 46 )
2X-RAY DIFFRACTION2chain 'B' and (resid 47 through 61 )
3X-RAY DIFFRACTION3chain 'B' and (resid 62 through 178 )
4X-RAY DIFFRACTION4chain 'B' and (resid 179 through 198 )
5X-RAY DIFFRACTION5chain 'B' and (resid 199 through 224 )
6X-RAY DIFFRACTION6chain 'A' and (resid 1 through 11 )
7X-RAY DIFFRACTION7chain 'A' and (resid 12 through 46 )
8X-RAY DIFFRACTION8chain 'A' and (resid 47 through 61 )
9X-RAY DIFFRACTION9chain 'A' and (resid 62 through 124 )
10X-RAY DIFFRACTION10chain 'A' and (resid 125 through 148 )
11X-RAY DIFFRACTION11chain 'A' and (resid 149 through 178 )
12X-RAY DIFFRACTION12chain 'A' and (resid 179 through 197 )
13X-RAY DIFFRACTION13chain 'A' and (resid 198 through 223 )

+
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