[English] 日本語
Yorodumi
- PDB-6pr2: R261A/S128A S. typhimurium siroheme synthase -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 6pr2
TitleR261A/S128A S. typhimurium siroheme synthase
ComponentsSiroheme synthase
KeywordsTRANSFERASE / precorrin-2 / tetrapyrrole biosynthesis / CysG
Function / homology
Function and homology information


precorrin-2 dehydrogenase / precorrin-2 dehydrogenase activity / uroporphyrinogen-III C-methyltransferase / uroporphyrin-III C-methyltransferase activity / sirohydrochlorin ferrochelatase / sirohydrochlorin ferrochelatase activity / siroheme biosynthetic process / cobalamin biosynthetic process / NAD binding / methylation
Similarity search - Function
Sirohaem synthase / Sirohaem synthase, dimerisation domain / Sirohaem synthase, dimerisation domain superfamily / Sirohaem synthase dimerisation region / Sirohaem synthase, N-terminal / Siroheme synthase, central domain / Putative NAD(P)-binding / Sirohaem biosynthesis protein central / Uroporphyrin-III C-methyltransferase / Uroporphyrin-III C-methyltransferase signature 2. ...Sirohaem synthase / Sirohaem synthase, dimerisation domain / Sirohaem synthase, dimerisation domain superfamily / Sirohaem synthase dimerisation region / Sirohaem synthase, N-terminal / Siroheme synthase, central domain / Putative NAD(P)-binding / Sirohaem biosynthesis protein central / Uroporphyrin-III C-methyltransferase / Uroporphyrin-III C-methyltransferase signature 2. / : / Uroporphyrin-III C-methyltransferase signature 1. / Uroporphiryn-III C-methyltransferase, conserved site / Tetrapyrrole methylase, subdomain 2 / Tetrapyrrole methylase / Tetrapyrrole (Corrin/Porphyrin) Methylases / Tetrapyrrole methylase, subdomain 1 / Tetrapyrrole methylase superfamily / NAD(P)-binding domain superfamily
Similarity search - Domain/homology
S-ADENOSYL-L-HOMOCYSTEINE / Siroheme synthase / Siroheme synthase
Similarity search - Component
Biological speciesSalmonella typhimurium (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.16 Å
AuthorsPennington, J.M. / Stroupe, M.E.
Funding support United States, 1items
OrganizationGrant numberCountry
National Science Foundation (NSF, United States)MCB1149763 United States
CitationJournal: Nat Commun / Year: 2020
Title: Siroheme synthase orients substrates for dehydrogenase and chelatase activities in a common active site.
Authors: Pennington, J.M. / Kemp, M. / McGarry, L. / Chen, Y. / Stroupe, M.E.
History
DepositionJul 10, 2019Deposition site: RCSB / Processing site: RCSB
Revision 1.0Feb 26, 2020Provider: repository / Type: Initial release
Revision 1.1Oct 11, 2023Group: Data collection / Database references / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

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


Theoretical massNumber of molelcules
Total (without water)101,2798
Polymers100,2092
Non-polymers1,0706
Water5,603311
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: gel filtration
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area13200 Å2
ΔGint-98 kcal/mol
Surface area34790 Å2
MethodPISA
Unit cell
Length a, b, c (Å)59.438, 99.758, 146.587
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number19
Space group name H-MP212121
Space group name HallP2ac2ab
Symmetry operation#1: x,y,z
#2: x+1/2,-y+1/2,-z
#3: -x,y+1/2,-z+1/2
#4: -x+1/2,-y,z+1/2

-
Components

#1: Protein Siroheme synthase


Mass: 50104.383 Da / Num. of mol.: 2 / Mutation: R261A, S128A
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Salmonella typhimurium (bacteria)
Gene: cysG, cobA, AAP89_23165, ABO94_22995, AF480_23265, AF488_22710, AF489_21700, AIC76_23675, AXR84_23260, AXU58_22185, C2253_19735, CD48_22680, CE87_23070, CET98_25025, CVR97_13625, D7F20_23535, ...Gene: cysG, cobA, AAP89_23165, ABO94_22995, AF480_23265, AF488_22710, AF489_21700, AIC76_23675, AXR84_23260, AXU58_22185, C2253_19735, CD48_22680, CE87_23070, CET98_25025, CVR97_13625, D7F20_23535, D7H43_21790, DJ388_17225, E2F01_22980, FCJ89_03505, FGA22_01875, FGA24_01980, FGA25_01865, FGA26_01870, GW08_22845, JO10_22525, LZ63_24065, NCTC13348_03825, NG18_22490, NU83_22495, QA89_22165, QB40_24005, QD15_23475, RJ78_23420, SE14_03689, Y934_21155, YG50_22125, YI33_23225, YR17_23015, ZC54_23835
Production host: Escherichia coli (E. coli)
References: UniProt: A0A0F7JCI1, UniProt: P25924*PLUS, uroporphyrinogen-III C-methyltransferase, precorrin-2 dehydrogenase, sirohydrochlorin ferrochelatase
#2: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: Cl
#3: Chemical ChemComp-MES / 2-(N-MORPHOLINO)-ETHANESULFONIC ACID


Mass: 195.237 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C6H13NO4S / Comment: pH buffer*YM
#4: Chemical ChemComp-SAH / S-ADENOSYL-L-HOMOCYSTEINE


Type: L-peptide linking / Mass: 384.411 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C14H20N6O5S
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 311 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestN

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.21 Å3/Da / Density % sol: 44.3 %
Crystal growTemperature: 298 K / Method: vapor diffusion, hanging drop / pH: 5
Details: 4-14% PEG 4000, 100 mM 2-(N-morpholino)ethanesulfonic acid (MES) pH 5.0, 500mM sodium chloride, 7 mM 2-Mercaptoethanol (BME)

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: APS / Beamline: 22-ID / Wavelength: 1 Å
DetectorType: RAYONIX MX300-HS / Detector: CCD / Date: Nov 20, 2017
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 2.16→41.24 Å / Num. obs: 47523 / % possible obs: 99.8 % / Redundancy: 11.6 % / Biso Wilson estimate: 39.7 Å2 / Rmerge(I) obs: 0.2836 / Rpim(I) all: 0.087 / Net I/σ(I): 25.8
Reflection shellResolution: 2.16→2.237 Å / Num. unique obs: 4664 / Rpim(I) all: 0.696

-
Processing

Software
NameVersionClassification
PHENIX1.13_2998refinement
HKL-2000data reduction
HKL-2000data scaling
PHENIXphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 1PJS
Resolution: 2.16→41.24 Å / SU ML: 0.2265 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 21.5583
RfactorNum. reflection% reflection
Rfree0.216 1254 2.64 %
Rwork0.1656 --
obs0.1669 47501 99.82 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å
Displacement parametersBiso mean: 55.99 Å2
Refinement stepCycle: LAST / Resolution: 2.16→41.24 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms6910 0 15 311 7236
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00777115
X-RAY DIFFRACTIONf_angle_d0.96929650
X-RAY DIFFRACTIONf_chiral_restr0.05931111
X-RAY DIFFRACTIONf_plane_restr0.00581263
X-RAY DIFFRACTIONf_dihedral_angle_d5.20875912
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.16-2.250.27891380.2215052X-RAY DIFFRACTION99.77
2.25-2.350.24641370.21535081X-RAY DIFFRACTION99.85
2.35-2.470.26741380.19375086X-RAY DIFFRACTION99.94
2.47-2.630.24591370.18125080X-RAY DIFFRACTION99.89
2.63-2.830.23411400.17755120X-RAY DIFFRACTION99.98
2.83-3.120.23931380.18095113X-RAY DIFFRACTION99.92
3.12-3.570.23711390.16765137X-RAY DIFFRACTION100
3.57-4.490.17121410.1395203X-RAY DIFFRACTION99.91
4.49-41.240.20041460.15475375X-RAY DIFFRACTION99.14
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)
14.484794481531.519692598460.008241999219823.2740307416-0.2334506616031.980785119770.0747674363841-0.134789491643-0.2955471704380.0112107912246-0.0277202504841-0.04978455895290.2528009534780.0154246974102-0.02339552961830.1986743841320.0110998878806-0.01701251623930.220001926034-0.02993532101370.25192170242459.0810788678-20.982868819347.6140959999
23.945635967731.399734393632.405491622380.7839126952440.3221563951674.64506990556-0.0282437041579-0.476259618580.0206286366306-0.0891549093764-0.1600195735860.05656327912160.0876814677546-0.4510297619990.08438740248150.2345971458710.06314724283690.02643763217570.320962016697-0.03567204950740.2680526239186.7449043911-16.442031718946.4199705146
33.411986452110.8973141007470.263421488624.32616276946-0.007542782554132.732869656850.0320100695854-0.745889556263-0.4428575766390.162737277587-0.1559905503980.1147905516910.431388736808-0.07172233965610.1173591836610.31488906867-0.05782611250930.02142725097290.4719288990270.007073625052040.331815679386100.533305188-19.48725951357.0930140476
40.900651367487-0.451089280384-0.07813150484281.01915674525-0.8612700431111.08902997016-0.0410899889601-0.3105925758870.1663162389910.3182346711730.0660644897732-0.0205518957911-0.630406513791-0.0499701766539-0.03284682975370.568554049821-0.01579374698780.09486068976990.35052261855-0.05705101260590.32621002034896.0878711218-3.3169070785333.4636790348
51.97087715463-0.4340298662380.3810615035121.753115772010.8209040775013.072874439740.0585464319418-0.1739423371670.8888360434060.2218688887070.01264180144680.372353436732-1.11127636595-0.01839845527720.01025442123580.838484822374-0.009361019760450.1374969234750.365477474949-0.09221268249360.67193830832996.18516705025.4193777465528.703222974
64.344709080412.605532482120.1251935235283.3393029886-1.323251959942.82292170015-0.2505535450480.333407330470.451942627349-0.6484334982050.1153794924510.1769686359380.1709771149360.306963256630.06758625723890.357901747480.003890778469390.0304394901180.3342887444920.05974672907630.291149152151101.70246496-3.97955350674.79084042775
71.970131856610.474057137156-0.5496175572742.93582479857-2.488569886734.06274622183-0.02206372216880.5128904917510.197466218687-0.3709170995150.228602116790.2860878215210.1827138258-0.393478071686-0.152087852320.326649174448-0.00292210126202-0.03256254121450.3707852341290.07804174928560.30197031782994.7262423873-1.69884095158-0.127942529024
82.634434876711.86605925224-0.1685521902834.590363190750.8460448598372.41329601679-0.01856528193580.1175969292050.46025065284-0.3840327305810.1473330337990.216840227215-0.3689205939470.08889908055-0.1034739586260.285787843611-0.02207131530430.01663846068110.221063449438-0.01205701613210.37916517139869.08253909732.6862231877143.538129679
91.07189587361-0.661103654126-0.9120840529131.69042077530.6704048642851.170473337710.0192649705122-0.2157415535740.1764185337260.05237951406670.128844278551-0.170200442049-0.2178970588110.468246539711-0.06699889687640.244602152129-0.0548019872512-0.001535405642570.380477169526-0.08148391807360.34889059339175.7699293214-9.2602776752744.5233771916
101.90925681924-0.2633880386341.08026298972.37841033331-0.7555583771313.70178184245-0.07121978931060.464796697344-0.0942739090563-0.6388261315270.2358714195420.274836471260.4785067371560.0274360314067-0.09246677293170.389114510909-0.0933269791655-0.01178801660740.4299362034770.02069243102730.32671558895977.2290410121-23.686554759621.5161488599
112.24925616114-0.08402293107790.04283971018443.559149767880.4339719659183.22853441160.0406394245703-0.280076430785-0.5418278401340.006258383376430.02805562466390.09798169199460.6956962449690.0116516218198-0.02281584012510.399613216775-0.00537274306875-0.0009822565491370.2122280654850.05391684707220.31107828213697.236102026-26.022163430120.5662893633
122.72251254770.781211971407-0.5005994939963.17994906328-2.232013457463.1927159863-0.05350103348420.133631760039-0.0415612202479-0.234430662897-0.303582452625-0.6370748562180.0861257993530.6324393799360.2108619233870.2827810319710.05784898531130.03048653945820.3722683769120.05715638321870.383442586602111.42927944-9.7509486778613.2747452653
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1chain 'A' and (resid 1 through 114 )
2X-RAY DIFFRACTION2chain 'A' and (resid 115 through 184 )
3X-RAY DIFFRACTION3chain 'A' and (resid 185 through 209 )
4X-RAY DIFFRACTION4chain 'A' and (resid 210 through 247 )
5X-RAY DIFFRACTION5chain 'A' and (resid 248 through 331 )
6X-RAY DIFFRACTION6chain 'A' and (resid 332 through 367 )
7X-RAY DIFFRACTION7chain 'A' and (resid 368 through 456 )
8X-RAY DIFFRACTION8chain 'B' and (resid 1 through 96 )
9X-RAY DIFFRACTION9chain 'B' and (resid 97 through 132 )
10X-RAY DIFFRACTION10chain 'B' and (resid 133 through 209 )
11X-RAY DIFFRACTION11chain 'B' and (resid 210 through 278 )
12X-RAY DIFFRACTION12chain 'B' and (resid 279 through 455 )

+
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