[English] 日本語
Yorodumi
- PDB-8po6: Structure of Escherichia coli HrpA apo form -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 8po6
TitleStructure of Escherichia coli HrpA apo form
ComponentsATP-dependent RNA helicase HrpA
KeywordsHYDROLASE / Helicase
Function / homology
Function and homology information


RNA modification / 3'-5' RNA helicase activity / helicase activity / RNA helicase activity / RNA helicase / ATP hydrolysis activity / RNA binding / ATP binding
Similarity search - Function
RNA helicase HrpA / RNA helicase HrpA, C-terminal / Domain of unknown function (DUF3418) / : / Helicase associated domain (HA2), ratchet-like / DEAD-box helicase, OB fold / Oligonucleotide/oligosaccharide-binding (OB)-fold / Helicase-associated domain / Helicase associated domain (HA2), winged-helix / Helicase associated domain (HA2) Add an annotation ...RNA helicase HrpA / RNA helicase HrpA, C-terminal / Domain of unknown function (DUF3418) / : / Helicase associated domain (HA2), ratchet-like / DEAD-box helicase, OB fold / Oligonucleotide/oligosaccharide-binding (OB)-fold / Helicase-associated domain / Helicase associated domain (HA2), winged-helix / Helicase associated domain (HA2) Add an annotation / DEAD/DEAH box helicase / DEAD/DEAH box helicase domain / Helicase conserved C-terminal domain / helicase superfamily c-terminal domain / Superfamilies 1 and 2 helicase C-terminal domain profile. / Superfamilies 1 and 2 helicase ATP-binding type-1 domain profile. / DEAD-like helicases superfamily / Helicase, C-terminal / Helicase superfamily 1/2, ATP-binding domain / ATPases associated with a variety of cellular activities / AAA+ ATPase domain / P-loop containing nucleoside triphosphate hydrolase
Similarity search - Domain/homology
PHOSPHATE ION / ATP-dependent RNA helicase HrpA
Similarity search - Component
Biological speciesEscherichia coli K-12 (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.66 Å
AuthorsXin, B.G. / Yuan, L.G. / Zhang, L.L. / Xie, S.M. / Liu, N.N. / Ai, X. / Li, H.H. / Rety, S. / Xi, X.G.
Funding support China, 2items
OrganizationGrant numberCountry
National Natural Science Foundation of China (NSFC)31870788 China
Other governmentZ101021903 China
CitationJournal: Nucleic Acids Res. / Year: 2024
Title: Structural insights into the N-terminal APHB domain of HrpA: mediating canonical and i-motif recognition.
Authors: Xin, B.G. / Huang, L.Y. / Yuan, L.G. / Liu, N.N. / Li, H.H. / Ai, X. / Lei, D.S. / Hou, X.M. / Rety, S. / Xi, X.G.
History
DepositionJul 3, 2023Deposition site: PDBE / Processing site: PDBE
Revision 1.0May 8, 2024Provider: repository / Type: Initial release

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: ATP-dependent RNA helicase HrpA
hetero molecules


Theoretical massNumber of molelcules
Total (without water)86,4092
Polymers86,3141
Non-polymers951
Water64936
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area230 Å2
ΔGint-7 kcal/mol
Surface area35860 Å2
MethodPISA
Unit cell
Length a, b, c (Å)39.605, 114.897, 94.011
Angle α, β, γ (deg.)90.000, 100.857, 90.000
Int Tables number4
Space group name H-MP1211
Space group name HallP2yb
Symmetry operation#1: x,y,z
#2: -x,y+1/2,-z

-
Components

#1: Protein ATP-dependent RNA helicase HrpA


Mass: 86313.797 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Escherichia coli K-12 (bacteria) / Gene: hrpA, b1413, JW5905 / Plasmid: pET15b-SUMO / Production host: Escherichia coli (E. coli) / Strain (production host): C2566H / References: UniProt: P43329, RNA helicase
#2: Chemical ChemComp-PO4 / PHOSPHATE ION / Phosphate


Mass: 94.971 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: PO4
#3: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 36 / 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: 2.43 Å3/Da / Density % sol: 49.46 %
Crystal growTemperature: 298 K / Method: vapor diffusion, sitting drop / pH: 7 / Details: 0.1M Hepes 7% PEG 20000

-
Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: SSRF / Beamline: BL17U / Wavelength: 0.97852 Å
DetectorType: DECTRIS PILATUS 6M / Detector: PIXEL / Date: Jun 9, 2019
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.97852 Å / Relative weight: 1
ReflectionResolution: 2.656→92.328 Å / Num. obs: 23640 / % possible obs: 99 % / Redundancy: 6.3 % / Biso Wilson estimate: 55.79 Å2 / CC1/2: 0.998 / Rmerge(I) obs: 0.082 / Rpim(I) all: 0.035 / Rrim(I) all: 0.09 / Net I/σ(I): 14.6
Reflection shellResolution: 2.656→2.702 Å / Redundancy: 4.3 % / Rmerge(I) obs: 0.587 / Mean I/σ(I) obs: 2 / Num. unique obs: 1051 / CC1/2: 0.891 / Rpim(I) all: 0.314 / Rrim(I) all: 0.669 / % possible all: 88.8

-
Processing

Software
NameVersionClassification
PHENIX1.17rc5_3630refinement
PHENIX1.17rc5_3630refinement
SORTAVBUILT 20190315data reduction
Aimless0.7.4data scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.66→29.73 Å / SU ML: 0.4653 / Cross valid method: FREE R-VALUE / σ(F): 1.38 / Phase error: 31.5545
Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
RfactorNum. reflection% reflection
Rfree0.2574 1122 4.75 %
Rwork0.2062 22478 -
obs0.2086 23600 98.88 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso mean: 72.75 Å2
Refinement stepCycle: LAST / Resolution: 2.66→29.73 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms6031 0 5 36 6072
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.00286143
X-RAY DIFFRACTIONf_angle_d0.60338308
X-RAY DIFFRACTIONf_chiral_restr0.043932
X-RAY DIFFRACTIONf_plane_restr0.00361090
X-RAY DIFFRACTIONf_dihedral_angle_d18.10122378
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.66-2.780.491250.38332606X-RAY DIFFRACTION92.39
2.78-2.920.38571600.29392781X-RAY DIFFRACTION99.26
2.92-3.110.32831400.27012853X-RAY DIFFRACTION99.87
3.11-3.350.30331310.26982826X-RAY DIFFRACTION99.86
3.35-3.680.25251380.22062837X-RAY DIFFRACTION99.93
3.68-4.210.25091450.19562835X-RAY DIFFRACTION99.97
4.21-5.30.221440.16412855X-RAY DIFFRACTION99.97
5.3-29.730.19391390.15632885X-RAY DIFFRACTION99.74
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)
12.15012046703-1.029074730081.002211038593.73729540812-0.4494064246626.07885182-0.00734380660453-0.2157793430790.1562009611950.5212418406230.0533507905715-0.344114772978-0.256455426939-0.457003161913-0.02501262422220.385778112066-0.02520859756030.005394512579230.365594158382-0.02397182107010.43698315496214.857423163634.526988160259.8935984553
22.0488193959-0.8523335535290.7848875139124.46003528351-1.89612057431.72445298471-0.139172321421-0.2234009402010.4677551195090.3332063137210.0430659274748-0.267085987676-0.3617674913980.002833160075520.05275031183450.5231071714420.12358756819-0.05012612372440.459084909283-0.1619642161230.45778386358512.290447149448.346073823330.4237395264
31.5503024747-1.241297704410.7110040197316.93100268294-0.5042163832591.606350950850.04703032605290.02524924296020.0462557104876-0.2023903918-0.05437783808820.01227688066730.1341814191570.05418870274530.007203356182140.3259759742610.0616177330495-0.006920469297750.3712794702080.0002911456560420.33574623474426.199294890521.825023127713.3818451329
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1chain 'A' and (resid 5 through 240 )
2X-RAY DIFFRACTION2chain 'A' and (resid 241 through 471 )
3X-RAY DIFFRACTION3chain 'A' and (resid 472 through 758 )

+
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