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- PDB-5ub6: XAC2383 from Xanthomonas citri bound to pyrophosphate -

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Basic information

Entry
Database: PDB / ID: 5ub6
TitleXAC2383 from Xanthomonas citri bound to pyrophosphate
ComponentsPhosphate-binding protein
KeywordsMETAL BINDING PROTEIN / Periplasmic binding protein Periplasmic sensor Pyrophosphate Phosphonate-bd
Function / homologyABC transporter, phosphonate, periplasmic substrate-binding protein / PYROPHOSPHATE 2- / Phosphate-binding protein
Function and homology information
Biological speciesXanthomonas axonopodis pv. citri (bacteria)
MethodX-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 2.2 Å
AuthorsTeixeira, R.D. / Guzzo, C.R. / Farah, C.S.
Funding support Brazil, 1items
OrganizationGrant numberCountry
Sao Paulo Research Foundation (FAPESP) Brazil
CitationJournal: J. Biol. Chem. / Year: 2018
Title: A bipartite periplasmic receptor-diguanylate cyclase pair (XAC2383-XAC2382) in the bacteriumXanthomonas citri.
Authors: Teixeira, R.D. / Guzzo, C.R. / Arevalo, S.J. / Andrade, M.O. / Abrahao, J. / de Souza, R.F. / Farah, C.S.
History
DepositionDec 20, 2016Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jan 10, 2018Provider: repository / Type: Initial release
Revision 1.1Jan 23, 2019Group: Data collection / 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 1.2Apr 17, 2019Group: Author supporting evidence / Data collection / Category: pdbx_audit_support / Item: _pdbx_audit_support.funding_organization
Revision 1.3Jan 1, 2020Group: Author supporting evidence / Category: pdbx_audit_support / Item: _pdbx_audit_support.funding_organization
Revision 1.4Mar 6, 2024Group: Data collection / Database references / Category: chem_comp_atom / chem_comp_bond / database_2
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Phosphate-binding protein
B: Phosphate-binding protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)63,0864
Polymers62,7342
Non-polymers3522
Water3,387188
1
A: Phosphate-binding protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)31,5432
Polymers31,3671
Non-polymers1761
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
B: Phosphate-binding protein
hetero molecules


Theoretical massNumber of molelcules
Total (without water)31,5432
Polymers31,3671
Non-polymers1761
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)66.544, 66.860, 113.033
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number19
Space group name H-MP212121

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Components

#1: Protein Phosphate-binding protein


Mass: 31367.150 Da / Num. of mol.: 2 / Fragment: UNP residues 31-309
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Xanthomonas axonopodis pv. citri (strain 306) (bacteria)
Strain: 306 / Gene: XAC2383 / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: Q8PJZ4
#2: Chemical ChemComp-POP / PYROPHOSPHATE 2- / Pyrophosphate


Mass: 175.959 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: H2O7P2
#3: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 188 / Source method: isolated from a natural source / Formula: H2O

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Experimental details

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Experiment

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

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Sample preparation

CrystalDensity Matthews: 2 Å3/Da / Density % sol: 38.63 %
Crystal growTemperature: 298 K / Method: batch mode / Details: 20 mM Tris pH 8.0, 300 mM NaCl

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Data collection

DiffractionMean temperature: 93 K
Diffraction sourceSource: ROTATING ANODE / Type: RIGAKU MICROMAX-007 HF / Wavelength: 1.54 Å
DetectorType: RIGAKU RAXIS IV++ / Detector: IMAGE PLATE / Date: Feb 4, 2014
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.54 Å / Relative weight: 1
ReflectionResolution: 2.2→43.69 Å / Num. obs: 24778 / % possible obs: 98.51 % / Redundancy: 4.7 % / Net I/σ(I): 8.73

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Processing

Software
NameVersionClassification
REFMAC5.8.0135refinement
HKL-2000data reduction
SCALAdata scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.2→43.69 Å / Cor.coef. Fo:Fc: 0.961 / Cor.coef. Fo:Fc free: 0.925 / SU B: 6.414 / SU ML: 0.161 / Cross valid method: THROUGHOUT / ESU R: 0.318 / ESU R Free: 0.222 / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
RfactorNum. reflection% reflectionSelection details
Rfree0.229 1351 5.2 %RANDOM
Rwork0.16463 ---
obs0.16797 24778 97.63 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å
Displacement parametersBiso mean: 31.096 Å2
Baniso -1Baniso -2Baniso -3
1--0.15 Å2-0 Å20 Å2
2--0.18 Å2-0 Å2
3----0.03 Å2
Refinement stepCycle: 1 / Resolution: 2.2→43.69 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms4382 0 18 188 4588
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0130.0194532
X-RAY DIFFRACTIONr_bond_other_d0.0020.024441
X-RAY DIFFRACTIONr_angle_refined_deg1.731.986144
X-RAY DIFFRACTIONr_angle_other_deg1.005310156
X-RAY DIFFRACTIONr_dihedral_angle_1_deg6.5895566
X-RAY DIFFRACTIONr_dihedral_angle_2_deg33.61221.154208
X-RAY DIFFRACTIONr_dihedral_angle_3_deg14.64215786
X-RAY DIFFRACTIONr_dihedral_angle_4_deg18.9741566
X-RAY DIFFRACTIONr_chiral_restr0.090.2683
X-RAY DIFFRACTIONr_gen_planes_refined0.0080.0215092
X-RAY DIFFRACTIONr_gen_planes_other0.0020.021078
X-RAY DIFFRACTIONr_nbd_refined
X-RAY DIFFRACTIONr_nbd_other
X-RAY DIFFRACTIONr_nbtor_refined
X-RAY DIFFRACTIONr_nbtor_other
X-RAY DIFFRACTIONr_xyhbond_nbd_refined
X-RAY DIFFRACTIONr_xyhbond_nbd_other
X-RAY DIFFRACTIONr_metal_ion_refined
X-RAY DIFFRACTIONr_metal_ion_other
X-RAY DIFFRACTIONr_symmetry_vdw_refined
X-RAY DIFFRACTIONr_symmetry_vdw_other
X-RAY DIFFRACTIONr_symmetry_hbond_refined
X-RAY DIFFRACTIONr_symmetry_hbond_other
X-RAY DIFFRACTIONr_symmetry_metal_ion_refined
X-RAY DIFFRACTIONr_symmetry_metal_ion_other
X-RAY DIFFRACTIONr_mcbond_it2.0882.8682249
X-RAY DIFFRACTIONr_mcbond_other2.0842.8672248
X-RAY DIFFRACTIONr_mcangle_it3.0944.2952814
X-RAY DIFFRACTIONr_mcangle_other3.0934.2952815
X-RAY DIFFRACTIONr_scbond_it2.963.2982283
X-RAY DIFFRACTIONr_scbond_other2.9343.2942265
X-RAY DIFFRACTIONr_scangle_it
X-RAY DIFFRACTIONr_scangle_other4.5994.7953302
X-RAY DIFFRACTIONr_long_range_B_refined6.22623.1515033
X-RAY DIFFRACTIONr_long_range_B_other6.17523.0694993
X-RAY DIFFRACTIONr_rigid_bond_restr
X-RAY DIFFRACTIONr_sphericity_free
X-RAY DIFFRACTIONr_sphericity_bonded
LS refinement shellResolution: 2.187→2.243 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.293 90 -
Rwork0.199 1546 -
obs--84.72 %

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