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- PDB-5xu0: Structure of the membrane fusion protein Spr0693 from Streptococc... -

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Basic information

Entry
Database: PDB / ID: 5xu0
TitleStructure of the membrane fusion protein Spr0693 from Streptococcus pneumoniae R6
ComponentsMembrane-fusion protein
KeywordsTRANSPORT PROTEIN / membrane fusion protein / channel
Function / homologyRND efflux pump, membrane fusion protein / RND efflux pump, membrane fusion protein, barrel-sandwich domain / Barrel-sandwich domain of CusB or HlyD membrane-fusion / transmembrane transporter activity / membrane => GO:0016020 / Membrane-fusion protein
Function and homology information
Biological speciesStreptococcus pneumoniae (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / SAD / Resolution: 2.95 Å
AuthorsYang, H.B. / Jiang, Y.L. / Hou, W.T. / Chen, M.T. / Chen, Y. / Zhou, C.Z.
Funding support China, 2items
OrganizationGrant numberCountry
Ministry of Science and Technology2015CB910103 China
National Natural Science Foundation of China31400628 China
CitationJournal: Nat Commun / Year: 2018
Title: Structure of a MacAB-like efflux pump from Streptococcus pneumoniae.
Authors: Yang, H.B. / Hou, W.T. / Cheng, M.T. / Jiang, Y.L. / Chen, Y. / Zhou, C.Z.
History
DepositionJun 22, 2017Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0Jan 24, 2018Provider: repository / Type: Initial release
Revision 1.1Jan 31, 2018Group: 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.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_DOI / _citation.pdbx_database_id_PubMed / _citation.title / _citation.year / _citation_author.name
Revision 1.2Nov 22, 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

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Membrane-fusion protein
B: Membrane-fusion protein
C: Membrane-fusion protein


Theoretical massNumber of molelcules
Total (without water)87,0703
Polymers87,0703
Non-polymers00
Water0
1
A: Membrane-fusion protein
B: Membrane-fusion protein
C: Membrane-fusion protein

A: Membrane-fusion protein
B: Membrane-fusion protein
C: Membrane-fusion protein


Theoretical massNumber of molelcules
Total (without water)174,1396
Polymers174,1396
Non-polymers00
Water0
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
crystal symmetry operation7_555y,x,-z1
Buried area14390 Å2
ΔGint-47 kcal/mol
Surface area70130 Å2
MethodPISA
Unit cell
Length a, b, c (Å)159.210, 159.210, 99.400
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number92
Space group name H-MP41212

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Components

#1: Protein Membrane-fusion protein


Mass: 29023.213 Da / Num. of mol.: 3 / Fragment: UNP RESIDUES 59-324 / Mutation: T197M, I317M
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Streptococcus pneumoniae (bacteria) / Gene: ERS515107_03100 / Plasmid: pET29b / Production host: Escherichia coli (E. coli) / References: UniProt: A0A0Y3EE53

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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: 3.64 Å3/Da / Density % sol: 66.22 %
Description: The entry contains friedel pairs in F_plus/minus columns and I_plus/minus columns
Crystal growTemperature: 285 K / Method: vapor diffusion, hanging drop / pH: 4.5 / Details: 7.5 % PEG 4000, 100 mM CaCl2, 10%-20% MPD

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: NFPSS / Beamline: BL19U1 / Wavelength: 0.97775 Å
DetectorType: DECTRIS PILATUS3 6M / Detector: PIXEL / Date: May 20, 2017
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.97775 Å / Relative weight: 1
ReflectionResolution: 2.95→50 Å / Num. obs: 27463 / % possible obs: 99.8 % / Redundancy: 7 % / Net I/σ(I): 15.6
Reflection shellResolution: 3→3.1 Å

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Processing

Software
NameVersionClassification
PHENIX(1.11.1_2575)refinement
XDSdata reduction
XSCALEdata scaling
MOLREPphasing
RefinementMethod to determine structure: SAD
Starting model: 1F3O
Resolution: 2.95→48.981 Å / SU ML: 0.42 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 36.87
Details: The entry contains friedel pairs in F_plus/minus columns and I_plus/minus columns
RfactorNum. reflection% reflection
Rfree0.3052 1305 4.75 %
Rwork0.2478 --
obs0.2504 27463 99.83 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å
Refinement stepCycle: LAST / Resolution: 2.95→48.981 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms5102 0 0 0 5102
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0045142
X-RAY DIFFRACTIONf_angle_d0.7936958
X-RAY DIFFRACTIONf_dihedral_angle_d3.6963137
X-RAY DIFFRACTIONf_chiral_restr0.045814
X-RAY DIFFRACTIONf_plane_restr0.003912
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.9486-3.06660.45121350.40012844X-RAY DIFFRACTION99
3.0666-3.20610.40961410.36862862X-RAY DIFFRACTION100
3.2061-3.37510.38771350.32172853X-RAY DIFFRACTION100
3.3751-3.58650.34121420.28412871X-RAY DIFFRACTION100
3.5865-3.86330.31961650.26732861X-RAY DIFFRACTION100
3.8633-4.25190.29381430.24712897X-RAY DIFFRACTION100
4.2519-4.86670.25881660.21112888X-RAY DIFFRACTION100
4.8667-6.12970.26541520.24492954X-RAY DIFFRACTION100
6.1297-48.98750.30531260.21063128X-RAY DIFFRACTION100

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