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- PDB-6hzh: Apo structure of TP domain from Chlamydia trachomatis penicillin-... -

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Database: PDB / ID: 6hzh
TitleApo structure of TP domain from Chlamydia trachomatis penicillin-binding protein 3
ComponentsPenicillin-binding proteinPenicillin-binding proteins
KeywordsPEPTIDE BINDING PROTEIN / penicillin-binding protein / peptidoglycan / Transpeptidase
Function / homology
Function and homology information

peptidoglycan glycosyltransferase / peptidoglycan glycosyltransferase activity / penicillin binding / membrane => GO:0016020
Similarity search - Function
Penicillin-binding protein, dimerisation domain / Penicillin-binding Protein dimerisation domain / Penicillin-binding protein, dimerisation domain superfamily / Penicillin-binding protein, transpeptidase / Penicillin binding protein transpeptidase domain / Beta-lactamase/transpeptidase-like
Similarity search - Domain/homology
Penicillin-binding protein
Similarity search - Component
Biological speciesChlamydia trachomatis (bacteria)
AuthorsBellini, D. / Koekemoer, L. / Newman, H. / Dowson, C.G.
Funding support United Kingdom, 1items
OrganizationGrant numberCountry
Medical Research Council (United Kingdom)grant.MR/P007503/1 United Kingdom
CitationJournal: To Be Published
Title: Apo structure of TP domain from Chlamydia trachomatis penicillin-binding protein 3
Authors: Bellini, D. / Koekemoer, L. / Newman, H. / Dowson, C.G.
DepositionOct 23, 2018Deposition site: PDBE / Processing site: PDBE
Revision 1.0Nov 20, 2019Provider: repository / Type: Initial release
Revision 1.1Jan 24, 2024Group: 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:

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Deposited unit
A: Penicillin-binding protein
B: Penicillin-binding protein

Theoretical massNumber of molelcules
Total (without water)72,9362
A: Penicillin-binding protein

Theoretical massNumber of molelcules
Total (without water)36,4681
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
B: Penicillin-binding protein

Theoretical massNumber of molelcules
Total (without water)36,4681
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)105.444, 105.444, 118.522
Angle α, β, γ (deg.)90.00, 90.00, 120.00
Int Tables number154
Space group name H-MP3221


#1: Protein Penicillin-binding protein / Penicillin-binding proteins

Mass: 36467.785 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Chlamydia trachomatis (bacteria) / Gene: pbp_2, ERS133248_00492 / Production host: Escherichia coli BL21(DE3) (bacteria)
References: UniProt: A0A0E9FXJ8, peptidoglycan glycosyltransferase
#2: Water ChemComp-HOH / water / Water

Mass: 18.015 Da / Num. of mol.: 170 / Source method: isolated from a natural source / Formula: H2O

Experimental details


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

Sample preparation

CrystalDensity Matthews: 2.61 Å3/Da / Density % sol: 52.83 %
Crystal growTemperature: 294 K / Method: vapor diffusion, sitting drop
Details: 1 M sodium citrate and 0.1 M sodium cacodylate pH 6.5

Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: Diamond / Beamline: I03 / Wavelength: 0.976 Å
DetectorType: DECTRIS PILATUS 6M / Detector: PIXEL / Date: Jul 7, 2018
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.976 Å / Relative weight: 1
ReflectionResolution: 1.83→72.34 Å / Num. obs: 45711 / % possible obs: 93.9 % / Redundancy: 10.8 % / Rrim(I) all: 0.12 / Net I/σ(I): 13.9
Reflection shellResolution: 1.83→2.04 Å


xia2data reduction
Aimlessdata scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 4ye5
Resolution: 1.83→72.34 Å / Cor.coef. Fo:Fc: 0.954 / Cor.coef. Fo:Fc free: 0.927 / SU B: 3.849 / SU ML: 0.108 / Cross valid method: THROUGHOUT / ESU R: 0.2 / ESU R Free: 0.177
RfactorNum. reflection% reflectionSelection details
Rfree0.24226 2362 5.2 %RANDOM
Rwork0.19842 ---
obs0.20072 43356 67.23 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å
Displacement parametersBiso mean: 33.72 Å2
Baniso -1Baniso -2Baniso -3
1--0.23 Å2-0.11 Å20 Å2
2---0.23 Å20 Å2
3---0.34 Å2
Refinement stepCycle: 1 / Resolution: 1.83→72.34 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms4980 0 0 170 5150
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0070.025073
X-RAY DIFFRACTIONr_bond_other_d
X-RAY DIFFRACTIONr_angle_refined_deg1.2261.9576917
X-RAY DIFFRACTIONr_angle_other_deg
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.5865667
X-RAY DIFFRACTIONr_dihedral_angle_2_deg34.67224.767193
X-RAY DIFFRACTIONr_dihedral_angle_3_deg14.60415795
X-RAY DIFFRACTIONr_dihedral_angle_4_deg19.2841524
X-RAY DIFFRACTIONr_chiral_restr0.080.2813
X-RAY DIFFRACTIONr_gen_planes_refined0.0050.0213818
X-RAY DIFFRACTIONr_gen_planes_other
X-RAY DIFFRACTIONr_nbd_refined
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_other
X-RAY DIFFRACTIONr_mcangle_other
X-RAY DIFFRACTIONr_scbond_other
X-RAY DIFFRACTIONr_scangle_other
X-RAY DIFFRACTIONr_long_range_B_refined
X-RAY DIFFRACTIONr_long_range_B_other
X-RAY DIFFRACTIONr_rigid_bond_restr
X-RAY DIFFRACTIONr_sphericity_free
X-RAY DIFFRACTIONr_sphericity_bonded
LS refinement shellResolution: 1.83→1.873 Å
RfactorNum. reflection% reflection
Rwork0.369 30 -
Rfree-0 -
obs--0.61 %

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