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- PDB-1o27: Crystal structure of Thymidylate Synthase Complementing Protein (... -

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Basic information

Entry
Database: PDB / ID: 1o27
TitleCrystal structure of Thymidylate Synthase Complementing Protein (TM0449) from Thermotoga maritima with FAD and BrdUMP at 2.3 A resolution
ComponentsThymidylate synthase thyX
KeywordsTRANSFERASE / TM0449 / THYMIDYLATE SYNTHASE COMPLEMENTING PROTEIN / STRUCTURAL GENOMICS / JCSG / Joint Center for Structural Genomics / PSI / Protein Structure Initiative
Function / homology
Function and homology information


thymidylate synthase (FAD) / thymidylate synthase (FAD) activity / thymidylate synthase activity / dTMP biosynthetic process / dTTP biosynthetic process / NADPH binding / flavin adenine dinucleotide binding / methylation
Similarity search - Function
Gyrase A; domain 2 - #170 / Thymidylate synthase ThyX / Thymidylate synthase ThyX superfamily / Thymidylate synthase complementing protein / Flavin-dependent thymidylate synthase (thyX) domain profile. / Gyrase A; domain 2 / 2-Layer Sandwich / Alpha Beta
Similarity search - Domain/homology
5-BROMO-2'-DEOXYURIDINE-5'-MONOPHOSPHATE / FLAVIN-ADENINE DINUCLEOTIDE / Flavin-dependent thymidylate synthase
Similarity search - Component
Biological speciesThermotoga maritima (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / molecular replacement / Resolution: 2.3 Å
AuthorsMathews, I.I. / Deacon, A.M. / Canaves, J.M. / McMullan, D. / Lesley, S.A. / Agarwalla, S. / Kuhn, P. / Joint Center for Structural Genomics (JCSG)
CitationJournal: Structure / Year: 2003
Title: Functional Analysis of Substrate and Cofactor Complex Structures of a Thymidylate Synthase-Complementing Protein
Authors: Mathews, I.I. / Deacon, A.M. / Canaves, J.M. / McMullan, D. / Lesley, S.A. / Agarwalla, S. / Kuhn, P.
History
DepositionFeb 18, 2003Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jun 24, 2003Provider: repository / Type: Initial release
Revision 1.1Apr 26, 2008Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3Oct 4, 2017Group: Refinement description / Category: software
Revision 1.4Jul 18, 2018Group: Data collection / Database references / Category: pdbx_database_related
Revision 1.5Jan 25, 2023Group: Database references / Derived calculations / Category: database_2 / struct_ref_seq_dif / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_ref_seq_dif.details / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id
Revision 1.6Sep 20, 2023Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Thymidylate synthase thyX
B: Thymidylate synthase thyX
C: Thymidylate synthase thyX
D: Thymidylate synthase thyX
hetero molecules


Theoretical massNumber of molelcules
Total (without water)114,70512
Polymers110,0154
Non-polymers4,6918
Water3,621201
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area23440 Å2
ΔGint-65 kcal/mol
Surface area31160 Å2
MethodPISA
Unit cell
Length a, b, c (Å)54.349, 116.428, 140.557
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
Thymidylate synthase thyX / TS / TSase / thymidylate synthase complementing protein


Mass: 27503.680 Da / Num. of mol.: 4
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Thermotoga maritima (bacteria) / Gene: TM0449 / Production host: Escherichia coli (E. coli)
References: UniProt: Q9WYT0, Transferases; Transferring one-carbon groups; Methyltransferases
#2: Chemical
ChemComp-BRU / 5-BROMO-2'-DEOXYURIDINE-5'-MONOPHOSPHATE


Type: DNA linking / Mass: 387.078 Da / Num. of mol.: 4 / Source method: obtained synthetically / Formula: C9H12BrN2O8P
#3: Chemical
ChemComp-FAD / FLAVIN-ADENINE DINUCLEOTIDE


Mass: 785.550 Da / Num. of mol.: 4 / Source method: obtained synthetically / Formula: C27H33N9O15P2 / Comment: FAD*YM
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 201 / 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: 2.06 Å3/Da / Density % sol: 39.74 %
Crystal growTemperature: 295 K / Method: vapor diffusion, hanging drop / pH: 7.5
Details: 45% PEG 200, 0.1M HEPES, pH 7.5, VAPOR DIFFUSION,HANGING DROP, temperature 295K
Crystal grow
*PLUS
Method: vapor diffusion, sitting drop / Details: Kuhn, P., (2002) Proteins, 49, 142.
Components of the solutions
*PLUS
IDConc.Common nameCrystal-IDSol-IDDetails
1100 mMTris-HCl1reservoirpH8.0
249 %(w/v)PEG2001reservoiror 100mM HEPES, pH7.5
344 %PEG2001reservoir

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: SSRL / Beamline: BL9-1 / Wavelength: 0.99184
DetectorType: ADSC QUANTUM 4r / Detector: CCD / Date: Mar 20, 2002
Details: Flat mirror,single crystal Si(311) bent monochromator
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.99184 Å / Relative weight: 1
ReflectionResolution: 2.3→46.477 Å / Num. all: 39615 / Num. obs: 39615 / % possible obs: 98 % / Redundancy: 5.7 % / Biso Wilson estimate: 34.877 Å2 / Rsym value: 0.081 / Net I/σ(I): 17.5
Reflection shellResolution: 2.3→2.36 Å / Redundancy: 5.4 % / Mean I/σ(I) obs: 3.5 / Num. unique all: 2762 / Rsym value: 0.445 / % possible all: 93.1
Reflection
*PLUS
Highest resolution: 2.3 Å / Lowest resolution: 46.6 Å / Num. measured all: 226323 / Rmerge(I) obs: 0.081
Reflection shell
*PLUS
% possible obs: 93.1 % / Rmerge(I) obs: 0.445

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Processing

Software
NameVersionClassification
MOSFLMdata reduction
SCALAdata scaling
RESOLVEmodel building
SOLVEphasing
CNSrefinement
CCP4(SCALA)data scaling
RESOLVEphasing
RefinementMethod to determine structure: molecular replacement
Starting model: 1KQ4

1kq4


Resolution: 2.3→20 Å / Isotropic thermal model: Isotropic / Cross valid method: THROUGHOUT / σ(F): 2 / Stereochemistry target values: Engh and Huber
RfactorNum. reflection% reflection
Rfree0.23 1971 4.9 %
Rwork0.1882 --
all-39539 -
obs-39284 97.2 %
Solvent computationSolvent model: Bulk solvent correction / Bsol: 0.383022 Å2 / ksol: 37.8738 e/Å3
Displacement parametersBiso mean: 32.9 Å2
Baniso -1Baniso -2Baniso -3
1--6.698 Å20 Å20 Å2
2--1.942 Å20 Å2
3---4.756 Å2
Refine analyzeLuzzati coordinate error obs: 0.2591 Å
Refinement stepCycle: LAST / Resolution: 2.3→20 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms7221 0 296 201 7718
Refine LS restraints
Refine-IDTypeDev idealDev ideal target
X-RAY DIFFRACTIONc_bond_d0.007
X-RAY DIFFRACTIONc_angle_deg1.22
X-RAY DIFFRACTIONc_mcbond_it1.1761.5
X-RAY DIFFRACTIONc_scbond_it1.982
X-RAY DIFFRACTIONc_mcangle_it1.8652
X-RAY DIFFRACTIONc_scangle_it2.9352.5
LS refinement shellResolution: 2.3→2.32 Å / Total num. of bins used: 39
RfactorNum. reflection% reflection
Rfree0.2744 41 4.371 %
Rwork0.2232 897 -
Refinement
*PLUS
Rfactor Rfree: 0.23 / Rfactor Rwork: 0.188 / % reflection Rfree: 5 %
Solvent computation
*PLUS
Displacement parameters
*PLUS

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