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- PDB-1vhs: Crystal structure of a putative phosphinothricin N-acetyltransferase -

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Basic information

Entry
Database: PDB / ID: 1vhs
TitleCrystal structure of a putative phosphinothricin N-acetyltransferase
Componentssimilar to phosphinothricin acetyltransferase
KeywordsStructural genomics / unknown function
Function / homology
Function and homology information


phosphinothricin acetyltransferase / phosphinothricin N-acetyltransferase activity / response to herbicide / acyltransferase activity, transferring groups other than amino-acyl groups / response to antibiotic
Similarity search - Function
Acetyltransferase (GNAT) family / Gcn5-related N-acetyltransferase (GNAT) / Gcn5-related N-acetyltransferase (GNAT) domain profile. / GNAT domain / Acyl-CoA N-acyltransferase / Aminopeptidase / 3-Layer(aba) Sandwich / Alpha Beta
Similarity search - Domain/homology
Putative phosphinothricin acetyltransferase YwnH
Similarity search - Component
Biological speciesBacillus subtilis (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / Se-Met SAD phasing / Resolution: 1.8 Å
AuthorsStructural GenomiX
CitationJournal: Proteins / Year: 2005
Title: Structural analysis of a set of proteins resulting from a bacterial genomics project
Authors: Badger, J. / Sauder, J.M. / Adams, J.M. / Antonysamy, S. / Bain, K. / Bergseid, M.G. / Buchanan, S.G. / Buchanan, M.D. / Batiyenko, Y. / Christopher, J.A. / Emtage, S. / Eroshkina, A. / ...Authors: Badger, J. / Sauder, J.M. / Adams, J.M. / Antonysamy, S. / Bain, K. / Bergseid, M.G. / Buchanan, S.G. / Buchanan, M.D. / Batiyenko, Y. / Christopher, J.A. / Emtage, S. / Eroshkina, A. / Feil, I. / Furlong, E.B. / Gajiwala, K.S. / Gao, X. / He, D. / Hendle, J. / Huber, A. / Hoda, K. / Kearins, P. / Kissinger, C. / Laubert, B. / Lewis, H.A. / Lin, J. / Loomis, K. / Lorimer, D. / Louie, G. / Maletic, M. / Marsh, C.D. / Miller, I. / Molinari, J. / Muller-Dieckmann, H.J. / Newman, J.M. / Noland, B.W. / Pagarigan, B. / Park, F. / Peat, T.S. / Post, K.W. / Radojicic, S. / Ramos, A. / Romero, R. / Rutter, M.E. / Sanderson, W.E. / Schwinn, K.D. / Tresser, J. / Winhoven, J. / Wright, T.A. / Wu, L. / Xu, J. / Harris, T.J.
History
DepositionDec 1, 2003Deposition site: RCSB / Processing site: RCSB
Revision 1.0Dec 30, 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 / Item: _software.name
Revision 1.4Dec 27, 2023Group: Data collection / Database references / Derived calculations
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / struct_conn
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_conn.pdbx_leaving_atom_flag
Revision 1.5Oct 30, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: similar to phosphinothricin acetyltransferase
B: similar to phosphinothricin acetyltransferase


Theoretical massNumber of molelcules
Total (without water)39,9602
Polymers39,9602
Non-polymers00
Water4,396244
1
A: similar to phosphinothricin acetyltransferase


Theoretical massNumber of molelcules
Total (without water)19,9801
Polymers19,9801
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
2
B: similar to phosphinothricin acetyltransferase


Theoretical massNumber of molelcules
Total (without water)19,9801
Polymers19,9801
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)84.506, 50.827, 87.606
Angle α, β, γ (deg.)90.00, 116.67, 90.00
Int Tables number5
Space group name H-MC121

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Components

#1: Protein similar to phosphinothricin acetyltransferase


Mass: 19979.752 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Bacillus subtilis (bacteria) / Gene: ywnH / Production host: Escherichia coli (E. coli) / References: UniProt: P71043
#2: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 244 / Source method: isolated from a natural source / Formula: H2O
Has protein modificationY

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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: 2.1 Å3/Da / Density % sol: 41.53 %
Crystal grow
*PLUS
pH: 7.5 / Method: vapor diffusion, hanging drop
Components of the solutions
*PLUS
IDConc.Common nameCrystal-IDSol-IDDetailsChemical formula
110 mMHEPES1droppH7.5
2150 mM1dropNaCl
310 mMmethionine1drop
410 %glycerol1drop
55 mMdithiothreitol1drop
610 mg/mlprotein1drop

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Data collection

Diffraction sourceSource: SYNCHROTRON / Site: APS / Beamline: 32-ID / Wavelength: 0.9795 Å
DetectorType: MARRESEARCH / Detector: CCD
RadiationProtocol: SINGLE WAVELENGTH / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9795 Å / Relative weight: 1
ReflectionResolution: 1.7→42.22 Å / Num. all: 35908 / Num. obs: 35908 / % possible obs: 97.6 % / Redundancy: 7.3 % / Rmerge(I) obs: 0.115 / Net I/σ(I): 8.9
Reflection shellResolution: 1.7→1.79 Å / Redundancy: 7 % / Rmerge(I) obs: 0.747 / Mean I/σ(I) obs: 2 / % possible all: 97.6
Reflection shell
*PLUS
% possible obs: 97.6 %

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Processing

Software
NameVersionClassification
DENZOdata reduction
SCALAdata scaling
TRUNCATEdata reduction
REFMAC4refinement
CCP4(SCALAdata scaling
TRUNCATEdata scaling
RefinementMethod to determine structure: Se-Met SAD phasing / Resolution: 1.8→42.22 Å / σ(F): 0
RfactorNum. reflection
Rfree0.28 1528
Rwork0.238 -
obs-30360
Solvent computationSolvent model: Babinet bulk solvent correction / Bsol: 381.154 Å2 / ksol: 0.999 e/Å3
Displacement parametersBiso mean: 30.116 Å2
Baniso -1Baniso -2Baniso -3
1--0.39 Å20 Å2-0.603 Å2
2--1.277 Å20 Å2
3----1.429 Å2
Refine Biso Class: all / Treatment: isotropic
Refinement stepCycle: LAST / Resolution: 1.8→42.22 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2532 0 0 244 2776
Refine LS restraints
Refine-IDTypeDev ideal
X-RAY DIFFRACTIONp_bond_d0.005
X-RAY DIFFRACTIONp_angle_d1.272
X-RAY DIFFRACTIONp_planar_tor1.12
X-RAY DIFFRACTIONp_chiral_restr0.1
X-RAY DIFFRACTIONp_plane_restr0.005
X-RAY DIFFRACTIONp_mcbond_it2.189
X-RAY DIFFRACTIONp_mcangle_it3.744
X-RAY DIFFRACTIONp_scbond_it3.859
X-RAY DIFFRACTIONp_scangle_it5.54
Software
*PLUS
Version: 4 / Classification: refinement
Refinement
*PLUS
Rfactor Rfree: 0.28
Solvent computation
*PLUS
Displacement parameters
*PLUS
Refine LS restraints
*PLUS
Refine-IDTypeDev ideal
X-RAY DIFFRACTIONp_angle_d
X-RAY DIFFRACTIONp_angle_deg1.3

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