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- PDB-6kew: Crystal structure of oxidized phosphoribulokinase from Arabidopsi... -

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Basic information

Entry
Database: PDB / ID: 6kew
TitleCrystal structure of oxidized phosphoribulokinase from Arabidopsis thaliana
ComponentsPhosphoribulokinase
KeywordsTRANSFERASE / phosphoribulokinase oxidized
Function / homology
Function and homology information


phosphoribulokinase / phosphoribulokinase activity / supramolecular complex / stromule / apoplast / reductive pentose-phosphate cycle / chloroplast envelope / thylakoid / chloroplast stroma / chloroplast thylakoid membrane ...phosphoribulokinase / phosphoribulokinase activity / supramolecular complex / stromule / apoplast / reductive pentose-phosphate cycle / chloroplast envelope / thylakoid / chloroplast stroma / chloroplast thylakoid membrane / response to cold / chloroplast / disordered domain specific binding / phosphorylation / protein homodimerization activity / ATP binding / nucleus
Similarity search - Function
Phosphoribulokinase signature. / Phosphoribulokinase / Phosphoribulokinase/uridine kinase / Phosphoribulokinase / Uridine kinase family / P-loop containing nucleoside triphosphate hydrolase
Similarity search - Domain/homology
Phosphoribulokinase, chloroplastic
Similarity search - Component
Biological speciesArabidopsis thaliana (thale cress)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.29 Å
AuthorsYu, A. / Xie, Y. / Li, M.
Funding support China, 1items
OrganizationGrant numberCountry
National Natural Science Foundation of China31770778 China
CitationJournal: Plant Cell / Year: 2020
Title: Photosynthetic Phosphoribulokinase Structures: Enzymatic Mechanisms and the Redox Regulation of the Calvin-Benson-Bassham Cycle.
Authors: Yu, A. / Xie, Y. / Pan, X. / Zhang, H. / Cao, P. / Su, X. / Chang, W. / Li, M.
History
DepositionJul 5, 2019Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0May 13, 2020Provider: repository / Type: Initial release
Revision 1.1May 20, 2020Group: Database references / Category: citation
Item: _citation.journal_volume / _citation.page_first / _citation.page_last
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

Downloads & links

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Assembly

Deposited unit
A: Phosphoribulokinase
B: Phosphoribulokinase


Theoretical massNumber of molelcules
Total (without water)81,0042
Polymers81,0042
Non-polymers00
Water3,135174
1


  • Idetical with deposited unit
  • defined by author
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area960 Å2
ΔGint-7 kcal/mol
Surface area30530 Å2
Unit cell
Length a, b, c (Å)80.784, 50.315, 194.783
Angle α, β, γ (deg.)90.000, 91.810, 90.000
Int Tables number5
Space group name H-MC121
Space group name HallC2y
Symmetry operation#1: x,y,z
#2: -x,y,-z
#3: x+1/2,y+1/2,z
#4: -x+1/2,y+1/2,-z
Components on special symmetry positions
IDModelComponents
11A-468-

HOH

21A-492-

HOH

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Components

#1: Protein Phosphoribulokinase / / PRKase / Phosphopentokinase


Mass: 40501.918 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Arabidopsis thaliana (thale cress) / Gene: At1g32060, T12O21.4 / Production host: Escherichia coli (E. coli) / References: UniProt: P25697, phosphoribulokinase
#2: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 174 / 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: 2.44 Å3/Da / Density % sol: 49.64 %
Crystal growTemperature: 291.15 K / Method: vapor diffusion, sitting drop
Details: 4% v/v Tacsimate pH5.0, 12% w/v polyethylene glycol 3350

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Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: SSRF / Beamline: BL17U / Wavelength: 0.98 Å
DetectorType: ADSC QUANTUM 315r / Detector: CCD / Date: Apr 14, 2017
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.98 Å / Relative weight: 1
ReflectionResolution: 2.29→50 Å / Num. obs: 23859 / % possible obs: 95.1 % / Redundancy: 6.3 % / Rmerge(I) obs: 0.085 / Rpim(I) all: 0.036 / Rrim(I) all: 0.092 / Χ2: 0.881 / Net I/σ(I): 18.1
Reflection shellResolution: 2.29→2.33 Å / Redundancy: 6.5 % / Rmerge(I) obs: 0.553 / Mean I/σ(I) obs: 2.22 / Num. unique obs: 1703 / CC1/2: 0.978 / Rpim(I) all: 0.232 / Rrim(I) all: 0.601 / % possible all: 98.9

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Processing

Software
NameVersionClassification
PHENIX1.12_2829refinement
HKL-2000data reduction
HKL-2000data scaling
PHENIXphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 6KEX
Resolution: 2.29→42.7 Å / Cross valid method: FREE R-VALUE
RfactorNum. reflection% reflection
Rfree0.2593 --
Rwork0.2408 --
obs-23781 79.37 %
Displacement parametersBiso mean: 44.16 Å2
Refinement stepCycle: LAST / Resolution: 2.29→42.7 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms5431 0 0 174 5605
Refinement TLS params.

Method: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
12.04080.8466-1.06721.266-0.6934.5933-0.1422-0.08230.22040.10.26430.4862-0.4088-0.773-0.11240.23620.1432-0.00030.58190.06610.34-20.302317.439936.7304
22.73610.1482-0.3091.1757-0.16972.0452-0.0649-0.06610.52260.19190.0142-0.0186-0.3487-0.21430.03080.21630.0748-0.0510.17280.01530.2904-12.303126.816822.0378
33.08240.5550.32911.0543-0.51434.089-0.0445-0.2069-0.0661-0.0213-0.0087-0.0310.2457-0.55770.04080.1663-0.0095-0.00740.1094-0.03870.2258-10.207412.774910.5319
42.8321-1.0001-1.34581.60070.56783.3164-0.11050.1826-0.0784-0.54320.0286-0.83440.73291.07120.06790.48740.12150.08990.93060.07850.473-22.5895-0.056170.4439
52.37110.0121-1.90211.7522-0.55153.5576-0.14620.1757-0.2268-0.3388-0.2051-0.1510.48950.30440.25380.35160.10790.03290.46780.0280.2183-25.02046.117659.455
63.37670.4667-1.0591.399-0.12223.64150.2305-0.09180.83690.2958-0.0633-0.3518-0.34950.6239-0.22430.3226-0.01260.01340.3797-0.01510.4851-22.57823.852974.6025
72.6918-0.0189-1.49791.8214-0.34693.5061-0.08360.0442-0.00740.1180.03320.02910.13870.19660.09070.20560.01170.00770.28160.02860.1363-35.5819.87880.7639
82.8046-0.2154-0.78332.3035-0.17723.8855-0.2539-0.0952-0.26840.0072-0.0695-0.11560.70080.85450.27770.34460.15260.08110.58660.08460.2573-33.20510.218286.7859
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection detailsAuth asym-IDAuth seq-ID
1X-RAY DIFFRACTION1chain 'A' and (resid 5 through 127 )A5 - 127
2X-RAY DIFFRACTION2chain 'A' and (resid 128 through 232 )A128 - 232
3X-RAY DIFFRACTION3chain 'A' and (resid 233 through 346 )A233 - 346
4X-RAY DIFFRACTION4chain 'B' and (resid 5 through 40 )B5 - 40
5X-RAY DIFFRACTION5chain 'B' and (resid 41 through 149 )B41 - 149
6X-RAY DIFFRACTION6chain 'B' and (resid 150 through 186 )B150 - 186
7X-RAY DIFFRACTION7chain 'B' and (resid 187 through 232 )B187 - 232
8X-RAY DIFFRACTION8chain 'B' and (resid 233 through 347 )B233 - 347

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