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- PDB-4ian: Crystal Structure of apo Human PRPF4B kinase domain -

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Basic information

Entry
Database: PDB / ID: 4ian
TitleCrystal Structure of apo Human PRPF4B kinase domain
ComponentsSerine/threonine-protein kinase PRP4 homolog
KeywordsTRANSFERASE / kinase
Function / homology
Function and homology information


mRNA cis splicing, via spliceosome / catalytic step 2 spliceosome / mRNA Splicing - Major Pathway / RNA splicing / mRNA splicing, via spliceosome / chromosome / non-specific serine/threonine protein kinase / protein kinase activity / nuclear speck / protein phosphorylation ...mRNA cis splicing, via spliceosome / catalytic step 2 spliceosome / mRNA Splicing - Major Pathway / RNA splicing / mRNA splicing, via spliceosome / chromosome / non-specific serine/threonine protein kinase / protein kinase activity / nuclear speck / protein phosphorylation / protein serine kinase activity / protein serine/threonine kinase activity / RNA binding / nucleoplasm / ATP binding / nucleus
Similarity search - Function
Serine/threonine-protein PRP4, catalytic domain / Transferase(Phosphotransferase) domain 1 / Transferase(Phosphotransferase); domain 1 / Phosphorylase Kinase; domain 1 / Phosphorylase Kinase; domain 1 / Serine/threonine-protein kinase, active site / Serine/Threonine protein kinases active-site signature. / Protein kinase domain / Serine/Threonine protein kinases, catalytic domain / Protein kinase domain profile. ...Serine/threonine-protein PRP4, catalytic domain / Transferase(Phosphotransferase) domain 1 / Transferase(Phosphotransferase); domain 1 / Phosphorylase Kinase; domain 1 / Phosphorylase Kinase; domain 1 / Serine/threonine-protein kinase, active site / Serine/Threonine protein kinases active-site signature. / Protein kinase domain / Serine/Threonine protein kinases, catalytic domain / Protein kinase domain profile. / Protein kinase domain / Protein kinase-like domain superfamily / 2-Layer Sandwich / Orthogonal Bundle / Mainly Alpha / Alpha Beta
Similarity search - Domain/homology
Serine/threonine-protein kinase PRP4 homolog
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.44 Å
AuthorsMechin, I. / Haas, K. / Chen, X. / Zhang, Y. / McLean, L.
CitationJournal: J.Biol.Chem. / Year: 2013
Title: Evaluation of Cancer Dependence and Druggability of PRP4 Kinase Using Cellular, Biochemical, and Structural Approaches.
Authors: Gao, Q. / Mechin, I. / Kothari, N. / Guo, Z. / Deng, G. / Haas, K. / McManus, J. / Hoffmann, D. / Wang, A. / Wiederschain, D. / Rocnik, J. / Czechtizky, W. / Chen, X. / McLean, L. / Arlt, H. ...Authors: Gao, Q. / Mechin, I. / Kothari, N. / Guo, Z. / Deng, G. / Haas, K. / McManus, J. / Hoffmann, D. / Wang, A. / Wiederschain, D. / Rocnik, J. / Czechtizky, W. / Chen, X. / McLean, L. / Arlt, H. / Harper, D. / Liu, F. / Majid, T. / Patel, V. / Lengauer, C. / Garcia-Echeverria, C. / Zhang, B. / Cheng, H. / Dorsch, M. / Huang, S.M.
History
DepositionDec 6, 2012Deposition site: RCSB / Processing site: RCSB
Revision 1.0Aug 28, 2013Provider: repository / Type: Initial release
Revision 1.1Sep 4, 2013Group: Data collection
Revision 1.2Sep 18, 2013Group: Database references
Revision 1.3Nov 6, 2013Group: Database references
Revision 1.4Nov 15, 2017Group: Refinement description / Category: software
Item: _software.classification / _software.contact_author ..._software.classification / _software.contact_author / _software.contact_author_email / _software.date / _software.language / _software.location / _software.name / _software.type / _software.version

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Serine/threonine-protein kinase PRP4 homolog
B: Serine/threonine-protein kinase PRP4 homolog
hetero molecules


Theoretical massNumber of molelcules
Total (without water)84,4438
Polymers83,8672
Non-polymers5766
Water1,17165
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area1840 Å2
ΔGint-77 kcal/mol
Surface area30090 Å2
MethodPISA
Unit cell
Length a, b, c (Å)73.266, 75.286, 148.003
Angle α, β, γ (deg.)90.000, 97.210, 90.000
Int Tables number5
Space group name H-MC121

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Components

#1: Protein Serine/threonine-protein kinase PRP4 homolog / PRP4 kinase / PRP4 pre-mRNA-processing factor 4 homolog


Mass: 41933.469 Da / Num. of mol.: 2 / Fragment: kinase domain
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: KIAA0536, PRP4, PRP4H, PRP4K, PRPF4B / Plasmid: pFastBac1 / Production host: Spodoptera frugiperda (fall armyworm) / Strain (production host): Sf9
References: UniProt: Q13523, non-specific serine/threonine protein kinase
#2: Chemical
ChemComp-SO4 / SULFATE ION / Sulfate


Mass: 96.063 Da / Num. of mol.: 6 / Source method: obtained synthetically / Formula: SO4
#3: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 65 / 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: 2.41 Å3/Da / Density % sol: 49.05 %
Crystal growTemperature: 291 K / Method: vapor diffusion, hanging drop / pH: 7
Details: 0.2M ammonium sulfate, 20-30% PEG 3350 and 0.1M HEPES pH7.0, vapor diffusion, hanging drop, temperature 291K

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: APS / Beamline: 22-BM / Wavelength: 1 Å
DetectorType: MARMOSAIC 225 mm CCD / Detector: CCD / Date: Oct 17, 2010
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 2.44→50 Å / Num. obs: 29966 / % possible obs: 99.3 % / Redundancy: 3.7 % / Rmerge(I) obs: 0.109 / Χ2: 1.057 / Net I/σ(I): 7.6
Reflection shell
Resolution (Å)Redundancy (%)Rmerge(I) obsNum. unique allΧ2Diffraction-ID% possible all
2.44-2.533.10.53328361.081193.5
2.53-2.633.70.44229811.087199.9
2.63-2.753.80.33729791.0931100
2.75-2.893.80.25829951.0841100
2.89-3.073.80.19330181.0931100
3.07-3.313.80.13630111.0121100
3.31-3.643.80.10129931.021100
3.64-4.173.80.08730151.0041100
4.17-5.253.80.0930631.0911100
5.25-503.70.0730751.009199.6

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Processing

Software
NameVersionClassificationNB
DENZOdata reduction
SCALEPACKdata scaling
CNSrefinement
PDB_EXTRACT3.11data extraction
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.44→50 Å / Occupancy max: 1 / Occupancy min: 1 / σ(F): 0
RfactorNum. reflection% reflection
Rfree0.2878 1395 4.7 %
Rwork0.2283 --
obs-28266 94.5 %
Displacement parametersBiso max: 100.32 Å2 / Biso mean: 44.6414 Å2 / Biso min: 11.67 Å2
Baniso -1Baniso -2Baniso -3
1-0.416 Å20 Å20.216 Å2
2---0.301 Å20 Å2
3----0.115 Å2
Refinement stepCycle: LAST / Resolution: 2.44→50 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms5238 0 30 65 5333
Refine LS restraints
Refine-IDTypeDev idealDev ideal target
X-RAY DIFFRACTIONc_bond_d0.006
X-RAY DIFFRACTIONc_angle_d1.039
X-RAY DIFFRACTIONc_mcbond_it1.5231.5
X-RAY DIFFRACTIONc_scbond_it2.1022
X-RAY DIFFRACTIONc_mcangle_it2.6192
X-RAY DIFFRACTIONc_scangle_it3.1922.5
Xplor file
Refine-IDSerial noParam file
X-RAY DIFFRACTION1protein_rep.param
X-RAY DIFFRACTION2dna-rna_rep.param
X-RAY DIFFRACTION3water_rep.param
X-RAY DIFFRACTION4ion.param

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