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- PDB-5wnk: Crystal structure of murine receptor-interacting protein 4 (Ripk4... -

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Basic information

Entry
Database: PDB / ID: 5wnk
TitleCrystal structure of murine receptor-interacting protein 4 (Ripk4) D143N bound to TG100-115
ComponentsReceptor-interacting serine/threonine-protein kinase 4
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / Kinase / Inhibitor / Complex / TRANSFERASE / TRANSFERASE-TRANSFERASE INHIBITOR complex
Function / homology
Function and homology information


morphogenesis of an epithelium / non-specific serine/threonine protein kinase / protein serine kinase activity / protein serine/threonine kinase activity / ATP binding / membrane / cytoplasm
Similarity search - Function
Ankyrin repeats (many copies) / Ankyrin repeats (3 copies) / Ankyrin repeat profile. / Ankyrin repeat region circular profile. / ankyrin repeats / Ankyrin repeat / Ankyrin repeat-containing domain superfamily / Transferase(Phosphotransferase) domain 1 / Transferase(Phosphotransferase); domain 1 / Serine/threonine-protein kinase, active site ...Ankyrin repeats (many copies) / Ankyrin repeats (3 copies) / Ankyrin repeat profile. / Ankyrin repeat region circular profile. / ankyrin repeats / Ankyrin repeat / Ankyrin repeat-containing domain superfamily / Transferase(Phosphotransferase) domain 1 / Transferase(Phosphotransferase); 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, ATP binding site / Protein kinases ATP-binding region signature. / Protein kinase domain profile. / Protein kinase domain / Protein kinase-like domain superfamily / Orthogonal Bundle / Mainly Alpha
Similarity search - Domain/homology
3,3'-(2,4-diaminopteridine-6,7-diyl)diphenol / Receptor-interacting serine/threonine-protein kinase 4
Similarity search - Component
Biological speciesMus musculus (house mouse)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 3.11 Å
AuthorsHuang, C.S. / Hymowitz, S.G.
CitationJournal: Structure / Year: 2018
Title: Crystal Structure of Ripk4 Reveals Dimerization-Dependent Kinase Activity.
Authors: Huang, C.S. / Oberbeck, N. / Hsiao, Y.C. / Liu, P. / Johnson, A.R. / Dixit, V.M. / Hymowitz, S.G.
History
DepositionAug 1, 2017Deposition site: RCSB / Processing site: RCSB
Revision 1.0May 9, 2018Provider: repository / Type: Initial release
Revision 1.1May 16, 2018Group: Data collection / Database references / Category: citation / citation_author
Item: _citation.journal_id_ISSN / _citation.journal_volume ..._citation.journal_id_ISSN / _citation.journal_volume / _citation.page_first / _citation.pdbx_database_id_PubMed / _citation.title / _citation_author.name
Revision 1.2Mar 13, 2024Group: Data collection / Database references / Category: chem_comp_atom / chem_comp_bond / database_2
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Receptor-interacting serine/threonine-protein kinase 4
hetero molecules


Theoretical massNumber of molelcules
Total (without water)39,3703
Polymers38,9881
Non-polymers3822
Water362
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: mass spectrometry
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)69.769, 110.231, 146.277
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number24
Space group name H-MI212121

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Components

#1: Protein Receptor-interacting serine/threonine-protein kinase 4 / Ankyrin repeat domain-containing protein 3 / PKC-associated protein kinase / PKC-regulated protein kinase


Mass: 38988.039 Da / Num. of mol.: 1 / Fragment: residues 1-342
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Mus musculus (house mouse) / Gene: Ripk4, Ankrd3, Pkk / Production host: Spodoptera frugiperda (fall armyworm)
References: UniProt: Q9ERK0, non-specific serine/threonine protein kinase
#2: Chemical ChemComp-CL / CHLORIDE ION


Mass: 35.453 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Cl
#3: Chemical ChemComp-B6J / 3,3'-(2,4-diaminopteridine-6,7-diyl)diphenol


Mass: 346.343 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C18H14N6O2
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 2 / 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: 3.65 Å3/Da / Density % sol: 66.3 %
Crystal growTemperature: 292 K / Method: microbatch
Details: 0.1M HEPES pH 7.5, 200 mM magnesium chloride, 10% isopropanol, 15% ethylene glycol, 10% PEG 4000

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: ALS / Beamline: 5.0.2 / Wavelength: 1 Å
DetectorType: DECTRIS PILATUS 6M / Detector: PIXEL / Date: Jun 3, 2015
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 3.11→50.01 Å / Num. obs: 16445 / % possible obs: 98.3 % / Redundancy: 3.8 % / Rmerge(I) obs: 0.0139 / Net I/σ(I): 9.4

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Processing

Software
NameVersionClassification
REFMAC5.8.0158refinement
HKL-2000data reduction
HKL-2000data scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 3.11→50.01 Å / Cor.coef. Fo:Fc: 0.924 / Cor.coef. Fo:Fc free: 0.884 / SU B: 20.123 / SU ML: 0.335 / Cross valid method: THROUGHOUT / ESU R: 0.782 / ESU R Free: 0.394 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
RfactorNum. reflection% reflectionSelection details
Rfree0.27248 547 5.3 %RANDOM
Rwork0.2251 ---
obs0.22771 9839 99.05 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK
Displacement parametersBiso mean: 83.873 Å2
Baniso -1Baniso -2Baniso -3
1-7.32 Å20 Å20 Å2
2--0.94 Å20 Å2
3----8.26 Å2
Refinement stepCycle: 1 / Resolution: 3.11→50.01 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2006 0 27 2 2035
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0080.0192090
X-RAY DIFFRACTIONr_bond_other_d0.0010.021841
X-RAY DIFFRACTIONr_angle_refined_deg1.2191.9682848
X-RAY DIFFRACTIONr_angle_other_deg0.91934243
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.6935260
X-RAY DIFFRACTIONr_dihedral_angle_2_deg35.41922.85784
X-RAY DIFFRACTIONr_dihedral_angle_3_deg14.10415311
X-RAY DIFFRACTIONr_dihedral_angle_4_deg11.6711513
X-RAY DIFFRACTIONr_chiral_restr0.0660.2310
X-RAY DIFFRACTIONr_gen_planes_refined0.0060.0212335
X-RAY DIFFRACTIONr_gen_planes_other0.0010.02430
X-RAY DIFFRACTIONr_nbd_refined
X-RAY DIFFRACTIONr_nbd_other
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_it3.9278.9361049
X-RAY DIFFRACTIONr_mcbond_other3.9238.9331048
X-RAY DIFFRACTIONr_mcangle_it6.32813.391306
X-RAY DIFFRACTIONr_mcangle_other6.32813.3931307
X-RAY DIFFRACTIONr_scbond_it4.0318.9061041
X-RAY DIFFRACTIONr_scbond_other4.0218.9171013
X-RAY DIFFRACTIONr_scangle_it
X-RAY DIFFRACTIONr_scangle_other6.35213.2861500
X-RAY DIFFRACTIONr_long_range_B_refined8.4142334
X-RAY DIFFRACTIONr_long_range_B_other8.3862270
X-RAY DIFFRACTIONr_rigid_bond_restr
X-RAY DIFFRACTIONr_sphericity_free
X-RAY DIFFRACTIONr_sphericity_bonded
LS refinement shellResolution: 3.111→3.192 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.358 37 -
Rwork0.342 636 -
obs--89.49 %

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