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- PDB-7dyg: Histone lysine demethylase 4D (KDM4D) in complex with the inhibit... -

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Basic information

Entry
Database: PDB / ID: 7dyg
TitleHistone lysine demethylase 4D (KDM4D) in complex with the inhibitor 2-(1H-pyrazol-3-yl)isonicotinic acid
ComponentsLysine-specific demethylase 4D
KeywordsOXIDOREDUCTASE / Complex / Inhibitor
Function / homology
Function and homology information


positive regulation of chromatin binding / [histone H3]-trimethyl-L-lysine9 demethylase / histone H3K9me2/H3K9me3 demethylase activity / positive regulation of double-strand break repair via nonhomologous end joining / histone H3K9 demethylase activity / regulation of protein phosphorylation / histone demethylase activity / pericentric heterochromatin / cellular response to ionizing radiation / HDMs demethylate histones ...positive regulation of chromatin binding / [histone H3]-trimethyl-L-lysine9 demethylase / histone H3K9me2/H3K9me3 demethylase activity / positive regulation of double-strand break repair via nonhomologous end joining / histone H3K9 demethylase activity / regulation of protein phosphorylation / histone demethylase activity / pericentric heterochromatin / cellular response to ionizing radiation / HDMs demethylate histones / double-strand break repair via homologous recombination / chromatin DNA binding / site of double-strand break / regulation of gene expression / blood microparticle / damaged DNA binding / chromatin remodeling / inflammatory response / chromatin / nucleoplasm / metal ion binding / nucleus
Similarity search - Function
JmjN domain / jmjN domain / JmjN domain profile. / Small domain found in the jumonji family of transcription factors / JmjC domain, hydroxylase / A domain family that is part of the cupin metalloenzyme superfamily. / JmjC domain / JmjC domain profile.
Similarity search - Domain/homology
2-(1H-pyrazol-3-yl)pyridine-4-carboxylic acid / : / Lysine-specific demethylase 4D
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2 Å
AuthorsWang, T. / Yang, L.
CitationJournal: To Be Published
Title: Crystal structure of histone lysine demethylase 4D (KDM4D) in complex with the inhibitor 2-(1H-pyrazol-3-yl)isonicotinic acid
Authors: Wang, T. / Yang, L.
History
DepositionJan 21, 2021Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0Jan 26, 2022Provider: repository / Type: Initial release
Revision 1.1Nov 29, 2023Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model
Revision 1.2Nov 20, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature / Item: _pdbx_entry_details.has_protein_modification

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Lysine-specific demethylase 4D
hetero molecules


Theoretical massNumber of molelcules
Total (without water)38,3383
Polymers38,0931
Non-polymers2452
Water5,891327
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: gel filtration
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area140 Å2
ΔGint-14 kcal/mol
Surface area15000 Å2
MethodPISA
Unit cell
Length a, b, c (Å)71.720, 71.720, 151.242
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number96
Space group name H-MP43212
Components on special symmetry positions
IDModelComponents
11A-530-

HOH

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Components

#1: Protein Lysine-specific demethylase 4D / JmjC domain-containing histone demethylation protein 3D / Jumonji domain-containing protein 2D / ...JmjC domain-containing histone demethylation protein 3D / Jumonji domain-containing protein 2D / [histone H3]-trimethyl-L-lysine(9) demethylase 4D / Histone lysine demethylase 4D


Mass: 38093.156 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: KDM4D, JHDM3D, JMJD2D / Production host: Escherichia coli (E. coli)
References: UniProt: Q6B0I6, [histone H3]-trimethyl-L-lysine9 demethylase
#2: Chemical ChemComp-0WS / 2-(1H-pyrazol-3-yl)pyridine-4-carboxylic acid


Mass: 189.171 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C9H7N3O2 / Feature type: SUBJECT OF INVESTIGATION
#3: Chemical ChemComp-FE / FE (III) ION


Mass: 55.845 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Fe
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 327 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestY
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: 2.55 Å3/Da / Density % sol: 51.82 %
Crystal growTemperature: 291.15 K / Method: vapor diffusion, sitting drop
Details: 0.2M potassium citrate tribasic monohydrate PH 8.3, 20% w/v PEG 3350

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Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: NFPSS / Beamline: BL19U1 / Wavelength: 0.9793 Å
DetectorType: DECTRIS PILATUS3 X CdTe 1M / Detector: PIXEL / Date: Jan 13, 2020
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9793 Å / Relative weight: 1
ReflectionResolution: 2→50 Å / Num. obs: 27588 / % possible obs: 100 % / Redundancy: 25.6 % / Rmerge(I) obs: 0.095 / Net I/σ(I): 38.2
Reflection shellResolution: 2→2.03 Å / Rmerge(I) obs: 0.238 / Num. unique obs: 1333

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Processing

Software
NameVersionClassification
PHENIX1.12_2829refinement
PDB_EXTRACT3.27data extraction
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 4d6q

4d6q


Resolution: 2→25.978 Å / SU ML: 0.14 / Cross valid method: THROUGHOUT / σ(F): 1.34 / Phase error: 17.29 / Stereochemistry target values: ML
RfactorNum. reflection% reflection
Rfree0.1857 1364 4.97 %
Rwork0.1609 26089 -
obs0.1622 27453 99.83 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Displacement parametersBiso max: 100.83 Å2 / Biso mean: 27.7658 Å2 / Biso min: 5.44 Å2
Refinement stepCycle: final / Resolution: 2→25.978 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2660 0 21 327 3008
Biso mean--43.86 34.94 -
Num. residues----330
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0122780
X-RAY DIFFRACTIONf_angle_d1.1773767
X-RAY DIFFRACTIONf_chiral_restr0.226380
X-RAY DIFFRACTIONf_plane_restr0.008490
X-RAY DIFFRACTIONf_dihedral_angle_d12.4151625
LS refinement shell

Refine-ID: X-RAY DIFFRACTION / Rfactor Rfree error: 0

Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection Rwork% reflection obs (%)
2-2.07090.18061390.14662550100
2.0709-2.15380.18911320.15652548100
2.1538-2.25180.22351220.16432582100
2.2518-2.37040.19971370.1622560100
2.3704-2.51880.19681330.15442564100
2.5188-2.71310.17291350.15572591100
2.7131-2.98580.20651170.16062649100
2.9858-3.4170.17761410.15582619100
3.417-4.30190.17281580.1472625100
4.3019-25.9780.1841500.184280199

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