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- PDB-3sw9: GLP (G9a-like protein) SET domain in complex with Dnmt3aK44me0 peptide -

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Basic information

Entry
Database: PDB / ID: 3sw9
TitleGLP (G9a-like protein) SET domain in complex with Dnmt3aK44me0 peptide
Components
  • DNA (cytosine-5)-methyltransferase 3A
  • Histone-lysine N-methyltransferase EHMT1
KeywordsTRANSFERASE / epigenetics / non-histone lysine methylation / SET domain / protein lysine methyltransferase
Function / homology
Function and homology information


DNA (cytosine-5-)-methyltransferase activity, acting on CpN substrates / transposable element silencing by piRNA-mediated DNA methylation / epigenetic programming of gene expression / PRC2 methylates histones and DNA / positive regulation of cellular response to hypoxia / [histone H3]-lysine9 N-methyltransferase / cellular response to bisphenol A / peptidyl-lysine monomethylation / peptidyl-lysine dimethylation / histone H3K27 methyltransferase activity ...DNA (cytosine-5-)-methyltransferase activity, acting on CpN substrates / transposable element silencing by piRNA-mediated DNA methylation / epigenetic programming of gene expression / PRC2 methylates histones and DNA / positive regulation of cellular response to hypoxia / [histone H3]-lysine9 N-methyltransferase / cellular response to bisphenol A / peptidyl-lysine monomethylation / peptidyl-lysine dimethylation / histone H3K27 methyltransferase activity / protein-cysteine methyltransferase activity / histone H3K9 methyltransferase activity / histone H3K9me2 methyltransferase activity / RMTs methylate histone arginines / genomic imprinting / DNA (cytosine-5-)-methyltransferase / DNA (cytosine-5-)-methyltransferase activity / autosome genomic imprinting / S-adenosylmethionine metabolic process / protein-lysine N-methyltransferase activity / XY body / C2H2 zinc finger domain binding / response to vitamin A / cellular response to ethanol / DNA methylation-dependent constitutive heterochromatin formation / lncRNA binding / negative regulation of gene expression via chromosomal CpG island methylation / response to ionizing radiation / hepatocyte apoptotic process / Transcriptional Regulation by E2F6 / regulation of embryonic development / Transcriptional Regulation by VENTX / chromosome, centromeric region / catalytic complex / heterochromatin / response to fungicide / Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex / transcription corepressor binding / Transferases; Transferring one-carbon groups; Methyltransferases / methyltransferase activity / response to cocaine / response to lead ion / cellular response to amino acid stimulus / euchromatin / Regulation of TP53 Activity through Methylation / heterochromatin formation / neuron differentiation / PKMTs methylate histone lysines / nuclear matrix / response to toxic substance / p53 binding / response to estradiol / chromatin organization / positive regulation of cold-induced thermogenesis / cellular response to hypoxia / Senescence-Associated Secretory Phenotype (SASP) / spermatogenesis / RNA polymerase II-specific DNA-binding transcription factor binding / methylation / nuclear body / response to xenobiotic stimulus / RNA polymerase II cis-regulatory region sequence-specific DNA binding / negative regulation of DNA-templated transcription / chromatin binding / chromatin / negative regulation of transcription by RNA polymerase II / DNA binding / zinc ion binding / nucleoplasm / identical protein binding / nucleus / metal ion binding / cytoplasm
Similarity search - Function
Histone-lysine N-methyltransferase EHMT1 / DNA (cytosine-5)-methyltransferase 3A, ADD domain / DNA (cytosine-5-)-methyltransferase, N-terminal / Histone-lysine N-methyltransferase EHMT1/EHMT2 / : / Histone-lysine N-methyltransferase EHMT1/EHMT2, Cys-rich region / DNMT3, cysteine rich ADD domain / : / DNMT3, cysteine rich ADD domain, GATA1-like zinc finger / DNMT3, ADD PHD zinc finger ...Histone-lysine N-methyltransferase EHMT1 / DNA (cytosine-5)-methyltransferase 3A, ADD domain / DNA (cytosine-5-)-methyltransferase, N-terminal / Histone-lysine N-methyltransferase EHMT1/EHMT2 / : / Histone-lysine N-methyltransferase EHMT1/EHMT2, Cys-rich region / DNMT3, cysteine rich ADD domain / : / DNMT3, cysteine rich ADD domain, GATA1-like zinc finger / DNMT3, ADD PHD zinc finger / ADD domain / ADD domain profile. / Pre-SET motif / Pre-SET domain / Pre-SET domain profile. / N-terminal to some SET domains / DNA methylase, C-5 cytosine-specific, active site / C-5 cytosine-specific DNA methylases active site. / C-5 cytosine-specific DNA methylase (Dnmt) domain profile. / C-5 cytosine methyltransferase / C-5 cytosine-specific DNA methylase / Beta-clip-like / SET domain / Ankyrin repeats (many copies) / SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain / SET domain / SET domain superfamily / SET domain profile. / SET domain / domain with conserved PWWP motif / PWWP domain / PWWP domain profile. / PWWP domain / Beta Complex / Ankyrin repeats (3 copies) / Ankyrin repeat profile. / Ankyrin repeat region circular profile. / ankyrin repeats / Ankyrin repeat / Ankyrin repeat-containing domain superfamily / S-adenosyl-L-methionine-dependent methyltransferase superfamily / Mainly Beta
Similarity search - Domain/homology
SINEFUNGIN / DNA (cytosine-5)-methyltransferase 3A / Histone-lysine N-methyltransferase EHMT1
Similarity search - Component
Biological speciesHomo sapiens (human)
Mus musculus (house mouse)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 3.05 Å
AuthorsChang, Y. / Horton, J.R. / Zhang, X. / Cheng, X.
CitationJournal: Nat Commun / Year: 2011
Title: MPP8 mediates the interactions between DNA methyltransferase Dnmt3a and H3K9 methyltransferase GLP/G9a.
Authors: Chang, Y. / Sun, L. / Kokura, K. / Horton, J.R. / Fukuda, M. / Espejo, A. / Izumi, V. / Koomen, J.M. / Bedford, M.T. / Zhang, X. / Shinkai, Y. / Fang, J. / Cheng, X.
History
DepositionJul 13, 2011Deposition site: RCSB / Processing site: RCSB
Revision 1.0Dec 7, 2011Provider: repository / Type: Initial release
Revision 1.1Apr 18, 2018Group: Data collection / Category: diffrn_detector / Item: _diffrn_detector.detector
Revision 1.2Sep 13, 2023Group: Data collection / Database references ...Data collection / Database references / Derived calculations / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model / pdbx_struct_conn_angle / struct_conn / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _pdbx_struct_conn_angle.ptnr1_auth_asym_id / _pdbx_struct_conn_angle.ptnr1_auth_seq_id / _pdbx_struct_conn_angle.ptnr1_label_asym_id / _pdbx_struct_conn_angle.ptnr1_label_seq_id / _pdbx_struct_conn_angle.ptnr2_auth_asym_id / _pdbx_struct_conn_angle.ptnr2_auth_seq_id / _pdbx_struct_conn_angle.ptnr2_label_asym_id / _pdbx_struct_conn_angle.ptnr3_auth_asym_id / _pdbx_struct_conn_angle.ptnr3_auth_seq_id / _pdbx_struct_conn_angle.ptnr3_label_asym_id / _pdbx_struct_conn_angle.ptnr3_label_seq_id / _pdbx_struct_conn_angle.value / _struct_conn.pdbx_dist_value / _struct_conn.ptnr1_auth_asym_id / _struct_conn.ptnr1_auth_comp_id / _struct_conn.ptnr1_auth_seq_id / _struct_conn.ptnr1_label_asym_id / _struct_conn.ptnr1_label_atom_id / _struct_conn.ptnr1_label_comp_id / _struct_conn.ptnr1_label_seq_id / _struct_conn.ptnr2_auth_asym_id / _struct_conn.ptnr2_auth_comp_id / _struct_conn.ptnr2_auth_seq_id / _struct_conn.ptnr2_label_asym_id / _struct_conn.ptnr2_label_atom_id / _struct_conn.ptnr2_label_comp_id / _struct_conn.ptnr2_label_seq_id / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Histone-lysine N-methyltransferase EHMT1
P: DNA (cytosine-5)-methyltransferase 3A
B: Histone-lysine N-methyltransferase EHMT1
Q: DNA (cytosine-5)-methyltransferase 3A
hetero molecules


Theoretical massNumber of molelcules
Total (without water)69,46514
Polymers68,1794
Non-polymers1,28610
Water41423
1
A: Histone-lysine N-methyltransferase EHMT1
P: DNA (cytosine-5)-methyltransferase 3A
hetero molecules


Theoretical massNumber of molelcules
Total (without water)34,7337
Polymers34,0902
Non-polymers6435
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area1220 Å2
ΔGint-3 kcal/mol
Surface area12800 Å2
MethodPISA
2
B: Histone-lysine N-methyltransferase EHMT1
Q: DNA (cytosine-5)-methyltransferase 3A
hetero molecules


Theoretical massNumber of molelcules
Total (without water)34,7337
Polymers34,0902
Non-polymers6435
Water362
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area1280 Å2
ΔGint-3 kcal/mol
Surface area12680 Å2
MethodPISA
3


  • Idetical with deposited unit
  • defined by software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area4510 Å2
ΔGint-17 kcal/mol
Surface area23460 Å2
MethodPISA
Unit cell
Length a, b, c (Å)80.140, 91.140, 95.070
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number19
Space group name H-MP212121

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Components

#1: Protein Histone-lysine N-methyltransferase EHMT1 / Euchromatic histone-lysine N-methyltransferase 1 / Eu-HMTase1 / G9a-like protein 1 / GLP / GLP1 / ...Euchromatic histone-lysine N-methyltransferase 1 / Eu-HMTase1 / G9a-like protein 1 / GLP / GLP1 / Histone H3-K9 methyltransferase 5 / H3-K9-HMTase 5 / Lysine N-methyltransferase 1D


Mass: 32830.219 Da / Num. of mol.: 2 / Fragment: unp residues 982-1266
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: EHMT1, EUHMTASE1, GLP, KIAA1876, KMT1D / Plasmid: pXC681 / Production host: Escherichia coli (E. coli)
References: UniProt: Q9H9B1, Transferases; Transferring one-carbon groups; Methyltransferases, histone-lysine N-methyltransferase
#2: Protein/peptide DNA (cytosine-5)-methyltransferase 3A / Dnmt3a / DNA methyltransferase MmuIIIA / DNA MTase MmuIIIA / M.MmuIIIA


Mass: 1259.463 Da / Num. of mol.: 2 / Fragment: unp residues 39-50 / Source method: obtained synthetically / Source: (synth.) Mus musculus (house mouse)
References: UniProt: O88508, DNA (cytosine-5-)-methyltransferase
#3: Chemical
ChemComp-ZN / ZINC ION


Mass: 65.409 Da / Num. of mol.: 8 / Source method: obtained synthetically / Formula: Zn
#4: Chemical ChemComp-SFG / SINEFUNGIN / ADENOSYL-ORNITHINE


Mass: 381.387 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C15H23N7O5
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 23 / 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: 2.55 Å3/Da / Density % sol: 51.69 %
Crystal growTemperature: 289 K / Method: vapor diffusion, hanging drop / pH: 7.5
Details: 0.1 M Hepes, 16% polyethylene glycol 4000 and 8% isopropanol, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: APS / Beamline: 22-BM / Wavelength: 1.07169 Å
DetectorType: MARMOSAIC 225 mm CCD / Detector: CCD / Date: Mar 19, 2010
RadiationMonochromator: Si(111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1.07169 Å / Relative weight: 1
ReflectionResolution: 3.05→28.69 Å / Num. obs: 13788 / % possible obs: 99.7 % / Observed criterion σ(I): -3 / Redundancy: 6.2 % / Rmerge(I) obs: 0.12 / Net I/σ(I): 13
Reflection shellResolution: 3.05→3.16 Å / Redundancy: 6.1 % / Rmerge(I) obs: 0.445 / Mean I/σ(I) obs: 3.9 / Num. unique all: 1325 / % possible all: 98.7

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Processing

Software
NameVersionClassification
HKL-2000data collection
PHENIXmodel building
PHENIX(phenix.refine: 1.6_289)refinement
HKL-2000data reduction
HKL-2000data scaling
PHENIXphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: PDB entry 3MO5

3mo5


Resolution: 3.05→28.689 Å / SU ML: 0.36 / Cross valid method: THROUGHOUT / σ(F): 0.02 / Phase error: 23.13 / Stereochemistry target values: ML
RfactorNum. reflection% reflectionSelection details
Rfree0.2485 674 5 %random
Rwork0.1727 ---
obs0.1765 13472 97.55 %-
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL / Bsol: 12.896 Å2 / ksol: 0.327 e/Å3
Displacement parameters
Baniso -1Baniso -2Baniso -3
1--0.3629 Å20 Å2-0 Å2
2--2.7737 Å20 Å2
3----2.4108 Å2
Refinement stepCycle: LAST / Resolution: 3.05→28.689 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms4258 0 62 23 4343
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0084416
X-RAY DIFFRACTIONf_angle_d1.2225981
X-RAY DIFFRACTIONf_dihedral_angle_d17.6831669
X-RAY DIFFRACTIONf_chiral_restr0.085626
X-RAY DIFFRACTIONf_plane_restr0.006791
LS refinement shell

Refine-ID: X-RAY DIFFRACTION

Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkNum. reflection obs% reflection obs (%)
3.0466-3.28160.31531190.21832354235491
3.2816-3.61120.29431390.1872516251698
3.6112-4.13240.24551320.1552586258699
4.1324-5.20140.21131390.14612599259999
5.2014-28.690.23521450.173627432743100

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